JP4560688B2

JP4560688B2 - Compound having tetrahydronaphthalene skeleton and liquid crystal composition containing the same

Info

Publication number: JP4560688B2
Application number: JP21338199A
Authority: JP
Inventors: 哲夫楠本; 貞夫竹原; 晴義高津
Original assignee: DIC Corp
Current assignee: DIC Corp
Priority date: 1999-07-28
Filing date: 1999-07-28
Publication date: 2010-10-13
Anticipated expiration: 2019-07-28
Also published as: JP2001039906A

Description

【０００１】
【発明の属する技術分野】
本発明は電気光学的液晶表示材料として有用な、テトラヒドロナフタレン誘導体である新規液晶性化合物とそれを含む液晶組成物及びそれを用いた液晶表示素子に関する。
【０００２】
【従来の技術】
液晶表示素子は、時計、電卓をはじめとして、各種測定機器、自動車用パネル、ワープロ、電子手帳、プリンター、コンピューター、テレビ等に用いられるようになっている。液晶表示方式としては、その代表的なものにTN(捩れネマチック)型、STN(超捩れネマチック)型、DS(動的光散乱)型、GH(ゲスト・ホスト)型あるいは高速応答が可能なFLC(強誘電性液晶)やAFLC(反強誘電性液晶)等を挙げることができる。また駆動方式としても従来のスタティック駆動からマルチプレックス駆動が一般的になり、さらに単純マトリックス方式、最近ではアクティブマトリックス方式が実用化されている。
【０００３】
これらに用いられる液晶材料として、これまでにも非常に多種類の液晶性化合物が合成されており、これらはその表示方式や駆動方式あるいはその用途に応じて使用されている。しかしながら、液晶表示素子の性能向上(表示品位の向上や表示画面の大型化等)に対する要求は年々強くなる一方であり、それを満足させるために新しい液晶化合物の開発が続けられている。
【０００４】
液晶化合物は通常コアと呼ばれる中心骨格部分と両側の末端部分から構成されている。通常、液晶化合物のコア部分を構成する環構造としては1,4-フェニレン基(1〜2個のハロゲン原子、シアノ基、メチル基等により置換されていることもある)及びトランス-1,4-シクロヘキシレン基がその大部分を占める。しかしながら1,4-フェニレン基とトランス-1,4-シクロヘキシレン基のみによって構成された液晶性化合物にはその種類や特性にも限界があり、それらだけでは前記要求に応えきれなくなっているのが実情である。
【０００５】
1,4-フェニレン基とトランス-1,4-シクロヘキシレン基以外の環構造としては、例えばピリジン-2,5-ジイル基、ピリミジン-2,5-ジイル基、1,3-ジオキサン-トランス-2,5-ジイル基等の複素環系や、トランス-デカリン-2,6-ジイル基、ナフタレン-2,6-ジイル基、テトラヒドロナフタレン-2-6-ジイル基、ビシクロ[2.2.2]オクタン-1,4-ジイル基、スピロ[3.3]ヘプタン-2,6-ジイル基等の縮合環系等も検討されているが、製造上(技術、コスト等)の問題、安定性の問題等から、現在のところ実用化されているものはわずかに過ぎない。
【０００６】
これらの縮合環系において、テトラヒドロナフタレン-2-6-ジイル基は古くから報告されている環構造であるにもかかわらず、その合成例は極端に少なく、また、液晶性(相転移温度)以外の特性、特にネマチック液晶としての特性はほとんど知られていない。(最近、テトラヒドロナフタレン-2-カルボン酸の光学活性アルコールエステルがスメクチック液晶、特に強誘電性液晶や反強誘電性液晶として興味ある特性を示すことが報告されている。)
通常液晶化合物において、末端部分の少なくとも一方は鎖状(側鎖)基であり、誘電率異方性が正のいわゆるp型液晶の場合には、他方は極性基であることが多い。
【０００７】
TNあるいはSTN表示方式においてその駆動電圧を低減するためには、誘電率異方性が正で大きい化合物(p型)が必要である。こうした目的には分子末端にシアノ基を有し、さらに分子の同方向に1個以上のフッ素原子を含有する化合物が通常用いられている。現在報告されているテトラヒドロナフタレン誘導体は誘電率異方性が0〜負のいわゆるn型液晶がほとんどであり、テトラヒドロナフタレン骨格に極性基が導入されたp型液晶としてはわずかにフェニルテトラヒドロナフタレン骨格やテトラヒドロナフタレン-2-カルボン酸フェニル骨格を有する化合物のみが報告されているにすぎず、電気光学特性や応用例の記載はない(Helv. Chim. Acta, 65, 1318-1330 (1982))。
【０００８】
前述のアクティブマトリックス駆動方式に用いるべきp型化合物としては、極性基としてフッ素原子やフルオロアルコキシル基、フルオロアルキル基のみを有するような化合物が用いられるが、テトラヒドロナフタレン化合物としてはこのような報告例はない。また、テトラヒドロナフタレン誘導体である液晶性化合物は一般的に他の液晶化合物との相溶性が優れないことが多いが、その改善のためにはテトラヒドロナフタレン骨格への側方置換基(特にフッ素原子が望ましい)の導入が有効と考えられる。前記アクティブマトリックス方式への使用において、テトラヒドロナフタレン環に直接極性基を導入する場合にも、フッ素原子による置換は有効と考えられる。このようなフルオロテトラリン誘導体は実際に合成された例はなく、そうした化合物がどの様な特性値を有するのか推定することもできないのが実情である。
【０００９】
液晶化合物において、側鎖部分として通常用いられているアルキル基に換えて、アルケニル基を導入することにより、液晶性の向上、粘度の減少、表示特性における急峻性の改善等の優れた効果が得られることが知られている。しかしながら、これらアルケニル基は通常、シクロヘキサン環に直結する形態で導入されることが多く、芳香環特にテトラヒドロナフタレン環に導入した化合物は報告されていない。
【００１０】
同様に、側鎖としてアルコキシルアルキル基、フルオロアルキル基、フルオロアルケニル基、フルオロアルケニルオキシ基等を有するテトラヒドロナフタレン誘導体は報告されていない。
【００１１】
液晶化合物においてコアにおける環構造の連結基としては、単結合やエステル基(-COO-,-OCO-)以外にも1,2-エチレン基(-CH₂CH₂-)、エチニレン基(-C≡C-)、ジフルオロエテニレン基(-CF=CF-)など多くの2価の有機基が知られているが、テトラヒドロナフタレン誘導体では知られていない。
【００１２】
【発明が解決しようとする課題】
本発明が解決しようとする課題は、テトラヒドロナフタレン骨格を有する新規化合物を提供することにあり、またそれを用いて実用的な液晶組成物を提供することにある。
【００１３】
【課題を解決するための手段】
本発明者らは上記課題を解決するために鋭意検討した結果、テトラヒドロナフタレン骨格を有する化合物が容易に製造でき、これらの多くが広い温度範囲で液晶性を示すこと、さらに単独で液晶性の有無に関わらず、これを組成物に添加すると、応答速度を遅くすることなく(多くの場合は応答速度を速め)、目的とする液晶温度範囲を著しく狭めることなく(多くの場合は温度範囲を広げ)、層分離することなく混合することが出来ることを見出し、本発明を完成するに至った。
【００１４】
すなわち本発明は、
１．一般式(I)
【００１５】
【化２】

【００１６】
(式中Rは1〜7個のフッ素原子または炭素原子数1〜7のアルコキシル基によって置換されていてもよく、分岐鎖を含んでもよい飽和または不飽和の炭素数1〜20のアルキル基を表し、連結基Vは単結合、酸素原子、イオウ原子、-COO-、-OCO-、-OCOO-、-COS-または-SCO-を表し、連結基W、XおよびYはそれぞれ独立的に、単結合、-CH₂CH₂-、-CH=CH-、-CH(CH₃)CH₂-、-CH₂CH(CH₃)-、-CH(CH₃)CH(CH₃)-、-CF₂CF₂-、-CF=CF-、-CH₂O-、-OCH₂-、-OCH(CH₃)-、-CH(CH₃)O-、-C≡C-、-CF₂O-、-OCF₂-、-COO-、-OCO-、-COS-または-SCO-を表し、Zはフッ素原子、塩素原子、シアノ基、シアナト基、トリフルオロメチル基、トリフルオロメトキシ基、ジフルオロメトキシ基または水素原子を表し、Q¹、Q²およびQ³はそれぞれ独立的に水素原子またはフッ素原子を表し、環Aおよび環Bはそれぞれ独立的にトランス-1,4-シクロヘキシレン基、トランス-デカヒドロナフタレン-2,6-ジイル基、トランス-1,3-ジオキサン-2,5-ジイル基または一個または二個のフッ素原子で置換されてもよい1,4-フェニレン基、ピリジン-2,5-ジイル基、ピリミジン-2,5-ジイル基、ピラジン-2,5-ジイル基、ピリダジン-3,6-ジイル基および一個または二個のフッ素原子で置換されてもよいナフタレン-2,6-ジイル基を表し、環Cは一個または二個のフッ素原子で置換されてもよい1,4-フェニレン基または一個または二個のフッ素原子で置換されてもよいナフタレン-2,6-ジイル基を表し、mおよびnはそれぞれ独立的に0または1を表す。ただし、Zが水素原子である場合、環Cは一個または二個のフッ素原子で置換された1,4-フェニレン基または一個または二個のフッ素原子で置換されてもよいナフタレン-2,6-ジイル基を表し、Q¹、Q²およびQ³がすべて水素原子であり、かつmおよびnがともに0であり、かつYが-COO-であり、かつZがフッ素原子である場合、環Cは一個または二個のフッ素原子で置換された1,4-フェニレン基または一個または二個のフッ素原子で置換されてもよいナフタレン-2,6-ジイル基を表し、Q¹、Q²およびQ³がすべて水素原子であり、かつmおよびnがともに0であり、かつYが単結合または-COO-であり、かつZがシアノ基である場合、環Cは一個または二個のフッ素原子で置換された1,4-フェニレン基または一個または二個のフッ素原子で置換されてもよいナフタレン-2,6-ジイル基を表す。)で表されるテトラヒドロナフタレン誘導体。
を提供する。
【００１７】
さらに、本発明は上記一般式(I)の化合物を1種類以上含有する液晶組成物、およびそれを構成要素とする液晶素子、すなわち、
２．一般式(I)においてmが0であるところの上記1記載の化合物。
３．一般式(I)においてnが0であるところの上記1記載の化合物。
４．一般式(I)においてQ¹およびQ²がともに水素原子であるところの上記1〜3記載の化合物。
５．一般式(I)において連結基W、XおよびYがそれぞれ独立的に、単結合または-CH₂CH₂-から選ばれるところの上記1〜4記載の化合物。
６．一般式(I)において環Aおよび環Bがそれぞれ独立的にトランス-1,4-シクロヘキシレン基、トランス-デカヒドロナフタレン-2,6-ジイル基または一個または二個のフッ素原子で置換されてもよい1,4-フェニレン基およびナフタレン-2,6-ジイル基から選ばれるところの上記1〜5記載の化合物。
７．一般式(I)において環Cが一個または二個のフッ素原子で置換された1,4-フェニレン基またはナフタレン-2,6-ジイル基から選ばれるところの上記1〜6記載の化合物。
８．一般式(I)においてZがフッ素原子、塩素原子、トリフルオロメチル基、トリフルオロメトキシ基、ジフルオロメトキシ基または水素原子から選ばれるところの上記1〜7記載の化合物。
９．一般式(I)においてZがフッ素原子またはトリフルオロメトキシ基から選ばれるところの上記8記載の化合物。
１０．一般式(I)においてVが単結合を表すところの上記1〜9記載の化合物。
１１．一般式(I)においてRが炭素数1〜10の直鎖状アルキル基から選ばれるところの上記1〜10記載の化合物。
１２．上記1〜11記載の一般式(I)の化合物を1種類以上含有する液晶組成物。
１３．アクティブマトリックス駆動用に用いられる上記12記載の液晶組成物。
１４．上記13記載の液晶組成物を構成要素とする液晶素子。
１５．上記14記載の液晶組成物を用いたアクティブマトリックス駆動液晶表示素子。
を提供する。
【００１８】
【発明の実施の形態】
上述のように上記一般式(I)の化合物においては、そのm、n、R、V、W、X、Y、Z、Q¹、Q²、Q³、環A、環Bおよび環Cとしては以下のようなものが挙げられる。
【００１９】
mおよびnは0または1であり、m=n=0、m=0でn=1、m=1でn=0、m=n=1のどの組み合わせも可能であるが、m=n=1の場合融点と粘性が高くなるので、m=n=0、m=0でn=1、m=1でn=0の組み合わせが好ましい。
【００２０】
R-としては、メチル基、エチル基、プロピル基、ブチル基、ペンチル基、ヘキシル基、ペプチル基、オクチル基、ノニル基、デシル基、ウンデシル基、ドデシル基、トリデシル基、テトラデシル基、ペンタデシル基、ヘキサデシル基、ヘプタデシル基、オクタデシル基、ノナデシル基、エイコシル基の直鎖型飽和アルキル基、1-メチルエチル基、1-メチルプロピル基、2-メチルプロピル基、1,2-ジメチルプロピル基、1-メチルブチル基、2-メチルブチル基、3-メチルブチル基、1,2-ジメチルブチル基、1,3-ジメチルブチル基、2,3-ジメチルブチル基、1-メチルペンチル基、2-メチルペンチル基、3-メチルペンチル基、4-メチルペンチル基、1,2-ジメチルペンチル基、1,3-ジメチルペンチル基、1-メチルヘキシル基、2-メチルヘキシル基、3-メチルヘキシル基、4-メチルヘキシル基、5-メチルヘキシル基、1,2-ジメチルヘキシル基、1,3-ジメチルヘキシル基、1-メチルヘプチル基、2-メチルヘプチル基、3-メチルヘプチル基、4-メチルヘプチル基、5-メチルヘプチル基、6-メチルヘプチル基、1,2-ジメチルヘプチル基、1,3-ジメチルヘプチル基、1-メチルオクチル基、2-メチルオクチル基、3-メチルオクチル基、4-メチルオクチル基、5-メチルオクチル基、6-メチルオクチル基、7-メチルオクチル基、1,2-ジメチルオクチル基、1,3-ジメチルオクチル基、1-メチルノニル基、2-メチルノニル基、3-メチルノニル基、4-メチルノニル基、5-メチルノニル基、6-メチルノニル基、7-メチルノニル基、8-メチルノニル基、1,2-ジメチルノニル基、1,3-ジメチルノニル基、1-メチルデシル基、2-メチルデシル基、3-メチルデシル基、1,2-ジメチルデシル基、1,3-ジメチルデシル基、1-メチルウンデシル基、2-メチルウンデシル基、3-メチルウンデシル基、1,2-ジメチルウンデシル基、1,3-ジメチルウンデシル基、1-メチルドデシル基、2-メチルドデシル基、3-メチルドデシル基、1,2-ジメチルドデシル基、1,3-ジメチルドデシル基、1-メチルトリデシル基、2-メチルトリデシル基、3-メチルトリデシル基、1,2-ジメチルトリデシル基、1,3-ジメチルトリデシル基等の分岐型飽和アルキル基、ビニル基、トランス-1-プロペニル基、2-プロペニル基、トランス-1-ブテニル基、トランス-2-ブテニル基、3-ブテニル基、トランス-1-ペンテニル基、トランス-2-ペンテニル基、トランス-3-ペンテニル基、4-ペンテニル基、トランス-1-ヘキセニル基、トランス-2-ヘキセニル基、トランス-3-ヘキセニル基、トランス-4-ヘキセニル基、5-ヘキセニル基、トランス-1-ヘプテニル基、トランス-2-ヘプテニル基、トランス-3-ヘプテニル基、トランス-4-ヘプテニル基、トランス-5-ヘプテニル基、6-ヘプテニル基、トランス-1-オクテニル基、トランス-2-オクテニル基、トランス-3-オクテニル基、トランス-4-オクテニル基、トランス-5-オクテニル基、トランス-6-オクテニル基、7-オクテニル基、トランス-1-ノネニル基、8-ノネニル基、トランス-1-デセニル基、9-デセニル基、トランス-1-ウンデセニル基、10-ウンデセニル基、トランス-1-ドデセニル基、11-ドデセニル基、エチニル基、1-プロピニル基、2-プロピニル基、1-ブチニル基、2-ブチニル基、3-ブチニル基、1-ペンテニル基、2-ペンテニル基、3-ペンテニル基、4-ペンテニル基、1-ヘキシニル基、2-ヘキシニル基、3-ヘキシニル基、4-ヘキシニル基、5-ヘキシニル基、1-ヘプチニル基、2-ヘプチニル基、3-ヘプチニル基、4-ヘプチニル基、5-ヘプチニル基、6-ヘプチニル基、1-オクチニル基、2-オクチニル基、3-オクチニル基、4-オクチニル基、5-オクチニル基、6-オクチニル基、7-オクチニル基、1-ノニニル基、8-ノニニル基、1-デシニル基、9-デシニル基、1-ウンデシニル基、10-ウンデシニル基、1-ドデシニル基、11-ドデシニル基、1-トリデシニル基、12-トリデシニル基等の不飽和アルキル基、フルオロメチル基、ジフルオロメチル基、トリフルオロメチル基、2-フルオロメチル基、2,2-ジフルオロエチル基、2,2,2-トリフルオロエチル基、1,1,2,2,2-ペンタフルオロエチル基、3-フルオロプロピル基、2-フルオロプロピル基、1-フルオロプロピル基、3,3-ジフルオロプロピル基、3,3,3-トリフルオロプロピル基、2,2,3,3-テトラフルオロプロピル基、2,2,3,3,3-ペンタフルオロプロピル基、1,1,2,2,3,3,3-ヘプタフルオロプロピル基、4-フルオロブチル基、3-フルオロブチル基、2-フルオロブチル基、1-フルオロブチル基、4,4-ジフルオロブチル基、4,4,4-トリフルオロブチル基、3,3,4,4-テトラフルオロブチル基、3,3,4,4,4-ペンタフルオロブチル基、2,2,3,3,4,4,4-ヘプタフルオロブチル基、5-フルオロペンチル基、4-フルオロペンチル基、3-フルオロペンチル基、2-フルオロペンチル基、1-フルオロペンチル基、5,5-ジフルオロペンチル基、5,5,5-トリフルオロペンチル基、4,4,5,5-テトラフルオロペンチル基、4,4,5,5,5-ペンタフルオロペンチル基、3,3,4,4,5,5,5-ヘプタフルオロペンチル基、6-フルオロヘキシル基、5-フルオロヘキシル基、4-フルオロヘキシル基、3-フルオロヘキシル基、2-フルオロヘキシル基、1-フルオロヘキシル基、6,6-ジフルオロヘキシル基、6,6,6-トリフルオロヘキシル基、5,5,6,6,6-ペンタフルオロヘキシル基、4,4,5,5,6,6,6-ヘプタフルオロヘキシル基、7-フルオロヘプチル基、6-フルオロヘプチル基、5-フルオロヘプチル基、4-フルオロヘプチル基、3-フルオロヘプチル基、2-フルオロヘプチル基、1-フルオロヘプチル基、7,7-ジフルオロヘプチル基、7,7,7-トリフルオロヘプチル基、6,6,7,7-テトラフルオロヘプチル基、6,6,7,7,7-ペンタフルオロヘプチル基、5,5,6,6,7,7,7-ヘプタフルオロヘプチル基、8-フルオロオクチル基、7-フルオロオクチル基、6-フルオロオクチル基、5-フルオロオクチル基、4-フルオロオクチル基、3-フルオロオクチル基、2-フルオロオクチル基、1-フルオロオクチル基、8,8-ジフルオロオクチル基、8,8,8-トリフルオロオクチル基、7,7,8,8-テトラフルオロオクチル基、7,7,8,8,8-ペンタフルオロオクチル基、6,6,7,7,8,8,8-ヘプタフルオロオクチル基等のフッ素置換アルキル基、
【００２１】
2,2-ジフルオロエテニル基、(E)-1,2-ジフルオロエテニル基、(Z)-1,2-ジフルオロエテニル基、3,3-ジフルオロ-2-プロペニル基、(E)-2,3-ジフルオロ-2-プロペニル基、(Z)-2,3-ジフルオロ-2-プロペニル基、4,4-ジフルオロ-3-ブテニル基、(E)-3,4-ジフルオロ-3-ブテニル基、(Z)-3,4-ジフルオロ-3-ブテニル基、5,5-ジフルオロ-4-ペンテニル基、(E)-4,5-ジフルオロ-4-ペンテニル基、(Z)-4,5-ジフルオロ-4-ペンテニル基、6,6-ジフルオロ-5-ヘキセニル基、(E)-5,6-ジフルオロ-5-ヘキセニル基、(Z)-5,6-ジフルオロ-5-ヘキセニル基、(E)-1,2-ジフルオロ-1-プロペニル基、(E)-1,2-ジフルオロ-1-ブテニル基、(E)-1,2-ジフルオロ-1-ペンテニル基、(E)-1,2-ジフルオロ-1-ヘキセニル基、(Z)-1-フルオロ-1-プロペニル基、(Z)-1-フルオロ-1-ブテニル基、(Z)-1-フルオロ-1-ペンテニル基、(Z)-1-フルオロ-1-ヘキセニル基、(Z)-2-フルオロ-1-プロペニル基、(Z)-2-フルオロ-1-ブテニル基、(Z)-2-フルオロ-1-ペンテニル基、(Z)-2-フルオロ-1-ヘキセニル基、 (E)-2,3-ジフルオロ-2-ブテニル基、(E)-2,3-ジフルオロ-2-ペンテニル基、(E)-2,3-ジフルオロ-2-ヘキセニル基、 (Z)-2-フルオロ-2-ブテニル基、(Z)-2-フルオロ-2-ペンテニル基、(Z)-2-フルオロ-2-ヘキセニル基、(Z)-3-フルオロ-2-ブテニル基、(Z)-3-フルオロ-2-ペンテニル基、(Z)-3-フルオロ-2-ヘキセニル基等のフッ素置換不飽和アルキル基、メトキシメチル基、エトキシメチル基、プロポキシメチル基、ブトキシメチル基、ペンチルオキシメチル基、ヘキシルオキシメチル基、ヘプチルオキシメチル基、1-メトキシエチル基、1-エトキシエチル基、1-プロポキシエチル基、1-ブトキシエチル基、1-ペンチルオキシエチル基、1-ヘキシルオキシエチル基、1-ヘプチルオキシエチル基、2-メトキシエチル基、2-エトキシエチル基、2-プロポキシエチル基、2-ブトキシエチル基、2-ペンチルオキシエチル基、2-ヘキシルオキシエチル基、2-ヘプチルオキシエチル基、1-メトキシプロピル基、1-エトキシプロピル基、1-プロポキシプロピル基、1-ブトキシプロピル基、1-ペンチルオキシプロピル基、1-ヘキシルオキシプロピル基、1-ヘプチルオキシプロピル基、2-メトキシプロピル基、2-エトキシプロピル基、2-プロポキシプロピル基、2-ブトキシプロピル基、2-ペンチルオキシプロピル基、2-ヘキシルオキシプロピル基、2-ヘプチルオキシプロピル基、3-メトキシプロピル基、3-エトキシプロピル基、3-プロポキシプロピル基、3-ブトキシプロピル基、3-ペンチルオキシプロピル基、3-ヘキシルオキシプロピル基、3-ヘプチルオキシプロピル基、4-メトキシブチル基、4-エトキシブチル基、4-プロポキシブチル基、4-ブトキシブチル基、4-ペンチルオキシブチル基、4-ヘキシルオキシブチル基、4-ヘプチルオキシブチル基、5-メトキシペンチル基、5-エトキシペンチル基、5-プロポキシペンチル基、5-ブトキシペンチル基、5-ペンチルオキシペンチル基、5-ヘキシルオキシペンチル基、5-ヘプチルオキシペンチル基、6-メトキシヘキシル基、6-エトキシヘキシル基、6-プロポキシヘキシル基、6-ブトキシヘキシル基、6-ペンチルオキシヘキシル基、6-ヘキシルオキシヘキシル基、6-ヘプチルオキシヘキシル基等のアルコキシル基置換アルキル基が挙げられるが、中でも直鎖型飽和アルキル基と不飽和アルキル基が好ましく、メチル基、エチル基、プロピル基、ブチル基、ペンチル基、ヘキシル基、ペプチル基、オクチル基、ビニル基、トランス-1-プロペニル基、2-プロペニル基、トランス-1-ブテニル基、トランス-2-ブテニル基、3-ブテニル基、トランス-1-ペンテニル基、トランス-2-ペンテニル基、トランス-3-ペンテニル基、4-ペンテニル基、トランス-1-ヘキセニル基、トランス-2-ヘキセニル基、トランス-3-ヘキセニル基、トランス-4-ヘキセニル基、5-ヘキセニル基、トランス-1-ヘプテニル基、トランス-2-ヘプテニル基、トランス-3-ヘプテニル基、トランス-4-ヘプテニル基、トランス-5-ヘプテニル基、6-ヘプテニル基が特に好ましい。
【００２２】
連結基Vとしては単結合、酸素原子、イオウ原子、-COO-、-OCO-、-OCOO-、-COS-、-SCO-が挙げられるが、単結合および酸素原子が好ましく、単結合が特に好ましい。
【００２３】
W、XおよびYとしては、単結合、-CH₂CH₂-、-CH=CH-、-CH(CH₃)CH₂-、-CH₂CH(CH₃)-、-CH(CH₃)CH(CH₃)-、-CF₂CF₂-、-CF=CF-、-CH₂O-、-OCH₂-、-OCH(CH₃)-、-CH(CH₃)O-、-C≡C-、-CF₂O-、-OCF₂-、-COO-、-OCO-、-COS-、-SCO-を挙げることができ、中でも単結合、-CH₂CH₂-、-C≡C-が好ましく、単結合が特に好ましい。
【００２４】
Zとしてはフッ素原子、塩素原子、シアノ基、シアナト基、トリフルオロメチル基、トリフルオロメトキシ基、ジフルオロメトキシ基、水素原子を挙げることができるが、フッ素原子、シアノ基、トリフルオロメトキシ基が好ましく、フッ素およびトリフルオロメトキシ基が特に好ましい。
【００２５】
Q¹、Q²およびQ³は水素原子またはフッ素原子を表すが、Q¹、Q²およびQ³が水素原子の場合と、Q¹およびQ²が水素原子でQ³がフッ素原子の場合が好ましい。
【００２６】
環Aおよび環Bとしては式群1に示すような構造が挙げられる。
【００２７】
【化３】

【００２８】
中でも、式群2に記載した構造が好ましい。
【００２９】
【化４】

【００３０】
中でも、式群3に記載した構造が特に好ましい。
【００３１】
【化５】

【００３２】
環Cとしては式群4に示すような構造が挙げられる。
【００３３】
【化６】

【００３４】
中でも、式群5に記載した構造が好ましい。
【００３５】
【化７】

【００３６】
中でも、式群6に記載した構造が特に好ましい。
【００３７】
【化８】

【００３８】
ただし、Zが水素原子である場合、Q¹、Q²およびQ³がすべて水素原子であり、かつmおよびnがともに0であり、かつYが-COO-であり、かつZがフッ素原子である場合、または、Q¹、Q²およびQ³がすべて水素原子であり、かつmおよびnがともに0であり、かつYが単結合または-COO-であり、かつZがシアノ基である場合、1,4-フェニレン基を除く。
【００３９】
上述のように上記一般式(I)の化合物はそのm、n、 R、V、W、X、Y、Z、Q¹、Q²、Q³、環A、環Bおよび環Cの選択によって非常に多種の化合物を包含しうる訳であるが、その各構造部位を選択することによってより広い用途分野に適合した化合物とすることができ、その結果、一般式(I)の化合物は広いネマチック温度範囲、光・熱に対する安定性、高い電圧保持率などの電気光学素子、特にSTN-LCDおよびAM-LCDに好ましい特徴を有するので非常に有用である。さらに詳述すると、一般式(I)の化合物の中で、特に好ましい化合物として以下の化合物を挙げることができる。
【００４０】
なお、化合物記載には下記の略号を使用し、R¹はメチル基、エチル基、プロピル基、ブチル基、ペンチル基、ヘキシル基、ペプチル基、オクチル基、ビニル基、トランス-1-プロペニル基、2-プロペニル基、トランス-1-ブテニル基、トランス-2-ブテニル基、3-ブテニル基、トランス-1-ペンテニル基、トランス-2-ペンテニル基、トランス-3-ペンテニル基、4-ペンテニル基、トランス-1-ヘキセニル基、トランス-2-ヘキセニル基、トランス-3-ヘキセニル基、トランス-4-ヘキセニル基、5-ヘキセニル基、トランス-1-ヘプテニル基、トランス-2-ヘプテニル基、トランス-3-ヘプテニル基、トランス-4-ヘプテニル基、トランス-5-ヘプテニル基、6-ヘプテニル基のいずれかを表す。
【００４１】
【化９】

【００４２】
m=n=0、Vが単結合、Zがフッ素原子の場合、
【００４３】
R¹-Te1-Ph1-F、R¹-Te1-Ph2-F、R¹-Te1-Ph3-F、R¹-Te1-Np1-F、R¹-Te1-Np2-F、R¹-Te1-Np3-F、R¹-Te1-Np4-F、R¹-Te2-Ph1-F、R¹-Te2-Ph2-F、R¹-Te2-Ph3-F、R¹-Te2-Np1-F、R¹-Te2-Np2-F、R¹-Te2-Np3-F、R¹-Te2-Np4-F、R¹-Te1-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Np4-F、
【００４４】
m=n=0、Vが単結合、Zがシアノ基の場合、
【００４５】
R¹-Te1-Ph2-CN、R¹-Te1-Ph3-CN、R¹-Te1-Np1-CN、R¹-Te1-Np2-CN、R¹-Te1-Np3-CN、R¹-Te1-Np4-CN、R¹-Te2-Ph1-CN、R¹-Te2-Ph2-CN、R¹-Te2-Ph3-CN、R¹-Te2-Np1-CN、R¹-Te2-Np2-CN、R¹-Te2-Np3-CN、R¹-Te2-Np4-CN、R¹-Te1-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Np4-CN、
【００４６】
m=n=0、Vが単結合、Zがトリフルオロメトキシ基の場合、
【００４７】
R¹-Te1-Ph1-OCF₃、R¹-Te1-Ph2-OCF₃、R¹-Te1-Ph3-OCF₃、R¹-Te1-Np1-OCF₃、R¹-Te1-Np2-OCF₃、R¹-Te1-Np3-OCF₃、R¹-Te1-Np4-OCF₃、R¹-Te2-Ph1-OCF₃、R¹-Te2-Ph2-OCF₃、R¹-Te2-Ph3-OCF₃、R¹-Te2-Np1-OCF₃、R¹-Te2-Np2-OCF₃、R¹-Te2-Np3-OCF₃、R¹-Te2-Np4-OCF₃、R¹-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Te1-CH₂CH₂-Np1-OCF₃、R¹-Te1-CH₂CH₂-Np2-OCF₃、R¹-Te1-CH₂CH₂-Np3-OCF₃、R¹-Te1-CH₂CH₂-Np4-OCF₃、R¹-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Te2-CH₂CH₂-Np1-OCF₃、R¹-Te2-CH₂CH₂-Np2-OCF₃、R¹-Te2-CH₂CH₂-Np3-OCF₃、R¹-Te2-CH₂CH₂-Np4-OCF₃、
【００４８】
m=1、n=0、Vが単結合、Zがフッ素原子の場合、
【００４９】
R¹-Cy-Te1-Ph1-F、R¹-Cy-Te1-Ph2-F、R¹-Cy-Te1-Ph3-F、R¹-Cy-Te1-Np1-F、R¹-Cy-Te1-Np2-F、R¹-Cy-Te1-Np3-F、R¹-Cy-Te1-Np4-F、R¹-Cy-Te2-Ph1-F、R¹-Cy-Te2-Ph2-F、R¹-Cy-Te2-Ph3-F、R¹-Cy-Te2-Np1-F、R¹-Cy-Te2-Np2-F、R¹-Cy-Te2-Np3-F、R¹-Cy-Te2-Np4-F、R¹-Cy-Te1-CH₂CH₂-Ph2-F、R¹-Cy-Te1-CH₂CH₂-Ph3-F、R¹-Cy-Te1-CH₂CH₂-Np1-F、R¹-Cy-Te1-CH₂CH₂-Np2-F、R¹-Cy-Te1-CH₂CH₂-Np3-F、R¹-Cy-Te1-CH₂CH₂-Np4-F、R¹-Cy-Te2-CH₂CH₂-Ph1-F、R¹-Cy-Te2-CH₂CH₂-Ph2-F、R¹-Cy-Te2-CH₂CH₂-Ph3-F、R¹-Cy-Te2-CH₂CH₂-Np1-F、R¹-Cy-Te2-CH₂CH₂-Np2-F、R¹-Cy-Te2-CH₂CH₂-Np3-F、R¹-Cy-Te2-CH₂CH₂-Np4-F、
【００５０】
R¹-Ph1-Te1-Ph1-F、R¹-Ph1-Te1-Ph2-F、R¹-Ph1-Te1-Ph3-F、R¹-Ph1-Te1-Np1-F、R¹-Ph1-Te1-Np2-F、R¹-Ph1-Te1-Np3-F、R¹-Ph1-Te1-Np4-F、R¹-Ph1-Te2-Ph1-F、R¹-Ph1-Te2-Ph2-F、R¹-Ph1-Te2-Ph3-F、R¹-Ph1-Te2-Np1-F、R¹-Ph1-Te2-Np2-F、R¹-Ph1-Te2-Np3-F、R¹-Ph1-Te2-Np4-F、R¹-Ph1-Te1-CH₂CH₂-Ph2-F、R¹-Ph1-Te1-CH₂CH₂-Ph3-F、R¹-Ph1-Te1-CH₂CH₂-Np1-F、R¹-Ph1-Te1-CH₂CH₂-Np2-F、R¹-Ph1-Te1-CH₂CH₂-Np3-F、R¹-Ph1-Te1-CH₂CH₂-Np4-F、R¹-Ph1-Te2-CH₂CH₂-Ph1-F、R¹-Ph1-Te2-CH₂CH₂-Ph2-F、R¹-Ph1-Te2-CH₂CH₂-Ph3-F、R¹-Ph1-Te2-CH₂CH₂-Np1-F、R¹-Ph1-Te2-CH₂CH₂-Np2-F、R¹-Ph1-Te2-CH₂CH₂-Np3-F、R¹-Ph1-Te2-CH₂CH₂-Np4-F、
【００５１】
R¹-Ph2-Te1-Ph1-F、R¹-Ph2-Te1-Ph2-F、R¹-Ph2-Te1-Ph3-F、R¹-Ph2-Te1-Np1-F、R¹-Ph2-Te1-Np2-F、R¹-Ph2-Te1-Np3-F、R¹-Ph2-Te1-Np4-F、R¹-Ph2-Te2-Ph1-F、R¹-Ph2-Te2-Ph2-F、R¹-Ph2-Te2-Ph3-F、R¹-Ph2-Te2-Np1-F、R¹-Ph2-Te2-Np2-F、R¹-Ph2-Te2-Np3-F、R¹-Ph2-Te2-Np4-F、R¹-Ph2-Te1-CH₂CH₂-Ph2-F、R¹-Ph2-Te1-CH₂CH₂-Ph3-F、R¹-Ph2-Te1-CH₂CH₂-Np1-F、R¹-Ph2-Te1-CH₂CH₂-Np2-F、R¹-Ph2-Te1-CH₂CH₂-Np3-F、R¹-Ph2-Te1-CH₂CH₂-Np4-F、R¹-Ph2-Te2-CH₂CH₂-Ph1-F、R¹-Ph2-Te2-CH₂CH₂-Ph2-F、R¹-Ph2-Te2-CH₂CH₂-Ph3-F、R¹-Ph2-Te2-CH₂CH₂-Np1-F、R¹-Ph2-Te2-CH₂CH₂-Np2-F、R¹-Ph2-Te2-CH₂CH₂-Np3-F、R¹-Ph2-Te2-CH₂CH₂-Np4-F、
【００５２】
R¹-Ph3-Te1-Ph1-F、R¹-Ph3-Te1-Ph2-F、R¹-Ph3-Te1-Ph3-F、R¹-Ph3-Te1-Np1-F、R¹-Ph3-Te1-Np2-F、R¹-Ph3-Te1-Np3-F、R¹-Ph3-Te1-Np4-F、R¹-Ph3-Te2-Ph1-F、R¹-Ph3-Te2-Ph2-F、R¹-Ph3-Te2-Ph3-F、R¹-Ph3-Te2-Np1-F、R¹-Ph3-Te2-Np2-F、R¹-Ph3-Te2-Np3-F、R¹-Ph3-Te2-Np4-F、R¹-Ph3-Te1-CH₂CH₂-Ph2-F、R¹-Ph3-Te1-CH₂CH₂-Ph3-F、R¹-Ph3-Te1-CH₂CH₂-Np1-F、R¹-Ph3-Te1-CH₂CH₂-Np2-F、R¹-Ph3-Te1-CH₂CH₂-Np3-F、R¹-Ph3-Te1-CH₂CH₂-Np4-F、R¹-Ph3-Te2-CH₂CH₂-Ph1-F、R¹-Ph3-Te2-CH₂CH₂-Ph2-F、R¹-Ph3-Te2-CH₂CH₂-Ph3-F、R¹-Ph3-Te2-CH₂CH₂-Np1-F、R¹-Ph3-Te2-CH₂CH₂-Np2-F、R¹-Ph3-Te2-CH₂CH₂-Np3-F、R¹-Ph3-Te2-CH₂CH₂-Np4-F、
【００５３】
R¹-Np1-Te1-Ph1-F、R¹-Np1-Te1-Ph2-F、R¹-Np1-Te1-Ph3-F、R¹-Np1-Te1-Np1-F、R¹-Np1-Te1-Np2-F、R¹-Np1-Te1-Np3-F、R¹-Np1-Te1-Np4-F、R¹-Np1-Te2-Ph1-F、R¹-Np1-Te2-Ph2-F、R¹-Np1-Te2-Ph3-F、R¹-Np1-Te2-Np1-F、R¹-Np1-Te2-Np2-F、R¹-Np1-Te2-Np3-F、R¹-Np1-Te2-Np4-F、R¹-Np1-Te1-CH₂CH₂-Ph2-F、R¹-Np1-Te1-CH₂CH₂-Ph3-F、R¹-Np1-Te1-CH₂CH₂-Np1-F、R¹-Np1-Te1-CH₂CH₂-Np2-F、R¹-Np1-Te1-CH₂CH₂-Np3-F、R¹-Np1-Te1-CH₂CH₂-Np4-F、R¹-Np1-Te2-CH₂CH₂-Ph1-F、R¹-Np1-Te2-CH₂CH₂-Ph2-F、R¹-Np1-Te2-CH₂CH₂-Ph3-F、R¹-Np1-Te2-CH₂CH₂-Np1-F、R¹-Np1-Te2-CH₂CH₂-Np2-F、R¹-Np1-Te2-CH₂CH₂-Np3-F、R¹-Np1-Te2-CH₂CH₂-Np4-F、
【００５４】
R¹-Np2-Te1-Ph1-F、R¹-Np2-Te1-Ph2-F、R¹-Np2-Te1-Ph3-F、R¹-Np2-Te1-Np1-F、R¹-Np2-Te1-Np2-F、R¹-Np2-Te1-Np3-F、R¹-Np2-Te1-Np4-F、R¹-Np2-Te2-Ph1-F、R¹-Np2-Te2-Ph2-F、R¹-Np2-Te2-Ph3-F、R¹-Np2-Te2-Np1-F、R¹-Np2-Te2-Np2-F、R¹-Np2-Te2-Np3-F、R¹-Np2-Te2-Np4-F、R¹-Np2-Te1-CH₂CH₂-Ph2-F、R¹-Np2-Te1-CH₂CH₂-Ph3-F、R¹-Np2-Te1-CH₂CH₂-Np1-F、R¹-Np2-Te1-CH₂CH₂-Np2-F、R¹-Np2-Te1-CH₂CH₂-Np3-F、R¹-Np2-Te1-CH₂CH₂-Np4-F、R¹-Np2-Te2-CH₂CH₂-Ph1-F、R¹-Np2-Te2-CH₂CH₂-Ph2-F、R¹-Np2-Te2-CH₂CH₂-Ph3-F、R¹-Np2-Te2-CH₂CH₂-Np1-F、R¹-Np2-Te2-CH₂CH₂-Np2-F、R¹-Np2-Te2-CH₂CH₂-Np3-F、R¹-Np2-Te2-CH₂CH₂-Np4-F、
【００５５】
R¹-Np3-Te1-Ph1-F、R¹-Np3-Te1-Ph2-F、R¹-Np3-Te1-Ph3-F、R¹-Np3-Te1-Np1-F、R¹-Np3-Te1-Np2-F、R¹-Np3-Te1-Np3-F、R¹-Np3-Te1-Np4-F、R¹-Np3-Te2-Ph1-F、R¹-Np3-Te2-Ph2-F、R¹-Np3-Te2-Ph3-F、R¹-Np3-Te2-Np1-F、R¹-Np3-Te2-Np2-F、R¹-Np3-Te2-Np3-F、R¹-Np3-Te2-Np4-F、R¹-Np3-Te1-CH₂CH₂-Ph2-F、R¹-Np3-Te1-CH₂CH₂-Ph3-F、R¹-Np3-Te1-CH₂CH₂-Np1-F、R¹-Np3-Te1-CH₂CH₂-Np2-F、R¹-Np3-Te1-CH₂CH₂-Np3-F、R¹-Np3-Te1-CH₂CH₂-Np4-F、R¹-Np3-Te2-CH₂CH₂-Ph1-F、R¹-Np3-Te2-CH₂CH₂-Ph2-F、R¹-Np3-Te2-CH₂CH₂-Ph3-F、R¹-Np3-Te2-CH₂CH₂-Np1-F、R¹-Np3-Te2-CH₂CH₂-Np2-F、R¹-Np3-Te2-CH₂CH₂-Np3-F、R¹-Np3-Te2-CH₂CH₂-Np4-F、
【００５６】
R¹-Np4-Te1-Ph1-F、R¹-Np4-Te1-Ph2-F、R¹-Np4-Te1-Ph3-F、R¹-Np4-Te1-Np1-F、R¹-Np4-Te1-Np2-F、R¹-Np4-Te1-Np3-F、R¹-Np4-Te1-Np4-F、R¹-Np4-Te2-Ph1-F、R¹-Np4-Te2-Ph2-F、R¹-Np4-Te2-Ph3-F、R¹-Np4-Te2-Np1-F、R¹-Np4-Te2-Np2-F、R¹-Np4-Te2-Np3-F、R¹-Np4-Te2-Np4-F、R¹-Np4-Te1-CH₂CH₂-Ph2-F、R¹-Np4-Te1-CH₂CH₂-Ph3-F、R¹-Np4-Te1-CH₂CH₂-Np1-F、R¹-Np4-Te1-CH₂CH₂-Np2-F、R¹-Np4-Te1-CH₂CH₂-Np3-F、R¹-Np4-Te1-CH₂CH₂-Np4-F、R¹-Np4-Te2-CH₂CH₂-Ph1-F、R¹-Np4-Te2-CH₂CH₂-Ph2-F、R¹-Np4-Te2-CH₂CH₂-Ph3-F、R¹-Np4-Te2-CH₂CH₂-Np1-F、R¹-Np4-Te2-CH₂CH₂-Np2-F、R¹-Np4-Te2-CH₂CH₂-Np3-F、R¹-Np4-Te2-CH₂CH₂-Np4-F、
【００５７】
R¹-Cy-CH₂CH₂-Te1-Ph1-F、R¹-Cy-CH₂CH₂-Te1-Ph2-F、R¹-Cy-CH₂CH₂-Te1-Ph3-F、R¹-Cy-CH₂CH₂-Te1-Np1-F、R¹-Cy-CH₂CH₂-Te1-Np2-F、R¹-Cy-CH₂CH₂-Te1-Np3-F、R¹-Cy-CH₂CH₂-Te1-Np4-F、R¹-Cy-CH₂CH₂-Te2-Ph1-F、R¹-Cy-CH₂CH₂-Te2-Ph2-F、R¹-Cy-CH₂CH₂-Te2-Ph3-F、R¹-Cy-CH₂CH₂-Te2-Np1-F、R¹-Cy-CH₂CH₂-Te2-Np2-F、R¹-Cy-CH₂CH₂-Te2-Np3-F、R¹-Cy-CH₂CH₂-Te2-Np4-F、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００５８】
R¹-Ph1-CH₂CH₂-Te1-Ph1-F、R¹-Ph1-CH₂CH₂-Te1-Ph2-F、R¹-Ph1-CH₂CH₂-Te1-Ph3-F、R¹-Ph1-CH₂CH₂-Te1-Np1-F、R¹-Ph1-CH₂CH₂-Te1-Np2-F、R¹-Ph1-CH₂CH₂-Te1-Np3-F、R¹-Ph1-CH₂CH₂-Te1-Np4-F、R¹-Ph1-CH₂CH₂-Te2-Ph1-F、R¹-Ph1-CH₂CH₂-Te2-Ph2-F、R¹-Ph1-CH₂CH₂-Te2-Ph3-F、R¹-Ph1-CH₂CH₂-Te2-Np1-F、R¹-Ph1-CH₂CH₂-Te2-Np2-F、R¹-Ph1-CH₂CH₂-Te2-Np3-F、R¹-Ph1-CH₂CH₂-Te2-Np4-F、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００５９】
R¹-Ph2-CH₂CH₂-Te1-Ph1-F、R¹-Ph2-CH₂CH₂-Te1-Ph2-F、R¹-Ph2-CH₂CH₂-Te1-Ph3-F、R¹-Ph2-CH₂CH₂-Te1-Np1-F、R¹-Ph2-CH₂CH₂-Te1-Np2-F、R¹-Ph2-CH₂CH₂-Te1-Np3-F、R¹-Ph2-CH₂CH₂-Te1-Np4-F、R¹-Ph2-CH₂CH₂-Te2-Ph1-F、R¹-Ph2-CH₂CH₂-Te2-Ph2-F、R¹-Ph2-CH₂CH₂-Te2-Ph3-F、R¹-Ph2-CH₂CH₂-Te2-Np1-F、R¹-Ph2-CH₂CH₂-Te2-Np2-F、R¹-Ph2-CH₂CH₂-Te2-Np3-F、R¹-Ph2-CH₂CH₂-Te2-Np4-F、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００６０】
R¹-Ph3-CH₂CH₂-Te1-Ph1-F、R¹-Ph3-CH₂CH₂-Te1-Ph2-F、R¹-Ph3-CH₂CH₂-Te1-Ph3-F、R¹-Ph3-CH₂CH₂-Te1-Np1-F、R¹-Ph3-CH₂CH₂-Te1-Np2-F、R¹-Ph3-CH₂CH₂-Te1-Np3-F、R¹-Ph3-CH₂CH₂-Te1-Np4-F、R¹-Ph3-CH₂CH₂-Te2-Ph1-F、R¹-Ph3-CH₂CH₂-Te2-Ph2-F、R¹-Ph3-CH₂CH₂-Te2-Ph3-F、R¹-Ph3-CH₂CH₂-Te2-Np1-F、R¹-Ph3-CH₂CH₂-Te2-Np2-F、R¹-Ph3-CH₂CH₂-Te2-Np3-F、R¹-Ph3-CH₂CH₂-Te2-Np4-F、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００６１】
R¹-Np1-CH₂CH₂-Te1-Ph1-F、R¹-Np1-CH₂CH₂-Te1-Ph2-F、R¹-Np1-CH₂CH₂-Te1-Ph3-F、R¹-Np1-CH₂CH₂-Te1-Np1-F、R¹-Np1-CH₂CH₂-Te1-Np2-F、R¹-Np1-CH₂CH₂-Te1-Np3-F、R¹-Np1-CH₂CH₂-Te1-Np4-F、R¹-Np1-CH₂CH₂-Te2-Ph1-F、R¹-Np1-CH₂CH₂-Te2-Ph2-F、R¹-Np1-CH₂CH₂-Te2-Ph3-F、R¹-Np1-CH₂CH₂-Te2-Np1-F、R¹-Np1-CH₂CH₂-Te2-Np2-F、R¹-Np1-CH₂CH₂-Te2-Np3-F、R¹-Np1-CH₂CH₂-Te2-Np4-F、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００６２】
R¹-Np2-CH₂CH₂-Te1-Ph1-F、R¹-Np2-CH₂CH₂-Te1-Ph2-F、R¹-Np2-CH₂CH₂-Te1-Ph3-F、R¹-Np2-CH₂CH₂-Te1-Np1-F、R¹-Np2-CH₂CH₂-Te1-Np2-F、R¹-Np2-CH₂CH₂-Te1-Np3-F、R¹-Np2-CH₂CH₂-Te1-Np4-F、R¹-Np2-CH₂CH₂-Te2-Ph1-F、R¹-Np2-CH₂CH₂-Te2-Ph2-F、R¹-Np2-CH₂CH₂-Te2-Ph3-F、R¹-Np2-CH₂CH₂-Te2-Np1-F、R¹-Np2-CH₂CH₂-Te2-Np2-F、R¹-Np2-CH₂CH₂-Te2-Np3-F、R¹-Np2-CH₂CH₂-Te2-Np4-F、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００６３】
R¹-Np3-CH₂CH₂-Te1-Ph1-F、R¹-Np3-CH₂CH₂-Te1-Ph2-F、R¹-Np3-CH₂CH₂-Te1-Ph3-F、R¹-Np3-CH₂CH₂-Te1-Np1-F、R¹-Np3-CH₂CH₂-Te1-Np2-F、R¹-Np3-CH₂CH₂-Te1-Np3-F、R¹-Np3-CH₂CH₂-Te1-Np4-F、R¹-Np3-CH₂CH₂-Te2-Ph1-F、R¹-Np3-CH₂CH₂-Te2-Ph2-F、R¹-Np3-CH₂CH₂-Te2-Ph3-F、R¹-Np3-CH₂CH₂-Te2-Np1-F、R¹-Np3-CH₂CH₂-Te2-Np2-F、R¹-Np3-CH₂CH₂-Te2-Np3-F、R¹-Np3-CH₂CH₂-Te2-Np4-F、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００６４】
R¹-Np4-CH₂CH₂-Te1-Ph1-F、R¹-Np4-CH₂CH₂-Te1-Ph2-F、R¹-Np4-CH₂CH₂-Te1-Ph3-F、R¹-Np4-CH₂CH₂-Te1-Np1-F、R¹-Np4-CH₂CH₂-Te1-Np2-F、R¹-Np4-CH₂CH₂-Te1-Np3-F、R¹-Np4-CH₂CH₂-Te1-Np4-F、R¹-Np4-CH₂CH₂-Te2-Ph1-F、R¹-Np4-CH₂CH₂-Te2-Ph2-F、R¹-Np4-CH₂CH₂-Te2-Ph3-F、R¹-Np4-CH₂CH₂-Te2-Np1-F、R¹-Np4-CH₂CH₂-Te2-Np2-F、R¹-Np4-CH₂CH₂-Te2-Np3-F、R¹-Np4-CH₂CH₂-Te2-Np4-F、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Ph2-F、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Ph3-F、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np1-F、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np2-F、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np3-F、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np4-F、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph1-F、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph2-F、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph3-F、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np1-F、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np2-F、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np3-F、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np4-F、
【００６５】
R¹-Ph1-C≡C-Te1-Ph1-F、R¹-Ph1-C≡C-Te1-Ph2-F、R¹-Ph1-C≡C-Te1-Ph3-F、R¹-Ph1-C≡C-Te1-Np1-F、R¹-Ph1-C≡C-Te1-Np2-F、R¹-Ph1-C≡C-Te1-Np3-F、R¹-Ph1-C≡C-Te1-Np4-F、R¹-Ph1-C≡C-Te2-Ph1-F、R¹-Ph1-C≡C-Te2-Ph2-F、R¹-Ph1-C≡C-Te2-Ph3-F、R¹-Ph1-C≡C-Te2-Np1-F、R¹-Ph1-C≡C-Te2-Np2-F、R¹-Ph1-C≡C-Te2-Np3-F、R¹-Ph1-C≡C-Te2-Np4-F、R¹-Ph1-C≡C-Te1-CH₂CH₂-Ph2-F、R¹-Ph1-C≡C-Te1-CH₂CH₂-Ph3-F、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np1-F、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np2-F、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np3-F、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np4-F、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph1-F、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph2-F、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph3-F、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np1-F、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np2-F、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np3-F、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np4-F、
【００６６】
R¹-Ph2-C≡C-Te1-Ph1-F、R¹-Ph2-C≡C-Te1-Ph2-F、R¹-Ph2-C≡C-Te1-Ph3-F、R¹-Ph2-C≡C-Te1-Np1-F、R¹-Ph2-C≡C-Te1-Np2-F、R¹-Ph2-C≡C-Te1-Np3-F、R¹-Ph2-C≡C-Te1-Np4-F、R¹-Ph2-C≡C-Te2-Ph1-F、R¹-Ph2-C≡C-Te2-Ph2-F、R¹-Ph2-C≡C-Te2-Ph3-F、R¹-Ph2-C≡C-Te2-Np1-F、R¹-Ph2-C≡C-Te2-Np2-F、R¹-Ph2-C≡C-Te2-Np3-F、R¹-Ph2-C≡C-Te2-Np4-F、R¹-Ph2-C≡C-Te1-CH₂CH₂-Ph2-F、R¹-Ph2-C≡C-Te1-CH₂CH₂-Ph3-F、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np1-F、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np2-F、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np3-F、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np4-F、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph1-F、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph2-F、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph3-F、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np1-F、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np2-F、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np3-F、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np4-F、
【００６７】
R¹-Ph3-C≡C-Te1-Ph1-F、R¹-Ph3-C≡C-Te1-Ph2-F、R¹-Ph3-C≡C-Te1-Ph3-F、R¹-Ph3-C≡C-Te1-Np1-F、R¹-Ph3-C≡C-Te1-Np2-F、R¹-Ph3-C≡C-Te1-Np3-F、R¹-Ph3-C≡C-Te1-Np4-F、R¹-Ph3-C≡C-Te2-Ph1-F、R¹-Ph3-C≡C-Te2-Ph2-F、R¹-Ph3-C≡C-Te2-Ph3-F、R¹-Ph3-C≡C-Te2-Np1-F、R¹-Ph3-C≡C-Te2-Np2-F、R¹-Ph3-C≡C-Te2-Np3-F、R¹-Ph3-C≡C-Te2-Np4-F、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph2-F、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph3-F、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np1-F、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np2-F、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np3-F、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np4-F、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph1-F、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph2-F、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph3-F、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np1-F、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np2-F、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np3-F、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np4-F、
【００６８】
R¹-Np1-C≡C-Te1-Ph1-F、R¹-Np1-C≡C-Te1-Ph2-F、R¹-Np1-C≡C-Te1-Ph3-F、R¹-Np1-C≡C-Te1-Np1-F、R¹-Np1-C≡C-Te1-Np2-F、R¹-Np1-C≡C-Te1-Np3-F、R¹-Np1-C≡C-Te1-Np4-F、R¹-Np1-C≡C-Te2-Ph1-F、R¹-Np1-C≡C-Te2-Ph2-F、R¹-Np1-C≡C-Te2-Ph3-F、R¹-Np1-C≡C-Te2-Np1-F、R¹-Np1-C≡C-Te2-Np2-F、R¹-Np1-C≡C-Te2-Np3-F、R¹-Np1-C≡C-Te2-Np4-F、R¹-Np1-C≡C-Te1-CH₂CH₂-Ph2-F、R¹-Np1-C≡C-Te1-CH₂CH₂-Ph3-F、R¹-Np1-C≡C-Te1-CH₂CH₂-Np1-F、R¹-Np1-C≡C-Te1-CH₂CH₂-Np2-F、R¹-Np1-C≡C-Te1-CH₂CH₂-Np3-F、R¹-Np1-C≡C-Te1-CH₂CH₂-Np4-F、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph1-F、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph2-F、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph3-F、R¹-Np1-C≡C-Te2-CH₂CH₂-Np1-F、R¹-Np1-C≡C-Te2-CH₂CH₂-Np2-F、R¹-Np1-C≡C-Te2-CH₂CH₂-Np3-F、R¹-Np1-C≡C-Te2-CH₂CH₂-Np4-F、
【００６９】
R¹-Np2-C≡C-Te1-Ph1-F、R¹-Np2-C≡C-Te1-Ph2-F、R¹-Np2-C≡C-Te1-Ph3-F、R¹-Np2-C≡C-Te1-Np1-F、R¹-Np2-C≡C-Te1-Np2-F、R¹-Np2-C≡C-Te1-Np3-F、R¹-Np2-C≡C-Te1-Np4-F、R¹-Np2-C≡C-Te2-Ph1-F、R¹-Np2-C≡C-Te2-Ph2-F、R¹-Np2-C≡C-Te2-Ph3-F、R¹-Np2-C≡C-Te2-Np1-F、R¹-Np2-C≡C-Te2-Np2-F、R¹-Np2-C≡C-Te2-Np3-F、R¹-Np2-C≡C-Te2-Np4-F、R¹-Np2-C≡C-Te1-CH₂CH₂-Ph2-F、R¹-Np2-C≡C-Te1-CH₂CH₂-Ph3-F、R¹-Np2-C≡C-Te1-CH₂CH₂-Np1-F、R¹-Np2-C≡C-Te1-CH₂CH₂-Np2-F、R¹-Np2-C≡C-Te1-CH₂CH₂-Np3-F、R¹-Np2-C≡C-Te1-CH₂CH₂-Np4-F、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph1-F、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph2-F、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph3-F、R¹-Np2-C≡C-Te2-CH₂CH₂-Np1-F、R¹-Np2-C≡C-Te2-CH₂CH₂-Np2-F、R¹-Np2-C≡C-Te2-CH₂CH₂-Np3-F、R¹-Np2-C≡C-Te2-CH₂CH₂-Np4-F、
【００７０】
R¹-Np3-C≡C-Te1-Ph1-F、R¹-Np3-C≡C-Te1-Ph2-F、R¹-Np3-C≡C-Te1-Ph3-F、R¹-Np3-C≡C-Te1-Np1-F、R¹-Np3-C≡C-Te1-Np2-F、R¹-Np3-C≡C-Te1-Np3-F、R¹-Np3-C≡C-Te1-Np4-F、R¹-Np3-C≡C-Te2-Ph1-F、R¹-Np3-C≡C-Te2-Ph2-F、R¹-Np3-C≡C-Te2-Ph3-F、R¹-Np3-C≡C-Te2-Np1-F、R¹-Np3-C≡C-Te2-Np2-F、R¹-Np3-C≡C-Te2-Np3-F、R¹-Np3-C≡C-Te2-Np4-F、R¹-Np3-C≡C-Te1-CH₂CH₂-Ph2-F、R¹-Np3-C≡C-Te1-CH₂CH₂-Ph3-F、R¹-Np3-C≡C-Te1-CH₂CH₂-Np1-F、R¹-Np3-C≡C-Te1-CH₂CH₂-Np2-F、R¹-Np3-C≡C-Te1-CH₂CH₂-Np3-F、R¹-Np3-C≡C-Te1-CH₂CH₂-Np4-F、R¹-Np3-C≡C-Te2-CH₂CH₂-Ph1-F、R¹-Np3-C≡C-Te2-CH₂CH₂-Ph2-F、R¹-Np3-C≡C-Te2-CH₂CH₂-Ph3-F、R¹-Np3-C≡C-Te2-CH₂CH₂-Np1-F、R¹-Np3-C≡C-Te2-CH₂CH₂-Np2-F、R¹-Np3-C≡C-Te2-CH₂CH₂-Np3-F、R¹-Np3-C≡C-Te2-CH₂CH₂-Np4-F、
【００７１】
R¹-Np4-C≡C-Te1-Ph1-F、R¹-Np4-C≡C-Te1-Ph2-F、R¹-Np4-C≡C-Te1-Ph3-F、R¹-Np4-C≡C-Te1-Np1-F、R¹-Np4-C≡C-Te1-Np2-F、R¹-Np4-C≡C-Te1-Np3-F、R¹-Np4-C≡C-Te1-Np4-F、R¹-Np4-C≡C-Te2-Ph1-F、R¹-Np4-C≡C-Te2-Ph2-F、R¹-Np4-C≡C-Te2-Ph3-F、R¹-Np4-C≡C-Te2-Np1-F、R¹-Np4-C≡C-Te2-Np2-F、R¹-Np4-C≡C-Te2-Np3-F、R¹-Np4-C≡C-Te2-Np4-F、R¹-Np4-C≡C-Te1-CH₂CH₂-Ph2-F、R¹-Np4-C≡C-Te1-CH₂CH₂-Ph3-F、R¹-Np4-C≡C-Te1-CH₂CH₂-Np1-F、R¹-Np4-C≡C-Te1-CH₂CH₂-Np2-F、R¹-Np4-C≡C-Te1-CH₂CH₂-Np3-F、R¹-Np4-C≡C-Te1-CH₂CH₂-Np4-F、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph1-F、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph2-F、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph3-F、R¹-Np4-C≡C-Te2-CH₂CH₂-Np1-F、R¹-Np4-C≡C-Te2-CH₂CH₂-Np2-F、R¹-Np4-C≡C-Te2-CH₂CH₂-Np3-F、R¹-Np4-C≡C-Te2-CH₂CH₂-Np4-F、
【００７２】
m=1、n=0、Vが単結合、Zがシアノ基の場合、
【００７３】
R¹-Cy-Te1-Ph1-CN、R¹-Cy-Te1-Ph2-CN、R¹-Cy-Te1-Ph3-CN、R¹-Cy-Te1-Np1-CN、R¹-Cy-Te1-Np2-CN、R¹-Cy-Te1-Np3-CN、R¹-Cy-Te1-Np4-CN、R¹-Cy-Te2-Ph1-CN、R¹-Cy-Te2-Ph2-CN、R¹-Cy-Te2-Ph3-CN、R¹-Cy-Te2-Np1-CN、R¹-Cy-Te2-Np2-CN、R¹-Cy-Te2-Np3-CN、R¹-Cy-Te2-Np4-CN、R¹-Cy-Te1-CH₂CH₂-Ph2-CN、R¹-Cy-Te1-CH₂CH₂-Ph3-CN、R¹-Cy-Te1-CH₂CH₂-Np1-CN、R¹-Cy-Te1-CH₂CH₂-Np2-CN、R¹-Cy-Te1-CH₂CH₂-Np3-CN、R¹-Cy-Te1-CH₂CH₂-Np4-CN、R¹-Cy-Te2-CH₂CH₂-Ph1-CN、R¹-Cy-Te2-CH₂CH₂-Ph2-CN、R¹-Cy-Te2-CH₂CH₂-Ph3-CN、R¹-Cy-Te2-CH₂CH₂-Np1-CN、R¹-Cy-Te2-CH₂CH₂-Np2-CN、R¹-Cy-Te2-CH₂CH₂-Np3-CN、R¹-Cy-Te2-CH₂CH₂-Np4-CN、
【００７４】
R¹-Ph1-Te1-Ph1-CN、R¹-Ph1-Te1-Ph2-CN、R¹-Ph1-Te1-Ph3-CN、R¹-Ph1-Te1-Np1-CN、R¹-Ph1-Te1-Np2-CN、R¹-Ph1-Te1-Np3-CN、R¹-Ph1-Te1-Np4-CN、R¹-Ph1-Te2-Ph1-CN、R¹-Ph1-Te2-Ph2-CN、R¹-Ph1-Te2-Ph3-CN、R¹-Ph1-Te2-Np1-CN、R¹-Ph1-Te2-Np2-CN、R¹-Ph1-Te2-Np3-CN、R¹-Ph1-Te2-Np4-CN、R¹-Ph1-Te1-CH₂CH₂-Ph2-CN、R¹-Ph1-Te1-CH₂CH₂-Ph3-CN、R¹-Ph1-Te1-CH₂CH₂-Np1-CN、R¹-Ph1-Te1-CH₂CH₂-Np2-CN、R¹-Ph1-Te1-CH₂CH₂-Np3-CN、R¹-Ph1-Te1-CH₂CH₂-Np4-CN、R¹-Ph1-Te2-CH₂CH₂-Ph1-CN、R¹-Ph1-Te2-CH₂CH₂-Ph2-CN、R¹-Ph1-Te2-CH₂CH₂-Ph3-CN、R¹-Ph1-Te2-CH₂CH₂-Np1-CN、R¹-Ph1-Te2-CH₂CH₂-Np2-CN、R¹-Ph1-Te2-CH₂CH₂-Np3-CN、R¹-Ph1-Te2-CH₂CH₂-Np4-CN、
【００７５】
R¹-Ph2-Te1-Ph1-CN、R¹-Ph2-Te1-Ph2-CN、R¹-Ph2-Te1-Ph3-CN、R¹-Ph2-Te1-Np1-CN、R¹-Ph2-Te1-Np2-CN、R¹-Ph2-Te1-Np3-CN、R¹-Ph2-Te1-Np4-CN、R¹-Ph2-Te2-Ph1-CN、R¹-Ph2-Te2-Ph2-CN、R¹-Ph2-Te2-Ph3-CN、R¹-Ph2-Te2-Np1-CN、R¹-Ph2-Te2-Np2-CN、R¹-Ph2-Te2-Np3-CN、R¹-Ph2-Te2-Np4-CN、R¹-Ph2-Te1-CH₂CH₂-Ph2-CN、R¹-Ph2-Te1-CH₂CH₂-Ph3-CN、R¹-Ph2-Te1-CH₂CH₂-Np1-CN、R¹-Ph2-Te1-CH₂CH₂-Np2-CN、R¹-Ph2-Te1-CH₂CH₂-Np3-CN、R¹-Ph2-Te1-CH₂CH₂-Np4-CN、R¹-Ph2-Te2-CH₂CH₂-Ph1-CN、R¹-Ph2-Te2-CH₂CH₂-Ph2-CN、R¹-Ph2-Te2-CH₂CH₂-Ph3-CN、R¹-Ph2-Te2-CH₂CH₂-Np1-CN、R¹-Ph2-Te2-CH₂CH₂-Np2-CN、R¹-Ph2-Te2-CH₂CH₂-Np3-CN、R¹-Ph2-Te2-CH₂CH₂-Np4-CN、
【００７６】
R¹-Ph3-Te1-Ph1-CN、R¹-Ph3-Te1-Ph2-CN、R¹-Ph3-Te1-Ph3-CN、R¹-Ph3-Te1-Np1-CN、R¹-Ph3-Te1-Np2-CN、R¹-Ph3-Te1-Np3-CN、R¹-Ph3-Te1-Np4-CN、R¹-Ph3-Te2-Ph1-CN、R¹-Ph3-Te2-Ph2-CN、R¹-Ph3-Te2-Ph3-CN、R¹-Ph3-Te2-Np1-CN、R¹-Ph3-Te2-Np2-CN、R¹-Ph3-Te2-Np3-CN、R¹-Ph3-Te2-Np4-CN、R¹-Ph3-Te1-CH₂CH₂-Ph2-CN、R¹-Ph3-Te1-CH₂CH₂-Ph3-CN、R¹-Ph3-Te1-CH₂CH₂-Np1-CN、R¹-Ph3-Te1-CH₂CH₂-Np2-CN、R¹-Ph3-Te1-CH₂CH₂-Np3-CN、R¹-Ph3-Te1-CH₂CH₂-Np4-CN、R¹-Ph3-Te2-CH₂CH₂-Ph1-CN、R¹-Ph3-Te2-CH₂CH₂-Ph2-CN、R¹-Ph3-Te2-CH₂CH₂-Ph3-CN、R¹-Ph3-Te2-CH₂CH₂-Np1-CN、R¹-Ph3-Te2-CH₂CH₂-Np2-CN、R¹-Ph3-Te2-CH₂CH₂-Np3-CN、R¹-Ph3-Te2-CH₂CH₂-Np4-CN、
【００７７】
R¹-Np1-Te1-Ph1-CN、R¹-Np1-Te1-Ph2-CN、R¹-Np1-Te1-Ph3-CN、R¹-Np1-Te1-Np1-CN、R¹-Np1-Te1-Np2-CN、R¹-Np1-Te1-Np3-CN、R¹-Np1-Te1-Np4-CN、R¹-Np1-Te2-Ph1-CN、R¹-Np1-Te2-Ph2-CN、R¹-Np1-Te2-Ph3-CN、R¹-Np1-Te2-Np1-CN、R¹-Np1-Te2-Np2-CN、R¹-Np1-Te2-Np3-CN、R¹-Np1-Te2-Np4-CN、R¹-Np1-Te1-CH₂CH₂-Ph2-CN、R¹-Np1-Te1-CH₂CH₂-Ph3-CN、R¹-Np1-Te1-CH₂CH₂-Np1-CN、R¹-Np1-Te1-CH₂CH₂-Np2-CN、R¹-Np1-Te1-CH₂CH₂-Np3-CN、R¹-Np1-Te1-CH₂CH₂-Np4-CN、R¹-Np1-Te2-CH₂CH₂-Ph1-CN、R¹-Np1-Te2-CH₂CH₂-Ph2-CN、R¹-Np1-Te2-CH₂CH₂-Ph3-CN、R¹-Np1-Te2-CH₂CH₂-Np1-CN、R¹-Np1-Te2-CH₂CH₂-Np2-CN、R¹-Np1-Te2-CH₂CH₂-Np3-CN、R¹-Np1-Te2-CH₂CH₂-Np4-CN、
【００７８】
R¹-Np2-Te1-Ph1-CN、R¹-Np2-Te1-Ph2-CN、R¹-Np2-Te1-Ph3-CN、R¹-Np2-Te1-Np1-CN、R¹-Np2-Te1-Np2-CN、R¹-Np2-Te1-Np3-CN、R¹-Np2-Te1-Np4-CN、R¹-Np2-Te2-Ph1-CN、R¹-Np2-Te2-Ph2-CN、R¹-Np2-Te2-Ph3-CN、R¹-Np2-Te2-Np1-CN、R¹-Np2-Te2-Np2-CN、R¹-Np2-Te2-Np3-CN、R¹-Np2-Te2-Np4-CN、R¹-Np2-Te1-CH₂CH₂-Ph2-CN、R¹-Np2-Te1-CH₂CH₂-Ph3-CN、R¹-Np2-Te1-CH₂CH₂-Np1-CN、R¹-Np2-Te1-CH₂CH₂-Np2-CN、R¹-Np2-Te1-CH₂CH₂-Np3-CN、R¹-Np2-Te1-CH₂CH₂-Np4-CN、R¹-Np2-Te2-CH₂CH₂-Ph1-CN、R¹-Np2-Te2-CH₂CH₂-Ph2-CN、R¹-Np2-Te2-CH₂CH₂-Ph3-CN、R¹-Np2-Te2-CH₂CH₂-Np1-CN、R¹-Np2-Te2-CH₂CH₂-Np2-CN、R¹-Np2-Te2-CH₂CH₂-Np3-CN、R¹-Np2-Te2-CH₂CH₂-Np4-CN、
【００７９】
R¹-Np3-Te1-Ph1-CN、R¹-Np3-Te1-Ph2-CN、R¹-Np3-Te1-Ph3-CN、R¹-Np3-Te1-Np1-CN、R¹-Np3-Te1-Np2-CN、R¹-Np3-Te1-Np3-CN、R¹-Np3-Te1-Np4-CN、R¹-Np3-Te2-Ph1-CN、R¹-Np3-Te2-Ph2-CN、R¹-Np3-Te2-Ph3-CN、R¹-Np3-Te2-Np1-CN、R¹-Np3-Te2-Np2-CN、R¹-Np3-Te2-Np3-CN、R¹-Np3-Te2-Np4-CN、R¹-Np3-Te1-CH₂CH₂-Ph2-CN、R¹-Np3-Te1-CH₂CH₂-Ph3-CN、R¹-Np3-Te1-CH₂CH₂-Np1-CN、R¹-Np3-Te1-CH₂CH₂-Np2-CN、R¹-Np3-Te1-CH₂CH₂-Np3-CN、R¹-Np3-Te1-CH₂CH₂-Np4-CN、R¹-Np3-Te2-CH₂CH₂-Ph1-CN、R¹-Np3-Te2-CH₂CH₂-Ph2-CN、R¹-Np3-Te2-CH₂CH₂-Ph3-CN、R¹-Np3-Te2-CH₂CH₂-Np1-CN、R¹-Np3-Te2-CH₂CH₂-Np2-CN、R¹-Np3-Te2-CH₂CH₂-Np3-CN、R¹-Np3-Te2-CH₂CH₂-Np4-CN、
【００８０】
R¹-Np4-Te1-Ph1-CN、R¹-Np4-Te1-Ph2-CN、R¹-Np4-Te1-Ph3-CN、R¹-Np4-Te1-Np1-CN、R¹-Np4-Te1-Np2-CN、R¹-Np4-Te1-Np3-CN、R¹-Np4-Te1-Np4-CN、R¹-Np4-Te2-Ph1-CN、R¹-Np4-Te2-Ph2-CN、R¹-Np4-Te2-Ph3-CN、R¹-Np4-Te2-Np1-CN、R¹-Np4-Te2-Np2-CN、R¹-Np4-Te2-Np3-CN、R¹-Np4-Te2-Np4-CN、R¹-Np4-Te1-CH₂CH₂-Ph2-CN、R¹-Np4-Te1-CH₂CH₂-Ph3-CN、R¹-Np4-Te1-CH₂CH₂-Np1-CN、R¹-Np4-Te1-CH₂CH₂-Np2-CN、R¹-Np4-Te1-CH₂CH₂-Np3-CN、R¹-Np4-Te1-CH₂CH₂-Np4-CN、R¹-Np4-Te2-CH₂CH₂-Ph1-CN、R¹-Np4-Te2-CH₂CH₂-Ph2-CN、R¹-Np4-Te2-CH₂CH₂-Ph3-CN、R¹-Np4-Te2-CH₂CH₂-Np1-CN、R¹-Np4-Te2-CH₂CH₂-Np2-CN、R¹-Np4-Te2-CH₂CH₂-Np3-CN、R¹-Np4-Te2-CH₂CH₂-Np4-CN、
【００８１】
R¹-Cy-CH₂CH₂-Te1-Ph1-CN、R¹-Cy-CH₂CH₂-Te1-Ph2-CN、R¹-Cy-CH₂CH₂-Te1-Ph3-CN、R¹-Cy-CH₂CH₂-Te1-Np1-CN、R¹-Cy-CH₂CH₂-Te1-Np2-CN、R¹-Cy-CH₂CH₂-Te1-Np3-CN、R¹-Cy-CH₂CH₂-Te1-Np4-CN、R¹-Cy-CH₂CH₂-Te2-Ph1-CN、R¹-Cy-CH₂CH₂-Te2-Ph2-CN、R¹-Cy-CH₂CH₂-Te2-Ph3-CN、R¹-Cy-CH₂CH₂-Te2-Np1-CN、R¹-Cy-CH₂CH₂-Te2-Np2-CN、R¹-Cy-CH₂CH₂-Te2-Np3-CN、R¹-Cy-CH₂CH₂-Te2-Np4-CN、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８２】
R¹-Ph1-CH₂CH₂-Te1-Ph1-CN、R¹-Ph1-CH₂CH₂-Te1-Ph2-CN、R¹-Ph1-CH₂CH₂-Te1-Ph3-CN、R¹-Ph1-CH₂CH₂-Te1-Np1-CN、R¹-Ph1-CH₂CH₂-Te1-Np2-CN、R¹-Ph1-CH₂CH₂-Te1-Np3-CN、R¹-Ph1-CH₂CH₂-Te1-Np4-CN、R¹-Ph1-CH₂CH₂-Te2-Ph1-CN、R¹-Ph1-CH₂CH₂-Te2-Ph2-CN、R¹-Ph1-CH₂CH₂-Te2-Ph3-CN、R¹-Ph1-CH₂CH₂-Te2-Np1-CN、R¹-Ph1-CH₂CH₂-Te2-Np2-CN、R¹-Ph1-CH₂CH₂-Te2-Np3-CN、R¹-Ph1-CH₂CH₂-Te2-Np4-CN、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８３】
R¹-Ph2-CH₂CH₂-Te1-Ph1-CN、R¹-Ph2-CH₂CH₂-Te1-Ph2-CN、R¹-Ph2-CH₂CH₂-Te1-Ph3-CN、R¹-Ph2-CH₂CH₂-Te1-Np1-CN、R¹-Ph2-CH₂CH₂-Te1-Np2-CN、R¹-Ph2-CH₂CH₂-Te1-Np3-CN、R¹-Ph2-CH₂CH₂-Te1-Np4-CN、R¹-Ph2-CH₂CH₂-Te2-Ph1-CN、R¹-Ph2-CH₂CH₂-Te2-Ph2-CN、R¹-Ph2-CH₂CH₂-Te2-Ph3-CN、R¹-Ph2-CH₂CH₂-Te2-Np1-CN、R¹-Ph2-CH₂CH₂-Te2-Np2-CN、R¹-Ph2-CH₂CH₂-Te2-Np3-CN、R¹-Ph2-CH₂CH₂-Te2-Np4-CN、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８４】
R¹-Ph3-CH₂CH₂-Te1-Ph1-CN、R¹-Ph3-CH₂CH₂-Te1-Ph2-CN、R¹-Ph3-CH₂CH₂-Te1-Ph3-CN、R¹-Ph3-CH₂CH₂-Te1-Np1-CN、R¹-Ph3-CH₂CH₂-Te1-Np2-CN、R¹-Ph3-CH₂CH₂-Te1-Np3-CN、R¹-Ph3-CH₂CH₂-Te1-Np4-CN、R¹-Ph3-CH₂CH₂-Te2-Ph1-CN、R¹-Ph3-CH₂CH₂-Te2-Ph2-CN、R¹-Ph3-CH₂CH₂-Te2-Ph3-CN、R¹-Ph3-CH₂CH₂-Te2-Np1-CN、R¹-Ph3-CH₂CH₂-Te2-Np2-CN、R¹-Ph3-CH₂CH₂-Te2-Np3-CN、R¹-Ph3-CH₂CH₂-Te2-Np4-CN、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８５】
R¹-Np1-CH₂CH₂-Te1-Ph1-CN、R¹-Np1-CH₂CH₂-Te1-Ph2-CN、R¹-Np1-CH₂CH₂-Te1-Ph3-CN、R¹-Np1-CH₂CH₂-Te1-Np1-CN、R¹-Np1-CH₂CH₂-Te1-Np2-CN、R¹-Np1-CH₂CH₂-Te1-Np3-CN、R¹-Np1-CH₂CH₂-Te1-Np4-CN、R¹-Np1-CH₂CH₂-Te2-Ph1-CN、R¹-Np1-CH₂CH₂-Te2-Ph2-CN、R¹-Np1-CH₂CH₂-Te2-Ph3-CN、R¹-Np1-CH₂CH₂-Te2-Np1-CN、R¹-Np1-CH₂CH₂-Te2-Np2-CN、R¹-Np1-CH₂CH₂-Te2-Np3-CN、R¹-Np1-CH₂CH₂-Te2-Np4-CN、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８６】
R¹-Np2-CH₂CH₂-Te1-Ph1-CN、R¹-Np2-CH₂CH₂-Te1-Ph2-CN、R¹-Np2-CH₂CH₂-Te1-Ph3-CN、R¹-Np2-CH₂CH₂-Te1-Np1-CN、R¹-Np2-CH₂CH₂-Te1-Np2-CN、R¹-Np2-CH₂CH₂-Te1-Np3-CN、R¹-Np2-CH₂CH₂-Te1-Np4-CN、R¹-Np2-CH₂CH₂-Te2-Ph1-CN、R¹-Np2-CH₂CH₂-Te2-Ph2-CN、R¹-Np2-CH₂CH₂-Te2-Ph3-CN、R¹-Np2-CH₂CH₂-Te2-Np1-CN、R¹-Np2-CH₂CH₂-Te2-Np2-CN、R¹-Np2-CH₂CH₂-Te2-Np3-CN、R¹-Np2-CH₂CH₂-Te2-Np4-CN、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８７】
R¹-Np3-CH₂CH₂-Te1-Ph1-CN、R¹-Np3-CH₂CH₂-Te1-Ph2-CN、R¹-Np3-CH₂CH₂-Te1-Ph3-CN、R¹-Np3-CH₂CH₂-Te1-Np1-CN、R¹-Np3-CH₂CH₂-Te1-Np2-CN、R¹-Np3-CH₂CH₂-Te1-Np3-CN、R¹-Np3-CH₂CH₂-Te1-Np4-CN、R¹-Np3-CH₂CH₂-Te2-Ph1-CN、R¹-Np3-CH₂CH₂-Te2-Ph2-CN、R¹-Np3-CH₂CH₂-Te2-Ph3-CN、R¹-Np3-CH₂CH₂-Te2-Np1-CN、R¹-Np3-CH₂CH₂-Te2-Np2-CN、R¹-Np3-CH₂CH₂-Te2-Np3-CN、R¹-Np3-CH₂CH₂-Te2-Np4-CN、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Np3-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Np3-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８８】
R¹-Np4-CH₂CH₂-Te1-Ph1-CN、R¹-Np4-CH₂CH₂-Te1-Ph2-CN、R¹-Np4-CH₂CH₂-Te1-Ph3-CN、R¹-Np4-CH₂CH₂-Te1-Np1-CN、R¹-Np4-CH₂CH₂-Te1-Np2-CN、R¹-Np4-CH₂CH₂-Te1-Np3-CN、R¹-Np4-CH₂CH₂-Te1-Np4-CN、R¹-Np4-CH₂CH₂-Te2-Ph1-CN、R¹-Np4-CH₂CH₂-Te2-Ph2-CN、R¹-Np4-CH₂CH₂-Te2-Ph3-CN、R¹-Np4-CH₂CH₂-Te2-Np1-CN、R¹-Np4-CH₂CH₂-Te2-Np2-CN、R¹-Np4-CH₂CH₂-Te2-Np3-CN、R¹-Np4-CH₂CH₂-Te2-Np4-CN、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Ph2-CN、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Ph3-CN、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np1-CN、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np2-CN、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np3-CN、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np4-CN、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph1-CN、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph2-CN、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph3-CN、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np1-CN、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np2-CN、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np3-CN、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np4-CN、
【００８９】
R¹-Ph1-C≡C-Te1-Ph1-CN、R¹-Ph1-C≡C-Te1-Ph2-CN、R¹-Ph1-C≡C-Te1-Ph3-CN、R¹-Ph1-C≡C-Te1-Np1-CN、R¹-Ph1-C≡C-Te1-Np2-CN、R¹-Ph1-C≡C-Te1-Np3-CN、R¹-Ph1-C≡C-Te1-Np4-CN、R¹-Ph1-C≡C-Te2-Ph1-CN、R¹-Ph1-C≡C-Te2-Ph2-CN、R¹-Ph1-C≡C-Te2-Ph3-CN、R¹-Ph1-C≡C-Te2-Np1-CN、R¹-Ph1-C≡C-Te2-Np2-CN、R¹-Ph1-C≡C-Te2-Np3-CN、R¹-Ph1-C≡C-Te2-Np4-CN、R¹-Ph1-C≡C-Te1-CH₂CH₂-Ph2-CN、R¹-Ph1-C≡C-Te1-CH₂CH₂-Ph3-CN、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np1-CN、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np2-CN、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np3-CN、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np4-CN、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph1-CN、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph2-CN、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph3-CN、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np1-CN、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np2-CN、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np3-CN、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np4-CN、
【００９０】
R¹-Ph2-C≡C-Te1-Ph1-CN、R¹-Ph2-C≡C-Te1-Ph2-CN、R¹-Ph2-C≡C-Te1-Ph3-CN、R¹-Ph2-C≡C-Te1-Np1-CN、R¹-Ph2-C≡C-Te1-Np2-CN、R¹-Ph2-C≡C-Te1-Np3-CN、R¹-Ph2-C≡C-Te1-Np4-CN、R¹-Ph2-C≡C-Te2-Ph1-CN、R¹-Ph2-C≡C-Te2-Ph2-CN、R¹-Ph2-C≡C-Te2-Ph3-CN、R¹-Ph2-C≡C-Te2-Np1-CN、R¹-Ph2-C≡C-Te2-Np2-CN、R¹-Ph2-C≡C-Te2-Np3-CN、R¹-Ph2-C≡C-Te2-Np4-CN、R¹-Ph2-C≡C-Te1-CH₂CH₂-Ph2-CN、R¹-Ph2-C≡C-Te1-CH₂CH₂-Ph3-CN、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np1-CN、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np2-CN、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np3-CN、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np4-CN、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph1-CN、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph2-CN、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph3-CN、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np1-CN、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np2-CN、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np3-CN、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np4-CN、
【００９１】
R¹-Ph3-C≡C-Te1-Ph1-CN、R¹-Ph3-C≡C-Te1-Ph2-CN、R¹-Ph3-C≡C-Te1-Ph3-CN、R¹-Ph3-C≡C-Te1-Np1-CN、R¹-Ph3-C≡C-Te1-Np2-CN、R¹-Ph3-C≡C-Te1-Np3-CN、R¹-Ph3-C≡C-Te1-Np4-CN、R¹-Ph3-C≡C-Te2-Ph1-CN、R¹-Ph3-C≡C-Te2-Ph2-CN、R¹-Ph3-C≡C-Te2-Ph3-CN、R¹-Ph3-C≡C-Te2-Np1-CN、R¹-Ph3-C≡C-Te2-Np2-CN、R¹-Ph3-C≡C-Te2-Np3-CN、R¹-Ph3-C≡C-Te2-Np4-CN、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph2-CN、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph3-CN、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np1-CN、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np2-CN、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np3-CN、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np4-CN、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph1-CN、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph2-CN、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph3-CN、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np1-CN、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np2-CN、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np3-CN、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np4-CN、
【００９２】
R¹-Np1-C≡C-Te1-Ph1-CN、R¹-Np1-C≡C-Te1-Ph2-CN、R¹-Np1-C≡C-Te1-Ph3-CN、R¹-Np1-C≡C-Te1-Np1-CN、R¹-Np1-C≡C-Te1-Np2-CN、R¹-Np1-C≡C-Te1-Np3-CN、R¹-Np1-C≡C-Te1-Np4-CN、R¹-Np1-C≡C-Te2-Ph1-CN、R¹-Np1-C≡C-Te2-Ph2-CN、R¹-Np1-C≡C-Te2-Ph3-CN、R¹-Np1-C≡C-Te2-Np1-CN、R¹-Np1-C≡C-Te2-Np2-CN、R¹-Np1-C≡C-Te2-Np3-CN、R¹-Np1-C≡C-Te2-Np4-CN、R¹-Np1-C≡C-Te1-CH₂CH₂-Ph2-CN、R¹-Np1-C≡C-Te1-CH₂CH₂-Ph3-CN、R¹-Np1-C≡C-Te1-CH₂CH₂-Np1-CN、R¹-Np1-C≡C-Te1-CH₂CH₂-Np2-CN、R¹-Np1-C≡C-Te1-CH₂CH₂-Np3-CN、R¹-Np1-C≡C-Te1-CH₂CH₂-Np4-CN、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph1-CN、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph2-CN、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph3-CN、R¹-Np1-C≡C-Te2-CH₂CH₂-Np1-CN、R¹-Np1-C≡C-Te2-CH₂CH₂-Np2-CN、R¹-Np1-C≡C-Te2-CH₂CH₂-Np3-CN、R¹-Np1-C≡C-Te2-CH₂CH₂-Np4-CN、
【００９３】
R¹-Np2-C≡C-Te1-Ph1-CN、R¹-Np2-C≡C-Te1-Ph2-CN、R¹-Np2-C≡C-Te1-Ph3-CN、R¹-Np2-C≡C-Te1-Np1-CN、R¹-Np2-C≡C-Te1-Np2-CN、R¹-Np2-C≡C-Te1-Np3-CN、R¹-Np2-C≡C-Te1-Np4-CN、R¹-Np2-C≡C-Te2-Ph1-CN、R¹-Np2-C≡C-Te2-Ph2-CN、R¹-Np2-C≡C-Te2-Ph3-CN、R¹-Np2-C≡C-Te2-Np1-CN、R¹-Np2-C≡C-Te2-Np2-CN、R¹-Np2-C≡C-Te2-Np3-CN、R¹-Np2-C≡C-Te2-Np4-CN、R¹-Np2-C≡C-Te1-CH₂CH₂-Ph2-CN、R¹-Np2-C≡C-Te1-CH₂CH₂-Ph3-CN、R¹-Np2-C≡C-Te1-CH₂CH₂-Np1-CN、R¹-Np2-C≡C-Te1-CH₂CH₂-Np2-CN、R¹-Np2-C≡C-Te1-CH₂CH₂-Np3-CN、R¹-Np2-C≡C-Te1-CH₂CH₂-Np4-CN、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph1-CN、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph2-CN、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph3-CN、R¹-Np2-C≡C-Te2-CH₂CH₂-Np1-CN、R¹-Np2-C≡C-Te2-CH₂CH₂-Np2-CN、R¹-Np2-C≡C-Te2-CH₂CH₂-Np3-CN、R¹-Np2-C≡C-Te2-CH₂CH₂-Np4-CN、
【００９４】
R¹-Np3-C≡C-Te1-Ph1-CN、R¹-Np3-C≡C-Te1-Ph2-CN、R¹-Np3-C≡C-Te1-Ph3-CN、R¹-Np3-C≡C-Te1-Np1-CN、R¹-Np3-C≡C-Te1-Np2-CN、R¹-Np3-C≡C-Te1-Np3-CN、R¹-Np3-C≡C-Te1-Np4-CN、R¹-Np3-C≡C-Te2-Ph1-CN、R¹-Np3-C≡C-Te2-Ph2-CN、R¹-Np3-C≡C-Te2-Ph3-CN、R¹-Np3-C≡C-Te2-Np1-CN、R¹-Np3-C≡C-Te2-Np2-CN、R¹-Np3-C≡C-Te2-Np3-CN、R¹-Np3-C≡C-Te2-Np4-CN、R¹-Np3-C≡C-Te1-CH₂CH₂-Ph2-CN、R¹-Np3-C≡C-Te1-CH₂CH₂-Ph3-CN、R¹-Np3-C≡C-Te1-CH₂CH₂-Np1-CN、R¹-Np3-C≡C-Te1-CH₂CH₂-Np2-CN、R¹-Np3-C≡C-Te1-CH₂CH₂-Np3-CN、R¹-Np3-C≡C-Te1-CH₂CH₂-Np4-CN、R¹-Np3-C≡C-Te2-CH₂CH₂-Ph1-CN、R¹-Np3-C≡C-Te2-CH₂CH₂-Ph2-CN、R¹-Np3-C≡C-Te2-CH₂CH₂-Ph3-CN、R¹-Np3-C≡C-Te2-CH₂CH₂-Np1-CN、R¹-Np3-C≡C-Te2-CH₂CH₂-Np2-CN、R¹-Np3-C≡C-Te2-CH₂CH₂-Np3-CN、R¹-Np3-C≡C-Te2-CH₂CH₂-Np4-CN、
【００９５】
R¹-Np4-C≡C-Te1-Ph1-CN、R¹-Np4-C≡C-Te1-Ph2-CN、R¹-Np4-C≡C-Te1-Ph3-CN、R¹-Np4-C≡C-Te1-Np1-CN、R¹-Np4-C≡C-Te1-Np2-CN、R¹-Np4-C≡C-Te1-Np3-CN、R¹-Np4-C≡C-Te1-Np4-CN、R¹-Np4-C≡C-Te2-Ph1-CN、R¹-Np4-C≡C-Te2-Ph2-CN、R¹-Np4-C≡C-Te2-Ph3-CN、R¹-Np4-C≡C-Te2-Np1-CN、R¹-Np4-C≡C-Te2-Np2-CN、R¹-Np4-C≡C-Te2-Np3-CN、R¹-Np4-C≡C-Te2-Np4-CN、R¹-Np4-C≡C-Te1-CH₂CH₂-Ph2-CN、R¹-Np4-C≡C-Te1-CH₂CH₂-Ph3-CN、R¹-Np4-C≡C-Te1-CH₂CH₂-Np1-CN、R¹-Np4-C≡C-Te1-CH₂CH₂-Np2-CN、R¹-Np4-C≡C-Te1-CH₂CH₂-Np3-CN、R¹-Np4-C≡C-Te1-CH₂CH₂-Np4-CN、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph1-CN、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph2-CN、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph3-CN、R¹-Np4-C≡C-Te2-CH₂CH₂-Np1-CN、R¹-Np4-C≡C-Te2-CH₂CH₂-Np2-CN、R¹-Np4-C≡C-Te2-CH₂CH₂-Np3-CN、R¹-Np4-C≡C-Te2-CH₂CH₂-Np4-CN、
【００９６】
m=1、n=0、Vが単結合、Zがトリフルオロメトキシ基の場合、
【００９７】
R¹-Cy-Te1-Ph1-OCF₃、R¹-Cy-Te1-Ph2-OCF₃、R¹-Cy-Te1-Ph3-OCF₃、R¹-Cy-Te1-Np1-OCF₃、R¹-Cy-Te1-Np2-OCF₃、R¹-Cy-Te1-Ph3-OCF₃、R¹-Cy-Te1-Np4-OCF₃、R¹-Cy-Te2-Ph1-OCF₃、R¹-Cy-Te2-Ph2-OCF₃、R¹-Cy-Te2-Ph3-OCF₃、R¹-Cy-Te2-Np1-OCF₃、R¹-Cy-Te2-Np2-OCF₃、R¹-Cy-Te2-Ph3-OCF₃、R¹-Cy-Te2-Np4-OCF₃、R¹-Cy-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Cy-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Cy-Te1-CH₂CH₂-Np1-OCF₃、R¹-Cy-Te1-CH₂CH₂-Np2-OCF₃、R¹-Cy-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Cy-Te1-CH₂CH₂-Np4-OCF₃、R¹-Cy-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Cy-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Cy-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Cy-Te2-CH₂CH₂-Np1-OCF₃、R¹-Cy-Te2-CH₂CH₂-Np2-OCF₃、R¹-Cy-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Cy-Te2-CH₂CH₂-Np4-OCF₃、
【００９８】
R¹-Ph1-Te1-Ph1-OCF₃、R¹-Ph1-Te1-Ph2-OCF₃、R¹-Ph1-Te1-Ph3-OCF₃、R¹-Ph1-Te1-Np1-OCF₃、R¹-Ph1-Te1-Np2-OCF₃、R¹-Ph1-Te1-Ph3-OCF₃、R¹-Ph1-Te1-Np4-OCF₃、R¹-Ph1-Te2-Ph1-OCF₃、R¹-Ph1-Te2-Ph2-OCF₃、R¹-Ph1-Te2-Ph3-OCF₃、R¹-Ph1-Te2-Np1-OCF₃、R¹-Ph1-Te2-Np2-OCF₃、R¹-Ph1-Te2-Ph3-OCF₃、R¹-Ph1-Te2-Np4-OCF₃、R¹-Ph1-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph1-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph1-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph1-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph1-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph1-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph1-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph1-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph1-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-Te2-CH₂CH₂-Np4-OCF₃、
【００９９】
R¹-Ph2-Te1-Ph1-OCF₃、R¹-Ph2-Te1-Ph2-OCF₃、R¹-Ph2-Te1-Ph3-OCF₃、R¹-Ph2-Te1-Np1-OCF₃、R¹-Ph2-Te1-Np2-OCF₃、R¹-Ph2-Te1-Ph3-OCF₃、R¹-Ph2-Te1-Np4-OCF₃、R¹-Ph2-Te2-Ph1-OCF₃、R¹-Ph2-Te2-Ph2-OCF₃、R¹-Ph2-Te2-Ph3-OCF₃、R¹-Ph2-Te2-Np1-OCF₃、R¹-Ph2-Te2-Np2-OCF₃、R¹-Ph2-Te2-Ph3-OCF₃、R¹-Ph2-Te2-Np4-OCF₃、R¹-Ph2-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph2-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph2-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph2-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph2-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph2-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph2-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph2-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph2-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-Te2-CH₂CH₂-Np4-OCF₃、
【０１００】
R¹-Ph3-Te1-Ph1-OCF₃、R¹-Ph3-Te1-Ph2-OCF₃、R¹-Ph3-Te1-Ph3-OCF₃、R¹-Ph3-Te1-Np1-OCF₃、R¹-Ph3-Te1-Np2-OCF₃、R¹-Ph3-Te1-Ph3-OCF₃、R¹-Ph3-Te1-Np4-OCF₃、R¹-Ph3-Te2-Ph1-OCF₃、R¹-Ph3-Te2-Ph2-OCF₃、R¹-Ph3-Te2-Ph3-OCF₃、R¹-Ph3-Te2-Np1-OCF₃、R¹-Ph3-Te2-Np2-OCF₃、R¹-Ph3-Te2-Ph3-OCF₃、R¹-Ph3-Te2-Np4-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Np4-OCF₃、
【０１０１】
R¹-Np1-Te1-Ph1-OCF₃、R¹-Np1-Te1-Ph2-OCF₃、R¹-Np1-Te1-Ph3-OCF₃、R¹-Np1-Te1-Np1-OCF₃、R¹-Np1-Te1-Np2-OCF₃、R¹-Np1-Te1-Ph3-OCF₃、R¹-Np1-Te1-Np4-OCF₃、R¹-Np1-Te2-Ph1-OCF₃、R¹-Np1-Te2-Ph2-OCF₃、R¹-Np1-Te2-Ph3-OCF₃、R¹-Np1-Te2-Np1-OCF₃、R¹-Np1-Te2-Np2-OCF₃、R¹-Np1-Te2-Ph3-OCF₃、R¹-Np1-Te2-Np4-OCF₃、R¹-Np1-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np1-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np1-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np1-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np1-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np1-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np1-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np1-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np1-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np1-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np1-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np1-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np1-Te2-CH₂CH₂-Np4-OCF₃、
【０１０２】
R¹-Np2-Te1-Ph1-OCF₃、R¹-Np2-Te1-Ph2-OCF₃、R¹-Np2-Te1-Ph3-OCF₃、R¹-Np2-Te1-Np1-OCF₃、R¹-Np2-Te1-Np2-OCF₃、R¹-Np2-Te1-Ph3-OCF₃、R¹-Np2-Te1-Np4-OCF₃、R¹-Np2-Te2-Ph1-OCF₃、R¹-Np2-Te2-Ph2-OCF₃、R¹-Np2-Te2-Ph3-OCF₃、R¹-Np2-Te2-Np1-OCF₃、R¹-Np2-Te2-Np2-OCF₃、R¹-Np2-Te2-Ph3-OCF₃、R¹-Np2-Te2-Np4-OCF₃、R¹-Np2-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np2-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np2-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np2-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np2-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np2-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np2-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np2-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np2-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np2-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np2-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np2-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np2-Te2-CH₂CH₂-Np4-OCF₃、
【０１０３】
R¹-Ph3-Te1-Ph1-OCF₃、R¹-Ph3-Te1-Ph2-OCF₃、R¹-Ph3-Te1-Ph3-OCF₃、R¹-Ph3-Te1-Np1-OCF₃、R¹-Ph3-Te1-Np2-OCF₃、R¹-Ph3-Te1-Ph3-OCF₃、R¹-Ph3-Te1-Np4-OCF₃、R¹-Ph3-Te2-Ph1-OCF₃、R¹-Ph3-Te2-Ph2-OCF₃、R¹-Ph3-Te2-Ph3-OCF₃、R¹-Ph3-Te2-Np1-OCF₃、R¹-Ph3-Te2-Np2-OCF₃、R¹-Ph3-Te2-Ph3-OCF₃、R¹-Ph3-Te2-Np4-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-Te2-CH₂CH₂-Np4-OCF₃、
【０１０４】
R¹-Np4-Te1-Ph1-OCF₃、R¹-Np4-Te1-Ph2-OCF₃、R¹-Np4-Te1-Ph3-OCF₃、R¹-Np4-Te1-Np1-OCF₃、R¹-Np4-Te1-Np2-OCF₃、R¹-Np4-Te1-Ph3-OCF₃、R¹-Np4-Te1-Np4-OCF₃、R¹-Np4-Te2-Ph1-OCF₃、R¹-Np4-Te2-Ph2-OCF₃、R¹-Np4-Te2-Ph3-OCF₃、R¹-Np4-Te2-Np1-OCF₃、R¹-Np4-Te2-Np2-OCF₃、R¹-Np4-Te2-Ph3-OCF₃、R¹-Np4-Te2-Np4-OCF₃、R¹-Np4-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np4-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np4-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np4-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np4-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np4-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np4-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np4-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np4-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np4-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np4-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np4-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np4-Te2-CH₂CH₂-Np4-OCF₃、
【０１０５】
R¹-Cy-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Cy-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Cy-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te1-Np1-OCF₃、R¹-Cy-CH₂CH₂-Te1-Np2-OCF₃、R¹-Cy-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te1-Np4-OCF₃、R¹-Cy-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Cy-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Cy-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te2-Np1-OCF₃、R¹-Cy-CH₂CH₂-Te2-Np2-OCF₃、R¹-Cy-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te2-Np4-OCF₃、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Cy-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１０６】
R¹-Ph1-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Ph1-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Ph1-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te1-Np1-OCF₃、R¹-Ph1-CH₂CH₂-Te1-Np2-OCF₃、R¹-Ph1-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te1-Np4-OCF₃、R¹-Ph1-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Ph1-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Ph1-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te2-Np1-OCF₃、R¹-Ph1-CH₂CH₂-Te2-Np2-OCF₃、R¹-Ph1-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te2-Np4-OCF₃、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１０７】
R¹-Ph2-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Ph2-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Ph2-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te1-Np1-OCF₃、R¹-Ph2-CH₂CH₂-Te1-Np2-OCF₃、R¹-Ph2-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te1-Np4-OCF₃、R¹-Ph2-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Ph2-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Ph2-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te2-Np1-OCF₃、R¹-Ph2-CH₂CH₂-Te2-Np2-OCF₃、R¹-Ph2-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te2-Np4-OCF₃、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１０８】
R¹-Ph3-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Np4-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Np4-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１０９】
R¹-Np1-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Np1-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Np1-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te1-Np1-OCF₃、R¹-Np1-CH₂CH₂-Te1-Np2-OCF₃、R¹-Np1-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te1-Np4-OCF₃、R¹-Np1-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Np1-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Np1-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te2-Np1-OCF₃、R¹-Np1-CH₂CH₂-Te2-Np2-OCF₃、R¹-Np1-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te2-Np4-OCF₃、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np1-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１１０】
R¹-Np2-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Np2-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Np2-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te1-Np1-OCF₃、R¹-Np2-CH₂CH₂-Te1-Np2-OCF₃、R¹-Np2-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te1-Np4-OCF₃、R¹-Np2-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Np2-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Np2-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te2-Np1-OCF₃、R¹-Np2-CH₂CH₂-Te2-Np2-OCF₃、R¹-Np2-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te2-Np4-OCF₃、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np2-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１１１】
R¹-Ph3-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-Np4-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-Np4-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１１２】
R¹-Np4-CH₂CH₂-Te1-Ph1-OCF₃、R¹-Np4-CH₂CH₂-Te1-Ph2-OCF₃、R¹-Np4-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te1-Np1-OCF₃、R¹-Np4-CH₂CH₂-Te1-Np2-OCF₃、R¹-Np4-CH₂CH₂-Te1-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te1-Np4-OCF₃、R¹-Np4-CH₂CH₂-Te2-Ph1-OCF₃、R¹-Np4-CH₂CH₂-Te2-Ph2-OCF₃、R¹-Np4-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te2-Np1-OCF₃、R¹-Np4-CH₂CH₂-Te2-Np2-OCF₃、R¹-Np4-CH₂CH₂-Te2-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te2-Np4-OCF₃、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np4-CH₂CH₂-Te2-CH₂CH₂-Np4-OCF₃、
【０１１３】
R¹-Ph1-C≡C-Te1-Ph1-OCF₃、R¹-Ph1-C≡C-Te1-Ph2-OCF₃、R¹-Ph1-C≡C-Te1-Ph3-OCF₃、R¹-Ph1-C≡C-Te1-Np1-OCF₃、R¹-Ph1-C≡C-Te1-Np2-OCF₃、R¹-Ph1-C≡C-Te1-Ph3-OCF₃、R¹-Ph1-C≡C-Te1-Np4-OCF₃、R¹-Ph1-C≡C-Te2-Ph1-OCF₃、R¹-Ph1-C≡C-Te2-Ph2-OCF₃、R¹-Ph1-C≡C-Te2-Ph3-OCF₃、R¹-Ph1-C≡C-Te2-Np1-OCF₃、R¹-Ph1-C≡C-Te2-Np2-OCF₃、R¹-Ph1-C≡C-Te2-Ph3-OCF₃、R¹-Ph1-C≡C-Te2-Np4-OCF₃、R¹-Ph1-C≡C-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph1-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph1-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-C≡C-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph1-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph1-C≡C-Te2-CH₂CH₂-Np4-OCF₃、
【０１１４】
R¹-Ph2-C≡C-Te1-Ph1-OCF₃、R¹-Ph2-C≡C-Te1-Ph2-OCF₃、R¹-Ph2-C≡C-Te1-Ph3-OCF₃、R¹-Ph2-C≡C-Te1-Np1-OCF₃、R¹-Ph2-C≡C-Te1-Np2-OCF₃、R¹-Ph2-C≡C-Te1-Ph3-OCF₃、R¹-Ph2-C≡C-Te1-Np4-OCF₃、R¹-Ph2-C≡C-Te2-Ph1-OCF₃、R¹-Ph2-C≡C-Te2-Ph2-OCF₃、R¹-Ph2-C≡C-Te2-Ph3-OCF₃、R¹-Ph2-C≡C-Te2-Np1-OCF₃、R¹-Ph2-C≡C-Te2-Np2-OCF₃、R¹-Ph2-C≡C-Te2-Ph3-OCF₃、R¹-Ph2-C≡C-Te2-Np4-OCF₃、R¹-Ph2-C≡C-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph2-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph2-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-C≡C-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph2-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph2-C≡C-Te2-CH₂CH₂-Np4-OCF₃、
【０１１５】
R¹-Ph3-C≡C-Te1-Ph1-OCF₃、R¹-Ph3-C≡C-Te1-Ph2-OCF₃、R¹-Ph3-C≡C-Te1-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-Np1-OCF₃、R¹-Ph3-C≡C-Te1-Np2-OCF₃、R¹-Ph3-C≡C-Te1-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-Np4-OCF₃、R¹-Ph3-C≡C-Te2-Ph1-OCF₃、R¹-Ph3-C≡C-Te2-Ph2-OCF₃、R¹-Ph3-C≡C-Te2-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-Np1-OCF₃、R¹-Ph3-C≡C-Te2-Np2-OCF₃、R¹-Ph3-C≡C-Te2-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-Np4-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np4-OCF₃、
【０１１６】
R¹-Np1-C≡C-Te1-Ph1-OCF₃、R¹-Np1-C≡C-Te1-Ph2-OCF₃、R¹-Np1-C≡C-Te1-Ph3-OCF₃、R¹-Np1-C≡C-Te1-Np1-OCF₃、R¹-Np1-C≡C-Te1-Np2-OCF₃、R¹-Np1-C≡C-Te1-Ph3-OCF₃、R¹-Np1-C≡C-Te1-Np4-OCF₃、R¹-Np1-C≡C-Te2-Ph1-OCF₃、R¹-Np1-C≡C-Te2-Ph2-OCF₃、R¹-Np1-C≡C-Te2-Ph3-OCF₃、R¹-Np1-C≡C-Te2-Np1-OCF₃、R¹-Np1-C≡C-Te2-Np2-OCF₃、R¹-Np1-C≡C-Te2-Ph3-OCF₃、R¹-Np1-C≡C-Te2-Np4-OCF₃、R¹-Np1-C≡C-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np1-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np1-C≡C-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np1-C≡C-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np1-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np1-C≡C-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np1-C≡C-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np1-C≡C-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np1-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np1-C≡C-Te2-CH₂CH₂-Np4-OCF₃、
【０１１７】
R¹-Np2-C≡C-Te1-Ph1-OCF₃、R¹-Np2-C≡C-Te1-Ph2-OCF₃、R¹-Np2-C≡C-Te1-Ph3-OCF₃、R¹-Np2-C≡C-Te1-Np1-OCF₃、R¹-Np2-C≡C-Te1-Np2-OCF₃、R¹-Np2-C≡C-Te1-Ph3-OCF₃、R¹-Np2-C≡C-Te1-Np4-OCF₃、R¹-Np2-C≡C-Te2-Ph1-OCF₃、R¹-Np2-C≡C-Te2-Ph2-OCF₃、R¹-Np2-C≡C-Te2-Ph3-OCF₃、R¹-Np2-C≡C-Te2-Np1-OCF₃、R¹-Np2-C≡C-Te2-Np2-OCF₃、R¹-Np2-C≡C-Te2-Ph3-OCF₃、R¹-Np2-C≡C-Te2-Np4-OCF₃、R¹-Np2-C≡C-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np2-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np2-C≡C-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np2-C≡C-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np2-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np2-C≡C-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np2-C≡C-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np2-C≡C-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np2-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np2-C≡C-Te2-CH₂CH₂-Np4-OCF₃、
【０１１８】
R¹-Ph3-C≡C-Te1-Ph1-OCF₃、R¹-Ph3-C≡C-Te1-Ph2-OCF₃、R¹-Ph3-C≡C-Te1-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-Np1-OCF₃、R¹-Ph3-C≡C-Te1-Np2-OCF₃、R¹-Ph3-C≡C-Te1-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-Np4-OCF₃、R¹-Ph3-C≡C-Te2-Ph1-OCF₃、R¹-Ph3-C≡C-Te2-Ph2-OCF₃、R¹-Ph3-C≡C-Te2-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-Np1-OCF₃、R¹-Ph3-C≡C-Te2-Np2-OCF₃、R¹-Ph3-C≡C-Te2-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-Np4-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np1-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np2-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te1-CH₂CH₂-Np4-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np1-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np2-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Ph3-C≡C-Te2-CH₂CH₂-Np4-OCF₃、
【０１１９】
R¹-Np4-C≡C-Te1-Ph1-OCF₃、R¹-Np4-C≡C-Te1-Ph2-OCF₃、R¹-Np4-C≡C-Te1-Ph3-OCF₃、R¹-Np4-C≡C-Te1-Np1-OCF₃、R¹-Np4-C≡C-Te1-Np2-OCF₃、R¹-Np4-C≡C-Te1-Ph3-OCF₃、R¹-Np4-C≡C-Te1-Np4-OCF₃、R¹-Np4-C≡C-Te2-Ph1-OCF₃、R¹-Np4-C≡C-Te2-Ph2-OCF₃、R¹-Np4-C≡C-Te2-Ph3-OCF₃、R¹-Np4-C≡C-Te2-Np1-OCF₃、R¹-Np4-C≡C-Te2-Np2-OCF₃、R¹-Np4-C≡C-Te2-Ph3-OCF₃、R¹-Np4-C≡C-Te2-Np4-OCF₃、R¹-Np4-C≡C-Te1-CH₂CH₂-Ph2-OCF₃、R¹-Np4-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np4-C≡C-Te1-CH₂CH₂-Np1-OCF₃、R¹-Np4-C≡C-Te1-CH₂CH₂-Np2-OCF₃、R¹-Np4-C≡C-Te1-CH₂CH₂-Ph3-OCF₃、R¹-Np4-C≡C-Te1-CH₂CH₂-Np4-OCF₃、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph1-OCF₃、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph2-OCF₃、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np4-C≡C-Te2-CH₂CH₂-Np1-OCF₃、R¹-Np4-C≡C-Te2-CH₂CH₂-Np2-OCF₃、R¹-Np4-C≡C-Te2-CH₂CH₂-Ph3-OCF₃、R¹-Np4-C≡C-Te2-CH₂CH₂-Np4-OCF₃、
【０１２０】
m=0、n=1、Vが単結合、Zがフッ素原子の場合、
【０１２１】
R¹-Te1-Cy-Ph1-F、R¹-Te1-Cy-Ph2-F、R¹-Te1-Cy-Ph3-F、R¹-Te1-Cy-Np1-F、R¹-Te1-Cy-Np2-F、R¹-Te1-Cy-Np3-F、R¹-Te1-Cy-Np4-F、R¹-Te2-Cy-Ph1-F、R¹-Te2-Cy-Ph2-F、R¹-Te2-Cy-Ph3-F、R¹-Te2-Cy-Np1-F、R¹-Te2-Cy-Np2-F、R¹-Te2-Cy-Np3-F、R¹-Te2-Cy-Np4-F、R¹-Te1-Cy-CH₂CH₂-Ph2-F、R¹-Te1-Cy-CH₂CH₂-Ph3-F、R¹-Te1-Cy-CH₂CH₂-Np1-F、R¹-Te1-Cy-CH₂CH₂-Np2-F、R¹-Te1-Cy-CH₂CH₂-Np3-F、R¹-Te1-Cy-CH₂CH₂-Np4-F、R¹-Te2-Cy-CH₂CH₂-Ph1-F、R¹-Te2-Cy-CH₂CH₂-Ph2-F、R¹-Te2-Cy-CH₂CH₂-Ph3-F、R¹-Te2-Cy-CH₂CH₂-Np1-F、R¹-Te2-Cy-CH₂CH₂-Np2-F、R¹-Te2-Cy-CH₂CH₂-Np3-F、R¹-Te2-Cy-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Cy-Ph1-F、R¹-Te1-CH₂CH₂-Cy-Ph2-F、R¹-Te1-CH₂CH₂-Cy-Ph3-F、R¹-Te1-CH₂CH₂-Cy-Np1-F、R¹-Te1-CH₂CH₂-Cy-Np2-F、R¹-Te1-CH₂CH₂-Cy-Np3-F、R¹-Te1-CH₂CH₂-Cy-Np4-F、R¹-Te2-CH₂CH₂-Cy-Ph1-F、R¹-Te2-CH₂CH₂-Cy-Ph2-F、R¹-Te2-CH₂CH₂-Cy-Ph3-F、R¹-Te2-CH₂CH₂-Cy-Np1-F、R¹-Te2-CH₂CH₂-Cy-Np2-F、R¹-Te2-CH₂CH₂-Cy-Np3-F、R¹-Te2-CH₂CH₂-Cy-Np4-F、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np4-F、
【０１２２】
R¹-Te1-Ph1-Ph1-F、R¹-Te1-Ph1-Ph2-F、R¹-Te1-Ph1-Ph3-F、R¹-Te1-Ph1-Np1-F、R¹-Te1-Ph1-Np2-F、R¹-Te1-Ph1-Np3-F、R¹-Te1-Ph1-Np4-F、R¹-Te2-Ph1-Ph1-F、R¹-Te2-Ph1-Ph2-F、R¹-Te2-Ph1-Ph3-F、R¹-Te2-Ph1-Np1-F、R¹-Te2-Ph1-Np2-F、R¹-Te2-Ph1-Np3-F、R¹-Te2-Ph1-Np4-F、R¹-Te1-Ph1-CH₂CH₂-Ph2-F、R¹-Te1-Ph1-CH₂CH₂-Ph3-F、R¹-Te1-Ph1-CH₂CH₂-Np1-F、R¹-Te1-Ph1-CH₂CH₂-Np2-F、R¹-Te1-Ph1-CH₂CH₂-Np3-F、R¹-Te1-Ph1-CH₂CH₂-Np4-F、R¹-Te2-Ph1-CH₂CH₂-Ph1-F、R¹-Te2-Ph1-CH₂CH₂-Ph2-F、R¹-Te2-Ph1-CH₂CH₂-Ph3-F、R¹-Te2-Ph1-CH₂CH₂-Np1-F、R¹-Te2-Ph1-CH₂CH₂-Np2-F、R¹-Te2-Ph1-CH₂CH₂-Np3-F、R¹-Te2-Ph1-CH₂CH₂-Np4-F、R¹-Te1-Ph1-C≡C-Ph2-F、R¹-Te1-Ph1-C≡C-Ph3-F、R¹-Te1-Ph1-C≡C-Np1-F、R¹-Te1-Ph1-C≡C-Np2-F、R¹-Te1-Ph1-C≡C-Np3-F、R¹-Te1-Ph1-C≡C-Np4-F、R¹-Te2-Ph1-C≡C-Ph1-F、R¹-Te2-Ph1-C≡C-Ph2-F、R¹-Te2-Ph1-C≡C-Ph3-F、R¹-Te2-Ph1-C≡C-Np1-F、R¹-Te2-Ph1-C≡C-Np2-F、R¹-Te2-Ph1-C≡C-Np3-F、R¹-Te2-Ph1-C≡C-Np4-F、
【０１２３】
R¹-Te1-Ph2-Ph1-F、R¹-Te1-Ph2-Ph2-F、R¹-Te1-Ph2-Ph3-F、R¹-Te1-Ph2-Np1-F、R¹-Te1-Ph2-Np2-F、R¹-Te1-Ph2-Np3-F、R¹-Te1-Ph2-Np4-F、R¹-Te2-Ph2-Ph1-F、R¹-Te2-Ph2-Ph2-F、R¹-Te2-Ph2-Ph3-F、R¹-Te2-Ph2-Np1-F、R¹-Te2-Ph2-Np2-F、R¹-Te2-Ph2-Np3-F、R¹-Te2-Ph2-Np4-F、R¹-Te1-Ph2-CH₂CH₂-Ph2-F、R¹-Te1-Ph2-CH₂CH₂-Ph3-F、R¹-Te1-Ph2-CH₂CH₂-Np1-F、R¹-Te1-Ph2-CH₂CH₂-Np2-F、R¹-Te1-Ph2-CH₂CH₂-Np3-F、R¹-Te1-Ph2-CH₂CH₂-Np4-F、R¹-Te2-Ph2-CH₂CH₂-Ph1-F、R¹-Te2-Ph2-CH₂CH₂-Ph2-F、R¹-Te2-Ph2-CH₂CH₂-Ph3-F、R¹-Te2-Ph2-CH₂CH₂-Np1-F、R¹-Te2-Ph2-CH₂CH₂-Np2-F、R¹-Te2-Ph2-CH₂CH₂-Np3-F、R¹-Te2-Ph2-CH₂CH₂-Np4-F、R¹-Te1-Ph2-C≡C-Ph2-F、R¹-Te1-Ph2-C≡C-Ph3-F、R¹-Te1-Ph2-C≡C-Np1-F、R¹-Te1-Ph2-C≡C-Np2-F、R¹-Te1-Ph2-C≡C-Np3-F、R¹-Te1-Ph2-C≡C-Np4-F、R¹-Te2-Ph2-C≡C-Ph1-F、R¹-Te2-Ph2-C≡C-Ph2-F、R¹-Te2-Ph2-C≡C-Ph3-F、R¹-Te2-Ph2-C≡C-Np1-F、R¹-Te2-Ph2-C≡C-Np2-F、R¹-Te2-Ph2-C≡C-Np3-F、R¹-Te2-Ph2-C≡C-Np4-F、
【０１２４】
R¹-Te1-Ph3-Ph1-F、R¹-Te1-Ph3-Ph2-F、R¹-Te1-Ph3-Ph3-F、R¹-Te1-Ph3-Np1-F、R¹-Te1-Ph3-Np2-F、R¹-Te1-Ph3-Np3-F、R¹-Te1-Ph3-Np4-F、R¹-Te2-Ph3-Ph1-F、R¹-Te2-Ph3-Ph2-F、R¹-Te2-Ph3-Ph3-F、R¹-Te2-Ph3-Np1-F、R¹-Te2-Ph3-Np2-F、R¹-Te2-Ph3-Np3-F、R¹-Te2-Ph3-Np4-F、R¹-Te1-Ph3-CH₂CH₂-Ph2-F、R¹-Te1-Ph3-CH₂CH₂-Ph3-F、R¹-Te1-Ph3-CH₂CH₂-Np1-F、R¹-Te1-Ph3-CH₂CH₂-Np2-F、R¹-Te1-Ph3-CH₂CH₂-Np3-F、R¹-Te1-Ph3-CH₂CH₂-Np4-F、R¹-Te2-Ph3-CH₂CH₂-Ph1-F、R¹-Te2-Ph3-CH₂CH₂-Ph2-F、R¹-Te2-Ph3-CH₂CH₂-Ph3-F、R¹-Te2-Ph3-CH₂CH₂-Np1-F、R¹-Te2-Ph3-CH₂CH₂-Np2-F、R¹-Te2-Ph3-CH₂CH₂-Np3-F、R¹-Te2-Ph3-CH₂CH₂-Np4-F、R¹-Te1-Ph3-C≡C-Ph2-F、R¹-Te1-Ph3-C≡C-Ph3-F、R¹-Te1-Ph3-C≡C-Np1-F、R¹-Te1-Ph3-C≡C-Np2-F、R¹-Te1-Ph3-C≡C-Np3-F、R¹-Te1-Ph3-C≡C-Np4-F、R¹-Te2-Ph3-C≡C-Ph1-F、R¹-Te2-Ph3-C≡C-Ph2-F、R¹-Te2-Ph3-C≡C-Ph3-F、R¹-Te2-Ph3-C≡C-Np1-F、R¹-Te2-Ph3-C≡C-Np2-F、R¹-Te2-Ph3-C≡C-Np3-F、R¹-Te2-Ph3-C≡C-Np4-F、
【０１２５】
R¹-Te1-Np1-Ph1-F、R¹-Te1-Np1-Ph2-F、R¹-Te1-Np1-Ph3-F、R¹-Te1-Np1-Np1-F、R¹-Te1-Np1-Np2-F、R¹-Te1-Np1-Np3-F、R¹-Te1-Np1-Np4-F、R¹-Te2-Np1-Ph1-F、R¹-Te2-Np1-Ph2-F、R¹-Te2-Np1-Ph3-F、R¹-Te2-Np1-Np1-F、R¹-Te2-Np1-Np2-F、R¹-Te2-Np1-Np3-F、R¹-Te2-Np1-Np4-F、R¹-Te1-Np1-CH₂CH₂-Ph2-F、R¹-Te1-Np1-CH₂CH₂-Ph3-F、R¹-Te1-Np1-CH₂CH₂-Np1-F、R¹-Te1-Np1-CH₂CH₂-Np2-F、R¹-Te1-Np1-CH₂CH₂-Np3-F、R¹-Te1-Np1-CH₂CH₂-Np4-F、R¹-Te2-Np1-CH₂CH₂-Ph1-F、R¹-Te2-Np1-CH₂CH₂-Ph2-F、R¹-Te2-Np1-CH₂CH₂-Ph3-F、R¹-Te2-Np1-CH₂CH₂-Np1-F、R¹-Te2-Np1-CH₂CH₂-Np2-F、R¹-Te2-Np1-CH₂CH₂-Np3-F、R¹-Te2-Np1-CH₂CH₂-Np4-F、R¹-Te1-Np1-C≡C-Ph2-F、R¹-Te1-Np1-C≡C-Ph3-F、R¹-Te1-Np1-C≡C-Np1-F、R¹-Te1-Np1-C≡C-Np2-F、R¹-Te1-Np1-C≡C-Np3-F、R¹-Te1-Np1-C≡C-Np4-F、R¹-Te2-Np1-C≡C-Ph1-F、R¹-Te2-Np1-C≡C-Ph2-F、R¹-Te2-Np1-C≡C-Ph3-F、R¹-Te2-Np1-C≡C-Np1-F、R¹-Te2-Np1-C≡C-Np2-F、R¹-Te2-Np1-C≡C-Np3-F、R¹-Te2-Np1-C≡C-Np4-F、
【０１２６】
R¹-Te1-Np2-Ph1-F、R¹-Te1-Np2-Ph2-F、R¹-Te1-Np2-Ph3-F、R¹-Te1-Np2-Np1-F、R¹-Te1-Np2-Np2-F、R¹-Te1-Np2-Np3-F、R¹-Te1-Np2-Np4-F、R¹-Te2-Np2-Ph1-F、R¹-Te2-Np2-Ph2-F、R¹-Te2-Np2-Ph3-F、R¹-Te2-Np2-Np1-F、R¹-Te2-Np2-Np2-F、R¹-Te2-Np2-Np3-F、R¹-Te2-Np2-Np4-F、R¹-Te1-Np2-CH₂CH₂-Ph2-F、R¹-Te1-Np2-CH₂CH₂-Ph3-F、R¹-Te1-Np2-CH₂CH₂-Np1-F、R¹-Te1-Np2-CH₂CH₂-Np2-F、R¹-Te1-Np2-CH₂CH₂-Np3-F、R¹-Te1-Np2-CH₂CH₂-Np4-F、R¹-Te2-Np2-CH₂CH₂-Ph1-F、R¹-Te2-Np2-CH₂CH₂-Ph2-F、R¹-Te2-Np2-CH₂CH₂-Ph3-F、R¹-Te2-Np2-CH₂CH₂-Np1-F、R¹-Te2-Np2-CH₂CH₂-Np2-F、R¹-Te2-Np2-CH₂CH₂-Np3-F、R¹-Te2-Np2-CH₂CH₂-Np4-F、R¹-Te1-Np2-C≡C-Ph2-F、R¹-Te1-Np2-C≡C-Ph3-F、R¹-Te1-Np2-C≡C-Np1-F、R¹-Te1-Np2-C≡C-Np2-F、R¹-Te1-Np2-C≡C-Np3-F、R¹-Te1-Np2-C≡C-Np4-F、R¹-Te2-Np2-C≡C-Ph1-F、R¹-Te2-Np2-C≡C-Ph2-F、R¹-Te2-Np2-C≡C-Ph3-F、R¹-Te2-Np2-C≡C-Np1-F、R¹-Te2-Np2-C≡C-Np2-F、R¹-Te2-Np2-C≡C-Np3-F、R¹-Te2-Np2-C≡C-Np4-F、
【０１２７】
R¹-Te1-Np3-Ph1-F、R¹-Te1-Np3-Ph2-F、R¹-Te1-Np3-Ph3-F、R¹-Te1-Np3-Np1-F、R¹-Te1-Np3-Np2-F、R¹-Te1-Np3-Np3-F、R¹-Te1-Np3-Np4-F、R¹-Te2-Np3-Ph1-F、R¹-Te2-Np3-Ph2-F、R¹-Te2-Np3-Ph3-F、R¹-Te2-Np3-Np1-F、R¹-Te2-Np3-Np2-F、R¹-Te2-Np3-Np3-F、R¹-Te2-Np3-Np4-F、R¹-Te1-Np3-CH₂CH₂-Ph2-F、R¹-Te1-Np3-CH₂CH₂-Ph3-F、R¹-Te1-Np3-CH₂CH₂-Np1-F、R¹-Te1-Np3-CH₂CH₂-Np2-F、R¹-Te1-Np3-CH₂CH₂-Np3-F、R¹-Te1-Np3-CH₂CH₂-Np4-F、R¹-Te2-Np3-CH₂CH₂-Ph1-F、R¹-Te2-Np3-CH₂CH₂-Ph2-F、R¹-Te2-Np3-CH₂CH₂-Ph3-F、R¹-Te2-Np3-CH₂CH₂-Np1-F、R¹-Te2-Np3-CH₂CH₂-Np2-F、R¹-Te2-Np3-CH₂CH₂-Np3-F、R¹-Te2-Np3-CH₂CH₂-Np4-F、R¹-Te1-Np3-C≡C-Ph2-F、R¹-Te1-Np3-C≡C-Ph3-F、R¹-Te1-Np3-C≡C-Np1-F、R¹-Te1-Np3-C≡C-Np2-F、R¹-Te1-Np3-C≡C-Np3-F、R¹-Te1-Np3-C≡C-Np4-F、R¹-Te2-Np3-C≡C-Ph1-F、R¹-Te2-Np3-C≡C-Ph2-F、R¹-Te2-Np3-C≡C-Ph3-F、R¹-Te2-Np3-C≡C-Np1-F、R¹-Te2-Np3-C≡C-Np2-F、R¹-Te2-Np3-C≡C-Np3-F、R¹-Te2-Np3-C≡C-Np4-F、
【０１２８】
R¹-Te1-Np4-Ph1-F、R¹-Te1-Np4-Ph2-F、R¹-Te1-Np4-Ph3-F、R¹-Te1-Np4-Np1-F、R¹-Te1-Np4-Np2-F、R¹-Te1-Np4-Np3-F、R¹-Te1-Np4-Np4-F、R¹-Te2-Np4-Ph1-F、R¹-Te2-Np4-Ph2-F、R¹-Te2-Np4-Ph3-F、R¹-Te2-Np4-Np1-F、R¹-Te2-Np4-Np2-F、R¹-Te2-Np4-Np3-F、R¹-Te2-Np4-Np4-F、R¹-Te1-Np4-CH₂CH₂-Ph2-F、R¹-Te1-Np4-CH₂CH₂-Ph3-F、R¹-Te1-Np4-CH₂CH₂-Np1-F、R¹-Te1-Np4-CH₂CH₂-Np2-F、R¹-Te1-Np4-CH₂CH₂-Np3-F、R¹-Te1-Np4-CH₂CH₂-Np4-F、R¹-Te2-Np4-CH₂CH₂-Ph1-F、R¹-Te2-Np4-CH₂CH₂-Ph2-F、R¹-Te2-Np4-CH₂CH₂-Ph3-F、R¹-Te2-Np4-CH₂CH₂-Np1-F、R¹-Te2-Np4-CH₂CH₂-Np2-F、R¹-Te2-Np4-CH₂CH₂-Np3-F、R¹-Te2-Np4-CH₂CH₂-Np4-F、R¹-Te1-Np4-C≡C-Ph2-F、R¹-Te1-Np4-C≡C-Ph3-F、R¹-Te1-Np4-C≡C-Np1-F、R¹-Te1-Np4-C≡C-Np2-F、R¹-Te1-Np4-C≡C-Np3-F、R¹-Te1-Np4-C≡C-Np4-F、R¹-Te2-Np4-C≡C-Ph1-F、R¹-Te2-Np4-C≡C-Ph2-F、R¹-Te2-Np4-C≡C-Ph3-F、R¹-Te2-Np4-C≡C-Np1-F、R¹-Te2-Np4-C≡C-Np2-F、R¹-Te2-Np4-C≡C-Np3-F、R¹-Te2-Np4-C≡C-Np4-F、
【０１２９】
R¹-Te1-CH₂CH₂-Ph1-Ph1-F、R¹-Te1-CH₂CH₂-Ph1-Ph2-F、R¹-Te1-CH₂CH₂-Ph1-Ph3-F、R¹-Te1-CH₂CH₂-Ph1-Np1-F、R¹-Te1-CH₂CH₂-Ph1-Np2-F、R¹-Te1-CH₂CH₂-Ph1-Np3-F、R¹-Te1-CH₂CH₂-Ph1-Np4-F、R¹-Te2-CH₂CH₂-Ph1-Ph1-F、R¹-Te2-CH₂CH₂-Ph1-Ph2-F、R¹-Te2-CH₂CH₂-Ph1-Ph3-F、R¹-Te2-CH₂CH₂-Ph1-Np1-F、R¹-Te2-CH₂CH₂-Ph1-Np2-F、R¹-Te2-CH₂CH₂-Ph1-Np3-F、R¹-Te2-CH₂CH₂-Ph1-Np4-F、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Ph1-C≡C-Ph2-F、R¹-Te1-CH₂CH₂-Ph1-C≡C-Ph3-F、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np1-F、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np2-F、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np3-F、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np4-F、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph1-F、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph2-F、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph3-F、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np1-F、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np2-F、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np3-F、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np4-F、
【０１３０】
R¹-Te1-CH₂CH₂-Ph2-Ph1-F、R¹-Te1-CH₂CH₂-Ph2-Ph2-F、R¹-Te1-CH₂CH₂-Ph2-Ph3-F、R¹-Te1-CH₂CH₂-Ph2-Np1-F、R¹-Te1-CH₂CH₂-Ph2-Np2-F、R¹-Te1-CH₂CH₂-Ph2-Np3-F、R¹-Te1-CH₂CH₂-Ph2-Np4-F、R¹-Te2-CH₂CH₂-Ph2-Ph1-F、R¹-Te2-CH₂CH₂-Ph2-Ph2-F、R¹-Te2-CH₂CH₂-Ph2-Ph3-F、R¹-Te2-CH₂CH₂-Ph2-Np1-F、R¹-Te2-CH₂CH₂-Ph2-Np2-F、R¹-Te2-CH₂CH₂-Ph2-Np3-F、R¹-Te2-CH₂CH₂-Ph2-Np4-F、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Ph2-C≡C-Ph2-F、R¹-Te1-CH₂CH₂-Ph2-C≡C-Ph3-F、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np1-F、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np2-F、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np3-F、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np4-F、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph1-F、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph2-F、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph3-F、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np1-F、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np2-F、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np3-F、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np4-F、
【０１３１】
R¹-Te1-CH₂CH₂-Ph3-Ph1-F、R¹-Te1-CH₂CH₂-Ph3-Ph2-F、R¹-Te1-CH₂CH₂-Ph3-Ph3-F、R¹-Te1-CH₂CH₂-Ph3-Np1-F、R¹-Te1-CH₂CH₂-Ph3-Np2-F、R¹-Te1-CH₂CH₂-Ph3-Np3-F、R¹-Te1-CH₂CH₂-Ph3-Np4-F、R¹-Te2-CH₂CH₂-Ph3-Ph1-F、R¹-Te2-CH₂CH₂-Ph3-Ph2-F、R¹-Te2-CH₂CH₂-Ph3-Ph3-F、R¹-Te2-CH₂CH₂-Ph3-Np1-F、R¹-Te2-CH₂CH₂-Ph3-Np2-F、R¹-Te2-CH₂CH₂-Ph3-Np3-F、R¹-Te2-CH₂CH₂-Ph3-Np4-F、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Ph3-C≡C-Ph2-F、R¹-Te1-CH₂CH₂-Ph3-C≡C-Ph3-F、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np1-F、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np2-F、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np3-F、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np4-F、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph1-F、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph2-F、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph3-F、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np1-F、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np2-F、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np3-F、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np4-F、
【０１３２】
R¹-Te1-CH₂CH₂-Np1-Ph1-F、R¹-Te1-CH₂CH₂-Np1-Ph2-F、R¹-Te1-CH₂CH₂-Np1-Ph3-F、R¹-Te1-CH₂CH₂-Np1-Np1-F、R¹-Te1-CH₂CH₂-Np1-Np2-F、R¹-Te1-CH₂CH₂-Np1-Np3-F、R¹-Te1-CH₂CH₂-Np1-Np4-F、R¹-Te2-CH₂CH₂-Np1-Ph1-F、R¹-Te2-CH₂CH₂-Np1-Ph2-F、R¹-Te2-CH₂CH₂-Np1-Ph3-F、R¹-Te2-CH₂CH₂-Np1-Np1-F、R¹-Te2-CH₂CH₂-Np1-Np2-F、R¹-Te2-CH₂CH₂-Np1-Np3-F、R¹-Te2-CH₂CH₂-Np1-Np4-F、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Np1-C≡C-Ph2-F、R¹-Te1-CH₂CH₂-Np1-C≡C-Ph3-F、R¹-Te1-CH₂CH₂-Np1-C≡C-Np1-F、R¹-Te1-CH₂CH₂-Np1-C≡C-Np2-F、R¹-Te1-CH₂CH₂-Np1-C≡C-Np3-F、R¹-Te1-CH₂CH₂-Np1-C≡C-Np4-F、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph1-F、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph2-F、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph3-F、R¹-Te2-CH₂CH₂-Np1-C≡C-Np1-F、R¹-Te2-CH₂CH₂-Np1-C≡C-Np2-F、R¹-Te2-CH₂CH₂-Np1-C≡C-Np3-F、R¹-Te2-CH₂CH₂-Np1-C≡C-Np4-F、
【０１３３】
R¹-Te1-CH₂CH₂-Np2-Ph1-F、R¹-Te1-CH₂CH₂-Np2-Ph2-F、R¹-Te1-CH₂CH₂-Np2-Ph3-F、R¹-Te1-CH₂CH₂-Np2-Np1-F、R¹-Te1-CH₂CH₂-Np2-Np2-F、R¹-Te1-CH₂CH₂-Np2-Np3-F、R¹-Te1-CH₂CH₂-Np2-Np4-F、R¹-Te2-CH₂CH₂-Np2-Ph1-F、R¹-Te2-CH₂CH₂-Np2-Ph2-F、R¹-Te2-CH₂CH₂-Np2-Ph3-F、R¹-Te2-CH₂CH₂-Np2-Np1-F、R¹-Te2-CH₂CH₂-Np2-Np2-F、R¹-Te2-CH₂CH₂-Np2-Np3-F、R¹-Te2-CH₂CH₂-Np2-Np4-F、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Np2-C≡C-Ph2-F、R¹-Te1-CH₂CH₂-Np2-C≡C-Ph3-F、R¹-Te1-CH₂CH₂-Np2-C≡C-Np1-F、R¹-Te1-CH₂CH₂-Np2-C≡C-Np2-F、R¹-Te1-CH₂CH₂-Np2-C≡C-Np3-F、R¹-Te1-CH₂CH₂-Np2-C≡C-Np4-F、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph1-F、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph2-F、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph3-F、R¹-Te2-CH₂CH₂-Np2-C≡C-Np1-F、R¹-Te2-CH₂CH₂-Np2-C≡C-Np2-F、R¹-Te2-CH₂CH₂-Np2-C≡C-Np3-F、R¹-Te2-CH₂CH₂-Np2-C≡C-Np4-F、
【０１３４】
R¹-Te1-CH₂CH₂-Np3-Ph1-F、R¹-Te1-CH₂CH₂-Np3-Ph2-F、R¹-Te1-CH₂CH₂-Np3-Ph3-F、R¹-Te1-CH₂CH₂-Np3-Np1-F、R¹-Te1-CH₂CH₂-Np3-Np2-F、R¹-Te1-CH₂CH₂-Np3-Np3-F、R¹-Te1-CH₂CH₂-Np3-Np4-F、R¹-Te2-CH₂CH₂-Np3-Ph1-F、R¹-Te2-CH₂CH₂-Np3-Ph2-F、R¹-Te2-CH₂CH₂-Np3-Ph3-F、R¹-Te2-CH₂CH₂-Np3-Np1-F、R¹-Te2-CH₂CH₂-Np3-Np2-F、R¹-Te2-CH₂CH₂-Np3-Np3-F、R¹-Te2-CH₂CH₂-Np3-Np4-F、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Np3-C≡C-Ph2-F、R¹-Te1-CH₂CH₂-Np3-C≡C-Ph3-F、R¹-Te1-CH₂CH₂-Np3-C≡C-Np1-F、R¹-Te1-CH₂CH₂-Np3-C≡C-Np2-F、R¹-Te1-CH₂CH₂-Np3-C≡C-Np3-F、R¹-Te1-CH₂CH₂-Np3-C≡C-Np4-F、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph1-F、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph2-F、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph3-F、R¹-Te2-CH₂CH₂-Np3-C≡C-Np1-F、R¹-Te2-CH₂CH₂-Np3-C≡C-Np2-F、R¹-Te2-CH₂CH₂-Np3-C≡C-Np3-F、R¹-Te2-CH₂CH₂-Np3-C≡C-Np4-F、
【０１３５】
R¹-Te1-CH₂CH₂-Np4-Ph1-F、R¹-Te1-CH₂CH₂-Np4-Ph2-F、R¹-Te1-CH₂CH₂-Np4-Ph3-F、R¹-Te1-CH₂CH₂-Np4-Np1-F、R¹-Te1-CH₂CH₂-Np4-Np2-F、R¹-Te1-CH₂CH₂-Np4-Np3-F、R¹-Te1-CH₂CH₂-Np4-Np4-F、R¹-Te2-CH₂CH₂-Np4-Ph1-F、R¹-Te2-CH₂CH₂-Np4-Ph2-F、R¹-Te2-CH₂CH₂-Np4-Ph3-F、R¹-Te2-CH₂CH₂-Np4-Np1-F、R¹-Te2-CH₂CH₂-Np4-Np2-F、R¹-Te2-CH₂CH₂-Np4-Np3-F、R¹-Te2-CH₂CH₂-Np4-Np4-F、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Ph2-F、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Ph3-F、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np1-F、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np2-F、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np3-F、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np4-F、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph1-F、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph2-F、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph3-F、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np1-F、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np2-F、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np3-F、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np4-F、R¹-Te1-CH₂CH₂-Np4-C≡C-Ph2-F、R¹-Te1-CH₂CH₂-Np4-C≡C-Ph3-F、R¹-Te1-CH₂CH₂-Np4-C≡C-Np1-F、R¹-Te1-CH₂CH₂-Np4-C≡C-Np2-F、R¹-Te1-CH₂CH₂-Np4-C≡C-Np3-F、R¹-Te1-CH₂CH₂-Np4-C≡C-Np4-F、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph1-F、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph2-F、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph3-F、R¹-Te2-CH₂CH₂-Np4-C≡C-Np1-F、R¹-Te2-CH₂CH₂-Np4-C≡C-Np2-F、R¹-Te2-CH₂CH₂-Np4-C≡C-Np3-F、R¹-Te2-CH₂CH₂-Np4-C≡C-Np4-F、
【０１３６】
R¹-Te1-C≡C-Ph1-Ph1-F、R¹-Te1-C≡C-Ph1-Ph2-F、R¹-Te1-C≡C-Ph1-Ph3-F、R¹-Te1-C≡C-Ph1-Np1-F、R¹-Te1-C≡C-Ph1-Np2-F、R¹-Te1-C≡C-Ph1-Np3-F、R¹-Te1-C≡C-Ph1-Np4-F、R¹-Te2-C≡C-Ph1-Ph1-F、R¹-Te2-C≡C-Ph1-Ph2-F、R¹-Te2-C≡C-Ph1-Ph3-F、R¹-Te2-C≡C-Ph1-Np1-F、R¹-Te2-C≡C-Ph1-Np2-F、R¹-Te2-C≡C-Ph1-Np3-F、R¹-Te2-C≡C-Ph1-Np4-F、R¹-Te1-C≡C-Ph1-CH₂CH₂-Ph2-F、R¹-Te1-C≡C-Ph1-CH₂CH₂-Ph3-F、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np1-F、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np2-F、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np3-F、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np4-F、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph1-F、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph2-F、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph3-F、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np1-F、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np2-F、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np3-F、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np4-F、R¹-Te1-C≡C-Ph1-C≡C-Ph2-F、R¹-Te1-C≡C-Ph1-C≡C-Ph3-F、R¹-Te1-C≡C-Ph1-C≡C-Np1-F、R¹-Te1-C≡C-Ph1-C≡C-Np2-F、R¹-Te1-C≡C-Ph1-C≡C-Np3-F、R¹-Te1-C≡C-Ph1-C≡C-Np4-F、R¹-Te2-C≡C-Ph1-C≡C-Ph1-F、R¹-Te2-C≡C-Ph1-C≡C-Ph2-F、R¹-Te2-C≡C-Ph1-C≡C-Ph3-F、R¹-Te2-C≡C-Ph1-C≡C-Np1-F、R¹-Te2-C≡C-Ph1-C≡C-Np2-F、R¹-Te2-C≡C-Ph1-C≡C-Np3-F、R¹-Te2-C≡C-Ph1-C≡C-Np4-F、
【０１３７】
R¹-Te1-C≡C-Ph2-Ph1-F、R¹-Te1-C≡C-Ph2-Ph2-F、R¹-Te1-C≡C-Ph2-Ph3-F、R¹-Te1-C≡C-Ph2-Np1-F、R¹-Te1-C≡C-Ph2-Np2-F、R¹-Te1-C≡C-Ph2-Np3-F、R¹-Te1-C≡C-Ph2-Np4-F、R¹-Te2-C≡C-Ph2-Ph1-F、R¹-Te2-C≡C-Ph2-Ph2-F、R¹-Te2-C≡C-Ph2-Ph3-F、R¹-Te2-C≡C-Ph2-Np1-F、R¹-Te2-C≡C-Ph2-Np2-F、R¹-Te2-C≡C-Ph2-Np3-F、R¹-Te2-C≡C-Ph2-Np4-F、R¹-Te1-C≡C-Ph2-CH₂CH₂-Ph2-F、R¹-Te1-C≡C-Ph2-CH₂CH₂-Ph3-F、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np1-F、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np2-F、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np3-F、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np4-F、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph1-F、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph2-F、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph3-F、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np1-F、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np2-F、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np3-F、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np4-F、R¹-Te1-C≡C-Ph2-C≡C-Ph2-F、R¹-Te1-C≡C-Ph2-C≡C-Ph3-F、R¹-Te1-C≡C-Ph2-C≡C-Np1-F、R¹-Te1-C≡C-Ph2-C≡C-Np2-F、R¹-Te1-C≡C-Ph2-C≡C-Np3-F、R¹-Te1-C≡C-Ph2-C≡C-Np4-F、R¹-Te2-C≡C-Ph2-C≡C-Ph1-F、R¹-Te2-C≡C-Ph2-C≡C-Ph2-F、R¹-Te2-C≡C-Ph2-C≡C-Ph3-F、R¹-Te2-C≡C-Ph2-C≡C-Np1-F、R¹-Te2-C≡C-Ph2-C≡C-Np2-F、R¹-Te2-C≡C-Ph2-C≡C-Np3-F、R¹-Te2-C≡C-Ph2-C≡C-Np4-F、
【０１３８】
R¹-Te1-C≡C-Ph3-Ph1-F、R¹-Te1-C≡C-Ph3-Ph2-F、R¹-Te1-C≡C-Ph3-Ph3-F、R¹-Te1-C≡C-Ph3-Np1-F、R¹-Te1-C≡C-Ph3-Np2-F、R¹-Te1-C≡C-Ph3-Np3-F、R¹-Te1-C≡C-Ph3-Np4-F、R¹-Te2-C≡C-Ph3-Ph1-F、R¹-Te2-C≡C-Ph3-Ph2-F、R¹-Te2-C≡C-Ph3-Ph3-F、R¹-Te2-C≡C-Ph3-Np1-F、R¹-Te2-C≡C-Ph3-Np2-F、R¹-Te2-C≡C-Ph3-Np3-F、R¹-Te2-C≡C-Ph3-Np4-F、R¹-Te1-C≡C-Ph3-CH₂CH₂-Ph2-F、R¹-Te1-C≡C-Ph3-CH₂CH₂-Ph3-F、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np1-F、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np2-F、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np3-F、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np4-F、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph1-F、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph2-F、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph3-F、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np1-F、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np2-F、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np3-F、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np4-F、R¹-Te1-C≡C-Ph3-C≡C-Ph2-F、R¹-Te1-C≡C-Ph3-C≡C-Ph3-F、R¹-Te1-C≡C-Ph3-C≡C-Np1-F、R¹-Te1-C≡C-Ph3-C≡C-Np2-F、R¹-Te1-C≡C-Ph3-C≡C-Np3-F、R¹-Te1-C≡C-Ph3-C≡C-Np4-F、R¹-Te2-C≡C-Ph3-C≡C-Ph1-F、R¹-Te2-C≡C-Ph3-C≡C-Ph2-F、R¹-Te2-C≡C-Ph3-C≡C-Ph3-F、R¹-Te2-C≡C-Ph3-C≡C-Np1-F、R¹-Te2-C≡C-Ph3-C≡C-Np2-F、R¹-Te2-C≡C-Ph3-C≡C-Np3-F、R¹-Te2-C≡C-Ph3-C≡C-Np4-F、
【０１３９】
R¹-Te1-C≡C-Np1-Ph1-F、R¹-Te1-C≡C-Np1-Ph2-F、R¹-Te1-C≡C-Np1-Ph3-F、R¹-Te1-C≡C-Np1-Np1-F、R¹-Te1-C≡C-Np1-Np2-F、R¹-Te1-C≡C-Np1-Np3-F、R¹-Te1-C≡C-Np1-Np4-F、R¹-Te2-C≡C-Np1-Ph1-F、R¹-Te2-C≡C-Np1-Ph2-F、R¹-Te2-C≡C-Np1-Ph3-F、R¹-Te2-C≡C-Np1-Np1-F、R¹-Te2-C≡C-Np1-Np2-F、R¹-Te2-C≡C-Np1-Np3-F、R¹-Te2-C≡C-Np1-Np4-F、R¹-Te1-C≡C-Np1-CH₂CH₂-Ph2-F、R¹-Te1-C≡C-Np1-CH₂CH₂-Ph3-F、R¹-Te1-C≡C-Np1-CH₂CH₂-Np1-F、R¹-Te1-C≡C-Np1-CH₂CH₂-Np2-F、R¹-Te1-C≡C-Np1-CH₂CH₂-Np3-F、R¹-Te1-C≡C-Np1-CH₂CH₂-Np4-F、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph1-F、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph2-F、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph3-F、R¹-Te2-C≡C-Np1-CH₂CH₂-Np1-F、R¹-Te2-C≡C-Np1-CH₂CH₂-Np2-F、R¹-Te2-C≡C-Np1-CH₂CH₂-Np3-F、R¹-Te2-C≡C-Np1-CH₂CH₂-Np4-F、R¹-Te1-C≡C-Np1-C≡C-Ph2-F、R¹-Te1-C≡C-Np1-C≡C-Ph3-F、R¹-Te1-C≡C-Np1-C≡C-Np1-F、R¹-Te1-C≡C-Np1-C≡C-Np2-F、R¹-Te1-C≡C-Np1-C≡C-Np3-F、R¹-Te1-C≡C-Np1-C≡C-Np4-F、R¹-Te2-C≡C-Np1-C≡C-Ph1-F、R¹-Te2-C≡C-Np1-C≡C-Ph2-F、R¹-Te2-C≡C-Np1-C≡C-Ph3-F、R¹-Te2-C≡C-Np1-C≡C-Np1-F、R¹-Te2-C≡C-Np1-C≡C-Np2-F、R¹-Te2-C≡C-Np1-C≡C-Np3-F、R¹-Te2-C≡C-Np1-C≡C-Np4-F、
【０１４０】
R¹-Te1-C≡C-Np2-Ph1-F、R¹-Te1-C≡C-Np2-Ph2-F、R¹-Te1-C≡C-Np2-Ph3-F、R¹-Te1-C≡C-Np2-Np1-F、R¹-Te1-C≡C-Np2-Np2-F、R¹-Te1-C≡C-Np2-Np3-F、R¹-Te1-C≡C-Np2-Np4-F、R¹-Te2-C≡C-Np2-Ph1-F、R¹-Te2-C≡C-Np2-Ph2-F、R¹-Te2-C≡C-Np2-Ph3-F、R¹-Te2-C≡C-Np2-Np1-F、R¹-Te2-C≡C-Np2-Np2-F、R¹-Te2-C≡C-Np2-Np3-F、R¹-Te2-C≡C-Np2-Np4-F、R¹-Te1-C≡C-Np2-CH₂CH₂-Ph2-F、R¹-Te1-C≡C-Np2-CH₂CH₂-Ph3-F、R¹-Te1-C≡C-Np2-CH₂CH₂-Np1-F、R¹-Te1-C≡C-Np2-CH₂CH₂-Np2-F、R¹-Te1-C≡C-Np2-CH₂CH₂-Np3-F、R¹-Te1-C≡C-Np2-CH₂CH₂-Np4-F、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph1-F、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph2-F、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph3-F、R¹-Te2-C≡C-Np2-CH₂CH₂-Np1-F、R¹-Te2-C≡C-Np2-CH₂CH₂-Np2-F、R¹-Te2-C≡C-Np2-CH₂CH₂-Np3-F、R¹-Te2-C≡C-Np2-CH₂CH₂-Np4-F、R¹-Te1-C≡C-Np2-C≡C-Ph2-F、R¹-Te1-C≡C-Np2-C≡C-Ph3-F、R¹-Te1-C≡C-Np2-C≡C-Np1-F、R¹-Te1-C≡C-Np2-C≡C-Np2-F、R¹-Te1-C≡C-Np2-C≡C-Np3-F、R¹-Te1-C≡C-Np2-C≡C-Np4-F、R¹-Te2-C≡C-Np2-C≡C-Ph1-F、R¹-Te2-C≡C-Np2-C≡C-Ph2-F、R¹-Te2-C≡C-Np2-C≡C-Ph3-F、R¹-Te2-C≡C-Np2-C≡C-Np1-F、R¹-Te2-C≡C-Np2-C≡C-Np2-F、R¹-Te2-C≡C-Np2-C≡C-Np3-F、R¹-Te2-C≡C-Np2-C≡C-Np4-F、
【０１４１】
R¹-Te1-C≡C-Np3-Ph1-F、R¹-Te1-C≡C-Np3-Ph2-F、R¹-Te1-C≡C-Np3-Ph3-F、R¹-Te1-C≡C-Np3-Np1-F、R¹-Te1-C≡C-Np3-Np2-F、R¹-Te1-C≡C-Np3-Np3-F、R¹-Te1-C≡C-Np3-Np4-F、R¹-Te2-C≡C-Np3-Ph1-F、R¹-Te2-C≡C-Np3-Ph2-F、R¹-Te2-C≡C-Np3-Ph3-F、R¹-Te2-C≡C-Np3-Np1-F、R¹-Te2-C≡C-Np3-Np2-F、R¹-Te2-C≡C-Np3-Np3-F、R¹-Te2-C≡C-Np3-Np4-F、R¹-Te1-C≡C-Np3-CH₂CH₂-Ph2-F、R¹-Te1-C≡C-Np3-CH₂CH₂-Ph3-F、R¹-Te1-C≡C-Np3-CH₂CH₂-Np1-F、R¹-Te1-C≡C-Np3-CH₂CH₂-Np2-F、R¹-Te1-C≡C-Np3-CH₂CH₂-Np3-F、R¹-Te1-C≡C-Np3-CH₂CH₂-Np4-F、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph1-F、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph2-F、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph3-F、R¹-Te2-C≡C-Np3-CH₂CH₂-Np1-F、R¹-Te2-C≡C-Np3-CH₂CH₂-Np2-F、R¹-Te2-C≡C-Np3-CH₂CH₂-Np3-F、R¹-Te2-C≡C-Np3-CH₂CH₂-Np4-F、R¹-Te1-C≡C-Np3-C≡C-Ph2-F、R¹-Te1-C≡C-Np3-C≡C-Ph3-F、R¹-Te1-C≡C-Np3-C≡C-Np1-F、R¹-Te1-C≡C-Np3-C≡C-Np2-F、R¹-Te1-C≡C-Np3-C≡C-Np3-F、R¹-Te1-C≡C-Np3-C≡C-Np4-F、R¹-Te2-C≡C-Np3-C≡C-Ph1-F、R¹-Te2-C≡C-Np3-C≡C-Ph2-F、R¹-Te2-C≡C-Np3-C≡C-Ph3-F、R¹-Te2-C≡C-Np3-C≡C-Np1-F、R¹-Te2-C≡C-Np3-C≡C-Np2-F、R¹-Te2-C≡C-Np3-C≡C-Np3-F、R¹-Te2-C≡C-Np3-C≡C-Np4-F、
【０１４２】
R¹-Te1-C≡C-Np4-Ph1-F、R¹-Te1-C≡C-Np4-Ph2-F、R¹-Te1-C≡C-Np4-Ph3-F、R¹-Te1-C≡C-Np4-Np1-F、R¹-Te1-C≡C-Np4-Np2-F、R¹-Te1-C≡C-Np4-Np3-F、R¹-Te1-C≡C-Np4-Np4-F、R¹-Te2-C≡C-Np4-Ph1-F、R¹-Te2-C≡C-Np4-Ph2-F、R¹-Te2-C≡C-Np4-Ph3-F、R¹-Te2-C≡C-Np4-Np1-F、R¹-Te2-C≡C-Np4-Np2-F、R¹-Te2-C≡C-Np4-Np3-F、R¹-Te2-C≡C-Np4-Np4-F、R¹-Te1-C≡C-Np4-CH₂CH₂-Ph2-F、R¹-Te1-C≡C-Np4-CH₂CH₂-Ph3-F、R¹-Te1-C≡C-Np4-CH₂CH₂-Np1-F、R¹-Te1-C≡C-Np4-CH₂CH₂-Np2-F、R¹-Te1-C≡C-Np4-CH₂CH₂-Np3-F、R¹-Te1-C≡C-Np4-CH₂CH₂-Np4-F、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph1-F、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph2-F、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph3-F、R¹-Te2-C≡C-Np4-CH₂CH₂-Np1-F、R¹-Te2-C≡C-Np4-CH₂CH₂-Np2-F、R¹-Te2-C≡C-Np4-CH₂CH₂-Np3-F、R¹-Te2-C≡C-Np4-CH₂CH₂-Np4-F、R¹-Te1-C≡C-Np4-C≡C-Ph2-F、R¹-Te1-C≡C-Np4-C≡C-Ph3-F、R¹-Te1-C≡C-Np4-C≡C-Np1-F、R¹-Te1-C≡C-Np4-C≡C-Np2-F、R¹-Te1-C≡C-Np4-C≡C-Np3-F、R¹-Te1-C≡C-Np4-C≡C-Np4-F、R¹-Te2-C≡C-Np4-C≡C-Ph1-F、R¹-Te2-C≡C-Np4-C≡C-Ph2-F、R¹-Te2-C≡C-Np4-C≡C-Ph3-F、R¹-Te2-C≡C-Np4-C≡C-Np1-F、R¹-Te2-C≡C-Np4-C≡C-Np2-F、R¹-Te2-C≡C-Np4-C≡C-Np3-F、R¹-Te2-C≡C-Np4-C≡C-Np4-F、
【０１４３】
m=0、n=1、Vが単結合、Zがシアノ基の場合、
【０１４４】
R¹-Te1-Cy-Ph1-CN、R¹-Te1-Cy-Ph2-CN、R¹-Te1-Cy-Ph3-CN、R¹-Te1-Cy-Np1-CN、R¹-Te1-Cy-Np2-CN、R¹-Te1-Cy-Np3-CN、R¹-Te1-Cy-Np4-CN、R¹-Te2-Cy-Ph1-CN、R¹-Te2-Cy-Ph2-CN、R¹-Te2-Cy-Ph3-CN、R¹-Te2-Cy-Np1-CN、R¹-Te2-Cy-Np2-CN、R¹-Te2-Cy-Np3-CN、R¹-Te2-Cy-Np4-CN、R¹-Te1-Cy-CH₂CH₂-Ph2-CN、R¹-Te1-Cy-CH₂CH₂-Ph3-CN、R¹-Te1-Cy-CH₂CH₂-Np1-CN、R¹-Te1-Cy-CH₂CH₂-Np2-CN、R¹-Te1-Cy-CH₂CH₂-Np3-CN、R¹-Te1-Cy-CH₂CH₂-Np4-CN、R¹-Te2-Cy-CH₂CH₂-Ph1-CN、R¹-Te2-Cy-CH₂CH₂-Ph2-CN、R¹-Te2-Cy-CH₂CH₂-Ph3-CN、R¹-Te2-Cy-CH₂CH₂-Np1-CN、R¹-Te2-Cy-CH₂CH₂-Np2-CN、R¹-Te2-Cy-CH₂CH₂-Np3-CN、R¹-Te2-Cy-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Cy-Ph1-CN、R¹-Te1-CH₂CH₂-Cy-Ph2-CN、R¹-Te1-CH₂CH₂-Cy-Ph3-CN、R¹-Te1-CH₂CH₂-Cy-Np1-CN、R¹-Te1-CH₂CH₂-Cy-Np2-CN、R¹-Te1-CH₂CH₂-Cy-Np3-CN、R¹-Te1-CH₂CH₂-Cy-Np4-CN、R¹-Te2-CH₂CH₂-Cy-Ph1-CN、R¹-Te2-CH₂CH₂-Cy-Ph2-CN、R¹-Te2-CH₂CH₂-Cy-Ph3-CN、R¹-Te2-CH₂CH₂-Cy-Np1-CN、R¹-Te2-CH₂CH₂-Cy-Np2-CN、R¹-Te2-CH₂CH₂-Cy-Np3-CN、R¹-Te2-CH₂CH₂-Cy-Np4-CN、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np4-CN、
【０１４５】
R¹-Te1-Ph1-Ph1-CN、R¹-Te1-Ph1-Ph2-CN、R¹-Te1-Ph1-Ph3-CN、R¹-Te1-Ph1-Np1-CN、R¹-Te1-Ph1-Np2-CN、R¹-Te1-Ph1-Np3-CN、R¹-Te1-Ph1-Np4-CN、R¹-Te2-Ph1-Ph1-CN、R¹-Te2-Ph1-Ph2-CN、R¹-Te2-Ph1-Ph3-CN、R¹-Te2-Ph1-Np1-CN、R¹-Te2-Ph1-Np2-CN、R¹-Te2-Ph1-Np3-CN、R¹-Te2-Ph1-Np4-CN、R¹-Te1-Ph1-CH₂CH₂-Ph2-CN、R¹-Te1-Ph1-CH₂CH₂-Ph3-CN、R¹-Te1-Ph1-CH₂CH₂-Np1-CN、R¹-Te1-Ph1-CH₂CH₂-Np2-CN、R¹-Te1-Ph1-CH₂CH₂-Np3-CN、R¹-Te1-Ph1-CH₂CH₂-Np4-CN、R¹-Te2-Ph1-CH₂CH₂-Ph1-CN、R¹-Te2-Ph1-CH₂CH₂-Ph2-CN、R¹-Te2-Ph1-CH₂CH₂-Ph3-CN、R¹-Te2-Ph1-CH₂CH₂-Np1-CN、R¹-Te2-Ph1-CH₂CH₂-Np2-CN、R¹-Te2-Ph1-CH₂CH₂-Np3-CN、R¹-Te2-Ph1-CH₂CH₂-Np4-CN、R¹-Te1-Ph1-C≡C-Ph2-CN、R¹-Te1-Ph1-C≡C-Ph3-CN、R¹-Te1-Ph1-C≡C-Np1-CN、R¹-Te1-Ph1-C≡C-Np2-CN、R¹-Te1-Ph1-C≡C-Np3-CN、R¹-Te1-Ph1-C≡C-Np4-CN、R¹-Te2-Ph1-C≡C-Ph1-CN、R¹-Te2-Ph1-C≡C-Ph2-CN、R¹-Te2-Ph1-C≡C-Ph3-CN、R¹-Te2-Ph1-C≡C-Np1-CN、R¹-Te2-Ph1-C≡C-Np2-CN、R¹-Te2-Ph1-C≡C-Np3-CN、R¹-Te2-Ph1-C≡C-Np4-CN、
【０１４６】
R¹-Te1-Ph2-Ph1-CN、R¹-Te1-Ph2-Ph2-CN、R¹-Te1-Ph2-Ph3-CN、R¹-Te1-Ph2-Np1-CN、R¹-Te1-Ph2-Np2-CN、R¹-Te1-Ph2-Np3-CN、R¹-Te1-Ph2-Np4-CN、R¹-Te2-Ph2-Ph1-CN、R¹-Te2-Ph2-Ph2-CN、R¹-Te2-Ph2-Ph3-CN、R¹-Te2-Ph2-Np1-CN、R¹-Te2-Ph2-Np2-CN、R¹-Te2-Ph2-Np3-CN、R¹-Te2-Ph2-Np4-CN、R¹-Te1-Ph2-CH₂CH₂-Ph2-CN、R¹-Te1-Ph2-CH₂CH₂-Ph3-CN、R¹-Te1-Ph2-CH₂CH₂-Np1-CN、R¹-Te1-Ph2-CH₂CH₂-Np2-CN、R¹-Te1-Ph2-CH₂CH₂-Np3-CN、R¹-Te1-Ph2-CH₂CH₂-Np4-CN、R¹-Te2-Ph2-CH₂CH₂-Ph1-CN、R¹-Te2-Ph2-CH₂CH₂-Ph2-CN、R¹-Te2-Ph2-CH₂CH₂-Ph3-CN、R¹-Te2-Ph2-CH₂CH₂-Np1-CN、R¹-Te2-Ph2-CH₂CH₂-Np2-CN、R¹-Te2-Ph2-CH₂CH₂-Np3-CN、R¹-Te2-Ph2-CH₂CH₂-Np4-CN、R¹-Te1-Ph2-C≡C-Ph2-CN、R¹-Te1-Ph2-C≡C-Ph3-CN、R¹-Te1-Ph2-C≡C-Np1-CN、R¹-Te1-Ph2-C≡C-Np2-CN、R¹-Te1-Ph2-C≡C-Np3-CN、R¹-Te1-Ph2-C≡C-Np4-CN、R¹-Te2-Ph2-C≡C-Ph1-CN、R¹-Te2-Ph2-C≡C-Ph2-CN、R¹-Te2-Ph2-C≡C-Ph3-CN、R¹-Te2-Ph2-C≡C-Np1-CN、R¹-Te2-Ph2-C≡C-Np2-CN、R¹-Te2-Ph2-C≡C-Np3-CN、R¹-Te2-Ph2-C≡C-Np4-CN、
【０１４７】
R¹-Te1-Ph3-Ph1-CN、R¹-Te1-Ph3-Ph2-CN、R¹-Te1-Ph3-Ph3-CN、R¹-Te1-Ph3-Np1-CN、R¹-Te1-Ph3-Np2-CN、R¹-Te1-Ph3-Np3-CN、R¹-Te1-Ph3-Np4-CN、R¹-Te2-Ph3-Ph1-CN、R¹-Te2-Ph3-Ph2-CN、R¹-Te2-Ph3-Ph3-CN、R¹-Te2-Ph3-Np1-CN、R¹-Te2-Ph3-Np2-CN、R¹-Te2-Ph3-Np3-CN、R¹-Te2-Ph3-Np4-CN、R¹-Te1-Ph3-CH₂CH₂-Ph2-CN、R¹-Te1-Ph3-CH₂CH₂-Ph3-CN、R¹-Te1-Ph3-CH₂CH₂-Np1-CN、R¹-Te1-Ph3-CH₂CH₂-Np2-CN、R¹-Te1-Ph3-CH₂CH₂-Np3-CN、R¹-Te1-Ph3-CH₂CH₂-Np4-CN、R¹-Te2-Ph3-CH₂CH₂-Ph1-CN、R¹-Te2-Ph3-CH₂CH₂-Ph2-CN、R¹-Te2-Ph3-CH₂CH₂-Ph3-CN、R¹-Te2-Ph3-CH₂CH₂-Np1-CN、R¹-Te2-Ph3-CH₂CH₂-Np2-CN、R¹-Te2-Ph3-CH₂CH₂-Np3-CN、R¹-Te2-Ph3-CH₂CH₂-Np4-CN、R¹-Te1-Ph3-C≡C-Ph2-CN、R¹-Te1-Ph3-C≡C-Ph3-CN、R¹-Te1-Ph3-C≡C-Np1-CN、R¹-Te1-Ph3-C≡C-Np2-CN、R¹-Te1-Ph3-C≡C-Np3-CN、R¹-Te1-Ph3-C≡C-Np4-CN、R¹-Te2-Ph3-C≡C-Ph1-CN、R¹-Te2-Ph3-C≡C-Ph2-CN、R¹-Te2-Ph3-C≡C-Ph3-CN、R¹-Te2-Ph3-C≡C-Np1-CN、R¹-Te2-Ph3-C≡C-Np2-CN、R¹-Te2-Ph3-C≡C-Np3-CN、R¹-Te2-Ph3-C≡C-Np4-CN、
【０１４８】
R¹-Te1-Np1-Ph1-CN、R¹-Te1-Np1-Ph2-CN、R¹-Te1-Np1-Ph3-CN、R¹-Te1-Np1-Np1-CN、R¹-Te1-Np1-Np2-CN、R¹-Te1-Np1-Np3-CN、R¹-Te1-Np1-Np4-CN、R¹-Te2-Np1-Ph1-CN、R¹-Te2-Np1-Ph2-CN、R¹-Te2-Np1-Ph3-CN、R¹-Te2-Np1-Np1-CN、R¹-Te2-Np1-Np2-CN、R¹-Te2-Np1-Np3-CN、R¹-Te2-Np1-Np4-CN、R¹-Te1-Np1-CH₂CH₂-Ph2-CN、R¹-Te1-Np1-CH₂CH₂-Ph3-CN、R¹-Te1-Np1-CH₂CH₂-Np1-CN、R¹-Te1-Np1-CH₂CH₂-Np2-CN、R¹-Te1-Np1-CH₂CH₂-Np3-CN、R¹-Te1-Np1-CH₂CH₂-Np4-CN、R¹-Te2-Np1-CH₂CH₂-Ph1-CN、R¹-Te2-Np1-CH₂CH₂-Ph2-CN、R¹-Te2-Np1-CH₂CH₂-Ph3-CN、R¹-Te2-Np1-CH₂CH₂-Np1-CN、R¹-Te2-Np1-CH₂CH₂-Np2-CN、R¹-Te2-Np1-CH₂CH₂-Np3-CN、R¹-Te2-Np1-CH₂CH₂-Np4-CN、R¹-Te1-Np1-C≡C-Ph2-CN、R¹-Te1-Np1-C≡C-Ph3-CN、R¹-Te1-Np1-C≡C-Np1-CN、R¹-Te1-Np1-C≡C-Np2-CN、R¹-Te1-Np1-C≡C-Np3-CN、R¹-Te1-Np1-C≡C-Np4-CN、R¹-Te2-Np1-C≡C-Ph1-CN、R¹-Te2-Np1-C≡C-Ph2-CN、R¹-Te2-Np1-C≡C-Ph3-CN、R¹-Te2-Np1-C≡C-Np1-CN、R¹-Te2-Np1-C≡C-Np2-CN、R¹-Te2-Np1-C≡C-Np3-CN、R¹-Te2-Np1-C≡C-Np4-CN、
【０１４９】
R¹-Te1-Np2-Ph1-CN、R¹-Te1-Np2-Ph2-CN、R¹-Te1-Np2-Ph3-CN、R¹-Te1-Np2-Np1-CN、R¹-Te1-Np2-Np2-CN、R¹-Te1-Np2-Np3-CN、R¹-Te1-Np2-Np4-CN、R¹-Te2-Np2-Ph1-CN、R¹-Te2-Np2-Ph2-CN、R¹-Te2-Np2-Ph3-CN、R¹-Te2-Np2-Np1-CN、R¹-Te2-Np2-Np2-CN、R¹-Te2-Np2-Np3-CN、R¹-Te2-Np2-Np4-CN、R¹-Te1-Np2-CH₂CH₂-Ph2-CN、R¹-Te1-Np2-CH₂CH₂-Ph3-CN、R¹-Te1-Np2-CH₂CH₂-Np1-CN、R¹-Te1-Np2-CH₂CH₂-Np2-CN、R¹-Te1-Np2-CH₂CH₂-Np3-CN、R¹-Te1-Np2-CH₂CH₂-Np4-CN、R¹-Te2-Np2-CH₂CH₂-Ph1-CN、R¹-Te2-Np2-CH₂CH₂-Ph2-CN、R¹-Te2-Np2-CH₂CH₂-Ph3-CN、R¹-Te2-Np2-CH₂CH₂-Np1-CN、R¹-Te2-Np2-CH₂CH₂-Np2-CN、R¹-Te2-Np2-CH₂CH₂-Np3-CN、R¹-Te2-Np2-CH₂CH₂-Np4-CN、R¹-Te1-Np2-C≡C-Ph2-CN、R¹-Te1-Np2-C≡C-Ph3-CN、R¹-Te1-Np2-C≡C-Np1-CN、R¹-Te1-Np2-C≡C-Np2-CN、R¹-Te1-Np2-C≡C-Np3-CN、R¹-Te1-Np2-C≡C-Np4-CN、R¹-Te2-Np2-C≡C-Ph1-CN、R¹-Te2-Np2-C≡C-Ph2-CN、R¹-Te2-Np2-C≡C-Ph3-CN、R¹-Te2-Np2-C≡C-Np1-CN、R¹-Te2-Np2-C≡C-Np2-CN、R¹-Te2-Np2-C≡C-Np3-CN、R¹-Te2-Np2-C≡C-Np4-CN、
【０１５０】
R¹-Te1-Np3-Ph1-CN、R¹-Te1-Np3-Ph2-CN、R¹-Te1-Np3-Ph3-CN、R¹-Te1-Np3-Np1-CN、R¹-Te1-Np3-Np2-CN、R¹-Te1-Np3-Np3-CN、R¹-Te1-Np3-Np4-CN、R¹-Te2-Np3-Ph1-CN、R¹-Te2-Np3-Ph2-CN、R¹-Te2-Np3-Ph3-CN、R¹-Te2-Np3-Np1-CN、R¹-Te2-Np3-Np2-CN、R¹-Te2-Np3-Np3-CN、R¹-Te2-Np3-Np4-CN、R¹-Te1-Np3-CH₂CH₂-Ph2-CN、R¹-Te1-Np3-CH₂CH₂-Ph3-CN、R¹-Te1-Np3-CH₂CH₂-Np1-CN、R¹-Te1-Np3-CH₂CH₂-Np2-CN、R¹-Te1-Np3-CH₂CH₂-Np3-CN、R¹-Te1-Np3-CH₂CH₂-Np4-CN、R¹-Te2-Np3-CH₂CH₂-Ph1-CN、R¹-Te2-Np3-CH₂CH₂-Ph2-CN、R¹-Te2-Np3-CH₂CH₂-Ph3-CN、R¹-Te2-Np3-CH₂CH₂-Np1-CN、R¹-Te2-Np3-CH₂CH₂-Np2-CN、R¹-Te2-Np3-CH₂CH₂-Np3-CN、R¹-Te2-Np3-CH₂CH₂-Np4-CN、R¹-Te1-Np3-C≡C-Ph2-CN、R¹-Te1-Np3-C≡C-Ph3-CN、R¹-Te1-Np3-C≡C-Np1-CN、R¹-Te1-Np3-C≡C-Np2-CN、R¹-Te1-Np3-C≡C-Np3-CN、R¹-Te1-Np3-C≡C-Np4-CN、R¹-Te2-Np3-C≡C-Ph1-CN、R¹-Te2-Np3-C≡C-Ph2-CN、R¹-Te2-Np3-C≡C-Ph3-CN、R¹-Te2-Np3-C≡C-Np1-CN、R¹-Te2-Np3-C≡C-Np2-CN、R¹-Te2-Np3-C≡C-Np3-CN、R¹-Te2-Np3-C≡C-Np4-CN、
【０１５１】
R¹-Te1-Np4-Ph1-CN、R¹-Te1-Np4-Ph2-CN、R¹-Te1-Np4-Ph3-CN、R¹-Te1-Np4-Np1-CN、R¹-Te1-Np4-Np2-CN、R¹-Te1-Np4-Np3-CN、R¹-Te1-Np4-Np4-CN、R¹-Te2-Np4-Ph1-CN、R¹-Te2-Np4-Ph2-CN、R¹-Te2-Np4-Ph3-CN、R¹-Te2-Np4-Np1-CN、R¹-Te2-Np4-Np2-CN、R¹-Te2-Np4-Np3-CN、R¹-Te2-Np4-Np4-CN、R¹-Te1-Np4-CH₂CH₂-Ph2-CN、R¹-Te1-Np4-CH₂CH₂-Ph3-CN、R¹-Te1-Np4-CH₂CH₂-Np1-CN、R¹-Te1-Np4-CH₂CH₂-Np2-CN、R¹-Te1-Np4-CH₂CH₂-Np3-CN、R¹-Te1-Np4-CH₂CH₂-Np4-CN、R¹-Te2-Np4-CH₂CH₂-Ph1-CN、R¹-Te2-Np4-CH₂CH₂-Ph2-CN、R¹-Te2-Np4-CH₂CH₂-Ph3-CN、R¹-Te2-Np4-CH₂CH₂-Np1-CN、R¹-Te2-Np4-CH₂CH₂-Np2-CN、R¹-Te2-Np4-CH₂CH₂-Np3-CN、R¹-Te2-Np4-CH₂CH₂-Np4-CN、R¹-Te1-Np4-C≡C-Ph2-CN、R¹-Te1-Np4-C≡C-Ph3-CN、R¹-Te1-Np4-C≡C-Np1-CN、R¹-Te1-Np4-C≡C-Np2-CN、R¹-Te1-Np4-C≡C-Np3-CN、R¹-Te1-Np4-C≡C-Np4-CN、R¹-Te2-Np4-C≡C-Ph1-CN、R¹-Te2-Np4-C≡C-Ph2-CN、R¹-Te2-Np4-C≡C-Ph3-CN、R¹-Te2-Np4-C≡C-Np1-CN、R¹-Te2-Np4-C≡C-Np2-CN、R¹-Te2-Np4-C≡C-Np3-CN、R¹-Te2-Np4-C≡C-Np4-CN、
【０１５２】
R¹-Te1-CH₂CH₂-Ph1-Ph1-CN、R¹-Te1-CH₂CH₂-Ph1-Ph2-CN、R¹-Te1-CH₂CH₂-Ph1-Ph3-CN、R¹-Te1-CH₂CH₂-Ph1-Np1-CN、R¹-Te1-CH₂CH₂-Ph1-Np2-CN、R¹-Te1-CH₂CH₂-Ph1-Np3-CN、R¹-Te1-CH₂CH₂-Ph1-Np4-CN、R¹-Te2-CH₂CH₂-Ph1-Ph1-CN、R¹-Te2-CH₂CH₂-Ph1-Ph2-CN、R¹-Te2-CH₂CH₂-Ph1-Ph3-CN、R¹-Te2-CH₂CH₂-Ph1-Np1-CN、R¹-Te2-CH₂CH₂-Ph1-Np2-CN、R¹-Te2-CH₂CH₂-Ph1-Np3-CN、R¹-Te2-CH₂CH₂-Ph1-Np4-CN、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Ph1-C≡C-Ph2-CN、R¹-Te1-CH₂CH₂-Ph1-C≡C-Ph3-CN、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np1-CN、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np2-CN、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np3-CN、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np4-CN、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph1-CN、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph2-CN、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph3-CN、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np1-CN、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np2-CN、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np3-CN、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np4-CN、
【０１５３】
R¹-Te1-CH₂CH₂-Ph2-Ph1-CN、R¹-Te1-CH₂CH₂-Ph2-Ph2-CN、R¹-Te1-CH₂CH₂-Ph2-Ph3-CN、R¹-Te1-CH₂CH₂-Ph2-Np1-CN、R¹-Te1-CH₂CH₂-Ph2-Np2-CN、R¹-Te1-CH₂CH₂-Ph2-Np3-CN、R¹-Te1-CH₂CH₂-Ph2-Np4-CN、R¹-Te2-CH₂CH₂-Ph2-Ph1-CN、R¹-Te2-CH₂CH₂-Ph2-Ph2-CN、R¹-Te2-CH₂CH₂-Ph2-Ph3-CN、R¹-Te2-CH₂CH₂-Ph2-Np1-CN、R¹-Te2-CH₂CH₂-Ph2-Np2-CN、R¹-Te2-CH₂CH₂-Ph2-Np3-CN、R¹-Te2-CH₂CH₂-Ph2-Np4-CN、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Ph2-C≡C-Ph2-CN、R¹-Te1-CH₂CH₂-Ph2-C≡C-Ph3-CN、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np1-CN、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np2-CN、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np3-CN、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np4-CN、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph1-CN、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph2-CN、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph3-CN、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np1-CN、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np2-CN、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np3-CN、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np4-CN、
【０１５４】
R¹-Te1-CH₂CH₂-Ph3-Ph1-CN、R¹-Te1-CH₂CH₂-Ph3-Ph2-CN、R¹-Te1-CH₂CH₂-Ph3-Ph3-CN、R¹-Te1-CH₂CH₂-Ph3-Np1-CN、R¹-Te1-CH₂CH₂-Ph3-Np2-CN、R¹-Te1-CH₂CH₂-Ph3-Np3-CN、R¹-Te1-CH₂CH₂-Ph3-Np4-CN、R¹-Te2-CH₂CH₂-Ph3-Ph1-CN、R¹-Te2-CH₂CH₂-Ph3-Ph2-CN、R¹-Te2-CH₂CH₂-Ph3-Ph3-CN、R¹-Te2-CH₂CH₂-Ph3-Np1-CN、R¹-Te2-CH₂CH₂-Ph3-Np2-CN、R¹-Te2-CH₂CH₂-Ph3-Np3-CN、R¹-Te2-CH₂CH₂-Ph3-Np4-CN、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Ph3-C≡C-Ph2-CN、R¹-Te1-CH₂CH₂-Ph3-C≡C-Ph3-CN、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np1-CN、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np2-CN、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np3-CN、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np4-CN、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph1-CN、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph2-CN、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph3-CN、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np1-CN、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np2-CN、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np3-CN、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np4-CN、
【０１５５】
R¹-Te1-CH₂CH₂-Np1-Ph1-CN、R¹-Te1-CH₂CH₂-Np1-Ph2-CN、R¹-Te1-CH₂CH₂-Np1-Ph3-CN、R¹-Te1-CH₂CH₂-Np1-Np1-CN、R¹-Te1-CH₂CH₂-Np1-Np2-CN、R¹-Te1-CH₂CH₂-Np1-Np3-CN、R¹-Te1-CH₂CH₂-Np1-Np4-CN、R¹-Te2-CH₂CH₂-Np1-Ph1-CN、R¹-Te2-CH₂CH₂-Np1-Ph2-CN、R¹-Te2-CH₂CH₂-Np1-Ph3-CN、R¹-Te2-CH₂CH₂-Np1-Np1-CN、R¹-Te2-CH₂CH₂-Np1-Np2-CN、R¹-Te2-CH₂CH₂-Np1-Np3-CN、R¹-Te2-CH₂CH₂-Np1-Np4-CN、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Np1-C≡C-Ph2-CN、R¹-Te1-CH₂CH₂-Np1-C≡C-Ph3-CN、R¹-Te1-CH₂CH₂-Np1-C≡C-Np1-CN、R¹-Te1-CH₂CH₂-Np1-C≡C-Np2-CN、R¹-Te1-CH₂CH₂-Np1-C≡C-Np3-CN、R¹-Te1-CH₂CH₂-Np1-C≡C-Np4-CN、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph1-CN、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph2-CN、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph3-CN、R¹-Te2-CH₂CH₂-Np1-C≡C-Np1-CN、R¹-Te2-CH₂CH₂-Np1-C≡C-Np2-CN、R¹-Te2-CH₂CH₂-Np1-C≡C-Np3-CN、R¹-Te2-CH₂CH₂-Np1-C≡C-Np4-CN、
【０１５６】
R¹-Te1-CH₂CH₂-Np2-Ph1-CN、R¹-Te1-CH₂CH₂-Np2-Ph2-CN、R¹-Te1-CH₂CH₂-Np2-Ph3-CN、R¹-Te1-CH₂CH₂-Np2-Np1-CN、R¹-Te1-CH₂CH₂-Np2-Np2-CN、R¹-Te1-CH₂CH₂-Np2-Np3-CN、R¹-Te1-CH₂CH₂-Np2-Np4-CN、R¹-Te2-CH₂CH₂-Np2-Ph1-CN、R¹-Te2-CH₂CH₂-Np2-Ph2-CN、R¹-Te2-CH₂CH₂-Np2-Ph3-CN、R¹-Te2-CH₂CH₂-Np2-Np1-CN、R¹-Te2-CH₂CH₂-Np2-Np2-CN、R¹-Te2-CH₂CH₂-Np2-Np3-CN、R¹-Te2-CH₂CH₂-Np2-Np4-CN、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Np2-C≡C-Ph2-CN、R¹-Te1-CH₂CH₂-Np2-C≡C-Ph3-CN、R¹-Te1-CH₂CH₂-Np2-C≡C-Np1-CN、R¹-Te1-CH₂CH₂-Np2-C≡C-Np2-CN、R¹-Te1-CH₂CH₂-Np2-C≡C-Np3-CN、R¹-Te1-CH₂CH₂-Np2-C≡C-Np4-CN、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph1-CN、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph2-CN、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph3-CN、R¹-Te2-CH₂CH₂-Np2-C≡C-Np1-CN、R¹-Te2-CH₂CH₂-Np2-C≡C-Np2-CN、R¹-Te2-CH₂CH₂-Np2-C≡C-Np3-CN、R¹-Te2-CH₂CH₂-Np2-C≡C-Np4-CN、
【０１５７】
R¹-Te1-CH₂CH₂-Np3-Ph1-CN、R¹-Te1-CH₂CH₂-Np3-Ph2-CN、R¹-Te1-CH₂CH₂-Np3-Ph3-CN、R¹-Te1-CH₂CH₂-Np3-Np1-CN、R¹-Te1-CH₂CH₂-Np3-Np2-CN、R¹-Te1-CH₂CH₂-Np3-Np3-CN、R¹-Te1-CH₂CH₂-Np3-Np4-CN、R¹-Te2-CH₂CH₂-Np3-Ph1-CN、R¹-Te2-CH₂CH₂-Np3-Ph2-CN、R¹-Te2-CH₂CH₂-Np3-Ph3-CN、R¹-Te2-CH₂CH₂-Np3-Np1-CN、R¹-Te2-CH₂CH₂-Np3-Np2-CN、R¹-Te2-CH₂CH₂-Np3-Np3-CN、R¹-Te2-CH₂CH₂-Np3-Np4-CN、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Np3-C≡C-Ph2-CN、R¹-Te1-CH₂CH₂-Np3-C≡C-Ph3-CN、R¹-Te1-CH₂CH₂-Np3-C≡C-Np1-CN、R¹-Te1-CH₂CH₂-Np3-C≡C-Np2-CN、R¹-Te1-CH₂CH₂-Np3-C≡C-Np3-CN、R¹-Te1-CH₂CH₂-Np3-C≡C-Np4-CN、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph1-CN、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph2-CN、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph3-CN、R¹-Te2-CH₂CH₂-Np3-C≡C-Np1-CN、R¹-Te2-CH₂CH₂-Np3-C≡C-Np2-CN、R¹-Te2-CH₂CH₂-Np3-C≡C-Np3-CN、R¹-Te2-CH₂CH₂-Np3-C≡C-Np4-CN、
【０１５８】
R¹-Te1-CH₂CH₂-Np4-Ph1-CN、R¹-Te1-CH₂CH₂-Np4-Ph2-CN、R¹-Te1-CH₂CH₂-Np4-Ph3-CN、R¹-Te1-CH₂CH₂-Np4-Np1-CN、R¹-Te1-CH₂CH₂-Np4-Np2-CN、R¹-Te1-CH₂CH₂-Np4-Np3-CN、R¹-Te1-CH₂CH₂-Np4-Np4-CN、R¹-Te2-CH₂CH₂-Np4-Ph1-CN、R¹-Te2-CH₂CH₂-Np4-Ph2-CN、R¹-Te2-CH₂CH₂-Np4-Ph3-CN、R¹-Te2-CH₂CH₂-Np4-Np1-CN、R¹-Te2-CH₂CH₂-Np4-Np2-CN、R¹-Te2-CH₂CH₂-Np4-Np3-CN、R¹-Te2-CH₂CH₂-Np4-Np4-CN、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Ph2-CN、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Ph3-CN、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np1-CN、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np2-CN、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np3-CN、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np4-CN、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph1-CN、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph2-CN、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph3-CN、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np1-CN、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np2-CN、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np3-CN、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np4-CN、R¹-Te1-CH₂CH₂-Np4-C≡C-Ph2-CN、R¹-Te1-CH₂CH₂-Np4-C≡C-Ph3-CN、R¹-Te1-CH₂CH₂-Np4-C≡C-Np1-CN、R¹-Te1-CH₂CH₂-Np4-C≡C-Np2-CN、R¹-Te1-CH₂CH₂-Np4-C≡C-Np3-CN、R¹-Te1-CH₂CH₂-Np4-C≡C-Np4-CN、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph1-CN、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph2-CN、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph3-CN、R¹-Te2-CH₂CH₂-Np4-C≡C-Np1-CN、R¹-Te2-CH₂CH₂-Np4-C≡C-Np2-CN、R¹-Te2-CH₂CH₂-Np4-C≡C-Np3-CN、R¹-Te2-CH₂CH₂-Np4-C≡C-Np4-CN、
【０１５９】
R¹-Te1-C≡C-Ph1-Ph1-CN、R¹-Te1-C≡C-Ph1-Ph2-CN、R¹-Te1-C≡C-Ph1-Ph3-CN、R¹-Te1-C≡C-Ph1-Np1-CN、R¹-Te1-C≡C-Ph1-Np2-CN、R¹-Te1-C≡C-Ph1-Np3-CN、R¹-Te1-C≡C-Ph1-Np4-CN、R¹-Te2-C≡C-Ph1-Ph1-CN、R¹-Te2-C≡C-Ph1-Ph2-CN、R¹-Te2-C≡C-Ph1-Ph3-CN、R¹-Te2-C≡C-Ph1-Np1-CN、R¹-Te2-C≡C-Ph1-Np2-CN、R¹-Te2-C≡C-Ph1-Np3-CN、R¹-Te2-C≡C-Ph1-Np4-CN、R¹-Te1-C≡C-Ph1-CH₂CH₂-Ph2-CN、R¹-Te1-C≡C-Ph1-CH₂CH₂-Ph3-CN、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np1-CN、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np2-CN、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np3-CN、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np4-CN、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph1-CN、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph2-CN、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph3-CN、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np1-CN、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np2-CN、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np3-CN、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np4-CN、R¹-Te1-C≡C-Ph1-C≡C-Ph2-CN、R¹-Te1-C≡C-Ph1-C≡C-Ph3-CN、R¹-Te1-C≡C-Ph1-C≡C-Np1-CN、R¹-Te1-C≡C-Ph1-C≡C-Np2-CN、R¹-Te1-C≡C-Ph1-C≡C-Np3-CN、R¹-Te1-C≡C-Ph1-C≡C-Np4-CN、R¹-Te2-C≡C-Ph1-C≡C-Ph1-CN、R¹-Te2-C≡C-Ph1-C≡C-Ph2-CN、R¹-Te2-C≡C-Ph1-C≡C-Ph3-CN、R¹-Te2-C≡C-Ph1-C≡C-Np1-CN、R¹-Te2-C≡C-Ph1-C≡C-Np2-CN、R¹-Te2-C≡C-Ph1-C≡C-Np3-CN、R¹-Te2-C≡C-Ph1-C≡C-Np4-CN、
【０１６０】
R¹-Te1-C≡C-Ph2-Ph1-CN、R¹-Te1-C≡C-Ph2-Ph2-CN、R¹-Te1-C≡C-Ph2-Ph3-CN、R¹-Te1-C≡C-Ph2-Np1-CN、R¹-Te1-C≡C-Ph2-Np2-CN、R¹-Te1-C≡C-Ph2-Np3-CN、R¹-Te1-C≡C-Ph2-Np4-CN、R¹-Te2-C≡C-Ph2-Ph1-CN、R¹-Te2-C≡C-Ph2-Ph2-CN、R¹-Te2-C≡C-Ph2-Ph3-CN、R¹-Te2-C≡C-Ph2-Np1-CN、R¹-Te2-C≡C-Ph2-Np2-CN、R¹-Te2-C≡C-Ph2-Np3-CN、R¹-Te2-C≡C-Ph2-Np4-CN、R¹-Te1-C≡C-Ph2-CH₂CH₂-Ph2-CN、R¹-Te1-C≡C-Ph2-CH₂CH₂-Ph3-CN、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np1-CN、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np2-CN、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np3-CN、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np4-CN、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph1-CN、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph2-CN、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph3-CN、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np1-CN、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np2-CN、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np3-CN、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np4-CN、R¹-Te1-C≡C-Ph2-C≡C-Ph2-CN、R¹-Te1-C≡C-Ph2-C≡C-Ph3-CN、R¹-Te1-C≡C-Ph2-C≡C-Np1-CN、R¹-Te1-C≡C-Ph2-C≡C-Np2-CN、R¹-Te1-C≡C-Ph2-C≡C-Np3-CN、R¹-Te1-C≡C-Ph2-C≡C-Np4-CN、R¹-Te2-C≡C-Ph2-C≡C-Ph1-CN、R¹-Te2-C≡C-Ph2-C≡C-Ph2-CN、R¹-Te2-C≡C-Ph2-C≡C-Ph3-CN、R¹-Te2-C≡C-Ph2-C≡C-Np1-CN、R¹-Te2-C≡C-Ph2-C≡C-Np2-CN、R¹-Te2-C≡C-Ph2-C≡C-Np3-CN、R¹-Te2-C≡C-Ph2-C≡C-Np4-CN、
【０１６１】
R¹-Te1-C≡C-Ph3-Ph1-CN、R¹-Te1-C≡C-Ph3-Ph2-CN、R¹-Te1-C≡C-Ph3-Ph3-CN、R¹-Te1-C≡C-Ph3-Np1-CN、R¹-Te1-C≡C-Ph3-Np2-CN、R¹-Te1-C≡C-Ph3-Np3-CN、R¹-Te1-C≡C-Ph3-Np4-CN、R¹-Te2-C≡C-Ph3-Ph1-CN、R¹-Te2-C≡C-Ph3-Ph2-CN、R¹-Te2-C≡C-Ph3-Ph3-CN、R¹-Te2-C≡C-Ph3-Np1-CN、R¹-Te2-C≡C-Ph3-Np2-CN、R¹-Te2-C≡C-Ph3-Np3-CN、R¹-Te2-C≡C-Ph3-Np4-CN、R¹-Te1-C≡C-Ph3-CH₂CH₂-Ph2-CN、R¹-Te1-C≡C-Ph3-CH₂CH₂-Ph3-CN、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np1-CN、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np2-CN、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np3-CN、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np4-CN、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph1-CN、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph2-CN、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph3-CN、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np1-CN、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np2-CN、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np3-CN、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np4-CN、R¹-Te1-C≡C-Ph3-C≡C-Ph2-CN、R¹-Te1-C≡C-Ph3-C≡C-Ph3-CN、R¹-Te1-C≡C-Ph3-C≡C-Np1-CN、R¹-Te1-C≡C-Ph3-C≡C-Np2-CN、R¹-Te1-C≡C-Ph3-C≡C-Np3-CN、R¹-Te1-C≡C-Ph3-C≡C-Np4-CN、R¹-Te2-C≡C-Ph3-C≡C-Ph1-CN、R¹-Te2-C≡C-Ph3-C≡C-Ph2-CN、R¹-Te2-C≡C-Ph3-C≡C-Ph3-CN、R¹-Te2-C≡C-Ph3-C≡C-Np1-CN、R¹-Te2-C≡C-Ph3-C≡C-Np2-CN、R¹-Te2-C≡C-Ph3-C≡C-Np3-CN、R¹-Te2-C≡C-Ph3-C≡C-Np4-CN、
【０１６２】
R¹-Te1-C≡C-Np1-Ph1-CN、R¹-Te1-C≡C-Np1-Ph2-CN、R¹-Te1-C≡C-Np1-Ph3-CN、R¹-Te1-C≡C-Np1-Np1-CN、R¹-Te1-C≡C-Np1-Np2-CN、R¹-Te1-C≡C-Np1-Np3-CN、R¹-Te1-C≡C-Np1-Np4-CN、R¹-Te2-C≡C-Np1-Ph1-CN、R¹-Te2-C≡C-Np1-Ph2-CN、R¹-Te2-C≡C-Np1-Ph3-CN、R¹-Te2-C≡C-Np1-Np1-CN、R¹-Te2-C≡C-Np1-Np2-CN、R¹-Te2-C≡C-Np1-Np3-CN、R¹-Te2-C≡C-Np1-Np4-CN、R¹-Te1-C≡C-Np1-CH₂CH₂-Ph2-CN、R¹-Te1-C≡C-Np1-CH₂CH₂-Ph3-CN、R¹-Te1-C≡C-Np1-CH₂CH₂-Np1-CN、R¹-Te1-C≡C-Np1-CH₂CH₂-Np2-CN、R¹-Te1-C≡C-Np1-CH₂CH₂-Np3-CN、R¹-Te1-C≡C-Np1-CH₂CH₂-Np4-CN、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph1-CN、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph2-CN、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph3-CN、R¹-Te2-C≡C-Np1-CH₂CH₂-Np1-CN、R¹-Te2-C≡C-Np1-CH₂CH₂-Np2-CN、R¹-Te2-C≡C-Np1-CH₂CH₂-Np3-CN、R¹-Te2-C≡C-Np1-CH₂CH₂-Np4-CN、R¹-Te1-C≡C-Np1-C≡C-Ph2-CN、R¹-Te1-C≡C-Np1-C≡C-Ph3-CN、R¹-Te1-C≡C-Np1-C≡C-Np1-CN、R¹-Te1-C≡C-Np1-C≡C-Np2-CN、R¹-Te1-C≡C-Np1-C≡C-Np3-CN、R¹-Te1-C≡C-Np1-C≡C-Np4-CN、R¹-Te2-C≡C-Np1-C≡C-Ph1-CN、R¹-Te2-C≡C-Np1-C≡C-Ph2-CN、R¹-Te2-C≡C-Np1-C≡C-Ph3-CN、R¹-Te2-C≡C-Np1-C≡C-Np1-CN、R¹-Te2-C≡C-Np1-C≡C-Np2-CN、R¹-Te2-C≡C-Np1-C≡C-Np3-CN、R¹-Te2-C≡C-Np1-C≡C-Np4-CN、
【０１６３】
R¹-Te1-C≡C-Np2-Ph1-CN、R¹-Te1-C≡C-Np2-Ph2-CN、R¹-Te1-C≡C-Np2-Ph3-CN、R¹-Te1-C≡C-Np2-Np1-CN、R¹-Te1-C≡C-Np2-Np2-CN、R¹-Te1-C≡C-Np2-Np3-CN、R¹-Te1-C≡C-Np2-Np4-CN、R¹-Te2-C≡C-Np2-Ph1-CN、R¹-Te2-C≡C-Np2-Ph2-CN、R¹-Te2-C≡C-Np2-Ph3-CN、R¹-Te2-C≡C-Np2-Np1-CN、R¹-Te2-C≡C-Np2-Np2-CN、R¹-Te2-C≡C-Np2-Np3-CN、R¹-Te2-C≡C-Np2-Np4-CN、R¹-Te1-C≡C-Np2-CH₂CH₂-Ph2-CN、R¹-Te1-C≡C-Np2-CH₂CH₂-Ph3-CN、R¹-Te1-C≡C-Np2-CH₂CH₂-Np1-CN、R¹-Te1-C≡C-Np2-CH₂CH₂-Np2-CN、R¹-Te1-C≡C-Np2-CH₂CH₂-Np3-CN、R¹-Te1-C≡C-Np2-CH₂CH₂-Np4-CN、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph1-CN、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph2-CN、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph3-CN、R¹-Te2-C≡C-Np2-CH₂CH₂-Np1-CN、R¹-Te2-C≡C-Np2-CH₂CH₂-Np2-CN、R¹-Te2-C≡C-Np2-CH₂CH₂-Np3-CN、R¹-Te2-C≡C-Np2-CH₂CH₂-Np4-CN、R¹-Te1-C≡C-Np2-C≡C-Ph2-CN、R¹-Te1-C≡C-Np2-C≡C-Ph3-CN、R¹-Te1-C≡C-Np2-C≡C-Np1-CN、R¹-Te1-C≡C-Np2-C≡C-Np2-CN、R¹-Te1-C≡C-Np2-C≡C-Np3-CN、R¹-Te1-C≡C-Np2-C≡C-Np4-CN、R¹-Te2-C≡C-Np2-C≡C-Ph1-CN、R¹-Te2-C≡C-Np2-C≡C-Ph2-CN、R¹-Te2-C≡C-Np2-C≡C-Ph3-CN、R¹-Te2-C≡C-Np2-C≡C-Np1-CN、R¹-Te2-C≡C-Np2-C≡C-Np2-CN、R¹-Te2-C≡C-Np2-C≡C-Np3-CN、R¹-Te2-C≡C-Np2-C≡C-Np4-CN、
【０１６４】
R¹-Te1-C≡C-Np3-Ph1-CN、R¹-Te1-C≡C-Np3-Ph2-CN、R¹-Te1-C≡C-Np3-Ph3-CN、R¹-Te1-C≡C-Np3-Np1-CN、R¹-Te1-C≡C-Np3-Np2-CN、R¹-Te1-C≡C-Np3-Np3-CN、R¹-Te1-C≡C-Np3-Np4-CN、R¹-Te2-C≡C-Np3-Ph1-CN、R¹-Te2-C≡C-Np3-Ph2-CN、R¹-Te2-C≡C-Np3-Ph3-CN、R¹-Te2-C≡C-Np3-Np1-CN、R¹-Te2-C≡C-Np3-Np2-CN、R¹-Te2-C≡C-Np3-Np3-CN、R¹-Te2-C≡C-Np3-Np4-CN、R¹-Te1-C≡C-Np3-CH₂CH₂-Ph2-CN、R¹-Te1-C≡C-Np3-CH₂CH₂-Ph3-CN、R¹-Te1-C≡C-Np3-CH₂CH₂-Np1-CN、R¹-Te1-C≡C-Np3-CH₂CH₂-Np2-CN、R¹-Te1-C≡C-Np3-CH₂CH₂-Np3-CN、R¹-Te1-C≡C-Np3-CH₂CH₂-Np4-CN、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph1-CN、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph2-CN、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph3-CN、R¹-Te2-C≡C-Np3-CH₂CH₂-Np1-CN、R¹-Te2-C≡C-Np3-CH₂CH₂-Np2-CN、R¹-Te2-C≡C-Np3-CH₂CH₂-Np3-CN、R¹-Te2-C≡C-Np3-CH₂CH₂-Np4-CN、R¹-Te1-C≡C-Np3-C≡C-Ph2-CN、R¹-Te1-C≡C-Np3-C≡C-Ph3-CN、R¹-Te1-C≡C-Np3-C≡C-Np1-CN、R¹-Te1-C≡C-Np3-C≡C-Np2-CN、R¹-Te1-C≡C-Np3-C≡C-Np3-CN、R¹-Te1-C≡C-Np3-C≡C-Np4-CN、R¹-Te2-C≡C-Np3-C≡C-Ph1-CN、R¹-Te2-C≡C-Np3-C≡C-Ph2-CN、R¹-Te2-C≡C-Np3-C≡C-Ph3-CN、R¹-Te2-C≡C-Np3-C≡C-Np1-CN、R¹-Te2-C≡C-Np3-C≡C-Np2-CN、R¹-Te2-C≡C-Np3-C≡C-Np3-CN、R¹-Te2-C≡C-Np3-C≡C-Np4-CN、
【０１６５】
R¹-Te1-C≡C-Np4-Ph1-CN、R¹-Te1-C≡C-Np4-Ph2-CN、R¹-Te1-C≡C-Np4-Ph3-CN、R¹-Te1-C≡C-Np4-Np1-CN、R¹-Te1-C≡C-Np4-Np2-CN、R¹-Te1-C≡C-Np4-Np3-CN、R¹-Te1-C≡C-Np4-Np4-CN、R¹-Te2-C≡C-Np4-Ph1-CN、R¹-Te2-C≡C-Np4-Ph2-CN、R¹-Te2-C≡C-Np4-Ph3-CN、R¹-Te2-C≡C-Np4-Np1-CN、R¹-Te2-C≡C-Np4-Np2-CN、R¹-Te2-C≡C-Np4-Np3-CN、R¹-Te2-C≡C-Np4-Np4-CN、R¹-Te1-C≡C-Np4-CH₂CH₂-Ph2-CN、R¹-Te1-C≡C-Np4-CH₂CH₂-Ph3-CN、R¹-Te1-C≡C-Np4-CH₂CH₂-Np1-CN、R¹-Te1-C≡C-Np4-CH₂CH₂-Np2-CN、R¹-Te1-C≡C-Np4-CH₂CH₂-Np3-CN、R¹-Te1-C≡C-Np4-CH₂CH₂-Np4-CN、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph1-CN、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph2-CN、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph3-CN、R¹-Te2-C≡C-Np4-CH₂CH₂-Np1-CN、R¹-Te2-C≡C-Np4-CH₂CH₂-Np2-CN、R¹-Te2-C≡C-Np4-CH₂CH₂-Np3-CN、R¹-Te2-C≡C-Np4-CH₂CH₂-Np4-CN、R¹-Te1-C≡C-Np4-C≡C-Ph2-CN、R¹-Te1-C≡C-Np4-C≡C-Ph3-CN、R¹-Te1-C≡C-Np4-C≡C-Np1-CN、R¹-Te1-C≡C-Np4-C≡C-Np2-CN、R¹-Te1-C≡C-Np4-C≡C-Np3-CN、R¹-Te1-C≡C-Np4-C≡C-Np4-CN、R¹-Te2-C≡C-Np4-C≡C-Ph1-CN、R¹-Te2-C≡C-Np4-C≡C-Ph2-CN、R¹-Te2-C≡C-Np4-C≡C-Ph3-CN、R¹-Te2-C≡C-Np4-C≡C-Np1-CN、R¹-Te2-C≡C-Np4-C≡C-Np2-CN、R¹-Te2-C≡C-Np4-C≡C-Np3-CN、R¹-Te2-C≡C-Np4-C≡C-Np4-CN、
【０１６６】
m=0、n=1、Vが単結合、Zがトリフルオロメチル基の場合、
【０１６７】
R¹-Te1-Cy-Ph1-CF₃、R¹-Te1-Cy-Ph2-CF₃、R¹-Te1-Cy-Ph3-CF₃、R¹-Te1-Cy-Np1-CF₃、R¹-Te1-Cy-Np2-CF₃、R¹-Te1-Cy-Np3-CF₃、R¹-Te1-Cy-Np4-CF₃、R¹-Te2-Cy-Ph1-CF₃、R¹-Te2-Cy-Ph2-CF₃、R¹-Te2-Cy-Ph3-CF₃、R¹-Te2-Cy-Np1-CF₃、R¹-Te2-Cy-Np2-CF₃、R¹-Te2-Cy-Np3-CF₃、R¹-Te2-Cy-Np4-CF₃、R¹-Te1-Cy-CH₂CH₂-Ph2-CF₃、R¹-Te1-Cy-CH₂CH₂-Ph3-CF₃、R¹-Te1-Cy-CH₂CH₂-Np1-CF₃、R¹-Te1-Cy-CH₂CH₂-Np2-CF₃、R¹-Te1-Cy-CH₂CH₂-Np3-CF₃、R¹-Te1-Cy-CH₂CH₂-Np4-CF₃、R¹-Te2-Cy-CH₂CH₂-Ph1-CF₃、R¹-Te2-Cy-CH₂CH₂-Ph2-CF₃、R¹-Te2-Cy-CH₂CH₂-Ph3-CF₃、R¹-Te2-Cy-CH₂CH₂-Np1-CF₃、R¹-Te2-Cy-CH₂CH₂-Np2-CF₃、R¹-Te2-Cy-CH₂CH₂-Np3-CF₃、R¹-Te2-Cy-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Cy-Ph1-CF₃、R¹-Te1-CH₂CH₂-Cy-Ph2-CF₃、R¹-Te1-CH₂CH₂-Cy-Ph3-CF₃、R¹-Te1-CH₂CH₂-Cy-Np1-CF₃、R¹-Te1-CH₂CH₂-Cy-Np2-CF₃、R¹-Te1-CH₂CH₂-Cy-Np3-CF₃、R¹-Te1-CH₂CH₂-Cy-Np4-CF₃、R¹-Te2-CH₂CH₂-Cy-Ph1-CF₃、R¹-Te2-CH₂CH₂-Cy-Ph2-CF₃、R¹-Te2-CH₂CH₂-Cy-Ph3-CF₃、R¹-Te2-CH₂CH₂-Cy-Np1-CF₃、R¹-Te2-CH₂CH₂-Cy-Np2-CF₃、R¹-Te2-CH₂CH₂-Cy-Np3-CF₃、R¹-Te2-CH₂CH₂-Cy-Np4-CF₃、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Cy-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Cy-CH₂CH₂-Np4-CF₃、
【０１６８】
R¹-Te1-Ph1-Ph1-CF₃、R¹-Te1-Ph1-Ph2-CF₃、R¹-Te1-Ph1-Ph3-CF₃、R¹-Te1-Ph1-Np1-CF₃、R¹-Te1-Ph1-Np2-CF₃、R¹-Te1-Ph1-Np3-CF₃、R¹-Te1-Ph1-Np4-CF₃、R¹-Te2-Ph1-Ph1-CF₃、R¹-Te2-Ph1-Ph2-CF₃、R¹-Te2-Ph1-Ph3-CF₃、R¹-Te2-Ph1-Np1-CF₃、R¹-Te2-Ph1-Np2-CF₃、R¹-Te2-Ph1-Np3-CF₃、R¹-Te2-Ph1-Np4-CF₃、R¹-Te1-Ph1-CH₂CH₂-Ph2-CF₃、R¹-Te1-Ph1-CH₂CH₂-Ph3-CF₃、R¹-Te1-Ph1-CH₂CH₂-Np1-CF₃、R¹-Te1-Ph1-CH₂CH₂-Np2-CF₃、R¹-Te1-Ph1-CH₂CH₂-Np3-CF₃、R¹-Te1-Ph1-CH₂CH₂-Np4-CF₃、R¹-Te2-Ph1-CH₂CH₂-Ph1-CF₃、R¹-Te2-Ph1-CH₂CH₂-Ph2-CF₃、R¹-Te2-Ph1-CH₂CH₂-Ph3-CF₃、R¹-Te2-Ph1-CH₂CH₂-Np1-CF₃、R¹-Te2-Ph1-CH₂CH₂-Np2-CF₃、R¹-Te2-Ph1-CH₂CH₂-Np3-CF₃、R¹-Te2-Ph1-CH₂CH₂-Np4-CF₃、R¹-Te1-Ph1-C≡C-Ph2-CF₃、R¹-Te1-Ph1-C≡C-Ph3-CF₃、R¹-Te1-Ph1-C≡C-Np1-CF₃、R¹-Te1-Ph1-C≡C-Np2-CF₃、R¹-Te1-Ph1-C≡C-Np3-CF₃、R¹-Te1-Ph1-C≡C-Np4-CF₃、R¹-Te2-Ph1-C≡C-Ph1-CF₃、R¹-Te2-Ph1-C≡C-Ph2-CF₃、R¹-Te2-Ph1-C≡C-Ph3-CF₃、R¹-Te2-Ph1-C≡C-Np1-CF₃、R¹-Te2-Ph1-C≡C-Np2-CF₃、R¹-Te2-Ph1-C≡C-Np3-CF₃、R¹-Te2-Ph1-C≡C-Np4-CF₃、
【０１６９】
R¹-Te1-Ph2-Ph1-CF₃、R¹-Te1-Ph2-Ph2-CF₃、R¹-Te1-Ph2-Ph3-CF₃、R¹-Te1-Ph2-Np1-CF₃、R¹-Te1-Ph2-Np2-CF₃、R¹-Te1-Ph2-Np3-CF₃、R¹-Te1-Ph2-Np4-CF₃、R¹-Te2-Ph2-Ph1-CF₃、R¹-Te2-Ph2-Ph2-CF₃、R¹-Te2-Ph2-Ph3-CF₃、R¹-Te2-Ph2-Np1-CF₃、R¹-Te2-Ph2-Np2-CF₃、R¹-Te2-Ph2-Np3-CF₃、R¹-Te2-Ph2-Np4-CF₃、R¹-Te1-Ph2-CH₂CH₂-Ph2-CF₃、R¹-Te1-Ph2-CH₂CH₂-Ph3-CF₃、R¹-Te1-Ph2-CH₂CH₂-Np1-CF₃、R¹-Te1-Ph2-CH₂CH₂-Np2-CF₃、R¹-Te1-Ph2-CH₂CH₂-Np3-CF₃、R¹-Te1-Ph2-CH₂CH₂-Np4-CF₃、R¹-Te2-Ph2-CH₂CH₂-Ph1-CF₃、R¹-Te2-Ph2-CH₂CH₂-Ph2-CF₃、R¹-Te2-Ph2-CH₂CH₂-Ph3-CF₃、R¹-Te2-Ph2-CH₂CH₂-Np1-CF₃、R¹-Te2-Ph2-CH₂CH₂-Np2-CF₃、R¹-Te2-Ph2-CH₂CH₂-Np3-CF₃、R¹-Te2-Ph2-CH₂CH₂-Np4-CF₃、R¹-Te1-Ph2-C≡C-Ph2-CF₃、R¹-Te1-Ph2-C≡C-Ph3-CF₃、R¹-Te1-Ph2-C≡C-Np1-CF₃、R¹-Te1-Ph2-C≡C-Np2-CF₃、R¹-Te1-Ph2-C≡C-Np3-CF₃、R¹-Te1-Ph2-C≡C-Np4-CF₃、R¹-Te2-Ph2-C≡C-Ph1-CF₃、R¹-Te2-Ph2-C≡C-Ph2-CF₃、R¹-Te2-Ph2-C≡C-Ph3-CF₃、R¹-Te2-Ph2-C≡C-Np1-CF₃、R¹-Te2-Ph2-C≡C-Np2-CF₃、R¹-Te2-Ph2-C≡C-Np3-CF₃、R¹-Te2-Ph2-C≡C-Np4-CF₃、
【０１７０】
R¹-Te1-Ph3-Ph1-CF₃、R¹-Te1-Ph3-Ph2-CF₃、R¹-Te1-Ph3-Ph3-CF₃、R¹-Te1-Ph3-Np1-CF₃、R¹-Te1-Ph3-Np2-CF₃、R¹-Te1-Ph3-Np3-CF₃、R¹-Te1-Ph3-Np4-CF₃、R¹-Te2-Ph3-Ph1-CF₃、R¹-Te2-Ph3-Ph2-CF₃、R¹-Te2-Ph3-Ph3-CF₃、R¹-Te2-Ph3-Np1-CF₃、R¹-Te2-Ph3-Np2-CF₃、R¹-Te2-Ph3-Np3-CF₃、R¹-Te2-Ph3-Np4-CF₃、R¹-Te1-Ph3-CH₂CH₂-Ph2-CF₃、R¹-Te1-Ph3-CH₂CH₂-Ph3-CF₃、R¹-Te1-Ph3-CH₂CH₂-Np1-CF₃、R¹-Te1-Ph3-CH₂CH₂-Np2-CF₃、R¹-Te1-Ph3-CH₂CH₂-Np3-CF₃、R¹-Te1-Ph3-CH₂CH₂-Np4-CF₃、R¹-Te2-Ph3-CH₂CH₂-Ph1-CF₃、R¹-Te2-Ph3-CH₂CH₂-Ph2-CF₃、R¹-Te2-Ph3-CH₂CH₂-Ph3-CF₃、R¹-Te2-Ph3-CH₂CH₂-Np1-CF₃、R¹-Te2-Ph3-CH₂CH₂-Np2-CF₃、R¹-Te2-Ph3-CH₂CH₂-Np3-CF₃、R¹-Te2-Ph3-CH₂CH₂-Np4-CF₃、R¹-Te1-Ph3-C≡C-Ph2-CF₃、R¹-Te1-Ph3-C≡C-Ph3-CF₃、R¹-Te1-Ph3-C≡C-Np1-CF₃、R¹-Te1-Ph3-C≡C-Np2-CF₃、R¹-Te1-Ph3-C≡C-Np3-CF₃、R¹-Te1-Ph3-C≡C-Np4-CF₃、R¹-Te2-Ph3-C≡C-Ph1-CF₃、R¹-Te2-Ph3-C≡C-Ph2-CF₃、R¹-Te2-Ph3-C≡C-Ph3-CF₃、R¹-Te2-Ph3-C≡C-Np1-CF₃、R¹-Te2-Ph3-C≡C-Np2-CF₃、R¹-Te2-Ph3-C≡C-Np3-CF₃、R¹-Te2-Ph3-C≡C-Np4-CF₃、
【０１７１】
R¹-Te1-Np1-Ph1-CF₃、R¹-Te1-Np1-Ph2-CF₃、R¹-Te1-Np1-Ph3-CF₃、R¹-Te1-Np1-Np1-CF₃、R¹-Te1-Np1-Np2-CF₃、R¹-Te1-Np1-Np3-CF₃、R¹-Te1-Np1-Np4-CF₃、R¹-Te2-Np1-Ph1-CF₃、R¹-Te2-Np1-Ph2-CF₃、R¹-Te2-Np1-Ph3-CF₃、R¹-Te2-Np1-Np1-CF₃、R¹-Te2-Np1-Np2-CF₃、R¹-Te2-Np1-Np3-CF₃、R¹-Te2-Np1-Np4-CF₃、R¹-Te1-Np1-CH₂CH₂-Ph2-CF₃、R¹-Te1-Np1-CH₂CH₂-Ph3-CF₃、R¹-Te1-Np1-CH₂CH₂-Np1-CF₃、R¹-Te1-Np1-CH₂CH₂-Np2-CF₃、R¹-Te1-Np1-CH₂CH₂-Np3-CF₃、R¹-Te1-Np1-CH₂CH₂-Np4-CF₃、R¹-Te2-Np1-CH₂CH₂-Ph1-CF₃、R¹-Te2-Np1-CH₂CH₂-Ph2-CF₃、R¹-Te2-Np1-CH₂CH₂-Ph3-CF₃、R¹-Te2-Np1-CH₂CH₂-Np1-CF₃、R¹-Te2-Np1-CH₂CH₂-Np2-CF₃、R¹-Te2-Np1-CH₂CH₂-Np3-CF₃、R¹-Te2-Np1-CH₂CH₂-Np4-CF₃、R¹-Te1-Np1-C≡C-Ph2-CF₃、R¹-Te1-Np1-C≡C-Ph3-CF₃、R¹-Te1-Np1-C≡C-Np1-CF₃、R¹-Te1-Np1-C≡C-Np2-CF₃、R¹-Te1-Np1-C≡C-Np3-CF₃、R¹-Te1-Np1-C≡C-Np4-CF₃、R¹-Te2-Np1-C≡C-Ph1-CF₃、R¹-Te2-Np1-C≡C-Ph2-CF₃、R¹-Te2-Np1-C≡C-Ph3-CF₃、R¹-Te2-Np1-C≡C-Np1-CF₃、R¹-Te2-Np1-C≡C-Np2-CF₃、R¹-Te2-Np1-C≡C-Np3-CF₃、R¹-Te2-Np1-C≡C-Np4-CF₃、
【０１７２】
R¹-Te1-Np2-Ph1-CF₃、R¹-Te1-Np2-Ph2-CF₃、R¹-Te1-Np2-Ph3-CF₃、R¹-Te1-Np2-Np1-CF₃、R¹-Te1-Np2-Np2-CF₃、R¹-Te1-Np2-Np3-CF₃、R¹-Te1-Np2-Np4-CF₃、R¹-Te2-Np2-Ph1-CF₃、R¹-Te2-Np2-Ph2-CF₃、R¹-Te2-Np2-Ph3-CF₃、R¹-Te2-Np2-Np1-CF₃、R¹-Te2-Np2-Np2-CF₃、R¹-Te2-Np2-Np3-CF₃、R¹-Te2-Np2-Np4-CF₃、R¹-Te1-Np2-CH₂CH₂-Ph2-CF₃、R¹-Te1-Np2-CH₂CH₂-Ph3-CF₃、R¹-Te1-Np2-CH₂CH₂-Np1-CF₃、R¹-Te1-Np2-CH₂CH₂-Np2-CF₃、R¹-Te1-Np2-CH₂CH₂-Np3-CF₃、R¹-Te1-Np2-CH₂CH₂-Np4-CF₃、R¹-Te2-Np2-CH₂CH₂-Ph1-CF₃、R¹-Te2-Np2-CH₂CH₂-Ph2-CF₃、R¹-Te2-Np2-CH₂CH₂-Ph3-CF₃、R¹-Te2-Np2-CH₂CH₂-Np1-CF₃、R¹-Te2-Np2-CH₂CH₂-Np2-CF₃、R¹-Te2-Np2-CH₂CH₂-Np3-CF₃、R¹-Te2-Np2-CH₂CH₂-Np4-CF₃、R¹-Te1-Np2-C≡C-Ph2-CF₃、R¹-Te1-Np2-C≡C-Ph3-CF₃、R¹-Te1-Np2-C≡C-Np1-CF₃、R¹-Te1-Np2-C≡C-Np2-CF₃、R¹-Te1-Np2-C≡C-Np3-CF₃、R¹-Te1-Np2-C≡C-Np4-CF₃、R¹-Te2-Np2-C≡C-Ph1-CF₃、R¹-Te2-Np2-C≡C-Ph2-CF₃、R¹-Te2-Np2-C≡C-Ph3-CF₃、R¹-Te2-Np2-C≡C-Np1-CF₃、R¹-Te2-Np2-C≡C-Np2-CF₃、R¹-Te2-Np2-C≡C-Np3-CF₃、R¹-Te2-Np2-C≡C-Np4-CF₃、
【０１７３】
R¹-Te1-Np3-Ph1-CF₃、R¹-Te1-Np3-Ph2-CF₃、R¹-Te1-Np3-Ph3-CF₃、R¹-Te1-Np3-Np1-CF₃、R¹-Te1-Np3-Np2-CF₃、R¹-Te1-Np3-Np3-CF₃、R¹-Te1-Np3-Np4-CF₃、R¹-Te2-Np3-Ph1-CF₃、R¹-Te2-Np3-Ph2-CF₃、R¹-Te2-Np3-Ph3-CF₃、R¹-Te2-Np3-Np1-CF₃、R¹-Te2-Np3-Np2-CF₃、R¹-Te2-Np3-Np3-CF₃、R¹-Te2-Np3-Np4-CF₃、R¹-Te1-Np3-CH₂CH₂-Ph2-CF₃、R¹-Te1-Np3-CH₂CH₂-Ph3-CF₃、R¹-Te1-Np3-CH₂CH₂-Np1-CF₃、R¹-Te1-Np3-CH₂CH₂-Np2-CF₃、R¹-Te1-Np3-CH₂CH₂-Np3-CF₃、R¹-Te1-Np3-CH₂CH₂-Np4-CF₃、R¹-Te2-Np3-CH₂CH₂-Ph1-CF₃、R¹-Te2-Np3-CH₂CH₂-Ph2-CF₃、R¹-Te2-Np3-CH₂CH₂-Ph3-CF₃、R¹-Te2-Np3-CH₂CH₂-Np1-CF₃、R¹-Te2-Np3-CH₂CH₂-Np2-CF₃、R¹-Te2-Np3-CH₂CH₂-Np3-CF₃、R¹-Te2-Np3-CH₂CH₂-Np4-CF₃、R¹-Te1-Np3-C≡C-Ph2-CF₃、R¹-Te1-Np3-C≡C-Ph3-CF₃、R¹-Te1-Np3-C≡C-Np1-CF₃、R¹-Te1-Np3-C≡C-Np2-CF₃、R¹-Te1-Np3-C≡C-Np3-CF₃、R¹-Te1-Np3-C≡C-Np4-CF₃、R¹-Te2-Np3-C≡C-Ph1-CF₃、R¹-Te2-Np3-C≡C-Ph2-CF₃、R¹-Te2-Np3-C≡C-Ph3-CF₃、R¹-Te2-Np3-C≡C-Np1-CF₃、R¹-Te2-Np3-C≡C-Np2-CF₃、R¹-Te2-Np3-C≡C-Np3-CF₃、R¹-Te2-Np3-C≡C-Np4-CF₃、
【０１７４】
R¹-Te1-Np4-Ph1-CF₃、R¹-Te1-Np4-Ph2-CF₃、R¹-Te1-Np4-Ph3-CF₃、R¹-Te1-Np4-Np1-CF₃、R¹-Te1-Np4-Np2-CF₃、R¹-Te1-Np4-Np3-CF₃、R¹-Te1-Np4-Np4-CF₃、R¹-Te2-Np4-Ph1-CF₃、R¹-Te2-Np4-Ph2-CF₃、R¹-Te2-Np4-Ph3-CF₃、R¹-Te2-Np4-Np1-CF₃、R¹-Te2-Np4-Np2-CF₃、R¹-Te2-Np4-Np3-CF₃、R¹-Te2-Np4-Np4-CF₃、R¹-Te1-Np4-CH₂CH₂-Ph2-CF₃、R¹-Te1-Np4-CH₂CH₂-Ph3-CF₃、R¹-Te1-Np4-CH₂CH₂-Np1-CF₃、R¹-Te1-Np4-CH₂CH₂-Np2-CF₃、R¹-Te1-Np4-CH₂CH₂-Np3-CF₃、R¹-Te1-Np4-CH₂CH₂-Np4-CF₃、R¹-Te2-Np4-CH₂CH₂-Ph1-CF₃、R¹-Te2-Np4-CH₂CH₂-Ph2-CF₃、R¹-Te2-Np4-CH₂CH₂-Ph3-CF₃、R¹-Te2-Np4-CH₂CH₂-Np1-CF₃、R¹-Te2-Np4-CH₂CH₂-Np2-CF₃、R¹-Te2-Np4-CH₂CH₂-Np3-CF₃、R¹-Te2-Np4-CH₂CH₂-Np4-CF₃、R¹-Te1-Np4-C≡C-Ph2-CF₃、R¹-Te1-Np4-C≡C-Ph3-CF₃、R¹-Te1-Np4-C≡C-Np1-CF₃、R¹-Te1-Np4-C≡C-Np2-CF₃、R¹-Te1-Np4-C≡C-Np3-CF₃、R¹-Te1-Np4-C≡C-Np4-CF₃、R¹-Te2-Np4-C≡C-Ph1-CF₃、R¹-Te2-Np4-C≡C-Ph2-CF₃、R¹-Te2-Np4-C≡C-Ph3-CF₃、R¹-Te2-Np4-C≡C-Np1-CF₃、R¹-Te2-Np4-C≡C-Np2-CF₃、R¹-Te2-Np4-C≡C-Np3-CF₃、R¹-Te2-Np4-C≡C-Np4-CF₃、
【０１７５】
R¹-Te1-CH₂CH₂-Ph1-Ph1-CF₃、R¹-Te1-CH₂CH₂-Ph1-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph1-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph1-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph1-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph1-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph1-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph1-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph1-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph1-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph1-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph1-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph1-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph1-Np4-CF₃、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph1-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph1-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Ph1-C≡C-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph1-C≡C-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph1-C≡C-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph1-C≡C-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph1-C≡C-Np4-CF₃、
【０１７６】
R¹-Te1-CH₂CH₂-Ph2-Ph1-CF₃、R¹-Te1-CH₂CH₂-Ph2-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph2-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph2-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph2-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph2-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph2-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph2-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph2-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph2-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph2-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph2-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph2-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph2-Np4-CF₃、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph2-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph2-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Ph2-C≡C-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph2-C≡C-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph2-C≡C-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph2-C≡C-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph2-C≡C-Np4-CF₃、
【０１７７】
R¹-Te1-CH₂CH₂-Ph3-Ph1-CF₃、R¹-Te1-CH₂CH₂-Ph3-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph3-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph3-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph3-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph3-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph3-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph3-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph3-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph3-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph3-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph3-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph3-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph3-Np4-CF₃、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph3-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph3-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Ph3-C≡C-Ph2-CF₃、R¹-Te1-CH₂CH₂-Ph3-C≡C-Ph3-CF₃、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np1-CF₃、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np2-CF₃、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np3-CF₃、R¹-Te1-CH₂CH₂-Ph3-C≡C-Np4-CF₃、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph1-CF₃、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph2-CF₃、R¹-Te2-CH₂CH₂-Ph3-C≡C-Ph3-CF₃、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np1-CF₃、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np2-CF₃、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np3-CF₃、R¹-Te2-CH₂CH₂-Ph3-C≡C-Np4-CF₃、
【０１７８】
R¹-Te1-CH₂CH₂-Np1-Ph1-CF₃、R¹-Te1-CH₂CH₂-Np1-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np1-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np1-Np1-CF₃、R¹-Te1-CH₂CH₂-Np1-Np2-CF₃、R¹-Te1-CH₂CH₂-Np1-Np3-CF₃、R¹-Te1-CH₂CH₂-Np1-Np4-CF₃、R¹-Te2-CH₂CH₂-Np1-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np1-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np1-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np1-Np1-CF₃、R¹-Te2-CH₂CH₂-Np1-Np2-CF₃、R¹-Te2-CH₂CH₂-Np1-Np3-CF₃、R¹-Te2-CH₂CH₂-Np1-Np4-CF₃、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Np1-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Np1-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Np1-C≡C-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np1-C≡C-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np1-C≡C-Np1-CF₃、R¹-Te1-CH₂CH₂-Np1-C≡C-Np2-CF₃、R¹-Te1-CH₂CH₂-Np1-C≡C-Np3-CF₃、R¹-Te1-CH₂CH₂-Np1-C≡C-Np4-CF₃、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np1-C≡C-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np1-C≡C-Np1-CF₃、R¹-Te2-CH₂CH₂-Np1-C≡C-Np2-CF₃、R¹-Te2-CH₂CH₂-Np1-C≡C-Np3-CF₃、R¹-Te2-CH₂CH₂-Np1-C≡C-Np4-CF₃、
【０１７９】
R¹-Te1-CH₂CH₂-Np2-Ph1-CF₃、R¹-Te1-CH₂CH₂-Np2-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np2-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np2-Np1-CF₃、R¹-Te1-CH₂CH₂-Np2-Np2-CF₃、R¹-Te1-CH₂CH₂-Np2-Np3-CF₃、R¹-Te1-CH₂CH₂-Np2-Np4-CF₃、R¹-Te2-CH₂CH₂-Np2-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np2-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np2-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np2-Np1-CF₃、R¹-Te2-CH₂CH₂-Np2-Np2-CF₃、R¹-Te2-CH₂CH₂-Np2-Np3-CF₃、R¹-Te2-CH₂CH₂-Np2-Np4-CF₃、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Np2-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Np2-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Np2-C≡C-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np2-C≡C-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np2-C≡C-Np1-CF₃、R¹-Te1-CH₂CH₂-Np2-C≡C-Np2-CF₃、R¹-Te1-CH₂CH₂-Np2-C≡C-Np3-CF₃、R¹-Te1-CH₂CH₂-Np2-C≡C-Np4-CF₃、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np2-C≡C-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np2-C≡C-Np1-CF₃、R¹-Te2-CH₂CH₂-Np2-C≡C-Np2-CF₃、R¹-Te2-CH₂CH₂-Np2-C≡C-Np3-CF₃、R¹-Te2-CH₂CH₂-Np2-C≡C-Np4-CF₃、
【０１８０】
R¹-Te1-CH₂CH₂-Np3-Ph1-CF₃、R¹-Te1-CH₂CH₂-Np3-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np3-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np3-Np1-CF₃、R¹-Te1-CH₂CH₂-Np3-Np2-CF₃、R¹-Te1-CH₂CH₂-Np3-Np3-CF₃、R¹-Te1-CH₂CH₂-Np3-Np4-CF₃、R¹-Te2-CH₂CH₂-Np3-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np3-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np3-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np3-Np1-CF₃、R¹-Te2-CH₂CH₂-Np3-Np2-CF₃、R¹-Te2-CH₂CH₂-Np3-Np3-CF₃、R¹-Te2-CH₂CH₂-Np3-Np4-CF₃、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Np3-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Np3-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Np3-C≡C-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np3-C≡C-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np3-C≡C-Np1-CF₃、R¹-Te1-CH₂CH₂-Np3-C≡C-Np2-CF₃、R¹-Te1-CH₂CH₂-Np3-C≡C-Np3-CF₃、R¹-Te1-CH₂CH₂-Np3-C≡C-Np4-CF₃、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np3-C≡C-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np3-C≡C-Np1-CF₃、R¹-Te2-CH₂CH₂-Np3-C≡C-Np2-CF₃、R¹-Te2-CH₂CH₂-Np3-C≡C-Np3-CF₃、R¹-Te2-CH₂CH₂-Np3-C≡C-Np4-CF₃、
【０１８１】
R¹-Te1-CH₂CH₂-Np4-Ph1-CF₃、R¹-Te1-CH₂CH₂-Np4-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np4-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np4-Np1-CF₃、R¹-Te1-CH₂CH₂-Np4-Np2-CF₃、R¹-Te1-CH₂CH₂-Np4-Np3-CF₃、R¹-Te1-CH₂CH₂-Np4-Np4-CF₃、R¹-Te2-CH₂CH₂-Np4-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np4-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np4-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np4-Np1-CF₃、R¹-Te2-CH₂CH₂-Np4-Np2-CF₃、R¹-Te2-CH₂CH₂-Np4-Np3-CF₃、R¹-Te2-CH₂CH₂-Np4-Np4-CF₃、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np1-CF₃、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np2-CF₃、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np3-CF₃、R¹-Te1-CH₂CH₂-Np4-CH₂CH₂-Np4-CF₃、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np1-CF₃、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np2-CF₃、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np3-CF₃、R¹-Te2-CH₂CH₂-Np4-CH₂CH₂-Np4-CF₃、R¹-Te1-CH₂CH₂-Np4-C≡C-Ph2-CF₃、R¹-Te1-CH₂CH₂-Np4-C≡C-Ph3-CF₃、R¹-Te1-CH₂CH₂-Np4-C≡C-Np1-CF₃、R¹-Te1-CH₂CH₂-Np4-C≡C-Np2-CF₃、R¹-Te1-CH₂CH₂-Np4-C≡C-Np3-CF₃、R¹-Te1-CH₂CH₂-Np4-C≡C-Np4-CF₃、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph1-CF₃、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph2-CF₃、R¹-Te2-CH₂CH₂-Np4-C≡C-Ph3-CF₃、R¹-Te2-CH₂CH₂-Np4-C≡C-Np1-CF₃、R¹-Te2-CH₂CH₂-Np4-C≡C-Np2-CF₃、R¹-Te2-CH₂CH₂-Np4-C≡C-Np3-CF₃、R¹-Te2-CH₂CH₂-Np4-C≡C-Np4-CF₃、
【０１８２】
R¹-Te1-C≡C-Ph1-Ph1-CF₃、R¹-Te1-C≡C-Ph1-Ph2-CF₃、R¹-Te1-C≡C-Ph1-Ph3-CF₃、R¹-Te1-C≡C-Ph1-Np1-CF₃、R¹-Te1-C≡C-Ph1-Np2-CF₃、R¹-Te1-C≡C-Ph1-Np3-CF₃、R¹-Te1-C≡C-Ph1-Np4-CF₃、R¹-Te2-C≡C-Ph1-Ph1-CF₃、R¹-Te2-C≡C-Ph1-Ph2-CF₃、R¹-Te2-C≡C-Ph1-Ph3-CF₃、R¹-Te2-C≡C-Ph1-Np1-CF₃、R¹-Te2-C≡C-Ph1-Np2-CF₃、R¹-Te2-C≡C-Ph1-Np3-CF₃、R¹-Te2-C≡C-Ph1-Np4-CF₃、R¹-Te1-C≡C-Ph1-CH₂CH₂-Ph2-CF₃、R¹-Te1-C≡C-Ph1-CH₂CH₂-Ph3-CF₃、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np1-CF₃、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np2-CF₃、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np3-CF₃、R¹-Te1-C≡C-Ph1-CH₂CH₂-Np4-CF₃、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph1-CF₃、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph2-CF₃、R¹-Te2-C≡C-Ph1-CH₂CH₂-Ph3-CF₃、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np1-CF₃、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np2-CF₃、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np3-CF₃、R¹-Te2-C≡C-Ph1-CH₂CH₂-Np4-CF₃、R¹-Te1-C≡C-Ph1-C≡C-Ph2-CF₃、R¹-Te1-C≡C-Ph1-C≡C-Ph3-CF₃、R¹-Te1-C≡C-Ph1-C≡C-Np1-CF₃、R¹-Te1-C≡C-Ph1-C≡C-Np2-CF₃、R¹-Te1-C≡C-Ph1-C≡C-Np3-CF₃、R¹-Te1-C≡C-Ph1-C≡C-Np4-CF₃、R¹-Te2-C≡C-Ph1-C≡C-Ph1-CF₃、R¹-Te2-C≡C-Ph1-C≡C-Ph2-CF₃、R¹-Te2-C≡C-Ph1-C≡C-Ph3-CF₃、R¹-Te2-C≡C-Ph1-C≡C-Np1-CF₃、R¹-Te2-C≡C-Ph1-C≡C-Np2-CF₃、R¹-Te2-C≡C-Ph1-C≡C-Np3-CF₃、R¹-Te2-C≡C-Ph1-C≡C-Np4-CF₃、
【０１８３】
R¹-Te1-C≡C-Ph2-Ph1-CF₃、R¹-Te1-C≡C-Ph2-Ph2-CF₃、R¹-Te1-C≡C-Ph2-Ph3-CF₃、R¹-Te1-C≡C-Ph2-Np1-CF₃、R¹-Te1-C≡C-Ph2-Np2-CF₃、R¹-Te1-C≡C-Ph2-Np3-CF₃、R¹-Te1-C≡C-Ph2-Np4-CF₃、R¹-Te2-C≡C-Ph2-Ph1-CF₃、R¹-Te2-C≡C-Ph2-Ph2-CF₃、R¹-Te2-C≡C-Ph2-Ph3-CF₃、R¹-Te2-C≡C-Ph2-Np1-CF₃、R¹-Te2-C≡C-Ph2-Np2-CF₃、R¹-Te2-C≡C-Ph2-Np3-CF₃、R¹-Te2-C≡C-Ph2-Np4-CF₃、R¹-Te1-C≡C-Ph2-CH₂CH₂-Ph2-CF₃、R¹-Te1-C≡C-Ph2-CH₂CH₂-Ph3-CF₃、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np1-CF₃、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np2-CF₃、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np3-CF₃、R¹-Te1-C≡C-Ph2-CH₂CH₂-Np4-CF₃、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph1-CF₃、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph2-CF₃、R¹-Te2-C≡C-Ph2-CH₂CH₂-Ph3-CF₃、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np1-CF₃、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np2-CF₃、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np3-CF₃、R¹-Te2-C≡C-Ph2-CH₂CH₂-Np4-CF₃、R¹-Te1-C≡C-Ph2-C≡C-Ph2-CF₃、R¹-Te1-C≡C-Ph2-C≡C-Ph3-CF₃、R¹-Te1-C≡C-Ph2-C≡C-Np1-CF₃、R¹-Te1-C≡C-Ph2-C≡C-Np2-CF₃、R¹-Te1-C≡C-Ph2-C≡C-Np3-CF₃、R¹-Te1-C≡C-Ph2-C≡C-Np4-CF₃、R¹-Te2-C≡C-Ph2-C≡C-Ph1-CF₃、R¹-Te2-C≡C-Ph2-C≡C-Ph2-CF₃、R¹-Te2-C≡C-Ph2-C≡C-Ph3-CF₃、R¹-Te2-C≡C-Ph2-C≡C-Np1-CF₃、R¹-Te2-C≡C-Ph2-C≡C-Np2-CF₃、R¹-Te2-C≡C-Ph2-C≡C-Np3-CF₃、R¹-Te2-C≡C-Ph2-C≡C-Np4-CF₃、
【０１８４】
R¹-Te1-C≡C-Ph3-Ph1-CF₃、R¹-Te1-C≡C-Ph3-Ph2-CF₃、R¹-Te1-C≡C-Ph3-Ph3-CF₃、R¹-Te1-C≡C-Ph3-Np1-CF₃、R¹-Te1-C≡C-Ph3-Np2-CF₃、R¹-Te1-C≡C-Ph3-Np3-CF₃、R¹-Te1-C≡C-Ph3-Np4-CF₃、R¹-Te2-C≡C-Ph3-Ph1-CF₃、R¹-Te2-C≡C-Ph3-Ph2-CF₃、R¹-Te2-C≡C-Ph3-Ph3-CF₃、R¹-Te2-C≡C-Ph3-Np1-CF₃、R¹-Te2-C≡C-Ph3-Np2-CF₃、R¹-Te2-C≡C-Ph3-Np3-CF₃、R¹-Te2-C≡C-Ph3-Np4-CF₃、R¹-Te1-C≡C-Ph3-CH₂CH₂-Ph2-CF₃、R¹-Te1-C≡C-Ph3-CH₂CH₂-Ph3-CF₃、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np1-CF₃、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np2-CF₃、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np3-CF₃、R¹-Te1-C≡C-Ph3-CH₂CH₂-Np4-CF₃、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph1-CF₃、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph2-CF₃、R¹-Te2-C≡C-Ph3-CH₂CH₂-Ph3-CF₃、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np1-CF₃、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np2-CF₃、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np3-CF₃、R¹-Te2-C≡C-Ph3-CH₂CH₂-Np4-CF₃、R¹-Te1-C≡C-Ph3-C≡C-Ph2-CF₃、R¹-Te1-C≡C-Ph3-C≡C-Ph3-CF₃、R¹-Te1-C≡C-Ph3-C≡C-Np1-CF₃、R¹-Te1-C≡C-Ph3-C≡C-Np2-CF₃、R¹-Te1-C≡C-Ph3-C≡C-Np3-CF₃、R¹-Te1-C≡C-Ph3-C≡C-Np4-CF₃、R¹-Te2-C≡C-Ph3-C≡C-Ph1-CF₃、R¹-Te2-C≡C-Ph3-C≡C-Ph2-CF₃、R¹-Te2-C≡C-Ph3-C≡C-Ph3-CF₃、R¹-Te2-C≡C-Ph3-C≡C-Np1-CF₃、R¹-Te2-C≡C-Ph3-C≡C-Np2-CF₃、R¹-Te2-C≡C-Ph3-C≡C-Np3-CF₃、R¹-Te2-C≡C-Ph3-C≡C-Np4-CF₃、
【０１８５】
R¹-Te1-C≡C-Np1-Ph1-CF₃、R¹-Te1-C≡C-Np1-Ph2-CF₃、R¹-Te1-C≡C-Np1-Ph3-CF₃、R¹-Te1-C≡C-Np1-Np1-CF₃、R¹-Te1-C≡C-Np1-Np2-CF₃、R¹-Te1-C≡C-Np1-Np3-CF₃、R¹-Te1-C≡C-Np1-Np4-CF₃、R¹-Te2-C≡C-Np1-Ph1-CF₃、R¹-Te2-C≡C-Np1-Ph2-CF₃、R¹-Te2-C≡C-Np1-Ph3-CF₃、R¹-Te2-C≡C-Np1-Np1-CF₃、R¹-Te2-C≡C-Np1-Np2-CF₃、R¹-Te2-C≡C-Np1-Np3-CF₃、R¹-Te2-C≡C-Np1-Np4-CF₃、R¹-Te1-C≡C-Np1-CH₂CH₂-Ph2-CF₃、R¹-Te1-C≡C-Np1-CH₂CH₂-Ph3-CF₃、R¹-Te1-C≡C-Np1-CH₂CH₂-Np1-CF₃、R¹-Te1-C≡C-Np1-CH₂CH₂-Np2-CF₃、R¹-Te1-C≡C-Np1-CH₂CH₂-Np3-CF₃、R¹-Te1-C≡C-Np1-CH₂CH₂-Np4-CF₃、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph1-CF₃、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph2-CF₃、R¹-Te2-C≡C-Np1-CH₂CH₂-Ph3-CF₃、R¹-Te2-C≡C-Np1-CH₂CH₂-Np1-CF₃、R¹-Te2-C≡C-Np1-CH₂CH₂-Np2-CF₃、R¹-Te2-C≡C-Np1-CH₂CH₂-Np3-CF₃、R¹-Te2-C≡C-Np1-CH₂CH₂-Np4-CF₃、R¹-Te1-C≡C-Np1-C≡C-Ph2-CF₃、R¹-Te1-C≡C-Np1-C≡C-Ph3-CF₃、R¹-Te1-C≡C-Np1-C≡C-Np1-CF₃、R¹-Te1-C≡C-Np1-C≡C-Np2-CF₃、R¹-Te1-C≡C-Np1-C≡C-Np3-CF₃、R¹-Te1-C≡C-Np1-C≡C-Np4-CF₃、R¹-Te2-C≡C-Np1-C≡C-Ph1-CF₃、R¹-Te2-C≡C-Np1-C≡C-Ph2-CF₃、R¹-Te2-C≡C-Np1-C≡C-Ph3-CF₃、R¹-Te2-C≡C-Np1-C≡C-Np1-CF₃、R¹-Te2-C≡C-Np1-C≡C-Np2-CF₃、R¹-Te2-C≡C-Np1-C≡C-Np3-CF₃、R¹-Te2-C≡C-Np1-C≡C-Np4-CF₃、
【０１８６】
R¹-Te1-C≡C-Np2-Ph1-CF₃、R¹-Te1-C≡C-Np2-Ph2-CF₃、R¹-Te1-C≡C-Np2-Ph3-CF₃、R¹-Te1-C≡C-Np2-Np1-CF₃、R¹-Te1-C≡C-Np2-Np2-CF₃、R¹-Te1-C≡C-Np2-Np3-CF₃、R¹-Te1-C≡C-Np2-Np4-CF₃、R¹-Te2-C≡C-Np2-Ph1-CF₃、R¹-Te2-C≡C-Np2-Ph2-CF₃、R¹-Te2-C≡C-Np2-Ph3-CF₃、R¹-Te2-C≡C-Np2-Np1-CF₃、R¹-Te2-C≡C-Np2-Np2-CF₃、R¹-Te2-C≡C-Np2-Np3-CF₃、R¹-Te2-C≡C-Np2-Np4-CF₃、R¹-Te1-C≡C-Np2-CH₂CH₂-Ph2-CF₃、R¹-Te1-C≡C-Np2-CH₂CH₂-Ph3-CF₃、R¹-Te1-C≡C-Np2-CH₂CH₂-Np1-CF₃、R¹-Te1-C≡C-Np2-CH₂CH₂-Np2-CF₃、R¹-Te1-C≡C-Np2-CH₂CH₂-Np3-CF₃、R¹-Te1-C≡C-Np2-CH₂CH₂-Np4-CF₃、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph1-CF₃、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph2-CF₃、R¹-Te2-C≡C-Np2-CH₂CH₂-Ph3-CF₃、R¹-Te2-C≡C-Np2-CH₂CH₂-Np1-CF₃、R¹-Te2-C≡C-Np2-CH₂CH₂-Np2-CF₃、R¹-Te2-C≡C-Np2-CH₂CH₂-Np3-CF₃、R¹-Te2-C≡C-Np2-CH₂CH₂-Np4-CF₃、R¹-Te1-C≡C-Np2-C≡C-Ph2-CF₃、R¹-Te1-C≡C-Np2-C≡C-Ph3-CF₃、R¹-Te1-C≡C-Np2-C≡C-Np1-CF₃、R¹-Te1-C≡C-Np2-C≡C-Np2-CF₃、R¹-Te1-C≡C-Np2-C≡C-Np3-CF₃、R¹-Te1-C≡C-Np2-C≡C-Np4-CF₃、R¹-Te2-C≡C-Np2-C≡C-Ph1-CF₃、R¹-Te2-C≡C-Np2-C≡C-Ph2-CF₃、R¹-Te2-C≡C-Np2-C≡C-Ph3-CF₃、R¹-Te2-C≡C-Np2-C≡C-Np1-CF₃、R¹-Te2-C≡C-Np2-C≡C-Np2-CF₃、R¹-Te2-C≡C-Np2-C≡C-Np3-CF₃、R¹-Te2-C≡C-Np2-C≡C-Np4-CF₃、
【０１８７】
R¹-Te1-C≡C-Np3-Ph1-CF₃、R¹-Te1-C≡C-Np3-Ph2-CF₃、R¹-Te1-C≡C-Np3-Ph3-CF₃、R¹-Te1-C≡C-Np3-Np1-CF₃、R¹-Te1-C≡C-Np3-Np2-CF₃、R¹-Te1-C≡C-Np3-Np3-CF₃、R¹-Te1-C≡C-Np3-Np4-CF₃、R¹-Te2-C≡C-Np3-Ph1-CF₃、R¹-Te2-C≡C-Np3-Ph2-CF₃、R¹-Te2-C≡C-Np3-Ph3-CF₃、R¹-Te2-C≡C-Np3-Np1-CF₃、R¹-Te2-C≡C-Np3-Np2-CF₃、R¹-Te2-C≡C-Np3-Np3-CF₃、R¹-Te2-C≡C-Np3-Np4-CF₃、R¹-Te1-C≡C-Np3-CH₂CH₂-Ph2-CF₃、R¹-Te1-C≡C-Np3-CH₂CH₂-Ph3-CF₃、R¹-Te1-C≡C-Np3-CH₂CH₂-Np1-CF₃、R¹-Te1-C≡C-Np3-CH₂CH₂-Np2-CF₃、R¹-Te1-C≡C-Np3-CH₂CH₂-Np3-CF₃、R¹-Te1-C≡C-Np3-CH₂CH₂-Np4-CF₃、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph1-CF₃、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph2-CF₃、R¹-Te2-C≡C-Np3-CH₂CH₂-Ph3-CF₃、R¹-Te2-C≡C-Np3-CH₂CH₂-Np1-CF₃、R¹-Te2-C≡C-Np3-CH₂CH₂-Np2-CF₃、R¹-Te2-C≡C-Np3-CH₂CH₂-Np3-CF₃、R¹-Te2-C≡C-Np3-CH₂CH₂-Np4-CF₃、R¹-Te1-C≡C-Np3-C≡C-Ph2-CF₃、R¹-Te1-C≡C-Np3-C≡C-Ph3-CF₃、R¹-Te1-C≡C-Np3-C≡C-Np1-CF₃、R¹-Te1-C≡C-Np3-C≡C-Np2-CF₃、R¹-Te1-C≡C-Np3-C≡C-Np3-CF₃、R¹-Te1-C≡C-Np3-C≡C-Np4-CF₃、R¹-Te2-C≡C-Np3-C≡C-Ph1-CF₃、R¹-Te2-C≡C-Np3-C≡C-Ph2-CF₃、R¹-Te2-C≡C-Np3-C≡C-Ph3-CF₃、R¹-Te2-C≡C-Np3-C≡C-Np1-CF₃、R¹-Te2-C≡C-Np3-C≡C-Np2-CF₃、R¹-Te2-C≡C-Np3-C≡C-Np3-CF₃、R¹-Te2-C≡C-Np3-C≡C-Np4-CF₃、
【０１８８】
R¹-Te1-C≡C-Np4-Ph1-CF₃、R¹-Te1-C≡C-Np4-Ph2-CF₃、R¹-Te1-C≡C-Np4-Ph3-CF₃、R¹-Te1-C≡C-Np4-Np1-CF₃、R¹-Te1-C≡C-Np4-Np2-CF₃、R¹-Te1-C≡C-Np4-Np3-CF₃、R¹-Te1-C≡C-Np4-Np4-CF₃、R¹-Te2-C≡C-Np4-Ph1-CF₃、R¹-Te2-C≡C-Np4-Ph2-CF₃、R¹-Te2-C≡C-Np4-Ph3-CF₃、R¹-Te2-C≡C-Np4-Np1-CF₃、R¹-Te2-C≡C-Np4-Np2-CF₃、R¹-Te2-C≡C-Np4-Np3-CF₃、R¹-Te2-C≡C-Np4-Np4-CF₃、R¹-Te1-C≡C-Np4-CH₂CH₂-Ph2-CF₃、R¹-Te1-C≡C-Np4-CH₂CH₂-Ph3-CF₃、R¹-Te1-C≡C-Np4-CH₂CH₂-Np1-CF₃、R¹-Te1-C≡C-Np4-CH₂CH₂-Np2-CF₃、R¹-Te1-C≡C-Np4-CH₂CH₂-Np3-CF₃、R¹-Te1-C≡C-Np4-CH₂CH₂-Np4-CF₃、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph1-CF₃、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph2-CF₃、R¹-Te2-C≡C-Np4-CH₂CH₂-Ph3-CF₃、R¹-Te2-C≡C-Np4-CH₂CH₂-Np1-CF₃、R¹-Te2-C≡C-Np4-CH₂CH₂-Np2-CF₃、R¹-Te2-C≡C-Np4-CH₂CH₂-Np3-CF₃、R¹-Te2-C≡C-Np4-CH₂CH₂-Np4-CF₃、R¹-Te1-C≡C-Np4-C≡C-Ph2-CF₃、R¹-Te1-C≡C-Np4-C≡C-Ph3-CF₃、R¹-Te1-C≡C-Np4-C≡C-Np1-CF₃、R¹-Te1-C≡C-Np4-C≡C-Np2-CF₃、R¹-Te1-C≡C-Np4-C≡C-Np3-CF₃、R¹-Te1-C≡C-Np4-C≡C-Np4-CF₃、R¹-Te2-C≡C-Np4-C≡C-Ph1-CF₃、R¹-Te2-C≡C-Np4-C≡C-Ph2-CF₃、R¹-Te2-C≡C-Np4-C≡C-Ph3-CF₃、R¹-Te2-C≡C-Np4-C≡C-Np1-CF₃、R¹-Te2-C≡C-Np4-C≡C-Np2-CF₃、R¹-Te2-C≡C-Np4-C≡C-Np3-CF₃、R¹-Te2-C≡C-Np4-C≡C-Np4-CF₃、
【０１８９】
一般式(I)の化合物はそのm、n、 R、V、W、X、Y、Z、Q¹、Q²、Q³、環A、環Bおよび環Cの選択によって、様々な合成法によって製造できるが、その代表的な例を以下に挙げる。
【０１９０】
たとえば、m=n=0、Yが単結合、Rが1〜7個のフッ素原子または炭素原子数1〜7のアルコキシル基によって置換されていてもよく、分岐鎖を含んでもよい飽和の炭素数1〜20のアルキル基で、Zがフッ素原子、塩素原子、トリフルオロメチル基、トリフルオロメトキシ基、ジフルオロメトキシ基または水素原子の時、下式に従って製造できる。
【０１９１】
【化１０】

【０１９２】
(式中、V、Q¹、Q²、Q³および環Cは一般式(I)におけると同じ意味を表し、R²は1〜7個のフッ素原子または炭素原子数1〜7のアルコキシル基によって置換されていてもよく、分岐鎖を含んでもよい飽和の炭素数1〜20のアルキル基を表し、Z¹はフッ素原子、塩素原子、トリフルオロメチル基、トリフルオロメトキシ基、ジフルオロメトキシ基または水素原子を表し、Mtl¹はLi、BrMg、IMgなどの金属イオンを表す。)
すなわち、一般式(II-a)で表されるケトンに、一般式(III-a)で表されるアリールリチウムまたはマグネシウム反応剤を、塩化セリウムや塩化マンガンなどの金属塩やルイス酸の共存下または非共存下に反応させることによって一般式(IV-a)で表されるアルコールを得た後、p-トルエンスルホン酸等の酸触媒存在下、加熱することによって、一般式(V-a)で表されるジヒドロナフタレン化合物を得、これをPd-C、Rh-C、Pt-C、Pd(OH)₂等の金属触媒存在下、水素添加することによって、目的の一般式(I-a)で表される化合物を得ることができる。
【０１９３】
ここで用いる、一般式(III-a)で表されるアリールリチウムまたはマグネシウム反応剤は液晶の製造ではよく用いられるもので、対応するハロゲン化物などから容易に調製できる。
【０１９４】
一般式(II-a)で表される化合物は、いくつかの方法で製造できるが、その代表的な方法としては下式に示すように、一般式(VI-a)で表されるフェニル酢酸誘導体を酸塩化物に変換した後、塩化アルミニウム存在下、エチレンと反応させる方法がある。
【０１９５】
【化１１】

【０１９６】
(式中、R²、V、Q¹、Q²およびQ³は上記と同じである。)
また、Q¹、Q²、およびQ³がすべて水素の場合、下式に示すように、一般式(II-a')で表される化合物は一般式(VII-a)で表されるナフトール誘導体をパラジウム、ロジウム、白金、ルテニウムなどの遷移金属触媒存在下で水素添加し、さらに必要に応じて酸化することによって合成できる。
【０１９７】
【化１２】

【０１９８】
(式中、R²およびVは上記と同じである。)
また、下式に示すように1,4-シクロヘキサジオンモノアセタールにピロリジン等のアミンを作用させ、さらにメチルビニルケトンを反応させて合成できるオクタヒドロナフタレンジオンモノアセタールに、R²-Mtl¹で表される有機金属反応剤を作用させさ、さらに、脱水反応によってオクタヒドロナフタレノンアセタールを得る。これに、脱水素触媒としてパラジウム、ロジウム、ルテニウム、白金などの金属触媒を用いて、または2,3-ジクロロ-5,6-ジシアノ-1,4-ベンゾキノンなどの酸化剤を作用させて、またはイオウ、臭素、ヨウ素などを用いて芳香化させた後、アセタールをケトンに変換することによって一般式(II-a'')で表される化合物を合成することができる。
【０１９９】
【化１３】

【０２００】
(式中、R²は上記と同じである。)
m=n=0、Yが-CH₂CH₂-、Rが1〜7個のフッ素原子または炭素原子数1〜7のアルコキシル基によって置換されていてもよく、分岐鎖を含んでもよい飽和の炭素数1〜20のアルキル基で、Zがフッ素原子、塩素原子、トリフルオロメチル基、トリフルオロメトキシ基、ジフルオロメトキシ基または水素原子の時、下式に従って製造できる。
【０２０１】
【化１４】

【０２０２】
(式中、V、Q¹、Q²、Q³および環Cは一般式(I)におけると同じ意味を表し、R²は1〜7個のフッ素原子または炭素原子数1〜7のアルコキシル基によって置換されていてもよく、分岐鎖を含んでもよい飽和の炭素数1〜20のアルキル基を表し、Z¹はフッ素原子、塩素原子、トリフルオロメチル基、トリフルオロメトキシ基、ジフルオロメトキシ基または水素原子を表し、Mtl¹はLi、BrMg、IMgなどの金属イオンを表す。)
すなわち、一般式(II-a)で表されるケトンに、一般式(III-b)で表されるアリールリチウムまたはマグネシウム反応剤を、塩化セリウムや塩化マンガンなどの金属塩やルイス酸の共存下または非共存下に反応させることによって一般式(IV-b)で表されるアルコールを得た後、p-トルエンスルホン酸等の酸触媒存在下、加熱することによって、一般式(V-b)で表されるジヒドロナフタレン化合物を得、これをPd-C、Rh-C、Pt-C、Pd(OH)₂等の金属触媒存在下、水素添加することによって、目的の一般式(I-b)で表される化合物を得ることができる。
【０２０３】
ここで用いる、一般式(III-b)で表されるエチニルリチウムまたはマグネシウム反応剤は液晶の製造ではよく用いられるもので、対応するアセチレン化合物にアルキルリチウムやアルキルマグネシウムハライドを作用させることによって容易に調製できる。
【０２０４】
また、上式の(III-a)および(III-b)の代わりに(III-c)および(III-d)を用いれば、一般式(I-c)および(I-d)で表される化合物を製造することができる。
【０２０５】
【化１５】

【０２０６】
(式中、V、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R²、Z¹およびMtl¹は上記と同じ意味を表し、Y¹は単結合または-CH₂CH₂-を表す。)この他にも、下式に示すように一般式(II-a)で表される化合物に、一般式(VIII-a)で表されるイリド化合物などを反応させ、得られたオレフィン化合物(IX-a)を水素添加することによって、一般式(I-b)で表される化合物を製造できる。
【０２０７】
【化１６】

【０２０８】
(式中、V、Z、Q¹、Q²、Q³および環Cは一般式(I)におけると同じ意味を表し、R²およびY¹は上記と同じ意味を表す。)
同様にして、(VIII-a)の代わりに(VIII-b)を用いることによって、一般式(I-d)で表される化合物を製造できる。
【０２０９】
【化１７】

【０２１０】
(式中、V、Z、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R²およびY¹は上記と同じ意味を表す。)
さらに下式に示すように、(II-a)で表されるテトラヒドロナフタレノンに、(VIII-c)で表されるイリド化合物を反応させ、酸で処理することによって、一般式(X-a)で表されるアルデヒドを得ることができる。これに(VIII-d)で表されるイリド化合物を反応させ、得られたオレフィン(XI-a)を水素添加することによって、一般式(I-b)で表される化合物を製造できる。
【０２１１】
【化１８】

【０２１２】
(式中、V、Z、Q¹、Q²、Q³および環Cは一般式(I)におけると同じ意味を表し、R²およびY¹は上記と同じ意味を表す。)
同様にして、(VIII-d)の代わりに(VIII-e)を用いることによって、一般式(I-d)で表される化合物を製造できる。
【０２１３】
【化１９】

【０２１４】
(式中、V、Z、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R²、Y¹は上記と同じ意味を表す。)
上記の方法において、(II-a)の代わりに(II-b)を用いると、一般式(XII-a)で表される化合物を製造することができる。
【０２１５】
【化２０】

【０２１６】
(式中、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R²、Z¹、Y¹は上記と同じ意味を表し、X¹は単結合または-CH₂CH₂-を表す。)
この化合物(XII-a)の臭素を置換することで一般式(I)の化合物の多くを製造することができる。
たとえば、(XIII-a)で表されるアセチレン化合物を、PdCl₂(PPh₃)₂やPd(PPh₃)₄などのパラジウム触媒とトリエチルアミンなどのアミン存在下、(XII-a)と反応させると、一般式(I-e)で表される化合物を得ることができる。さらに、金属触媒存在下、水素添加し、アセチレンジイル基(-C≡C-)をエチレン基(-CH₂CH₂-)に変換することもできる。
【０２１７】
【化２１】

【０２１８】
(式中、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、Y¹およびX¹は上記と同じ意味を表し、R²はRは1〜7個のフッ素原子または炭素原子数1〜7のアルコキシル基によって置換されていてもよく、分岐鎖を含んでもよい飽和または不飽和の炭素数1〜18のアルキル基を表す。)
さらに、(XIII-a)を(XIII-b)に代えることで、一般式(I-f)で表される化合物を得ることができる。さらにこれを金属触媒存在下、水素添加し、アセチレンジイル基(-C≡C-)をエチレン基(-CH₂CH₂-)に変換することもできる。
【０２１９】
【化２２】

【０２２０】
(式中、R、V、n、Q¹、Q²、Q³、環A、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、Y¹およびX¹は上記と同じ意味を表す。)
また、ニッケルやパラジウム触媒存在下、R-Mtl¹で表される有機リチウムや有機マグネシウム反応剤を(XII-a)に反応させることによって、一般式(I-g)で表される化合物を製造することができる。
【０２２１】
【化２３】

【０２２２】
(式中、R、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、Y¹、X¹およびMtl¹は上記と同じ意味を表す。)
また、ニッケルやパラジウム触媒存在下、(XIV-a)で表される有機リチウムや有機マグネシウム反応剤を(XII-a)に反応させることによって、または(XIV-a)で表される有機リチウムや有機マグネシウム反応剤をホウ素、スズ、ケイ素化合物に変換した後、ニッケルやパラジウム触媒存在下、(XII-a)に反応させることによって一般式(I-h)で表される化合物を製造することができる。
【０２２３】
【化２４】

【０２２４】
(式中、R、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、Y¹、X¹およびMtl¹は上記と同じ意味を表し、V¹は単結合または酸素原子を表し、環A¹は一個または二個のフッ素原子で置換されてもよい1,4-フェニレン基または二個のフッ素原子で置換されてもよいナフタレン-2,6-ジイル基を表す。)また、(XII-a)をマグネシウム、リチウム、アルキルリチウムなどと反応させ、(XV-a)に変換した後、ニッケルやパラジウム触媒存在下、(XVI-a)で表されるハロゲン化物と反応させることによって、または(XIV-a)をホウ素、スズ、ケイ素化合物に変換した後、ニッケルやパラジウム触媒存在下、(XVI-a)で表されるハロゲン化物に反応させることによって一般式(I-i)で表される化合物を製造することができる。
【０２２５】
【化２５】

【０２２６】
(式中、R、V、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、Y¹、X¹およびMtl¹は上記と同じ意味を表し、環A²は一個または二個のフッ素原子で置換されてもよい1,4-フェニレン基、ピリジン-2,5-ジイル基、ピリミジン-2,5-ジイル基、ピラジン-2,5-ジイル基、ピリダジン-3,6-ジイル基および一個または二個のフッ素原子で置換されてもよいナフタレン-2,6-ジイル基を表し、Halは塩素原子、臭素原子またはヨウ素原子を表す。)
(XV-a)で表される化合物は(XVII-a)で表されるシクロヘキサン誘導体と反応させることによって、アルコール(XVII-a)を与える。これを酸触媒存在下、加熱することにより脱水し、化合物(XVIII-a)を得ることができる。さらに、遷移金属触媒存在下で水素添加し、(I-j)で表される化合物を得ることができる。
【０２２７】
【化２６】

【０２２８】
(式中、V、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R²、Z¹、Y¹、X¹およびMtl¹は上記と同じ意味を表す。)
上記の方法において、(II-a)の代わりに(II-c)を用いると、一般式(I-k)で表される化合物を製造することができる。
【０２２９】
【化２７】

【０２３０】
(式中、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R²、Z¹、X¹、Y¹は上記と同じ意味を表す。)
(I-k)で表される化合物を、臭化水素酸、三臭化ホウ素や塩化アルミニウムなどを作用させて、脱メチル化すると、(XIX-a)
【０２３１】
【化２８】

【０２３２】
(式中、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、X¹、Y¹は上記と同じ意味を表す。)が得られる。これを、一般式(XX-a)および(XX-b)
【０２３３】
【化２９】

【０２３４】
(式中、R、Vおよび環Aは一般式(I)におけると同じ意味を表す。)で表されるカルボン酸をジシクロヘキシルカルボジイミドなどの脱水縮合剤と反応させるか、(XX-a)および(XX-b)を塩化チオニルなどを用いて酸ハロゲン化物にした後、アミン共存下で反応させることによって、一般式(I-l)および(I-m)
【０２３５】
【化３０】

【０２３６】
(式中、R、n、Q¹、Q²、Q³、環A、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、X¹、Y¹は上記と同じ意味を表す。)を得ることができる。
【０２３７】
(XIX-a)を、一般式(XXI-a)および(XXI-b)
【０２３８】
【化３１】

【０２３９】
(式中、R、Vおよび環Aは一般式(I)におけると同じ意味を表し、R³は1,2位が不飽和の場合を除く、1〜7個のフッ素原子または炭素原子数1〜7のアルコキシル基によって置換されていてもよく、分岐鎖を含んでもよい飽和または不飽和の炭素数1〜20のアルキル基を表す。)で表されるハロゲン化物と、水素化ナトリウムや水酸化ナトリウムなどの塩基存在下反応させることによって、一般式(I-n)および(I-o)
【０２４０】
【化３２】

【０２４１】
(式中、R、n、Q¹、Q²、Q³、環A、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R³、Z¹、X¹、Y¹は上記と同じ意味を表す。)を得ることができる。
【０２４２】
さらに、(XIX-a)をトリフルオロメタンスルホン酸塩化物や無水物と塩基存在下に反応させて得られる、一般式(XXII-a)
【０２４３】
【化３３】

【０２４４】
(式中、n、Q¹、Q²、Q³、環Bおよび環Cは一般式(I)におけると同じ意味を表し、Z¹、X¹、Y¹は上記と同じ意味を表す。)で表される化合物を、(XIII-a)、(XIII-b)、R-Mtl¹および(XIV-a)と(XII-a)と同様な条件下で反応させれば、(I-e)、(I-f)、(I-g)および(I-h)を得ることができる。
【０２４５】
下式に示すように、一般式(XXIII-a)で表されるシクロヘキサノン誘導体にピロリジン等のアミンを作用させ、さらにメチルビニルケトンを反応させて合成できるオクタヒドロナフタレノン誘導体に、R²-Mtl¹で表される有機金属反応剤を作用させさ、さらに、脱水反応によってオクタヒドロナフタレノン誘導体を得る。これに、脱水素触媒としてパラジウム、ロジウム、ルテニウム、白金などの金属触媒を用いて、または2,3-ジクロロ-5,6-ジシアノ-1,4-ベンゾキノンなどの酸化剤を作用させて、またはイオウ、臭素、ヨウ素などを用いて芳香化させて、一般式(I-p)で表される化合物を合成することができる。
【０２４６】
【化３４】

【０２４７】
(式中、n、X、Y、Z、環Bおよび環Cは一般式(I)におけると同じ意味を表し、R²およびMtl¹は上記と同じ意味を表す。)
ここで、一般式(XXIII-a)で表されるシクロヘキサノン誘導体は液晶の製造ではよく用いられるものであり、その入手は容易である。
【０２４８】
さらに、R²-Mtl¹に代えて、(XIV-a)、(XIV-b)および(XIV-c)
【０２４９】
【化３５】

【０２５０】
(式中、Rは一般式(I)におけると同じ意味を表し、V¹、環A¹およびMtl¹は上記と同じ意味を表す。)を用いると、一般式(I-q)
【０２５１】
【化３６】

【０２５２】
(式中、R、n、X、Y、Z、環Bおよび環Cは一般式(I)におけると同じ意味を表し、V¹、R²および環A¹は上記と同じ意味をあらわし、W¹は単結合、-C≡C-または-CH₂CH₂-を表す。)を製造できる。
【０２５３】
一般式(I)で表される化合物おいて、Zが塩素原子である(I-r)
【０２５４】
【化３７】

【０２５５】
(式中、m、n、 R、V、W、X、Y、Q¹、Q²、Q³、環A、環Bおよび環Cは一般式(I)におけると同じ意味を表す。)にシアン化銅を作用させると、一般式(I-s)
【０２５６】
【化３８】

【０２５７】
(式中、m、n、 R、V、W、X、Y、Q¹、Q²、Q³、環A、環Bおよび環Cは一般式(I)におけると同じ意味を表す。)で表される化合物を得ることができる。
【０２５８】
斯くして製造された一般式(I)で表される化合物の代表例を以下に挙げる。
【０２５９】
【化３９】

【０２６０】
本発明は、このように一般式(I)で表される化合物の少なくとも1種類をその構成成分として含有する液晶組成物をも提供するものである。
【０２６１】
一般式(I)で表される化合物の少なくとも1種類をその構成成分として含有する液晶組成物においては、その組成物が液晶性を示す限り、一般式(I)で表される化合物の他にどのような化合物を含んでいてもよいが、その第一成分として一般式(I)で表される化合物を少なくとも1種含有するが、その他の成分として特に以下の第二〜第四成分から少なくとも1種含有することが好ましい。
【０２６２】
即ち、第二成分はいわゆるフッ素系(ハロゲン系)のp型液晶化合物であって、以下の一般式(A1)〜(A3)で示される化合物からなるものである。
【０２６３】
【化４０】

【０２６４】
上式中、Alk^aは炭素原子数1〜12のアルキル基を表し、これらは直鎖状であってもメチルまたはエチル分岐を有していてもよく、3〜6員環の環状構造を有していてもよく、基内に存在する任意の-CH₂-は-O-、-CH=CH-、-CH=CF-、-CF=CH-、-CF=CF-または-C≡C-により交換されていてもよく、基内に存在する任意の水素原子はフッ素原子またはトリフルオロメトキシ基により置換されていてもよいが、炭素原子数2〜7の直鎖状アルキル基、炭素原子数2〜7の直鎖状1-アルケニル基、炭素原子数4〜7の直鎖状3-アルケニル基、末端が炭素原子数1〜3のアルコキシル基により置換された炭素原子数1〜5のアルキル基が好ましい。また、分岐により不斉炭素が生じる場合には、化合物として光学活性であってもラセミ体であってもよい。
【０２６５】
環Fa、環Fbおよび環Fcはそれぞれ独立的にトランス-1,4-シクロヘキシレン基、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよい1,4-フェニレン基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、フッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基を表すが、トランス-1,4-シクロヘキシレン基、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、フッ素原子により置換されていてもよいナフタレン-2,6-ジイル基または1〜2個のフッ素原子により置換されていてもよい1,4-フェニレン基が好ましい。特に環Fbがトランス-1,4-シクロヘキシレン基またはトランスデカヒドロナフタレン-トランス-2,6-ジイル基である場合に、環Faはトランス-1,4-シクロヘキシレン基であることが好ましく、環Fcがトランス-1,4-シクロヘキシレン基またはトランスデカヒドロナフタレン-トランス-2,6-ジイル基である場合に環Fbおよび環Faはトランス-1,4-シクロヘキシレン基であることが好ましい。また、(A3)において環Faはトランス-1,4-シクロヘキシレン基であることが好ましい。L^a、L^bおよびL^cは連結基であって、それぞれ独立的に単結合、エチレン基(-CH₂CH₂-)、1,2-プロピレン基(-CH(CH₃)CH₂-および-CH₂CH(CH₃)-)、1,4-ブチレン基、-COO-、-OCO-、-OCF₂-、-CF₂O-、-CH=CH-、-CH=CF-、-CF=CH-、-CF=CF-、-C≡C-または-CH=N-N=CH-を表すが、単結合、エチレン基、1,4-ブチレン基、-COO-、-OCF₂-、-CF₂O-、-CF=CF-または-C≡C-が好ましく、単結合またはエチレン基が特に好ましい。また、(A2)においてはその少なくとも1個が、(A3)においてはその少なくとも2個が単結合を表すことが好ましい。
【０２６６】
環Fzは芳香環であり以下の一般式(Ga)〜(Gc)で表すことができる。
【０２６７】
【化４１】

【０２６８】
式中、J^a〜J^jはそれぞれ独立的に水素原子あるいはフッ素原子を表すが、(Ga)において、J^aおよびJ^bの少なくとも1個はフッ素原子であることが好ましく、(Gb)において、J^d〜J^fの少なくとも1個はフッ素原子であることが好ましく、特にJ^dはフッ素原子であることがさらに好ましい。
【０２６９】
末端基P^aはフッ素原子、塩素原子、トリフルオロメトキシ基、ジフルオロメトキシ基、トリフルオロメチル基またはジフルオロメチル基あるいは2個以上のフッ素原子により置換された炭素原子数2または3のアルコキシル基、アルキル基、アルケニル基またはアルケニルオキシ基を表すが、フッ素原子、トリフルオロメトキシ基またはジフルオロメトキシ基が好ましく、フッ素原子が特に好ましい。
【０２７０】
また、(A1)〜(A3)においては本発明の一般式(I)の化合物は除く。
【０２７１】
第三成分はいわゆるシアノ系のp型液晶化合物であって、以下の一般式(B1)〜(B3)で示される化合物からなるものである。
【０２７２】
【化４２】

【０２７３】
上式中、Alk^bは炭素原子数1〜12のアルキル基を表し、これらは直鎖状であってもメチルまたはエチル分岐を有していてもよく、3〜6員環の環状構造を有していてもよく、基内に存在する任意の-CH₂-は-O-、-CH=CH-、-CH=CF-、-CF=CH-、-CF=CF-または-C≡C-により交換されていてもよく、基内に存在する任意の水素原子はフッ素原子またはトリフルオロメトキシ基により置換されていてもよいが、炭素原子数2〜7の直鎖状アルキル基、炭素原子数2〜7の直鎖状1-アルケニル基、炭素原子数4〜7の直鎖状3-アルケニル基、末端が炭素原子数1〜3のアルコキシル基により置換された炭素原子数1〜5のアルキル基が好ましい。また、分岐により不斉炭素が生じる場合には、化合物として光学活性であってもラセミ体であってもよい。
【０２７４】
環Fd、環Feおよび環Ffはそれぞれ独立的にトランス-1,4-シクロヘキシレン基、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよい1,4-フェニレン基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、フッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基を表すが、トランス-1,4-シクロヘキシレン基、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、フッ素原子により置換されていてもよいナフタレン-2,6-ジイル基または1〜2個のフッ素原子により置換されていてもよい1,4-フェニレン基が好ましい。特に環Feがトランス-1,4-シクロヘキシレン基またはトランスデカヒドロナフタレン-トランス-2,6-ジイル基である場合に、環Fdはトランス-1,4-シクロヘキシレン基であることが好ましく、環Ffがトランス-1,4-シクロヘキシレン基またはトランスデカヒドロナフタレン-トランス-2,6-ジイル基である場合に環Fdおよび環Feはトランス-1,4-シクロヘキシレン基であることが好ましい。また、(B3)において環Fdはトランス-1,4-シクロヘキシレン基であることが好ましい。
【０２７５】
L^d、L^eおよびL^fは連結基であって、それぞれ独立的に単結合、エチレン基(-CH₂CH₂-)、1,2-プロピレン基(-CH(CH₃)CH₂-および-CH₂CH(CH₃)-)、1,4-ブチレン基、-COO-、-OCO-、-OCF₂-、-CF₂O-、-CH=CH-、-CH=CF-、-CF=CH-、-CF=CF-、-C≡C-、-OCH₂-、-CH₂O-、または-CH=N-N=CH-を表すが、単結合、エチレン基、-COO-、-OCF₂-、-CF₂O-、-CF=CF-または-C≡C-が好ましく、単結合、エチレン基または-COO-が特に好ましい。また、(B2)においてはその少なくとも1個が、(B3)においてはその少なくとも2個が単結合を表すことが好ましい。
【０２７６】
環Fyは芳香環であり以下の一般式(Gd)〜(Gf)で表すことができる。
【０２７７】
【化４３】

【０２７８】
式中、J^k〜J^qはそれぞれ独立的に水素原子あるいはフッ素原子を表すが、(Ge)において、JⁿおよびJ^oは水素原子であることが好ましい。
末端基P^aはシアノ基(-CN)、シアナト基(-OCN)または-C≡CCNを表すが、シアノ基が好ましい。
【０２７９】
また、(B1)〜(B3)においては本発明の一般式(I)の化合物は除く。
【０２８０】
第四成分は誘電率異方性が0程度またはそれ以下である、いわゆるn型液晶であり、以下の一般式(C1)〜(C3)で示される化合物からなるものである。
【０２８１】
【化４４】

【０２８２】
上式中、Alk^cおよびAlk^dはそれぞれ独立的に炭素原子数1〜12のアルキル基を表し、これらは直鎖状であってもメチルまたはエチル分岐を有していてもよく、3〜6員環の環状構造を有していてもよく、基内に存在する任意の-CH₂-は-O-、-CH=CH-、-CH=CF-、-CF=CH-、-CF=CF-または-C≡C-により交換されていてもよく、基内に存在する任意の水素原子はフッ素原子またはトリフルオロメトキシ基により置換されていてもよいが、炭素原子数1〜7の直鎖状アルキル基、炭素原子数2〜7の直鎖状1-アルケニル基、炭素原子数4〜7の直鎖状3-アルケニル基、炭素原子数1〜3の直鎖状アルコキシル基または末端が炭素原子数1〜3のアルコキシル基により置換された炭素原子数1〜5の直鎖状アルキル基が好ましく、さらに少なくとも一方は炭素原子数1〜7の直鎖状アルキル基、炭素原子数2〜7の直鎖状1-アルケニル基または炭素原子数4〜7の直鎖状3-アルケニル基であることが特に好ましい。
【０２８３】
環Fg、環Fh、環Fiおよび環Fjはそれぞれ独立的に、トランス-1,4-シクロヘキシレン基、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1〜2個のフッ素原子あるいはメチル基により置換されていてもよい1,4-フェニレン基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基を表すが、各化合物において、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、フッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基は1個以内であることが好ましく、他の環はトランス-1,4-シクロヘキシレン基あるいは1〜2個のフッ素原子またはメチル基により置換されていてもよい1,4-フェニレン基であることが好ましい。
【０２８４】
L^g、L^hおよびLⁱは連結基であって、それぞれ独立的に単結合、エチレン基(-CH₂CH₂-)、1,2-プロピレン基(-CH(CH₃)CH₂-および-CH₂CH(CH₃)-)、1,4-ブチレン基、-COO-、-OCO-、-OCF₂-、-CF₂O-、-CH=CH-、-CH=CF-、-CF=CH-、-CF=CF-、-C≡C-または-CH=N-N=CH-を表すが、単結合、エチレン基、1,4-ブチレン基、-COO-、-OCO-、-OCF₂-、-CF₂O-、-CF=CF-、-C≡C-または-CH=N-N=CH-が好ましく、(C2)においてはその少なくとも1個が、(C3)においてはその少なくとも2個が単結合を表すことが好ましい。
【０２８５】
(C1)におけるより好ましい形態は以下の一般式(C1a)〜(C1h)で表すことができる。
【０２８６】
【化４５】

【０２８７】
上記各式中、Alk^eおよびAlk^fはそれぞれ独立的に炭素原子数1〜7の直鎖状アルキル基、炭素原子数2〜7の直鎖状1-アルケニル基、炭素原子数4〜7の直鎖状3-アルケニル基、炭素原子数1〜3の直鎖状アルコキシル基または末端が炭素原子数1〜3のアルコキシル基により置換された炭素原子数1〜5の直鎖状アルキル基を表すが、少なくとも一方は炭素原子数1〜7の直鎖状アルキル基、炭素原子数2〜7の直鎖状1-アルケニル基または炭素原子数4〜7の直鎖状3-アルケニル基を表す。ただし、環Fg1〜環Fg3が芳香環の場合、対応するAlk^eは1-アルケニル基およびアルコキシル基を除き、環Fh1〜環Fh3が芳香環の場合、対応するAlk^fは1-アルケニル基およびアルコキシル基を除く。
【０２８８】
環Fg1および環Fh1はそれぞれ独立的にトランス-1,4-シクロヘキシレン基、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1〜2個のフッ素原子あるいはメチル基により置換されていてもよい1,4-フェニレン基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基を表すが、各化合物において、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、フッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基は1個以内であることが好ましく、その場合の他方の環はトランス-1,4-シクロヘキシレン基あるいは1〜2個のフッ素原子またはメチル基により置換されていてもよい1,4-フェニレン基である。環Fg2および環Fh2はそれぞれ独立的にトランス-1,4-シクロヘキシレン基、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1〜2個のフッ素原子あるいはメチル基により置換されていてもよい1,4-フェニレン基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基を表すが、各化合物において、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基は1個以内であることが好ましく、その場合の他方の環はトランス-1,4-シクロヘキシレン基あるいは1〜2個のフッ素原子またはメチル基により置換されていてもよい1,4-フェニレン基である。環Fg3および環Fh3はそれぞれ独立的に1〜2個のフッ素原子あるいはメチル基により置換されていてもよい1,4-フェニレン基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基を表すが、各化合物において1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基は1個以内であることが好ましい。
【０２８９】
(C2)におけるより好ましい形態は以下の一般式(C2a)〜(C2m)で表すことができる。
【０２９０】
【化４６】

【０２９１】
上式中、環Fg1、環Fg2、環Fg3、環Fh1、環Fh2および環Fh3は前述の意味を表し、環Fi1は環Fg1と、環Fi2は環Fg2と、環Fi3は環Fg3とそれぞれ同じ意味を表す。
また、上記各化合物において、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、フッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基は1個以内であることが好ましく、その場合の他方の環はトランス-1,4-シクロヘキシレン基あるいは1〜2個のフッ素原子またはメチル基により置換されていてもよい1,4-フェニレン基である。
【０２９２】
次に(C3)におけるより好ましい形態は以下の一般式(C3a)〜(C3f)で表すことができる。
【０２９３】
【化４７】

【０２９４】
上式中、環Fg1、環Fg2、環Fh1、環Fh2、環Fi1および環Fi2は前述の意味を表し、環Fj1は環Fg1また環Fj2は環Fg2とそれぞれ同じ意味を表す。また、上記各化合物において、トランスデカヒドロナフタレン-トランス-2,6-ジイル基、1個以上のフッ素原子により置換されていてもよいナフタレン-2,6-ジイル基、1〜2個のフッ素原子により置換されていてもよいテトラヒドロナフタレン-2,6-ジイル基、フッ素原子により置換されていてもよい1,4-シクロヘキセニレン基、1,3-ジオキサン-トランス-2,5-ジイル基、ピリミジン-2,5-ジイル基またはピリジン-2,5-ジイル基は1個以内であることが好ましく、その場合の他方の環はトランス-1,4-シクロヘキシレン基あるいは1〜2個のフッ素原子またはメチル基により置換されていてもよい1,4-フェニレン基である。
【０２９５】
実際に上記化合物を用いて、ネマチック相の上限温度が117℃の液晶組成物を調製し、これに(I-2)で表される化合物を20重量%添加したところ、ネマチック相の上限温度は74℃であり、0℃で1週間保存しても析出しなかった。類似の構造を有する化合物として、トランス-4-プロピル-(3,4,5-トリフルオロフェニル)シクロヘキサンを添加した場合のネマチック相の上限温度が70℃であることから、(I-2)で表される化合物はホスト液晶組成物に対する優れた溶解性を有し、極めて広い温度範囲で液晶相を発現できることが判る。
【０２９６】
さらに、この組成物の電圧保持率を測定したところ、調製時、加熱後及び紫外線照射後ともにホスト液晶組成物と同様に充分高い値を示した。
【０２９７】
このように、本発明の化合物は、優れた液晶性、および現在汎用の液晶化合物、液晶組成物への優れた相溶性を有している。また、液晶相を示す温度範囲が広く、閾値電圧が低く、高速応答が可能な液晶組成物を調製するうえにおいて従来の化合物より優れた効果を有していることがわかる。
【０２９８】
従って、一般式(I)の化合物は、他のネマチック液晶化合物との混合物の状態で、TN型あるいはSTN型等の電界効果型表示セル用として、特に温度範囲が広く低電圧駆動が可能な液晶材料として好適に使用することができる。また(I)の化合物のなかでシアノ基やエステル結合を含まないものは、大きい比抵抗と高い電圧保持率を得ることが容易であり、アクティブマトリックス駆動用液晶材料の構成成分として使用することも可能である。さらに、ネマチック液晶に限らず、強誘電性液晶や反強誘電性液晶の高速応答の実現に不可欠な低粘剤としての利用も期待できる。
【０２９９】
【実施例】
以下に具体例を挙げて、本発明のテトラヒドロナフタレン誘導体とその製造方法、並びに本発明のテトラヒドロナフタレン誘導体を構成成分として得られる液晶組成物における利点に関してより詳しく説明するが、勿論本発明の主旨、及び適用範囲は、これら実施例により制限されるものではない。
【０３００】
(実施例1)
6-プロピル-2-(3,4,5-トリフルオロフェニル)-1,2,3,4-テトラヒドロナフタレン(I-2)の合成
【０３０１】
【化４８】

【０３０２】
マグネシウム(4.0 g)に、3,4,5-トリフルオロブロモベンゼン(30 g)のテトラヒドロフラン(100 ml)溶液を滴下し、グリニャール反応剤を調製した。これにトルエン(150 ml)を加えた後、室温、減圧下で溶媒約100 mlを留去した。これを60℃に加熱し、6-プロピル-1,2,3,4-テトラヒドロナフタレン-2-オン(25 g)のトルエン(50 ml)溶液を20分かけて滴下した。さらに30分撹拌した後、室温に戻し、反応液を10%塩酸にあけた。有機層を飽和食塩水で洗い、無水硫酸ナトリウムで乾燥後、濃縮した。残渣をシリカゲルカラムクロマトグラフィー(ヘキサン：酢酸エチル=6：1)で精製し、2-ヒドロキシ-6-プロピル-2-(3,4,5-トリフルオロフェニル)-1,2,3,4-テトラヒドロナフタレン(29 g)を得た。これにトルエン(100 ml)とp-トルエンスルホン酸(3 g)を加え、1時間加熱撹拌した。反応液を冷却後、濃縮し、残渣をシリカゲルカラムクロマトグラフィー(ヘキサン)で精製し、6-プロピル-2-(3,4,5-トリフルオロフェニル)-3,4-ジヒドロナフタレン(26 g)を得た。これに、エタノール(50 ml)、酢酸エチル(50 ml)と5%パラジウム-炭素(3 g)を加え、水素雰囲気下、室温で2時間撹拌した。反応液をセライトで濾過し、炉液を濃縮した。残渣をシリカゲルカラムクロマトグラフィー(ヘキサン)で精製し、6-プロピル-2-(3,4,5-トリフルオロフェニル)-1,2,3,4-テトラヒドロナフタレン(26 g)を得た。この化合物は、ガスクロマトグラフィーで純度が99%であり、質量分析で、分子量304であった。
【０３０３】
(実施例2)2-(3,4-ジフルオロフェニル)-6-プロピル-1,2,3,4-テトラヒドロナフタレン(I-1)の合成
実施例1と同様な条件下、3,4,5-トリフルオロブロモベンゼンの代わりに3,4-ジフルオロブロモベンゼンを用いて、2-(3,4-ジフルオロフェニル)-6-プロピル-1,2,3,4-テトラヒドロナフタレンを合成した。純度99%、分子量286。
【０３０４】
(実施例3)6-プロピル-2-(4-トリフルオロメトキシフェニル)-1,2,3,4-テトラヒドロナフタレン(I-3)の合成
実施例1と同様な条件下、3,4,5-トリフルオロブロモベンゼンの代わりに4-トリフルオロメトキシブロモベンゼンを用いて、6-プロピル-2-(4-トリフルオロメトキシフェニル)-1,2,3,4-テトラヒドロナフタレンを合成した。純度99%、分子量334。
【０３０５】
(実施例4) 2-(3,4-ジフルオロフェニル)-6-(トランス-4-プロピルシクロヘキシル)-1,2,3,4-テトラヒドロナフタレン(I-4)の合成
【０３０６】
【化４９】

【０３０７】
マグネシウム(3.5 g)に、3,4-ジフルオロブロモベンゼン(25 g)のテトラヒドロフラン(100 ml)溶液を滴下し、グリニャール反応剤を調製した。これをグラスフィルターで濾過し、濾液にトルエン(150 ml)を加えた後、室温、減圧下で溶媒約100 mlを留去した。これを60℃に加熱し、6-ブロモ-1,2,3,4-テトラヒドロナフタレン-2-オン(27 g)のトルエン(50 ml)溶液を20分かけて滴下した。さらに30分撹拌した後、室温に戻し、反応液を10%塩酸にあけた。有機層を飽和食塩水で洗い、無水硫酸ナトリウムで乾燥後、濃縮した。残渣をシリカゲルカラムクロマトグラフィー(ヘキサン：酢酸エチル=6：1)で精製し、6-ブロモ-2-(3,4-ジフルオロフェニル)-2-ヒドロキシ-1,2,3,4-テトラヒドロナフタレン(29 g)を得た。これにトルエン(100 ml)とp-トルエンスルホン酸(3 g)を加え、1時間加熱撹拌した。反応液を冷却後、濃縮し、残渣をシリカゲルカラムクロマトグラフィー(ヘキサン)で精製し、6-ブロモ-2-(3,4-ジフルオロフェニル)-3,4-ジヒドロナフタレン(26 g)を得た。これに、エタノール(50 ml)、酢酸エチル(50 ml)と5%ロジウム-炭素(3 g)を加え、水素雰囲気下、室温で2時間撹拌した。反応液をセライトで濾過し、炉液を濃縮した。残渣をシリカゲルカラムクロマトグラフィー(ヘキサン)で精製し、6-ブロモ-2-(3,4-ジフルオロフェニル)-1,2,3,4-テトラヒドロナフタレン(26 g)を得た。マグネシウム(2.3 g)に、6-ブロモ-2-(3,4-ジフルオロフェニル)-1,2,3,4-テトラヒドロナフタレン(26 g)のテトラヒドロフラン(70 ml)溶液を滴下し、グリニャール反応剤を調製した。これに4-プロピルシクロヘキサノン(13.5 g)のテトラヒドロフラン(30 ml)溶液を滴下した。さらに30分撹拌した後、反応液を10%塩酸にあけた。有機層を飽和食塩水で洗い、無水硫酸ナトリウムで乾燥後、濃縮した。残渣をシリカゲルカラムクロマトグラフィー(ヘキサン：酢酸エチル=6：1)で精製し、2-(3,4-ジフルオロフェニル)-2-ヒドロキシ-6-(トランス-4-プロピルシクロヘキシル)-1,2,3,4-テトラヒドロナフタレン(23 g)を得た。これにトルエン(80 ml)とp-トルエンスルホン酸(2 g)を加え、1時間加熱撹拌した。反応液を冷却後、濃縮し、残渣をシリカゲルカラムクロマトグラフィー(ヘキサン)で精製し、2-(3,4-ジフルオロフェニル)-6-(トランス-4-プロピルシクロヘキシル)-3,4-ジヒドロナフタレン(26 g)を得た。これに、エタノール(30 ml)、酢酸エチル(50 ml)と5%パラジウム-炭素(2 g)を加え、水素雰囲気下、室温で2時間撹拌した。反応液をセライトで濾過し、炉液を濃縮した。残渣にジメチルホルムアミド(50 ml)とt-ブトキシカリウム(5.5 g)を加え、70℃で2時間撹拌した。反応液に10%塩酸を加え、トルエンで抽出し、有機層を飽和食塩水で洗い、無水硫酸ナトリウムで乾燥後、濃縮した。残渣をシリカゲルカラムクロマトグラフィー(ヘキサン)で精製し、さらにエタノールで再結晶し、2-(3,4-ジフルオロフェニル)-6-(トランス-4-プロピルシクロヘキシル)-1,2,3,4-テトラヒドロナフタレン(20 g)を得た。この化合物は、ガスクロマトグラフィーで純度が99.8%であり、質量分析で分子量368であった。
【０３０８】
(実施例5) 2-(3,4-ジフルオロフェニル)-6-(4-プロピルフェニル)-1,2,3,4-テトラヒドロナフタレン(I-5)の合成
【０３０９】
【化５０】

【０３１０】
4-プロピルブロモベンゼンとマグネシウムから調製されるグリニャール反応剤とトリメチルホウ酸とを反応させた後、希塩酸で加水分解することによって得た4-プロピルフェニルホウ酸(4.5 g)、実施例4において合成した6-ブロモ-2-(3,4-ジフルオロフェニル)-1,2,3,4-テトラヒドロナフタレン(5.0 g)、テトラキス(トリフェニルホスフィン)パラジウム(0)(0.3 g)およびリン酸カリウム(3.0 g)をジメチルホルムアミド(30 ml)中、80℃で8時間撹拌した。反応液を室温まで冷却した後、水を加え、トルエンで抽出した。有機層を飽和食塩水で洗い、無水硫酸ナトリウムで乾燥後、濃縮した。残渣をシリカゲルカラムクロマトグラフィー(ヘキサン)で精製し、さらにエタノールで再結晶し、2-(3,4-ジフルオロフェニル)-6-(4-プロピルフェニル)-1,2,3,4-テトラヒドロナフタレン(4 g)を得た。この化合物は、ガスクロマトグラフィーで純度が99.7%であり、質量分析で分子量362であった。
【０３１１】
(実施例6)液晶組成物の調製
温度範囲が広く低粘性でアクティブマトリックス駆動にも使用可能な汎用のホスト液晶(H)を調製した。この(H)は116.7℃以下でネマチック相を示し、その融点は11℃である。この組成物の物性値ならびに、これを用いて作成したTNセル(セル厚4.5μm)の閾値電圧(Vth)の20℃における測定値は以下の通りであった。
【０３１２】
ネマチック相上限温度(T_N-I)116.7℃
誘電率異方性(Δε)4.80
閾値電圧(Vth)1.88 V
応答時間(τ) 21.5 m秒
次にこのホスト液晶(H)の80%と実施例1で得られた本発明の化合物である(I-2)20%からなる液晶組成物(M-1)を調製したところ、液晶相上限温度(T_N-I)は74℃であった。この(M-1)を150℃で20時間放置した後にそのT_N-Iを測定したが、加熱前と変化がみられなかった。また、紫外線を20時間照射したが、T_N-Iに変化はみられなかった。次にこの組成物の電圧保持率を測定したところ、調製時、加熱後及び紫外線照射後ともにホスト液晶(H)と同様に充分高い値を示した。
【０３１３】
次に、(M-1)をセル厚4.5μmのTNセルに充填して液晶素子を作成し、その電気光学特性を測定したところ、以下の通りであった。
【０３１４】
ネマチック相上限温度(T_N-I)74.0℃
誘電率異方性(Δε)5.50
閾値電圧(Vth)1.55 V
応答時間(τ) 30.5 m秒
従って、(I-2)を20%添加することにより、そのネマチック相上限温度(T_N-I)の降下を46°に抑えながら、その閾値電圧(Vth)を0.33 Vも低減することができた。さらにその応答時間も9 m秒の増加に抑えることができた。また、0℃で1週間放置しても結晶は析出しなかった。さらに急冷して結晶化させ、測定したその融点(T_C-N)は12℃でホスト液晶(H)とほとんど変化がなく、(I-2)がホスト液晶によく溶解していることがわかる。
【０３１５】
次に、この素子の室温及び80℃における電圧保持率を測定したがいずれも極めて良好でアクティブマトリックス駆動用としても充分使用可能であることがわかった。
【０３１６】
(比較例1)
実施例6において、(I-2)に換えて、トランス-4-プロピル-(3,4,5-トリフルオロフェニル)シクロヘキサンをホスト液晶(H)に同量(20%)添加して液晶組成物(M-2)を調製した。この組成物のネマチック相上限温度(T_N-I)は70℃であり、(I-2)と比較して液晶性が低いことがわかる。
【０３１７】
この組成物の他の物性値ならびに同様にして作成した素子の電気光学特性値は以下の通りである。
【０３１８】
ネマチック相上限温度(T_N-I)70.0℃
誘電率異方性(Δε)5.60
閾値電圧(Vth)1.58 V
応答時間(τ) 30.0 m秒
屈折率異方性(Δn)： 0.080
従って、(I-2)と比較してネマチック相上限温度(T_N-I)が4°降下しているにもかかわらず、閾値電圧(Vth)はほとんど変化がない、応答時間もほとんど変化がないことがわかる。
【０３１９】
【発明の効果】
本発明により提供されるテトラヒドロナフタレン誘導体は、液晶性及び現在汎用の液晶化合物あるいは組成物との相溶性に優れる。また、その添加により、応答性をほとんど悪化させずに閾値電圧を大きく低減させることが可能である。さらに、工業的にも製造が容易であり、無色で化学的にも安定である。従って、これを含有する液晶組成物は実用的液晶として、特に温度範囲が広く低電圧駆動と高速応答を必要とする液晶表示用として極めて有用である。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a novel liquid crystalline compound that is a tetrahydronaphthalene derivative, a liquid crystal composition containing the same, and a liquid crystal display device using the same, which are useful as an electro-optical liquid crystal display material.
[0002]
[Prior art]
Liquid crystal display elements are used in various measuring instruments, automobile panels, word processors, electronic notebooks, printers, computers, televisions, etc., including watches and calculators. Typical liquid crystal display methods include TN (twisted nematic), STN (super twisted nematic), DS (dynamic light scattering), GH (guest / host), or FLC capable of high-speed response. (Ferroelectric liquid crystal) and AFLC (antiferroelectric liquid crystal). As a drive system, a multiplex drive is generally used instead of a conventional static drive, and a simple matrix system and recently an active matrix system have been put into practical use.
[0003]
As a liquid crystal material used for these, a great variety of liquid crystalline compounds have been synthesized so far, and these are used according to the display method, driving method or use thereof. However, demands for improving the performance of liquid crystal display elements (improvement of display quality, enlargement of display screen, etc.) are increasing year by year, and new liquid crystal compounds are being developed to satisfy them.
[0004]
A liquid crystal compound is usually composed of a central skeleton part called a core and terminal parts on both sides. Usually, the ring structure constituting the core part of the liquid crystal compound includes a 1,4-phenylene group (which may be substituted by 1 to 2 halogen atoms, a cyano group, a methyl group, etc.) and trans-1,4 -Cyclohexylene group accounts for the majority. However, liquid crystal compounds composed only of 1,4-phenylene groups and trans-1,4-cyclohexylene groups have limitations in their types and characteristics, and these alone cannot meet the above requirements. It is a fact.
[0005]
Examples of the ring structure other than 1,4-phenylene group and trans-1,4-cyclohexylene group include pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, 1,3-dioxane-trans- Heterocyclic systems such as 2,5-diyl group, trans-decalin-2,6-diyl group, naphthalene-2,6-diyl group, tetrahydronaphthalene-2-6-diyl group, bicyclo [2.2.2] octane Condensed ring systems such as 1,4-diyl group and spiro [3.3] heptane-2,6-diyl group are also being studied, but due to manufacturing (technology, cost, etc.) problems, stability problems, etc. There are only a few that are currently in practical use.
[0006]
In these condensed ring systems, the tetrahydronaphthalene-2-6-diyl group is extremely rare in spite of its long-reported ring structure, and other than liquid crystallinity (phase transition temperature). The characteristics of these, particularly as nematic liquid crystals, are hardly known. (Recently, it has been reported that optically active alcohol esters of tetrahydronaphthalene-2-carboxylic acid exhibit interesting properties as smectic liquid crystals, especially ferroelectric liquid crystals and antiferroelectric liquid crystals.)
In general, in a liquid crystal compound, at least one of the terminal portions is a chain (side chain) group, and in the case of a so-called p-type liquid crystal having a positive dielectric anisotropy, the other is often a polar group.
[0007]
In order to reduce the driving voltage in the TN or STN display system, a compound (p-type) having a large positive dielectric anisotropy is required. For these purposes, compounds having a cyano group at the molecular end and further containing one or more fluorine atoms in the same direction of the molecule are usually used. Most of the currently reported tetrahydronaphthalene derivatives are so-called n-type liquid crystals having a dielectric anisotropy of 0 to negative, and as a p-type liquid crystal in which a polar group is introduced into the tetrahydronaphthalene skeleton, a slight amount of phenyltetrahydronaphthalene skeleton or Only a compound having a tetrahydronaphthalene-2-carboxylic acid phenyl skeleton has been reported, and there is no description of electro-optical properties and application examples (Helv. Chim. Acta, 65, 1318-1330 (1982)).
[0008]
As the p-type compound to be used for the active matrix driving method described above, a compound having only a fluorine atom, a fluoroalkoxyl group, or a fluoroalkyl group as a polar group is used, but such a report example as a tetrahydronaphthalene compound is not available. Absent. In addition, liquid crystalline compounds that are tetrahydronaphthalene derivatives generally do not have excellent compatibility with other liquid crystal compounds, but in order to improve this, lateral substituents on the tetrahydronaphthalene skeleton (especially fluorine atoms) Introduction is desirable. In the use in the active matrix system, substitution with a fluorine atom is considered effective even when a polar group is directly introduced into the tetrahydronaphthalene ring. There is no example of such a fluorotetralin derivative actually synthesized, and it is the actual situation that it is impossible to estimate what characteristic value such a compound has.
[0009]
In liquid crystal compounds, by introducing an alkenyl group instead of the alkyl group normally used as the side chain moiety, excellent effects such as improved liquid crystal properties, reduced viscosity, and improved steepness in display characteristics can be obtained. It is known that However, these alkenyl groups are usually introduced in a form directly linked to a cyclohexane ring, and no compound introduced into an aromatic ring, particularly a tetrahydronaphthalene ring, has been reported.
[0010]
Similarly, no tetrahydronaphthalene derivative having an alkoxylalkyl group, a fluoroalkyl group, a fluoroalkenyl group, a fluoroalkenyloxy group or the like as a side chain has been reported.
[0011]
As the linking group of the ring structure in the core of the liquid crystal compound, a 1,2-ethylene group (-CH ₂ CH ₂ Many divalent organic groups such as-), ethynylene group (-C≡C-) and difluoroethenylene group (-CF = CF-) are known, but not known for tetrahydronaphthalene derivatives.
[0012]
[Problems to be solved by the invention]
The problem to be solved by the present invention is to provide a novel compound having a tetrahydronaphthalene skeleton, and to provide a practical liquid crystal composition using the compound.
[0013]
[Means for Solving the Problems]
As a result of intensive investigations to solve the above problems, the present inventors have been able to easily produce compounds having a tetrahydronaphthalene skeleton, many of which exhibit liquid crystallinity over a wide temperature range, and whether or not they have liquid crystallinity alone. Regardless, adding this to the composition does not slow down the response speed (in many cases, increase the response speed) or significantly narrow the target liquid crystal temperature range (often expanding the temperature range). ), It was found that mixing can be performed without separating the layers, and the present invention has been completed.
[0014]
That is, the present invention
1. Formula (I)
[0015]
[Chemical 2]

[0016]
(In the formula, R represents a saturated or unsaturated alkyl group having 1 to 20 carbon atoms which may be substituted by 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms and may contain a branched chain. The linking group V represents a single bond, an oxygen atom, a sulfur atom, -COO-, -OCO-, -OCOO-, -COS- or -SCO-, and the linking groups W, X and Y are each independently Single bond, -CH ₂ CH ₂ -, -CH = CH-, -CH (CH _Three ) CH ₂ -, -CH ₂ CH (CH _Three )-, -CH (CH _Three ) CH (CH _Three )-, -CF ₂ CF ₂ -, -CF = CF-, -CH ₂ O-, -OCH ₂ -, -OCH (CH _Three )-, -CH (CH _Three ) O-, -C≡C-, -CF ₂ O-, -OCF ₂ -, -COO-, -OCO-, -COS- or -SCO-, where Z is a fluorine atom, chlorine atom, cyano group, cyanato group, trifluoromethyl group, trifluoromethoxy group, difluoromethoxy group or hydrogen atom Q ¹ , Q ² And Q ^Three Each independently represents a hydrogen atom or a fluorine atom, and ring A and ring B are each independently a trans-1,4-cyclohexylene group, trans-decahydronaphthalene-2,6-diyl group, trans-1, 1,4-phenylene group, pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, pyrazine which may be substituted with 3-dioxane-2,5-diyl group or one or two fluorine atoms Represents a -2,5-diyl group, a pyridazine-3,6-diyl group and a naphthalene-2,6-diyl group optionally substituted by one or two fluorine atoms, wherein ring C is one or two fluorine atoms Represents a 1,4-phenylene group which may be substituted with an atom or a naphthalene-2,6-diyl group which may be substituted with one or two fluorine atoms, m and n each independently represents 0 or 1; To express. However, when Z is a hydrogen atom, the ring C is a 1,4-phenylene group substituted with one or two fluorine atoms or naphthalene-2,6-, optionally substituted with one or two fluorine atoms Q represents a diyl group ¹ , Q ² And Q ^Three Are all hydrogen atoms, m and n are both 0, Y is -COO-, and Z is a fluorine atom, then ring C is substituted with one or two fluorine atoms. , 4-phenylene group or naphthalene-2,6-diyl group optionally substituted by one or two fluorine atoms, Q ¹ , Q ² And Q ^Three Are all hydrogen atoms, m and n are both 0, Y is a single bond or —COO—, and Z is a cyano group, then ring C is substituted with one or two fluorine atoms Or a naphthalene-2,6-diyl group which may be substituted with one or two fluorine atoms. ) A tetrahydronaphthalene derivative represented by:
I will provide a.
[0017]
Further, the present invention provides a liquid crystal composition containing one or more compounds of the above general formula (I), and a liquid crystal element comprising the same, that is,
2. 2. The compound according to 1 above, wherein m is 0 in the general formula (I).
3. 2. The compound according to 1 above, wherein n is 0 in the general formula (I).
4). Q in general formula (I) ¹ And Q ² The compound according to the above 1 to 3, wherein both are hydrogen atoms.
5). In the general formula (I), the linking groups W, X and Y are each independently a single bond or —CH ₂ CH ₂ 5. The compound according to the above 1 to 4, which is selected from-.
6). In general formula (I), ring A and ring B are each independently substituted with a trans-1,4-cyclohexylene group, a trans-decahydronaphthalene-2,6-diyl group, or one or two fluorine atoms. 6. The compound according to 1 to 5 above, which is selected from a 1,4-phenylene group and a naphthalene-2,6-diyl group.
7). 7. The compound according to 1 to 6 above, wherein in formula (I), ring C is selected from a 1,4-phenylene group or a naphthalene-2,6-diyl group substituted with one or two fluorine atoms.
8). 8. The compound according to 1 to 7 above, wherein in general formula (I), Z is selected from a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group, or a hydrogen atom.
9. 9. The compound according to 8 above, wherein Z in the general formula (I) is selected from a fluorine atom or a trifluoromethoxy group.
10. 10. The compound according to 1 to 9 above, wherein V represents a single bond in the general formula (I).
11. 11. The compound according to the above 1 to 10, wherein R in the general formula (I) is selected from linear alkyl groups having 1 to 10 carbon atoms.
12 A liquid crystal composition containing one or more compounds of the general formula (I) described in 1 to 11 above.
13. 13. The liquid crystal composition according to the above 12, which is used for driving an active matrix.
14 14. A liquid crystal device comprising the liquid crystal composition according to the above 13 as a constituent element.
15. 15. An active matrix drive liquid crystal display device using the liquid crystal composition according to the above 14.
I will provide a.
[0018]
DETAILED DESCRIPTION OF THE INVENTION
As described above, in the compound of the general formula (I), m, n, R, V, W, X, Y, Z, Q ¹ , Q ² , Q ^Three Examples of ring A, ring B and ring C include the following.
[0019]
m and n are 0 or 1, and any combination of m = n = 0, m = 0, n = 1, m = 1, n = 0, m = n = 1 is possible, but m = n = In the case of 1, since the melting point and the viscosity are increased, a combination of m = n = 0, m = 0, n = 1, and m = 1 and n = 0 is preferable.
[0020]
As R-, methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, peptyl group, octyl group, nonyl group, decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, Hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, eicosyl linear saturated alkyl group, 1-methylethyl group, 1-methylpropyl group, 2-methylpropyl group, 1,2-dimethylpropyl group, 1- Methylbutyl group, 2-methylbutyl group, 3-methylbutyl group, 1,2-dimethylbutyl group, 1,3-dimethylbutyl group, 2,3-dimethylbutyl group, 1-methylpentyl group, 2-methylpentyl group, 3 -Methylpentyl group, 4-methylpentyl group, 1,2-dimethylpentyl group, 1,3-dimethylpentyl group, 1-methylhexyl group, 2-methylhexyl group, 3-methylhexyl group, 4- Tylhexyl group, 5-methylhexyl group, 1,2-dimethylhexyl group, 1,3-dimethylhexyl group, 1-methylheptyl group, 2-methylheptyl group, 3-methylheptyl group, 4-methylheptyl group, 5 -Methylheptyl group, 6-methylheptyl group, 1,2-dimethylheptyl group, 1,3-dimethylheptyl group, 1-methyloctyl group, 2-methyloctyl group, 3-methyloctyl group, 4-methyloctyl group 5-methyloctyl group, 6-methyloctyl group, 7-methyloctyl group, 1,2-dimethyloctyl group, 1,3-dimethyloctyl group, 1-methylnonyl group, 2-methylnonyl group, 3-methylnonyl group, 4-methylnonyl group, 5-methylnonyl group, 6-methylnonyl group, 7-methylnonyl group, 8-methylnonyl group, 1,2-dimethylnonyl group, 1,3-dimethylnonyl group, 1-methyldecyl group, 2-methyldecyl group , 3-methyldecyl group, 1,2-dimethyl Decyl group, 1,3-dimethyldecyl group, 1-methylundecyl group, 2-methylundecyl group, 3-methylundecyl group, 1,2-dimethylundecyl group, 1,3-dimethylundecyl group, 1-methyldodecyl group, 2-methyldodecyl group, 3-methyldodecyl group, 1,2-dimethyldodecyl group, 1,3-dimethyldodecyl group, 1-methyltridecyl group, 2-methyltridecyl group, 3- Branched saturated alkyl groups such as methyltridecyl group, 1,2-dimethyltridecyl group, 1,3-dimethyltridecyl group, vinyl group, trans-1-propenyl group, 2-propenyl group, trans-1-butenyl Group, trans-2-butenyl group, 3-butenyl group, trans-1-pentenyl group, trans-2-pentenyl group, trans-3-pentenyl group, 4-pentenyl group, trans-1-hexenyl group, trans-2 -Hexenyl group, trans-3-hexenyl group, trans-4-hexe Nyl group, 5-hexenyl group, trans-1-heptenyl group, trans-2-heptenyl group, trans-3-heptenyl group, trans-4-heptenyl group, trans-5-heptenyl group, 6-heptenyl group, trans- 1-octenyl group, trans-2-octenyl group, trans-3-octenyl group, trans-4-octenyl group, trans-5-octenyl group, trans-6-octenyl group, 7-octenyl group, trans-1-nonenyl Group, 8-nonenyl group, trans-1-decenyl group, 9-decenyl group, trans-1-undecenyl group, 10-undecenyl group, trans-1-dodecenyl group, 11-dodecenyl group, ethynyl group, 1-propynyl group 2-propynyl group, 1-butynyl group, 2-butynyl group, 3-butynyl group, 1-pentenyl group, 2-pentenyl group, 3-pentenyl group, 4-pentenyl group, 1-hexynyl group, 2-hexynyl group , 3-hexynyl group, 4-he Sinyl group, 5-hexynyl group, 1-heptynyl group, 2-heptynyl group, 3-heptynyl group, 4-heptynyl group, 5-heptynyl group, 6-heptynyl group, 1-octynyl group, 2-octynyl group, 3- Octynyl group, 4-octynyl group, 5-octynyl group, 6-octynyl group, 7-octynyl group, 1-noninyl group, 8-noninyl group, 1-decynyl group, 9-decynyl group, 1-undecynyl group, 10- Undecynyl group, 1-dodecynyl group, 11-dodecynyl group, 1-tridecynyl group, unsaturated alkyl group such as 12-tridecynyl group, fluoromethyl group, difluoromethyl group, trifluoromethyl group, 2-fluoromethyl group, 2, 2-difluoroethyl group, 2,2,2-trifluoroethyl group, 1,1,2,2,2-pentafluoroethyl group, 3-fluoropropyl group, 2-fluoropropyl group, 1-fluoropropyl group, 3,3-difluoropropyl group, 3,3,3-trifluoropropyl Propyl group, 2,2,3,3-tetrafluoropropyl group, 2,2,3,3,3-pentafluoropropyl group, 1,1,2,2,3,3,3-heptafluoropropyl group, 4-fluorobutyl group, 3-fluorobutyl group, 2-fluorobutyl group, 1-fluorobutyl group, 4,4-difluorobutyl group, 4,4,4-trifluorobutyl group, 3,3,4,4 -Tetrafluorobutyl group, 3,3,4,4,4-pentafluorobutyl group, 2,2,3,3,4,4,4-heptafluorobutyl group, 5-fluoropentyl group, 4-fluoropentyl group Group, 3-fluoropentyl group, 2-fluoropentyl group, 1-fluoropentyl group, 5,5-difluoropentyl group, 5,5,5-trifluoropentyl group, 4,4,5,5-tetrafluoropentyl Group, 4,4,5,5,5-pentafluoropentyl group, 3,3,4,4,5,5,5-heptafluoropentyl group, 6-fluorohexyl group, 5-fluorohexyl group, 4- Fluorohexyl group, 3-fluorohexyl Group, 2-fluorohexyl group, 1-fluorohexyl group, 6,6-difluorohexyl group, 6,6,6-trifluorohexyl group, 5,5,6,6,6-pentafluorohexyl group, 4 , 4,5,5,6,6,6-heptafluorohexyl group, 7-fluoroheptyl group, 6-fluoroheptyl group, 5-fluoroheptyl group, 4-fluoroheptyl group, 3-fluoroheptyl group, 2- Fluoroheptyl group, 1-fluoroheptyl group, 7,7-difluoroheptyl group, 7,7,7-trifluoroheptyl group, 6,6,7,7-tetrafluoroheptyl group, 6,6,7,7, 7-pentafluoroheptyl group, 5,5,6,6,7,7,7-heptafluoroheptyl group, 8-fluorooctyl group, 7-fluorooctyl group, 6-fluorooctyl group, 5-fluorooctyl group, 4-fluorooctyl group, 3-fluorooctyl group, 2-fluorooctyl group, 1-fluorooctyl group, 8,8-difluorooctyl group, 8 , 8,8-trifluorooctyl group, 7,7,8,8-tetrafluorooctyl group, 7,7,8,8,8-pentafluorooctyl group, 6,6,7,7,8,8, Fluorine-substituted alkyl group such as 8-heptafluorooctyl group,
[0021]
2,2-difluoroethenyl group, (E) -1,2-difluoroethenyl group, (Z) -1,2-difluoroethenyl group, 3,3-difluoro-2-propenyl group, (E)- 2,3-difluoro-2-propenyl group, (Z) -2,3-difluoro-2-propenyl group, 4,4-difluoro-3-butenyl group, (E) -3,4-difluoro-3-butenyl Group, (Z) -3,4-difluoro-3-butenyl group, 5,5-difluoro-4-pentenyl group, (E) -4,5-difluoro-4-pentenyl group, (Z) -4,5 -Difluoro-4-pentenyl group, 6,6-difluoro-5-hexenyl group, (E) -5,6-difluoro-5-hexenyl group, (Z) -5,6-difluoro-5-hexenyl group, E) -1,2-difluoro-1-propenyl group, (E) -1,2-difluoro-1-butenyl group, (E) -1,2-difluoro-1-pentenyl group, (E) -1, 2-difluoro-1-hexenyl group, (Z) -1-fluoro-1-propenyl group, (Z) -1-fluoro-1-butenyl group, (Z) -1-fluoro-1-pentenyl group, (Z ) -1-Fluoro-1-hexeni Group, (Z) -2-fluoro-1-propenyl group, (Z) -2-fluoro-1-butenyl group, (Z) -2-fluoro-1-pentenyl group, (Z) -2-fluoro-1 -Hexenyl group, (E) -2,3-difluoro-2-butenyl group, (E) -2,3-difluoro-2-pentenyl group, (E) -2,3-difluoro-2-hexenyl group, Z) -2-fluoro-2-butenyl group, (Z) -2-fluoro-2-pentenyl group, (Z) -2-fluoro-2-hexenyl group, (Z) -3-fluoro-2-butenyl group , (Z) -3-fluoro-2-pentenyl group, (Z) -3-fluoro-2-hexenyl group and other fluorine-substituted unsaturated alkyl groups, methoxymethyl group, ethoxymethyl group, propoxymethyl group, butoxymethyl group Pentyloxymethyl group, hexyloxymethyl group, heptyloxymethyl group, 1-methoxyethyl group, 1-ethoxyethyl group, 1-propoxyethyl group, 1-butoxyethyl group, 1-pentyloxyethyl group, 1-hexyloxy Siethyl group, 1-heptyloxyethyl group, 2-methoxyethyl group, 2-ethoxyethyl group, 2-propoxyethyl group, 2-butoxyethyl group, 2-pentyloxyethyl group, 2-hexyloxyethyl group, 2- Heptyloxyethyl group, 1-methoxypropyl group, 1-ethoxypropyl group, 1-propoxypropyl group, 1-butoxypropyl group, 1-pentyloxypropyl group, 1-hexyloxypropyl group, 1-heptyloxypropyl group, 2-methoxypropyl group, 2-ethoxypropyl group, 2-propoxypropyl group, 2-butoxypropyl group, 2-pentyloxypropyl group, 2-hexyloxypropyl group, 2-heptyloxypropyl group, 3-methoxypropyl group 3-ethoxypropyl group, 3-propoxypropyl group, 3-butoxypropyl group, 3-pentyloxypropyl group, 3-hexyloxypro group Group, 3-heptyloxypropyl group, 4-methoxybutyl group, 4-ethoxybutyl group, 4-propoxybutyl group, 4-butoxybutyl group, 4-pentyloxybutyl group, 4-hexyloxybutyl group, 4- Heptyloxybutyl group, 5-methoxypentyl group, 5-ethoxypentyl group, 5-propoxypentyl group, 5-butoxypentyl group, 5-pentyloxypentyl group, 5-hexyloxypentyl group, 5-heptyloxypentyl group, Alkoxyl-substituted alkyl such as 6-methoxyhexyl group, 6-ethoxyhexyl group, 6-propoxyhexyl group, 6-butoxyhexyl group, 6-pentyloxyhexyl group, 6-hexyloxyhexyl group, 6-heptyloxyhexyl group, etc. Among them, a straight-chain saturated alkyl group and an unsaturated alkyl group are preferable, and a methyl group, an ethyl group, a propyl group, a buty Group, pentyl group, hexyl group, peptyl group, octyl group, vinyl group, trans-1-propenyl group, 2-propenyl group, trans-1-butenyl group, trans-2-butenyl group, 3-butenyl group, trans- 1-pentenyl group, trans-2-pentenyl group, trans-3-pentenyl group, 4-pentenyl group, trans-1-hexenyl group, trans-2-hexenyl group, trans-3-hexenyl group, trans-4-hexenyl group Particularly preferred are a group, 5-hexenyl group, trans-1-heptenyl group, trans-2-heptenyl group, trans-3-heptenyl group, trans-4-heptenyl group, trans-5-heptenyl group and 6-heptenyl group.
[0022]
Examples of the linking group V include a single bond, an oxygen atom, a sulfur atom, -COO-, -OCO-, -OCOO-, -COS-, and -SCO-. A single bond and an oxygen atom are preferable, and a single bond is particularly preferable. preferable.
[0023]
W, X and Y include a single bond, -CH ₂ CH ₂ -, -CH = CH-, -CH (CH _Three ) CH ₂ -, -CH ₂ CH (CH _Three )-, -CH (CH _Three ) CH (CH _Three )-, -CF ₂ CF ₂ -, -CF = CF-, -CH ₂ O-, -OCH ₂ -, -OCH (CH _Three )-, -CH (CH _Three ) O-, -C≡C-, -CF ₂ O-, -OCF ₂ -, -COO-, -OCO-, -COS-, -SCO- ₂ CH ₂ -And -C≡C- are preferred, and a single bond is particularly preferred.
[0024]
Examples of Z include a fluorine atom, a chlorine atom, a cyano group, a cyanato group, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group, and a hydrogen atom, and a fluorine atom, a cyano group, and a trifluoromethoxy group are preferable. Fluorine and trifluoromethoxy groups are particularly preferred.
[0025]
Q ¹ , Q ² And Q ^Three Represents a hydrogen atom or a fluorine atom, but Q ¹ , Q ² And Q ^Three Q is a hydrogen atom and Q ¹ And Q ² Is a hydrogen atom and Q ^Three Is preferably a fluorine atom.
[0026]
Examples of ring A and ring B include structures shown in Formula Group 1.
[0027]
[Chemical 3]

[0028]
Among them, the structure described in Formula Group 2 is preferable.
[0029]
[Formula 4]

[0030]
Among them, the structure described in Formula Group 3 is particularly preferable.
[0031]
[Chemical formula 5]

[0032]
Ring C includes structures shown in Formula Group 4.
[0033]
[Chemical 6]

[0034]
Among these, the structure described in Formula Group 5 is preferable.
[0035]
[Chemical 7]

[0036]
Among these, the structure described in Formula Group 6 is particularly preferable.
[0037]
[Chemical 8]

[0038]
However, when Z is a hydrogen atom, Q ¹ , Q ² And Q ^Three Are all hydrogen atoms, m and n are both 0, Y is -COO-, and Z is a fluorine atom, or Q ¹ , Q ² And Q ^Three Are all hydrogen atoms, m and n are both 0, Y is a single bond or —COO—, and Z is a cyano group, the 1,4-phenylene group is excluded.
[0039]
As mentioned above, the compound of the above general formula (I) is m, n, R, V, W, X, Y, Z, Q ¹ , Q ² , Q ^Three The selection of ring A, ring B and ring C can include a wide variety of compounds, but by selecting each structural site, the compound can be adapted to a wider range of applications. As a result, the compound of the general formula (I) is very useful because it has favorable characteristics for electro-optic elements such as STN-LCD and AM-LCD, such as wide nematic temperature range, stability to light and heat, and high voltage holding ratio. is there. More specifically, among the compounds of the general formula (I), the following compounds can be mentioned as particularly preferred compounds.
[0040]
In the compound description, the following abbreviations are used, and R ¹ Is methyl, ethyl, propyl, butyl, pentyl, hexyl, peptyl, octyl, vinyl, trans-1-propenyl, 2-propenyl, trans-1-butenyl, trans-2 -Butenyl group, 3-butenyl group, trans-1-pentenyl group, trans-2-pentenyl group, trans-3-pentenyl group, 4-pentenyl group, trans-1-hexenyl group, trans-2-hexenyl group, trans -3-hexenyl group, trans-4-hexenyl group, 5-hexenyl group, trans-1-heptenyl group, trans-2-heptenyl group, trans-3-heptenyl group, trans-4-heptenyl group, trans-5- It represents either a heptenyl group or a 6-heptenyl group.
[0041]
[Chemical 9]

[0042]
When m = n = 0, V is a single bond, and Z is a fluorine atom,
[0043]
R ¹ -Te1-Ph1-F, R ¹ -Te1-Ph2-F, R ¹ -Te1-Ph3-F, R ¹ -Te1-Np1-F, R ¹ -Te1-Np2-F, R ¹ -Te1-Np3-F, R ¹ -Te1-Np4-F, R ¹ -Te2-Ph1-F, R ¹ -Te2-Ph2-F, R ¹ -Te2-Ph3-F, R ¹ -Te2-Np1-F, R ¹ -Te2-Np2-F, R ¹ -Te2-Np3-F, R ¹ -Te2-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-F,
[0044]
When m = n = 0, V is a single bond and Z is a cyano group,
[0045]
R ¹ -Te1-Ph2-CN, R ¹ -Te1-Ph3-CN, R ¹ -Te1-Np1-CN, R ¹ -Te1-Np2-CN, R ¹ -Te1-Np3-CN, R ¹ -Te1-Np4-CN, R ¹ -Te2-Ph1-CN, R ¹ -Te2-Ph2-CN, R ¹ -Te2-Ph3-CN, R ¹ -Te2-Np1-CN, R ¹ -Te2-Np2-CN, R ¹ -Te2-Np3-CN, R ¹ -Te2-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CN,
[0046]
When m = n = 0, V is a single bond, and Z is a trifluoromethoxy group,
[0047]
R ¹ -Te1-Ph1-OCF _Three , R ¹ -Te1-Ph2-OCF _Three , R ¹ -Te1-Ph3-OCF _Three , R ¹ -Te1-Np1-OCF _Three , R ¹ -Te1-Np2-OCF _Three , R ¹ -Te1-Np3-OCF _Three , R ¹ -Te1-Np4-OCF _Three , R ¹ -Te2-Ph1-OCF _Three , R ¹ -Te2-Ph2-OCF _Three , R ¹ -Te2-Ph3-OCF _Three , R ¹ -Te2-Np1-OCF _Three , R ¹ -Te2-Np2-OCF _Three , R ¹ -Te2-Np3-OCF _Three , R ¹ -Te2-Np4-OCF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-OCF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-OCF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0048]
When m = 1, n = 0, V is a single bond, and Z is a fluorine atom,
[0049]
R ¹ -Cy-Te1-Ph1-F, R ¹ -Cy-Te1-Ph2-F, R ¹ -Cy-Te1-Ph3-F, R ¹ -Cy-Te1-Np1-F, R ¹ -Cy-Te1-Np2-F, R ¹ -Cy-Te1-Np3-F, R ¹ -Cy-Te1-Np4-F, R ¹ -Cy-Te2-Ph1-F, R ¹ -Cy-Te2-Ph2-F, R ¹ -Cy-Te2-Ph3-F, R ¹ -Cy-Te2-Np1-F, R ¹ -Cy-Te2-Np2-F, R ¹ -Cy-Te2-Np3-F, R ¹ -Cy-Te2-Np4-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np4-F,
[0050]
R ¹ -Ph1-Te1-Ph1-F, R ¹ -Ph1-Te1-Ph2-F, R ¹ -Ph1-Te1-Ph3-F, R ¹ -Ph1-Te1-Np1-F, R ¹ -Ph1-Te1-Np2-F, R ¹ -Ph1-Te1-Np3-F, R ¹ -Ph1-Te1-Np4-F, R ¹ -Ph1-Te2-Ph1-F, R ¹ -Ph1-Te2-Ph2-F, R ¹ -Ph1-Te2-Ph3-F, R ¹ -Ph1-Te2-Np1-F, R ¹ -Ph1-Te2-Np2-F, R ¹ -Ph1-Te2-Np3-F, R ¹ -Ph1-Te2-Np4-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np4-F,
[0051]
R ¹ -Ph2-Te1-Ph1-F, R ¹ -Ph2-Te1-Ph2-F, R ¹ -Ph2-Te1-Ph3-F, R ¹ -Ph2-Te1-Np1-F, R ¹ -Ph2-Te1-Np2-F, R ¹ -Ph2-Te1-Np3-F, R ¹ -Ph2-Te1-Np4-F, R ¹ -Ph2-Te2-Ph1-F, R ¹ -Ph2-Te2-Ph2-F, R ¹ -Ph2-Te2-Ph3-F, R ¹ -Ph2-Te2-Np1-F, R ¹ -Ph2-Te2-Np2-F, R ¹ -Ph2-Te2-Np3-F, R ¹ -Ph2-Te2-Np4-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np4-F,
[0052]
R ¹ -Ph3-Te1-Ph1-F, R ¹ -Ph3-Te1-Ph2-F, R ¹ -Ph3-Te1-Ph3-F, R ¹ -Ph3-Te1-Np1-F, R ¹ -Ph3-Te1-Np2-F, R ¹ -Ph3-Te1-Np3-F, R ¹ -Ph3-Te1-Np4-F, R ¹ -Ph3-Te2-Ph1-F, R ¹ -Ph3-Te2-Ph2-F, R ¹ -Ph3-Te2-Ph3-F, R ¹ -Ph3-Te2-Np1-F, R ¹ -Ph3-Te2-Np2-F, R ¹ -Ph3-Te2-Np3-F, R ¹ -Ph3-Te2-Np4-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np4-F,
[0053]
R ¹ -Np1-Te1-Ph1-F, R ¹ -Np1-Te1-Ph2-F, R ¹ -Np1-Te1-Ph3-F, R ¹ -Np1-Te1-Np1-F, R ¹ -Np1-Te1-Np2-F, R ¹ -Np1-Te1-Np3-F, R ¹ -Np1-Te1-Np4-F, R ¹ -Np1-Te2-Ph1-F, R ¹ -Np1-Te2-Ph2-F, R ¹ -Np1-Te2-Ph3-F, R ¹ -Np1-Te2-Np1-F, R ¹ -Np1-Te2-Np2-F, R ¹ -Np1-Te2-Np3-F, R ¹ -Np1-Te2-Np4-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np4-F,
[0054]
R ¹ -Np2-Te1-Ph1-F, R ¹ -Np2-Te1-Ph2-F, R ¹ -Np2-Te1-Ph3-F, R ¹ -Np2-Te1-Np1-F, R ¹ -Np2-Te1-Np2-F, R ¹ -Np2-Te1-Np3-F, R ¹ -Np2-Te1-Np4-F, R ¹ -Np2-Te2-Ph1-F, R ¹ -Np2-Te2-Ph2-F, R ¹ -Np2-Te2-Ph3-F, R ¹ -Np2-Te2-Np1-F, R ¹ -Np2-Te2-Np2-F, R ¹ -Np2-Te2-Np3-F, R ¹ -Np2-Te2-Np4-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np4-F,
[0055]
R ¹ -Np3-Te1-Ph1-F, R ¹ -Np3-Te1-Ph2-F, R ¹ -Np3-Te1-Ph3-F, R ¹ -Np3-Te1-Np1-F, R ¹ -Np3-Te1-Np2-F, R ¹ -Np3-Te1-Np3-F, R ¹ -Np3-Te1-Np4-F, R ¹ -Np3-Te2-Ph1-F, R ¹ -Np3-Te2-Ph2-F, R ¹ -Np3-Te2-Ph3-F, R ¹ -Np3-Te2-Np1-F, R ¹ -Np3-Te2-Np2-F, R ¹ -Np3-Te2-Np3-F, R ¹ -Np3-Te2-Np4-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np4-F,
[0056]
R ¹ -Np4-Te1-Ph1-F, R ¹ -Np4-Te1-Ph2-F, R ¹ -Np4-Te1-Ph3-F, R ¹ -Np4-Te1-Np1-F, R ¹ -Np4-Te1-Np2-F, R ¹ -Np4-Te1-Np3-F, R ¹ -Np4-Te1-Np4-F, R ¹ -Np4-Te2-Ph1-F, R ¹ -Np4-Te2-Ph2-F, R ¹ -Np4-Te2-Ph3-F, R ¹ -Np4-Te2-Np1-F, R ¹ -Np4-Te2-Np2-F, R ¹ -Np4-Te2-Np3-F, R ¹ -Np4-Te2-Np4-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np4-F,
[0057]
R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0058]
R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0059]
R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0060]
R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0061]
R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0062]
R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0063]
R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0064]
R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph1-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph2-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph3-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np1-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np2-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np3-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np4-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph1-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph2-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph3-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np1-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np2-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np3-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np4-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-F,
[0065]
R ¹ -Ph1-C≡C-Te1-Ph1-F, R ¹ -Ph1-C≡C-Te1-Ph2-F, R ¹ -Ph1-C≡C-Te1-Ph3-F, R ¹ -Ph1-C≡C-Te1-Np1-F, R ¹ -Ph1-C≡C-Te1-Np2-F, R ¹ -Ph1-C≡C-Te1-Np3-F, R ¹ -Ph1-C≡C-Te1-Np4-F, R ¹ -Ph1-C≡C-Te2-Ph1-F, R ¹ -Ph1-C≡C-Te2-Ph2-F, R ¹ -Ph1-C≡C-Te2-Ph3-F, R ¹ -Ph1-C≡C-Te2-Np1-F, R ¹ -Ph1-C≡C-Te2-Np2-F, R ¹ -Ph1-C≡C-Te2-Np3-F, R ¹ -Ph1-C≡C-Te2-Np4-F, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np4-F,
[0066]
R ¹ -Ph2-C≡C-Te1-Ph1-F, R ¹ -Ph2-C≡C-Te1-Ph2-F, R ¹ -Ph2-C≡C-Te1-Ph3-F, R ¹ -Ph2-C≡C-Te1-Np1-F, R ¹ -Ph2-C≡C-Te1-Np2-F, R ¹ -Ph2-C≡C-Te1-Np3-F, R ¹ -Ph2-C≡C-Te1-Np4-F, R ¹ -Ph2-C≡C-Te2-Ph1-F, R ¹ -Ph2-C≡C-Te2-Ph2-F, R ¹ -Ph2-C≡C-Te2-Ph3-F, R ¹ -Ph2-C≡C-Te2-Np1-F, R ¹ -Ph2-C≡C-Te2-Np2-F, R ¹ -Ph2-C≡C-Te2-Np3-F, R ¹ -Ph2-C≡C-Te2-Np4-F, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np4-F,
[0067]
R ¹ -Ph3-C≡C-Te1-Ph1-F, R ¹ -Ph3-C≡C-Te1-Ph2-F, R ¹ -Ph3-C≡C-Te1-Ph3-F, R ¹ -Ph3-C≡C-Te1-Np1-F, R ¹ -Ph3-C≡C-Te1-Np2-F, R ¹ -Ph3-C≡C-Te1-Np3-F, R ¹ -Ph3-C≡C-Te1-Np4-F, R ¹ -Ph3-C≡C-Te2-Ph1-F, R ¹ -Ph3-C≡C-Te2-Ph2-F, R ¹ -Ph3-C≡C-Te2-Ph3-F, R ¹ -Ph3-C≡C-Te2-Np1-F, R ¹ -Ph3-C≡C-Te2-Np2-F, R ¹ -Ph3-C≡C-Te2-Np3-F, R ¹ -Ph3-C≡C-Te2-Np4-F, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np4-F,
[0068]
R ¹ -Np1-C≡C-Te1-Ph1-F, R ¹ -Np1-C≡C-Te1-Ph2-F, R ¹ -Np1-C≡C-Te1-Ph3-F, R ¹ -Np1-C≡C-Te1-Np1-F, R ¹ -Np1-C≡C-Te1-Np2-F, R ¹ -Np1-C≡C-Te1-Np3-F, R ¹ -Np1-C≡C-Te1-Np4-F, R ¹ -Np1-C≡C-Te2-Ph1-F, R ¹ -Np1-C≡C-Te2-Ph2-F, R ¹ -Np1-C≡C-Te2-Ph3-F, R ¹ -Np1-C≡C-Te2-Np1-F, R ¹ -Np1-C≡C-Te2-Np2-F, R ¹ -Np1-C≡C-Te2-Np3-F, R ¹ -Np1-C≡C-Te2-Np4-F, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np4-F,
[0069]
R ¹ -Np2-C≡C-Te1-Ph1-F, R ¹ -Np2-C≡C-Te1-Ph2-F, R ¹ -Np2-C≡C-Te1-Ph3-F, R ¹ -Np2-C≡C-Te1-Np1-F, R ¹ -Np2-C≡C-Te1-Np2-F, R ¹ -Np2-C≡C-Te1-Np3-F, R ¹ -Np2-C≡C-Te1-Np4-F, R ¹ -Np2-C≡C-Te2-Ph1-F, R ¹ -Np2-C≡C-Te2-Ph2-F, R ¹ -Np2-C≡C-Te2-Ph3-F, R ¹ -Np2-C≡C-Te2-Np1-F, R ¹ -Np2-C≡C-Te2-Np2-F, R ¹ -Np2-C≡C-Te2-Np3-F, R ¹ -Np2-C≡C-Te2-Np4-F, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np4-F,
[0070]
R ¹ -Np3-C≡C-Te1-Ph1-F, R ¹ -Np3-C≡C-Te1-Ph2-F, R ¹ -Np3-C≡C-Te1-Ph3-F, R ¹ -Np3-C≡C-Te1-Np1-F, R ¹ -Np3-C≡C-Te1-Np2-F, R ¹ -Np3-C≡C-Te1-Np3-F, R ¹ -Np3-C≡C-Te1-Np4-F, R ¹ -Np3-C≡C-Te2-Ph1-F, R ¹ -Np3-C≡C-Te2-Ph2-F, R ¹ -Np3-C≡C-Te2-Ph3-F, R ¹ -Np3-C≡C-Te2-Np1-F, R ¹ -Np3-C≡C-Te2-Np2-F, R ¹ -Np3-C≡C-Te2-Np3-F, R ¹ -Np3-C≡C-Te2-Np4-F, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np4-F,
[0071]
R ¹ -Np4-C≡C-Te1-Ph1-F, R ¹ -Np4-C≡C-Te1-Ph2-F, R ¹ -Np4-C≡C-Te1-Ph3-F, R ¹ -Np4-C≡C-Te1-Np1-F, R ¹ -Np4-C≡C-Te1-Np2-F, R ¹ -Np4-C≡C-Te1-Np3-F, R ¹ -Np4-C≡C-Te1-Np4-F, R ¹ -Np4-C≡C-Te2-Ph1-F, R ¹ -Np4-C≡C-Te2-Ph2-F, R ¹ -Np4-C≡C-Te2-Ph3-F, R ¹ -Np4-C≡C-Te2-Np1-F, R ¹ -Np4-C≡C-Te2-Np2-F, R ¹ -Np4-C≡C-Te2-Np3-F, R ¹ -Np4-C≡C-Te2-Np4-F, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np4-F, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph1-F, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph2-F, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph3-F, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np1-F, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np2-F, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np3-F, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np4-F,
[0072]
When m = 1, n = 0, V is a single bond, and Z is a cyano group,
[0073]
R ¹ -Cy-Te1-Ph1-CN, R ¹ -Cy-Te1-Ph2-CN, R ¹ -Cy-Te1-Ph3-CN, R ¹ -Cy-Te1-Np1-CN, R ¹ -Cy-Te1-Np2-CN, R ¹ -Cy-Te1-Np3-CN, R ¹ -Cy-Te1-Np4-CN, R ¹ -Cy-Te2-Ph1-CN, R ¹ -Cy-Te2-Ph2-CN, R ¹ -Cy-Te2-Ph3-CN, R ¹ -Cy-Te2-Np1-CN, R ¹ -Cy-Te2-Np2-CN, R ¹ -Cy-Te2-Np3-CN, R ¹ -Cy-Te2-Np4-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Cy-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Cy-Te2-CH ₂ CH ₂ -Np4-CN,
[0074]
R ¹ -Ph1-Te1-Ph1-CN, R ¹ -Ph1-Te1-Ph2-CN, R ¹ -Ph1-Te1-Ph3-CN, R ¹ -Ph1-Te1-Np1-CN, R ¹ -Ph1-Te1-Np2-CN, R ¹ -Ph1-Te1-Np3-CN, R ¹ -Ph1-Te1-Np4-CN, R ¹ -Ph1-Te2-Ph1-CN, R ¹ -Ph1-Te2-Ph2-CN, R ¹ -Ph1-Te2-Ph3-CN, R ¹ -Ph1-Te2-Np1-CN, R ¹ -Ph1-Te2-Np2-CN, R ¹ -Ph1-Te2-Np3-CN, R ¹ -Ph1-Te2-Np4-CN, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np4-CN,
[0075]
R ¹ -Ph2-Te1-Ph1-CN, R ¹ -Ph2-Te1-Ph2-CN, R ¹ -Ph2-Te1-Ph3-CN, R ¹ -Ph2-Te1-Np1-CN, R ¹ -Ph2-Te1-Np2-CN, R ¹ -Ph2-Te1-Np3-CN, R ¹ -Ph2-Te1-Np4-CN, R ¹ -Ph2-Te2-Ph1-CN, R ¹ -Ph2-Te2-Ph2-CN, R ¹ -Ph2-Te2-Ph3-CN, R ¹ -Ph2-Te2-Np1-CN, R ¹ -Ph2-Te2-Np2-CN, R ¹ -Ph2-Te2-Np3-CN, R ¹ -Ph2-Te2-Np4-CN, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np4-CN,
[0076]
R ¹ -Ph3-Te1-Ph1-CN, R ¹ -Ph3-Te1-Ph2-CN, R ¹ -Ph3-Te1-Ph3-CN, R ¹ -Ph3-Te1-Np1-CN, R ¹ -Ph3-Te1-Np2-CN, R ¹ -Ph3-Te1-Np3-CN, R ¹ -Ph3-Te1-Np4-CN, R ¹ -Ph3-Te2-Ph1-CN, R ¹ -Ph3-Te2-Ph2-CN, R ¹ -Ph3-Te2-Ph3-CN, R ¹ -Ph3-Te2-Np1-CN, R ¹ -Ph3-Te2-Np2-CN, R ¹ -Ph3-Te2-Np3-CN, R ¹ -Ph3-Te2-Np4-CN, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np4-CN,
[0077]
R ¹ -Np1-Te1-Ph1-CN, R ¹ -Np1-Te1-Ph2-CN, R ¹ -Np1-Te1-Ph3-CN, R ¹ -Np1-Te1-Np1-CN, R ¹ -Np1-Te1-Np2-CN, R ¹ -Np1-Te1-Np3-CN, R ¹ -Np1-Te1-Np4-CN, R ¹ -Np1-Te2-Ph1-CN, R ¹ -Np1-Te2-Ph2-CN, R ¹ -Np1-Te2-Ph3-CN, R ¹ -Np1-Te2-Np1-CN, R ¹ -Np1-Te2-Np2-CN, R ¹ -Np1-Te2-Np3-CN, R ¹ -Np1-Te2-Np4-CN, R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np1-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np1-Te2-CH ₂ CH ₂ -Np4-CN,
[0078]
R ¹ -Np2-Te1-Ph1-CN, R ¹ -Np2-Te1-Ph2-CN, R ¹ -Np2-Te1-Ph3-CN, R ¹ -Np2-Te1-Np1-CN, R ¹ -Np2-Te1-Np2-CN, R ¹ -Np2-Te1-Np3-CN, R ¹ -Np2-Te1-Np4-CN, R ¹ -Np2-Te2-Ph1-CN, R ¹ -Np2-Te2-Ph2-CN, R ¹ -Np2-Te2-Ph3-CN, R ¹ -Np2-Te2-Np1-CN, R ¹ -Np2-Te2-Np2-CN, R ¹ -Np2-Te2-Np3-CN, R ¹ -Np2-Te2-Np4-CN, R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np2-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np2-Te2-CH ₂ CH ₂ -Np4-CN,
[0079]
R ¹ -Np3-Te1-Ph1-CN, R ¹ -Np3-Te1-Ph2-CN, R ¹ -Np3-Te1-Ph3-CN, R ¹ -Np3-Te1-Np1-CN, R ¹ -Np3-Te1-Np2-CN, R ¹ -Np3-Te1-Np3-CN, R ¹ -Np3-Te1-Np4-CN, R ¹ -Np3-Te2-Ph1-CN, R ¹ -Np3-Te2-Ph2-CN, R ¹ -Np3-Te2-Ph3-CN, R ¹ -Np3-Te2-Np1-CN, R ¹ -Np3-Te2-Np2-CN, R ¹ -Np3-Te2-Np3-CN, R ¹ -Np3-Te2-Np4-CN, R ¹ -Np3-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np3-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np3-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np3-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np3-Te2-CH ₂ CH ₂ -Np4-CN,
[0080]
R ¹ -Np4-Te1-Ph1-CN, R ¹ -Np4-Te1-Ph2-CN, R ¹ -Np4-Te1-Ph3-CN, R ¹ -Np4-Te1-Np1-CN, R ¹ -Np4-Te1-Np2-CN, R ¹ -Np4-Te1-Np3-CN, R ¹ -Np4-Te1-Np4-CN, R ¹ -Np4-Te2-Ph1-CN, R ¹ -Np4-Te2-Ph2-CN, R ¹ -Np4-Te2-Ph3-CN, R ¹ -Np4-Te2-Np1-CN, R ¹ -Np4-Te2-Np2-CN, R ¹ -Np4-Te2-Np3-CN, R ¹ -Np4-Te2-Np4-CN, R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np4-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np4-Te2-CH ₂ CH ₂ -Np4-CN,
[0081]
R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0082]
R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0083]
R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0084]
R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0085]
R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0086]
R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0087]
R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0088]
R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph1-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np1-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-Np4-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph1-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np1-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-Np4-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-CN,
[0089]
R ¹ -Ph1-C≡C-Te1-Ph1-CN, R ¹ -Ph1-C≡C-Te1-Ph2-CN, R ¹ -Ph1-C≡C-Te1-Ph3-CN, R ¹ -Ph1-C≡C-Te1-Np1-CN, R ¹ -Ph1-C≡C-Te1-Np2-CN, R ¹ -Ph1-C≡C-Te1-Np3-CN, R ¹ -Ph1-C≡C-Te1-Np4-CN, R ¹ -Ph1-C≡C-Te2-Ph1-CN, R ¹ -Ph1-C≡C-Te2-Ph2-CN, R ¹ -Ph1-C≡C-Te2-Ph3-CN, R ¹ -Ph1-C≡C-Te2-Np1-CN, R ¹ -Ph1-C≡C-Te2-Np2-CN, R ¹ -Ph1-C≡C-Te2-Np3-CN, R ¹ -Ph1-C≡C-Te2-Np4-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np4-CN,
[0090]
R ¹ -Ph2-C≡C-Te1-Ph1-CN, R ¹ -Ph2-C≡C-Te1-Ph2-CN, R ¹ -Ph2-C≡C-Te1-Ph3-CN, R ¹ -Ph2-C≡C-Te1-Np1-CN, R ¹ -Ph2-C≡C-Te1-Np2-CN, R ¹ -Ph2-C≡C-Te1-Np3-CN, R ¹ -Ph2-C≡C-Te1-Np4-CN, R ¹ -Ph2-C≡C-Te2-Ph1-CN, R ¹ -Ph2-C≡C-Te2-Ph2-CN, R ¹ -Ph2-C≡C-Te2-Ph3-CN, R ¹ -Ph2-C≡C-Te2-Np1-CN, R ¹ -Ph2-C≡C-Te2-Np2-CN, R ¹ -Ph2-C≡C-Te2-Np3-CN, R ¹ -Ph2-C≡C-Te2-Np4-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np4-CN,
[0091]
R ¹ -Ph3-C≡C-Te1-Ph1-CN, R ¹ -Ph3-C≡C-Te1-Ph2-CN, R ¹ -Ph3-C≡C-Te1-Ph3-CN, R ¹ -Ph3-C≡C-Te1-Np1-CN, R ¹ -Ph3-C≡C-Te1-Np2-CN, R ¹ -Ph3-C≡C-Te1-Np3-CN, R ¹ -Ph3-C≡C-Te1-Np4-CN, R ¹ -Ph3-C≡C-Te2-Ph1-CN, R ¹ -Ph3-C≡C-Te2-Ph2-CN, R ¹ -Ph3-C≡C-Te2-Ph3-CN, R ¹ -Ph3-C≡C-Te2-Np1-CN, R ¹ -Ph3-C≡C-Te2-Np2-CN, R ¹ -Ph3-C≡C-Te2-Np3-CN, R ¹ -Ph3-C≡C-Te2-Np4-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np4-CN,
[0092]
R ¹ -Np1-C≡C-Te1-Ph1-CN, R ¹ -Np1-C≡C-Te1-Ph2-CN, R ¹ -Np1-C≡C-Te1-Ph3-CN, R ¹ -Np1-C≡C-Te1-Np1-CN, R ¹ -Np1-C≡C-Te1-Np2-CN, R ¹ -Np1-C≡C-Te1-Np3-CN, R ¹ -Np1-C≡C-Te1-Np4-CN, R ¹ -Np1-C≡C-Te2-Ph1-CN, R ¹ -Np1-C≡C-Te2-Ph2-CN, R ¹ -Np1-C≡C-Te2-Ph3-CN, R ¹ -Np1-C≡C-Te2-Np1-CN, R ¹ -Np1-C≡C-Te2-Np2-CN, R ¹ -Np1-C≡C-Te2-Np3-CN, R ¹ -Np1-C≡C-Te2-Np4-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np4-CN,
[0093]
R ¹ -Np2-C≡C-Te1-Ph1-CN, R ¹ -Np2-C≡C-Te1-Ph2-CN, R ¹ -Np2-C≡C-Te1-Ph3-CN, R ¹ -Np2-C≡C-Te1-Np1-CN, R ¹ -Np2-C≡C-Te1-Np2-CN, R ¹ -Np2-C≡C-Te1-Np3-CN, R ¹ -Np2-C≡C-Te1-Np4-CN, R ¹ -Np2-C≡C-Te2-Ph1-CN, R ¹ -Np2-C≡C-Te2-Ph2-CN, R ¹ -Np2-C≡C-Te2-Ph3-CN, R ¹ -Np2-C≡C-Te2-Np1-CN, R ¹ -Np2-C≡C-Te2-Np2-CN, R ¹ -Np2-C≡C-Te2-Np3-CN, R ¹ -Np2-C≡C-Te2-Np4-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np4-CN,
[0094]
R ¹ -Np3-C≡C-Te1-Ph1-CN, R ¹ -Np3-C≡C-Te1-Ph2-CN, R ¹ -Np3-C≡C-Te1-Ph3-CN, R ¹ -Np3-C≡C-Te1-Np1-CN, R ¹ -Np3-C≡C-Te1-Np2-CN, R ¹ -Np3-C≡C-Te1-Np3-CN, R ¹ -Np3-C≡C-Te1-Np4-CN, R ¹ -Np3-C≡C-Te2-Ph1-CN, R ¹ -Np3-C≡C-Te2-Ph2-CN, R ¹ -Np3-C≡C-Te2-Ph3-CN, R ¹ -Np3-C≡C-Te2-Np1-CN, R ¹ -Np3-C≡C-Te2-Np2-CN, R ¹ -Np3-C≡C-Te2-Np3-CN, R ¹ -Np3-C≡C-Te2-Np4-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np3-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np3-C≡C-Te2-CH ₂ CH ₂ -Np4-CN,
[0095]
R ¹ -Np4-C≡C-Te1-Ph1-CN, R ¹ -Np4-C≡C-Te1-Ph2-CN, R ¹ -Np4-C≡C-Te1-Ph3-CN, R ¹ -Np4-C≡C-Te1-Np1-CN, R ¹ -Np4-C≡C-Te1-Np2-CN, R ¹ -Np4-C≡C-Te1-Np3-CN, R ¹ -Np4-C≡C-Te1-Np4-CN, R ¹ -Np4-C≡C-Te2-Ph1-CN, R ¹ -Np4-C≡C-Te2-Ph2-CN, R ¹ -Np4-C≡C-Te2-Ph3-CN, R ¹ -Np4-C≡C-Te2-Np1-CN, R ¹ -Np4-C≡C-Te2-Np2-CN, R ¹ -Np4-C≡C-Te2-Np3-CN, R ¹ -Np4-C≡C-Te2-Np4-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np1-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np2-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np3-CN, R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np4-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np1-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np2-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np3-CN, R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np4-CN,
[0096]
When m = 1, n = 0, V is a single bond, and Z is a trifluoromethoxy group,
[0097]
R ¹ -Cy-Te1-Ph1-OCF _Three , R ¹ -Cy-Te1-Ph2-OCF _Three , R ¹ -Cy-Te1-Ph3-OCF _Three , R ¹ -Cy-Te1-Np1-OCF _Three , R ¹ -Cy-Te1-Np2-OCF _Three , R ¹ -Cy-Te1-Ph3-OCF _Three , R ¹ -Cy-Te1-Np4-OCF _Three , R ¹ -Cy-Te2-Ph1-OCF _Three , R ¹ -Cy-Te2-Ph2-OCF _Three , R ¹ -Cy-Te2-Ph3-OCF _Three , R ¹ -Cy-Te2-Np1-OCF _Three , R ¹ -Cy-Te2-Np2-OCF _Three , R ¹ -Cy-Te2-Ph3-OCF _Three , R ¹ -Cy-Te2-Np4-OCF _Three , R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Cy-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Cy-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Cy-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Cy-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0098]
R ¹ -Ph1-Te1-Ph1-OCF _Three , R ¹ -Ph1-Te1-Ph2-OCF _Three , R ¹ -Ph1-Te1-Ph3-OCF _Three , R ¹ -Ph1-Te1-Np1-OCF _Three , R ¹ -Ph1-Te1-Np2-OCF _Three , R ¹ -Ph1-Te1-Ph3-OCF _Three , R ¹ -Ph1-Te1-Np4-OCF _Three , R ¹ -Ph1-Te2-Ph1-OCF _Three , R ¹ -Ph1-Te2-Ph2-OCF _Three , R ¹ -Ph1-Te2-Ph3-OCF _Three , R ¹ -Ph1-Te2-Np1-OCF _Three , R ¹ -Ph1-Te2-Np2-OCF _Three , R ¹ -Ph1-Te2-Ph3-OCF _Three , R ¹ -Ph1-Te2-Np4-OCF _Three , R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph1-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph1-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0099]
R ¹ -Ph2-Te1-Ph1-OCF _Three , R ¹ -Ph2-Te1-Ph2-OCF _Three , R ¹ -Ph2-Te1-Ph3-OCF _Three , R ¹ -Ph2-Te1-Np1-OCF _Three , R ¹ -Ph2-Te1-Np2-OCF _Three , R ¹ -Ph2-Te1-Ph3-OCF _Three , R ¹ -Ph2-Te1-Np4-OCF _Three , R ¹ -Ph2-Te2-Ph1-OCF _Three , R ¹ -Ph2-Te2-Ph2-OCF _Three , R ¹ -Ph2-Te2-Ph3-OCF _Three , R ¹ -Ph2-Te2-Np1-OCF _Three , R ¹ -Ph2-Te2-Np2-OCF _Three , R ¹ -Ph2-Te2-Ph3-OCF _Three , R ¹ -Ph2-Te2-Np4-OCF _Three , R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph2-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph2-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0100]
R ¹ -Ph3-Te1-Ph1-OCF _Three , R ¹ -Ph3-Te1-Ph2-OCF _Three , R ¹ -Ph3-Te1-Ph3-OCF _Three , R ¹ -Ph3-Te1-Np1-OCF _Three , R ¹ -Ph3-Te1-Np2-OCF _Three , R ¹ -Ph3-Te1-Ph3-OCF _Three , R ¹ -Ph3-Te1-Np4-OCF _Three , R ¹ -Ph3-Te2-Ph1-OCF _Three , R ¹ -Ph3-Te2-Ph2-OCF _Three , R ¹ -Ph3-Te2-Ph3-OCF _Three , R ¹ -Ph3-Te2-Np1-OCF _Three , R ¹ -Ph3-Te2-Np2-OCF _Three , R ¹ -Ph3-Te2-Ph3-OCF _Three , R ¹ -Ph3-Te2-Np4-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0101]
R ¹ -Np1-Te1-Ph1-OCF _Three , R ¹ -Np1-Te1-Ph2-OCF _Three , R ¹ -Np1-Te1-Ph3-OCF _Three , R ¹ -Np1-Te1-Np1-OCF _Three , R ¹ -Np1-Te1-Np2-OCF _Three , R ¹ -Np1-Te1-Ph3-OCF _Three , R ¹ -Np1-Te1-Np4-OCF _Three , R ¹ -Np1-Te2-Ph1-OCF _Three , R ¹ -Np1-Te2-Ph2-OCF _Three , R ¹ -Np1-Te2-Ph3-OCF _Three , R ¹ -Np1-Te2-Np1-OCF _Three , R ¹ -Np1-Te2-Np2-OCF _Three , R ¹ -Np1-Te2-Ph3-OCF _Three , R ¹ -Np1-Te2-Np4-OCF _Three , R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np1-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np1-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np1-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np1-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0102]
R ¹ -Np2-Te1-Ph1-OCF _Three , R ¹ -Np2-Te1-Ph2-OCF _Three , R ¹ -Np2-Te1-Ph3-OCF _Three , R ¹ -Np2-Te1-Np1-OCF _Three , R ¹ -Np2-Te1-Np2-OCF _Three , R ¹ -Np2-Te1-Ph3-OCF _Three , R ¹ -Np2-Te1-Np4-OCF _Three , R ¹ -Np2-Te2-Ph1-OCF _Three , R ¹ -Np2-Te2-Ph2-OCF _Three , R ¹ -Np2-Te2-Ph3-OCF _Three , R ¹ -Np2-Te2-Np1-OCF _Three , R ¹ -Np2-Te2-Np2-OCF _Three , R ¹ -Np2-Te2-Ph3-OCF _Three , R ¹ -Np2-Te2-Np4-OCF _Three , R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np2-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np2-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np2-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np2-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0103]
R ¹ -Ph3-Te1-Ph1-OCF _Three , R ¹ -Ph3-Te1-Ph2-OCF _Three , R ¹ -Ph3-Te1-Ph3-OCF _Three , R ¹ -Ph3-Te1-Np1-OCF _Three , R ¹ -Ph3-Te1-Np2-OCF _Three , R ¹ -Ph3-Te1-Ph3-OCF _Three , R ¹ -Ph3-Te1-Np4-OCF _Three , R ¹ -Ph3-Te2-Ph1-OCF _Three , R ¹ -Ph3-Te2-Ph2-OCF _Three , R ¹ -Ph3-Te2-Ph3-OCF _Three , R ¹ -Ph3-Te2-Np1-OCF _Three , R ¹ -Ph3-Te2-Np2-OCF _Three , R ¹ -Ph3-Te2-Ph3-OCF _Three , R ¹ -Ph3-Te2-Np4-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0104]
R ¹ -Np4-Te1-Ph1-OCF _Three , R ¹ -Np4-Te1-Ph2-OCF _Three , R ¹ -Np4-Te1-Ph3-OCF _Three , R ¹ -Np4-Te1-Np1-OCF _Three , R ¹ -Np4-Te1-Np2-OCF _Three , R ¹ -Np4-Te1-Ph3-OCF _Three , R ¹ -Np4-Te1-Np4-OCF _Three , R ¹ -Np4-Te2-Ph1-OCF _Three , R ¹ -Np4-Te2-Ph2-OCF _Three , R ¹ -Np4-Te2-Ph3-OCF _Three , R ¹ -Np4-Te2-Np1-OCF _Three , R ¹ -Np4-Te2-Np2-OCF _Three , R ¹ -Np4-Te2-Ph3-OCF _Three , R ¹ -Np4-Te2-Np4-OCF _Three , R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np4-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np4-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np4-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np4-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0105]
R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Cy-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0106]
R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0107]
R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0108]
R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0109]
R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0110]
R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0111]
R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0112]
R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph1-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-Np1-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-Np2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-Np4-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph1-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-Np1-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-Np2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-Np4-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-CH ₂ CH ₂ -Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0113]
R ¹ -Ph1-C≡C-Te1-Ph1-OCF _Three , R ¹ -Ph1-C≡C-Te1-Ph2-OCF _Three , R ¹ -Ph1-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te1-Np1-OCF _Three , R ¹ -Ph1-C≡C-Te1-Np2-OCF _Three , R ¹ -Ph1-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te1-Np4-OCF _Three , R ¹ -Ph1-C≡C-Te2-Ph1-OCF _Three , R ¹ -Ph1-C≡C-Te2-Ph2-OCF _Three , R ¹ -Ph1-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te2-Np1-OCF _Three , R ¹ -Ph1-C≡C-Te2-Np2-OCF _Three , R ¹ -Ph1-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te2-Np4-OCF _Three , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph1-C≡C-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0114]
R ¹ -Ph2-C≡C-Te1-Ph1-OCF _Three , R ¹ -Ph2-C≡C-Te1-Ph2-OCF _Three , R ¹ -Ph2-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te1-Np1-OCF _Three , R ¹ -Ph2-C≡C-Te1-Np2-OCF _Three , R ¹ -Ph2-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te1-Np4-OCF _Three , R ¹ -Ph2-C≡C-Te2-Ph1-OCF _Three , R ¹ -Ph2-C≡C-Te2-Ph2-OCF _Three , R ¹ -Ph2-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te2-Np1-OCF _Three , R ¹ -Ph2-C≡C-Te2-Np2-OCF _Three , R ¹ -Ph2-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te2-Np4-OCF _Three , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph2-C≡C-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0115]
R ¹ -Ph3-C≡C-Te1-Ph1-OCF _Three , R ¹ -Ph3-C≡C-Te1-Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-Np1-OCF _Three , R ¹ -Ph3-C≡C-Te1-Np2-OCF _Three , R ¹ -Ph3-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-Np4-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph1-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-Np1-OCF _Three , R ¹ -Ph3-C≡C-Te2-Np2-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-Np4-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0116]
R ¹ -Np1-C≡C-Te1-Ph1-OCF _Three , R ¹ -Np1-C≡C-Te1-Ph2-OCF _Three , R ¹ -Np1-C≡C-Te1-Ph3-OCF _Three , R ¹ -Np1-C≡C-Te1-Np1-OCF _Three , R ¹ -Np1-C≡C-Te1-Np2-OCF _Three , R ¹ -Np1-C≡C-Te1-Ph3-OCF _Three , R ¹ -Np1-C≡C-Te1-Np4-OCF _Three , R ¹ -Np1-C≡C-Te2-Ph1-OCF _Three , R ¹ -Np1-C≡C-Te2-Ph2-OCF _Three , R ¹ -Np1-C≡C-Te2-Ph3-OCF _Three , R ¹ -Np1-C≡C-Te2-Np1-OCF _Three , R ¹ -Np1-C≡C-Te2-Np2-OCF _Three , R ¹ -Np1-C≡C-Te2-Ph3-OCF _Three , R ¹ -Np1-C≡C-Te2-Np4-OCF _Three , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-C≡C-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np1-C≡C-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0117]
R ¹ -Np2-C≡C-Te1-Ph1-OCF _Three , R ¹ -Np2-C≡C-Te1-Ph2-OCF _Three , R ¹ -Np2-C≡C-Te1-Ph3-OCF _Three , R ¹ -Np2-C≡C-Te1-Np1-OCF _Three , R ¹ -Np2-C≡C-Te1-Np2-OCF _Three , R ¹ -Np2-C≡C-Te1-Ph3-OCF _Three , R ¹ -Np2-C≡C-Te1-Np4-OCF _Three , R ¹ -Np2-C≡C-Te2-Ph1-OCF _Three , R ¹ -Np2-C≡C-Te2-Ph2-OCF _Three , R ¹ -Np2-C≡C-Te2-Ph3-OCF _Three , R ¹ -Np2-C≡C-Te2-Np1-OCF _Three , R ¹ -Np2-C≡C-Te2-Np2-OCF _Three , R ¹ -Np2-C≡C-Te2-Ph3-OCF _Three , R ¹ -Np2-C≡C-Te2-Np4-OCF _Three , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-C≡C-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np2-C≡C-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0118]
R ¹ -Ph3-C≡C-Te1-Ph1-OCF _Three , R ¹ -Ph3-C≡C-Te1-Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-Np1-OCF _Three , R ¹ -Ph3-C≡C-Te1-Np2-OCF _Three , R ¹ -Ph3-C≡C-Te1-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-Np4-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph1-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-Np1-OCF _Three , R ¹ -Ph3-C≡C-Te2-Np2-OCF _Three , R ¹ -Ph3-C≡C-Te2-Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-Np4-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Ph3-C≡C-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0119]
R ¹ -Np4-C≡C-Te1-Ph1-OCF _Three , R ¹ -Np4-C≡C-Te1-Ph2-OCF _Three , R ¹ -Np4-C≡C-Te1-Ph3-OCF _Three , R ¹ -Np4-C≡C-Te1-Np1-OCF _Three , R ¹ -Np4-C≡C-Te1-Np2-OCF _Three , R ¹ -Np4-C≡C-Te1-Ph3-OCF _Three , R ¹ -Np4-C≡C-Te1-Np4-OCF _Three , R ¹ -Np4-C≡C-Te2-Ph1-OCF _Three , R ¹ -Np4-C≡C-Te2-Ph2-OCF _Three , R ¹ -Np4-C≡C-Te2-Ph3-OCF _Three , R ¹ -Np4-C≡C-Te2-Np1-OCF _Three , R ¹ -Np4-C≡C-Te2-Np2-OCF _Three , R ¹ -Np4-C≡C-Te2-Ph3-OCF _Three , R ¹ -Np4-C≡C-Te2-Np4-OCF _Three , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-C≡C-Te1-CH ₂ CH ₂ -Np4-OCF _Three , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph1-OCF _Three , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph2-OCF _Three , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np1-OCF _Three , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np2-OCF _Three , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Ph3-OCF _Three , R ¹ -Np4-C≡C-Te2-CH ₂ CH ₂ -Np4-OCF _Three ,
[0120]
When m = 0, n = 1, V is a single bond, and Z is a fluorine atom,
[0121]
R ¹ -Te1-Cy-Ph1-F, R ¹ -Te1-Cy-Ph2-F, R ¹ -Te1-Cy-Ph3-F, R ¹ -Te1-Cy-Np1-F, R ¹ -Te1-Cy-Np2-F, R ¹ -Te1-Cy-Np3-F, R ¹ -Te1-Cy-Np4-F, R ¹ -Te2-Cy-Ph1-F, R ¹ -Te2-Cy-Ph2-F, R ¹ -Te2-Cy-Ph3-F, R ¹ -Te2-Cy-Np1-F, R ¹ -Te2-Cy-Np2-F, R ¹ -Te2-Cy-Np3-F, R ¹ -Te2-Cy-Np4-F, R ¹ -Te1-Cy-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Cy-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np4-F,
[0122]
R ¹ -Te1-Ph1-Ph1-F, R ¹ -Te1-Ph1-Ph2-F, R ¹ -Te1-Ph1-Ph3-F, R ¹ -Te1-Ph1-Np1-F, R ¹ -Te1-Ph1-Np2-F, R ¹ -Te1-Ph1-Np3-F, R ¹ -Te1-Ph1-Np4-F, R ¹ -Te2-Ph1-Ph1-F, R ¹ -Te2-Ph1-Ph2-F, R ¹ -Te2-Ph1-Ph3-F, R ¹ -Te2-Ph1-Np1-F, R ¹ -Te2-Ph1-Np2-F, R ¹ -Te2-Ph1-Np3-F, R ¹ -Te2-Ph1-Np4-F, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-Ph1-C≡C-Ph2-F, R ¹ -Te1-Ph1-C≡C-Ph3-F, R ¹ -Te1-Ph1-C≡C-Np1-F, R ¹ -Te1-Ph1-C≡C-Np2-F, R ¹ -Te1-Ph1-C≡C-Np3-F, R ¹ -Te1-Ph1-C≡C-Np4-F, R ¹ -Te2-Ph1-C≡C-Ph1-F, R ¹ -Te2-Ph1-C≡C-Ph2-F, R ¹ -Te2-Ph1-C≡C-Ph3-F, R ¹ -Te2-Ph1-C≡C-Np1-F, R ¹ -Te2-Ph1-C≡C-Np2-F, R ¹ -Te2-Ph1-C≡C-Np3-F, R ¹ -Te2-Ph1-C≡C-Np4-F,
[0123]
R ¹ -Te1-Ph2-Ph1-F, R ¹ -Te1-Ph2-Ph2-F, R ¹ -Te1-Ph2-Ph3-F, R ¹ -Te1-Ph2-Np1-F, R ¹ -Te1-Ph2-Np2-F, R ¹ -Te1-Ph2-Np3-F, R ¹ -Te1-Ph2-Np4-F, R ¹ -Te2-Ph2-Ph1-F, R ¹ -Te2-Ph2-Ph2-F, R ¹ -Te2-Ph2-Ph3-F, R ¹ -Te2-Ph2-Np1-F, R ¹ -Te2-Ph2-Np2-F, R ¹ -Te2-Ph2-Np3-F, R ¹ -Te2-Ph2-Np4-F, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-Ph2-C≡C-Ph2-F, R ¹ -Te1-Ph2-C≡C-Ph3-F, R ¹ -Te1-Ph2-C≡C-Np1-F, R ¹ -Te1-Ph2-C≡C-Np2-F, R ¹ -Te1-Ph2-C≡C-Np3-F, R ¹ -Te1-Ph2-C≡C-Np4-F, R ¹ -Te2-Ph2-C≡C-Ph1-F, R ¹ -Te2-Ph2-C≡C-Ph2-F, R ¹ -Te2-Ph2-C≡C-Ph3-F, R ¹ -Te2-Ph2-C≡C-Np1-F, R ¹ -Te2-Ph2-C≡C-Np2-F, R ¹ -Te2-Ph2-C≡C-Np3-F, R ¹ -Te2-Ph2-C≡C-Np4-F,
[0124]
R ¹ -Te1-Ph3-Ph1-F, R ¹ -Te1-Ph3-Ph2-F, R ¹ -Te1-Ph3-Ph3-F, R ¹ -Te1-Ph3-Np1-F, R ¹ -Te1-Ph3-Np2-F, R ¹ -Te1-Ph3-Np3-F, R ¹ -Te1-Ph3-Np4-F, R ¹ -Te2-Ph3-Ph1-F, R ¹ -Te2-Ph3-Ph2-F, R ¹ -Te2-Ph3-Ph3-F, R ¹ -Te2-Ph3-Np1-F, R ¹ -Te2-Ph3-Np2-F, R ¹ -Te2-Ph3-Np3-F, R ¹ -Te2-Ph3-Np4-F, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-Ph3-C≡C-Ph2-F, R ¹ -Te1-Ph3-C≡C-Ph3-F, R ¹ -Te1-Ph3-C≡C-Np1-F, R ¹ -Te1-Ph3-C≡C-Np2-F, R ¹ -Te1-Ph3-C≡C-Np3-F, R ¹ -Te1-Ph3-C≡C-Np4-F, R ¹ -Te2-Ph3-C≡C-Ph1-F, R ¹ -Te2-Ph3-C≡C-Ph2-F, R ¹ -Te2-Ph3-C≡C-Ph3-F, R ¹ -Te2-Ph3-C≡C-Np1-F, R ¹ -Te2-Ph3-C≡C-Np2-F, R ¹ -Te2-Ph3-C≡C-Np3-F, R ¹ -Te2-Ph3-C≡C-Np4-F,
[0125]
R ¹ -Te1-Np1-Ph1-F, R ¹ -Te1-Np1-Ph2-F, R ¹ -Te1-Np1-Ph3-F, R ¹ -Te1-Np1-Np1-F, R ¹ -Te1-Np1-Np2-F, R ¹ -Te1-Np1-Np3-F, R ¹ -Te1-Np1-Np4-F, R ¹ -Te2-Np1-Ph1-F, R ¹ -Te2-Np1-Ph2-F, R ¹ -Te2-Np1-Ph3-F, R ¹ -Te2-Np1-Np1-F, R ¹ -Te2-Np1-Np2-F, R ¹ -Te2-Np1-Np3-F, R ¹ -Te2-Np1-Np4-F, R ¹ -Te1-Np1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Np1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-Np1-C≡C-Ph2-F, R ¹ -Te1-Np1-C≡C-Ph3-F, R ¹ -Te1-Np1-C≡C-Np1-F, R ¹ -Te1-Np1-C≡C-Np2-F, R ¹ -Te1-Np1-C≡C-Np3-F, R ¹ -Te1-Np1-C≡C-Np4-F, R ¹ -Te2-Np1-C≡C-Ph1-F, R ¹ -Te2-Np1-C≡C-Ph2-F, R ¹ -Te2-Np1-C≡C-Ph3-F, R ¹ -Te2-Np1-C≡C-Np1-F, R ¹ -Te2-Np1-C≡C-Np2-F, R ¹ -Te2-Np1-C≡C-Np3-F, R ¹ -Te2-Np1-C≡C-Np4-F,
[0126]
R ¹ -Te1-Np2-Ph1-F, R ¹ -Te1-Np2-Ph2-F, R ¹ -Te1-Np2-Ph3-F, R ¹ -Te1-Np2-Np1-F, R ¹ -Te1-Np2-Np2-F, R ¹ -Te1-Np2-Np3-F, R ¹ -Te1-Np2-Np4-F, R ¹ -Te2-Np2-Ph1-F, R ¹ -Te2-Np2-Ph2-F, R ¹ -Te2-Np2-Ph3-F, R ¹ -Te2-Np2-Np1-F, R ¹ -Te2-Np2-Np2-F, R ¹ -Te2-Np2-Np3-F, R ¹ -Te2-Np2-Np4-F, R ¹ -Te1-Np2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Np2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-Np2-C≡C-Ph2-F, R ¹ -Te1-Np2-C≡C-Ph3-F, R ¹ -Te1-Np2-C≡C-Np1-F, R ¹ -Te1-Np2-C≡C-Np2-F, R ¹ -Te1-Np2-C≡C-Np3-F, R ¹ -Te1-Np2-C≡C-Np4-F, R ¹ -Te2-Np2-C≡C-Ph1-F, R ¹ -Te2-Np2-C≡C-Ph2-F, R ¹ -Te2-Np2-C≡C-Ph3-F, R ¹ -Te2-Np2-C≡C-Np1-F, R ¹ -Te2-Np2-C≡C-Np2-F, R ¹ -Te2-Np2-C≡C-Np3-F, R ¹ -Te2-Np2-C≡C-Np4-F,
[0127]
R ¹ -Te1-Np3-Ph1-F, R ¹ -Te1-Np3-Ph2-F, R ¹ -Te1-Np3-Ph3-F, R ¹ -Te1-Np3-Np1-F, R ¹ -Te1-Np3-Np2-F, R ¹ -Te1-Np3-Np3-F, R ¹ -Te1-Np3-Np4-F, R ¹ -Te2-Np3-Ph1-F, R ¹ -Te2-Np3-Ph2-F, R ¹ -Te2-Np3-Ph3-F, R ¹ -Te2-Np3-Np1-F, R ¹ -Te2-Np3-Np2-F, R ¹ -Te2-Np3-Np3-F, R ¹ -Te2-Np3-Np4-F, R ¹ -Te1-Np3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Np3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-Np3-C≡C-Ph2-F, R ¹ -Te1-Np3-C≡C-Ph3-F, R ¹ -Te1-Np3-C≡C-Np1-F, R ¹ -Te1-Np3-C≡C-Np2-F, R ¹ -Te1-Np3-C≡C-Np3-F, R ¹ -Te1-Np3-C≡C-Np4-F, R ¹ -Te2-Np3-C≡C-Ph1-F, R ¹ -Te2-Np3-C≡C-Ph2-F, R ¹ -Te2-Np3-C≡C-Ph3-F, R ¹ -Te2-Np3-C≡C-Np1-F, R ¹ -Te2-Np3-C≡C-Np2-F, R ¹ -Te2-Np3-C≡C-Np3-F, R ¹ -Te2-Np3-C≡C-Np4-F,
[0128]
R ¹ -Te1-Np4-Ph1-F, R ¹ -Te1-Np4-Ph2-F, R ¹ -Te1-Np4-Ph3-F, R ¹ -Te1-Np4-Np1-F, R ¹ -Te1-Np4-Np2-F, R ¹ -Te1-Np4-Np3-F, R ¹ -Te1-Np4-Np4-F, R ¹ -Te2-Np4-Ph1-F, R ¹ -Te2-Np4-Ph2-F, R ¹ -Te2-Np4-Ph3-F, R ¹ -Te2-Np4-Np1-F, R ¹ -Te2-Np4-Np2-F, R ¹ -Te2-Np4-Np3-F, R ¹ -Te2-Np4-Np4-F, R ¹ -Te1-Np4-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-Np4-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-Np4-C≡C-Ph2-F, R ¹ -Te1-Np4-C≡C-Ph3-F, R ¹ -Te1-Np4-C≡C-Np1-F, R ¹ -Te1-Np4-C≡C-Np2-F, R ¹ -Te1-Np4-C≡C-Np3-F, R ¹ -Te1-Np4-C≡C-Np4-F, R ¹ -Te2-Np4-C≡C-Ph1-F, R ¹ -Te2-Np4-C≡C-Ph2-F, R ¹ -Te2-Np4-C≡C-Ph3-F, R ¹ -Te2-Np4-C≡C-Np1-F, R ¹ -Te2-Np4-C≡C-Np2-F, R ¹ -Te2-Np4-C≡C-Np3-F, R ¹ -Te2-Np4-C≡C-Np4-F,
[0129]
R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np4-F,
[0130]
R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np4-F,
[0131]
R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np4-F,
[0132]
R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np4-F,
[0133]
R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np4-F,
[0134]
R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np4-F,
[0135]
R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph1-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Ph2-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Ph3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np1-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np2-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np3-F, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np4-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph1-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph2-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np1-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np2-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np3-F, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np4-F,
[0136]
R ¹ -Te1-C≡C-Ph1-Ph1-F, R ¹ -Te1-C≡C-Ph1-Ph2-F, R ¹ -Te1-C≡C-Ph1-Ph3-F, R ¹ -Te1-C≡C-Ph1-Np1-F, R ¹ -Te1-C≡C-Ph1-Np2-F, R ¹ -Te1-C≡C-Ph1-Np3-F, R ¹ -Te1-C≡C-Ph1-Np4-F, R ¹ -Te2-C≡C-Ph1-Ph1-F, R ¹ -Te2-C≡C-Ph1-Ph2-F, R ¹ -Te2-C≡C-Ph1-Ph3-F, R ¹ -Te2-C≡C-Ph1-Np1-F, R ¹ -Te2-C≡C-Ph1-Np2-F, R ¹ -Te2-C≡C-Ph1-Np3-F, R ¹ -Te2-C≡C-Ph1-Np4-F, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-C≡C-Ph1-C≡C-Ph2-F, R ¹ -Te1-C≡C-Ph1-C≡C-Ph3-F, R ¹ -Te1-C≡C-Ph1-C≡C-Np1-F, R ¹ -Te1-C≡C-Ph1-C≡C-Np2-F, R ¹ -Te1-C≡C-Ph1-C≡C-Np3-F, R ¹ -Te1-C≡C-Ph1-C≡C-Np4-F, R ¹ -Te2-C≡C-Ph1-C≡C-Ph1-F, R ¹ -Te2-C≡C-Ph1-C≡C-Ph2-F, R ¹ -Te2-C≡C-Ph1-C≡C-Ph3-F, R ¹ -Te2-C≡C-Ph1-C≡C-Np1-F, R ¹ -Te2-C≡C-Ph1-C≡C-Np2-F, R ¹ -Te2-C≡C-Ph1-C≡C-Np3-F, R ¹ -Te2-C≡C-Ph1-C≡C-Np4-F,
[0137]
R ¹ -Te1-C≡C-Ph2-Ph1-F, R ¹ -Te1-C≡C-Ph2-Ph2-F, R ¹ -Te1-C≡C-Ph2-Ph3-F, R ¹ -Te1-C≡C-Ph2-Np1-F, R ¹ -Te1-C≡C-Ph2-Np2-F, R ¹ -Te1-C≡C-Ph2-Np3-F, R ¹ -Te1-C≡C-Ph2-Np4-F, R ¹ -Te2-C≡C-Ph2-Ph1-F, R ¹ -Te2-C≡C-Ph2-Ph2-F, R ¹ -Te2-C≡C-Ph2-Ph3-F, R ¹ -Te2-C≡C-Ph2-Np1-F, R ¹ -Te2-C≡C-Ph2-Np2-F, R ¹ -Te2-C≡C-Ph2-Np3-F, R ¹ -Te2-C≡C-Ph2-Np4-F, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-C≡C-Ph2-C≡C-Ph2-F, R ¹ -Te1-C≡C-Ph2-C≡C-Ph3-F, R ¹ -Te1-C≡C-Ph2-C≡C-Np1-F, R ¹ -Te1-C≡C-Ph2-C≡C-Np2-F, R ¹ -Te1-C≡C-Ph2-C≡C-Np3-F, R ¹ -Te1-C≡C-Ph2-C≡C-Np4-F, R ¹ -Te2-C≡C-Ph2-C≡C-Ph1-F, R ¹ -Te2-C≡C-Ph2-C≡C-Ph2-F, R ¹ -Te2-C≡C-Ph2-C≡C-Ph3-F, R ¹ -Te2-C≡C-Ph2-C≡C-Np1-F, R ¹ -Te2-C≡C-Ph2-C≡C-Np2-F, R ¹ -Te2-C≡C-Ph2-C≡C-Np3-F, R ¹ -Te2-C≡C-Ph2-C≡C-Np4-F,
[0138]
R ¹ -Te1-C≡C-Ph3-Ph1-F, R ¹ -Te1-C≡C-Ph3-Ph2-F, R ¹ -Te1-C≡C-Ph3-Ph3-F, R ¹ -Te1-C≡C-Ph3-Np1-F, R ¹ -Te1-C≡C-Ph3-Np2-F, R ¹ -Te1-C≡C-Ph3-Np3-F, R ¹ -Te1-C≡C-Ph3-Np4-F, R ¹ -Te2-C≡C-Ph3-Ph1-F, R ¹ -Te2-C≡C-Ph3-Ph2-F, R ¹ -Te2-C≡C-Ph3-Ph3-F, R ¹ -Te2-C≡C-Ph3-Np1-F, R ¹ -Te2-C≡C-Ph3-Np2-F, R ¹ -Te2-C≡C-Ph3-Np3-F, R ¹ -Te2-C≡C-Ph3-Np4-F, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-C≡C-Ph3-C≡C-Ph2-F, R ¹ -Te1-C≡C-Ph3-C≡C-Ph3-F, R ¹ -Te1-C≡C-Ph3-C≡C-Np1-F, R ¹ -Te1-C≡C-Ph3-C≡C-Np2-F, R ¹ -Te1-C≡C-Ph3-C≡C-Np3-F, R ¹ -Te1-C≡C-Ph3-C≡C-Np4-F, R ¹ -Te2-C≡C-Ph3-C≡C-Ph1-F, R ¹ -Te2-C≡C-Ph3-C≡C-Ph2-F, R ¹ -Te2-C≡C-Ph3-C≡C-Ph3-F, R ¹ -Te2-C≡C-Ph3-C≡C-Np1-F, R ¹ -Te2-C≡C-Ph3-C≡C-Np2-F, R ¹ -Te2-C≡C-Ph3-C≡C-Np3-F, R ¹ -Te2-C≡C-Ph3-C≡C-Np4-F,
[0139]
R ¹ -Te1-C≡C-Np1-Ph1-F, R ¹ -Te1-C≡C-Np1-Ph2-F, R ¹ -Te1-C≡C-Np1-Ph3-F, R ¹ -Te1-C≡C-Np1-Np1-F, R ¹ -Te1-C≡C-Np1-Np2-F, R ¹ -Te1-C≡C-Np1-Np3-F, R ¹ -Te1-C≡C-Np1-Np4-F, R ¹ -Te2-C≡C-Np1-Ph1-F, R ¹ -Te2-C≡C-Np1-Ph2-F, R ¹ -Te2-C≡C-Np1-Ph3-F, R ¹ -Te2-C≡C-Np1-Np1-F, R ¹ -Te2-C≡C-Np1-Np2-F, R ¹ -Te2-C≡C-Np1-Np3-F, R ¹ -Te2-C≡C-Np1-Np4-F, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-C≡C-Np1-C≡C-Ph2-F, R ¹ -Te1-C≡C-Np1-C≡C-Ph3-F, R ¹ -Te1-C≡C-Np1-C≡C-Np1-F, R ¹ -Te1-C≡C-Np1-C≡C-Np2-F, R ¹ -Te1-C≡C-Np1-C≡C-Np3-F, R ¹ -Te1-C≡C-Np1-C≡C-Np4-F, R ¹ -Te2-C≡C-Np1-C≡C-Ph1-F, R ¹ -Te2-C≡C-Np1-C≡C-Ph2-F, R ¹ -Te2-C≡C-Np1-C≡C-Ph3-F, R ¹ -Te2-C≡C-Np1-C≡C-Np1-F, R ¹ -Te2-C≡C-Np1-C≡C-Np2-F, R ¹ -Te2-C≡C-Np1-C≡C-Np3-F, R ¹ -Te2-C≡C-Np1-C≡C-Np4-F,
[0140]
R ¹ -Te1-C≡C-Np2-Ph1-F, R ¹ -Te1-C≡C-Np2-Ph2-F, R ¹ -Te1-C≡C-Np2-Ph3-F, R ¹ -Te1-C≡C-Np2-Np1-F, R ¹ -Te1-C≡C-Np2-Np2-F, R ¹ -Te1-C≡C-Np2-Np3-F, R ¹ -Te1-C≡C-Np2-Np4-F, R ¹ -Te2-C≡C-Np2-Ph1-F, R ¹ -Te2-C≡C-Np2-Ph2-F, R ¹ -Te2-C≡C-Np2-Ph3-F, R ¹ -Te2-C≡C-Np2-Np1-F, R ¹ -Te2-C≡C-Np2-Np2-F, R ¹ -Te2-C≡C-Np2-Np3-F, R ¹ -Te2-C≡C-Np2-Np4-F, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-C≡C-Np2-C≡C-Ph2-F, R ¹ -Te1-C≡C-Np2-C≡C-Ph3-F, R ¹ -Te1-C≡C-Np2-C≡C-Np1-F, R ¹ -Te1-C≡C-Np2-C≡C-Np2-F, R ¹ -Te1-C≡C-Np2-C≡C-Np3-F, R ¹ -Te1-C≡C-Np2-C≡C-Np4-F, R ¹ -Te2-C≡C-Np2-C≡C-Ph1-F, R ¹ -Te2-C≡C-Np2-C≡C-Ph2-F, R ¹ -Te2-C≡C-Np2-C≡C-Ph3-F, R ¹ -Te2-C≡C-Np2-C≡C-Np1-F, R ¹ -Te2-C≡C-Np2-C≡C-Np2-F, R ¹ -Te2-C≡C-Np2-C≡C-Np3-F, R ¹ -Te2-C≡C-Np2-C≡C-Np4-F,
[0141]
R ¹ -Te1-C≡C-Np3-Ph1-F, R ¹ -Te1-C≡C-Np3-Ph2-F, R ¹ -Te1-C≡C-Np3-Ph3-F, R ¹ -Te1-C≡C-Np3-Np1-F, R ¹ -Te1-C≡C-Np3-Np2-F, R ¹ -Te1-C≡C-Np3-Np3-F, R ¹ -Te1-C≡C-Np3-Np4-F, R ¹ -Te2-C≡C-Np3-Ph1-F, R ¹ -Te2-C≡C-Np3-Ph2-F, R ¹ -Te2-C≡C-Np3-Ph3-F, R ¹ -Te2-C≡C-Np3-Np1-F, R ¹ -Te2-C≡C-Np3-Np2-F, R ¹ -Te2-C≡C-Np3-Np3-F, R ¹ -Te2-C≡C-Np3-Np4-F, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-C≡C-Np3-C≡C-Ph2-F, R ¹ -Te1-C≡C-Np3-C≡C-Ph3-F, R ¹ -Te1-C≡C-Np3-C≡C-Np1-F, R ¹ -Te1-C≡C-Np3-C≡C-Np2-F, R ¹ -Te1-C≡C-Np3-C≡C-Np3-F, R ¹ -Te1-C≡C-Np3-C≡C-Np4-F, R ¹ -Te2-C≡C-Np3-C≡C-Ph1-F, R ¹ -Te2-C≡C-Np3-C≡C-Ph2-F, R ¹ -Te2-C≡C-Np3-C≡C-Ph3-F, R ¹ -Te2-C≡C-Np3-C≡C-Np1-F, R ¹ -Te2-C≡C-Np3-C≡C-Np2-F, R ¹ -Te2-C≡C-Np3-C≡C-Np3-F, R ¹ -Te2-C≡C-Np3-C≡C-Np4-F,
[0142]
R ¹ -Te1-C≡C-Np4-Ph1-F, R ¹ -Te1-C≡C-Np4-Ph2-F, R ¹ -Te1-C≡C-Np4-Ph3-F, R ¹ -Te1-C≡C-Np4-Np1-F, R ¹ -Te1-C≡C-Np4-Np2-F, R ¹ -Te1-C≡C-Np4-Np3-F, R ¹ -Te1-C≡C-Np4-Np4-F, R ¹ -Te2-C≡C-Np4-Ph1-F, R ¹ -Te2-C≡C-Np4-Ph2-F, R ¹ -Te2-C≡C-Np4-Ph3-F, R ¹ -Te2-C≡C-Np4-Np1-F, R ¹ -Te2-C≡C-Np4-Np2-F, R ¹ -Te2-C≡C-Np4-Np3-F, R ¹ -Te2-C≡C-Np4-Np4-F, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Ph2-F, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Ph3-F, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np1-F, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np2-F, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np3-F, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np4-F, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph1-F, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph2-F, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph3-F, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np1-F, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np2-F, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np3-F, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np4-F, R ¹ -Te1-C≡C-Np4-C≡C-Ph2-F, R ¹ -Te1-C≡C-Np4-C≡C-Ph3-F, R ¹ -Te1-C≡C-Np4-C≡C-Np1-F, R ¹ -Te1-C≡C-Np4-C≡C-Np2-F, R ¹ -Te1-C≡C-Np4-C≡C-Np3-F, R ¹ -Te1-C≡C-Np4-C≡C-Np4-F, R ¹ -Te2-C≡C-Np4-C≡C-Ph1-F, R ¹ -Te2-C≡C-Np4-C≡C-Ph2-F, R ¹ -Te2-C≡C-Np4-C≡C-Ph3-F, R ¹ -Te2-C≡C-Np4-C≡C-Np1-F, R ¹ -Te2-C≡C-Np4-C≡C-Np2-F, R ¹ -Te2-C≡C-Np4-C≡C-Np3-F, R ¹ -Te2-C≡C-Np4-C≡C-Np4-F,
[0143]
When m = 0, n = 1, V is a single bond, and Z is a cyano group,
[0144]
R ¹ -Te1-Cy-Ph1-CN, R ¹ -Te1-Cy-Ph2-CN, R ¹ -Te1-Cy-Ph3-CN, R ¹ -Te1-Cy-Np1-CN, R ¹ -Te1-Cy-Np2-CN, R ¹ -Te1-Cy-Np3-CN, R ¹ -Te1-Cy-Np4-CN, R ¹ -Te2-Cy-Ph1-CN, R ¹ -Te2-Cy-Ph2-CN, R ¹ -Te2-Cy-Ph3-CN, R ¹ -Te2-Cy-Np1-CN, R ¹ -Te2-Cy-Np2-CN, R ¹ -Te2-Cy-Np3-CN, R ¹ -Te2-Cy-Np4-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Cy-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Cy-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np4-CN,
[0145]
R ¹ -Te1-Ph1-Ph1-CN, R ¹ -Te1-Ph1-Ph2-CN, R ¹ -Te1-Ph1-Ph3-CN, R ¹ -Te1-Ph1-Np1-CN, R ¹ -Te1-Ph1-Np2-CN, R ¹ -Te1-Ph1-Np3-CN, R ¹ -Te1-Ph1-Np4-CN, R ¹ -Te2-Ph1-Ph1-CN, R ¹ -Te2-Ph1-Ph2-CN, R ¹ -Te2-Ph1-Ph3-CN, R ¹ -Te2-Ph1-Np1-CN, R ¹ -Te2-Ph1-Np2-CN, R ¹ -Te2-Ph1-Np3-CN, R ¹ -Te2-Ph1-Np4-CN, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-Ph1-C≡C-Ph2-CN, R ¹ -Te1-Ph1-C≡C-Ph3-CN, R ¹ -Te1-Ph1-C≡C-Np1-CN, R ¹ -Te1-Ph1-C≡C-Np2-CN, R ¹ -Te1-Ph1-C≡C-Np3-CN, R ¹ -Te1-Ph1-C≡C-Np4-CN, R ¹ -Te2-Ph1-C≡C-Ph1-CN, R ¹ -Te2-Ph1-C≡C-Ph2-CN, R ¹ -Te2-Ph1-C≡C-Ph3-CN, R ¹ -Te2-Ph1-C≡C-Np1-CN, R ¹ -Te2-Ph1-C≡C-Np2-CN, R ¹ -Te2-Ph1-C≡C-Np3-CN, R ¹ -Te2-Ph1-C≡C-Np4-CN,
[0146]
R ¹ -Te1-Ph2-Ph1-CN, R ¹ -Te1-Ph2-Ph2-CN, R ¹ -Te1-Ph2-Ph3-CN, R ¹ -Te1-Ph2-Np1-CN, R ¹ -Te1-Ph2-Np2-CN, R ¹ -Te1-Ph2-Np3-CN, R ¹ -Te1-Ph2-Np4-CN, R ¹ -Te2-Ph2-Ph1-CN, R ¹ -Te2-Ph2-Ph2-CN, R ¹ -Te2-Ph2-Ph3-CN, R ¹ -Te2-Ph2-Np1-CN, R ¹ -Te2-Ph2-Np2-CN, R ¹ -Te2-Ph2-Np3-CN, R ¹ -Te2-Ph2-Np4-CN, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-Ph2-C≡C-Ph2-CN, R ¹ -Te1-Ph2-C≡C-Ph3-CN, R ¹ -Te1-Ph2-C≡C-Np1-CN, R ¹ -Te1-Ph2-C≡C-Np2-CN, R ¹ -Te1-Ph2-C≡C-Np3-CN, R ¹ -Te1-Ph2-C≡C-Np4-CN, R ¹ -Te2-Ph2-C≡C-Ph1-CN, R ¹ -Te2-Ph2-C≡C-Ph2-CN, R ¹ -Te2-Ph2-C≡C-Ph3-CN, R ¹ -Te2-Ph2-C≡C-Np1-CN, R ¹ -Te2-Ph2-C≡C-Np2-CN, R ¹ -Te2-Ph2-C≡C-Np3-CN, R ¹ -Te2-Ph2-C≡C-Np4-CN,
[0147]
R ¹ -Te1-Ph3-Ph1-CN, R ¹ -Te1-Ph3-Ph2-CN, R ¹ -Te1-Ph3-Ph3-CN, R ¹ -Te1-Ph3-Np1-CN, R ¹ -Te1-Ph3-Np2-CN, R ¹ -Te1-Ph3-Np3-CN, R ¹ -Te1-Ph3-Np4-CN, R ¹ -Te2-Ph3-Ph1-CN, R ¹ -Te2-Ph3-Ph2-CN, R ¹ -Te2-Ph3-Ph3-CN, R ¹ -Te2-Ph3-Np1-CN, R ¹ -Te2-Ph3-Np2-CN, R ¹ -Te2-Ph3-Np3-CN, R ¹ -Te2-Ph3-Np4-CN, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-Ph3-C≡C-Ph2-CN, R ¹ -Te1-Ph3-C≡C-Ph3-CN, R ¹ -Te1-Ph3-C≡C-Np1-CN, R ¹ -Te1-Ph3-C≡C-Np2-CN, R ¹ -Te1-Ph3-C≡C-Np3-CN, R ¹ -Te1-Ph3-C≡C-Np4-CN, R ¹ -Te2-Ph3-C≡C-Ph1-CN, R ¹ -Te2-Ph3-C≡C-Ph2-CN, R ¹ -Te2-Ph3-C≡C-Ph3-CN, R ¹ -Te2-Ph3-C≡C-Np1-CN, R ¹ -Te2-Ph3-C≡C-Np2-CN, R ¹ -Te2-Ph3-C≡C-Np3-CN, R ¹ -Te2-Ph3-C≡C-Np4-CN,
[0148]
R ¹ -Te1-Np1-Ph1-CN, R ¹ -Te1-Np1-Ph2-CN, R ¹ -Te1-Np1-Ph3-CN, R ¹ -Te1-Np1-Np1-CN, R ¹ -Te1-Np1-Np2-CN, R ¹ -Te1-Np1-Np3-CN, R ¹ -Te1-Np1-Np4-CN, R ¹ -Te2-Np1-Ph1-CN, R ¹ -Te2-Np1-Ph2-CN, R ¹ -Te2-Np1-Ph3-CN, R ¹ -Te2-Np1-Np1-CN, R ¹ -Te2-Np1-Np2-CN, R ¹ -Te2-Np1-Np3-CN, R ¹ -Te2-Np1-Np4-CN, R ¹ -Te1-Np1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Np1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Np1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Np1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-Np1-C≡C-Ph2-CN, R ¹ -Te1-Np1-C≡C-Ph3-CN, R ¹ -Te1-Np1-C≡C-Np1-CN, R ¹ -Te1-Np1-C≡C-Np2-CN, R ¹ -Te1-Np1-C≡C-Np3-CN, R ¹ -Te1-Np1-C≡C-Np4-CN, R ¹ -Te2-Np1-C≡C-Ph1-CN, R ¹ -Te2-Np1-C≡C-Ph2-CN, R ¹ -Te2-Np1-C≡C-Ph3-CN, R ¹ -Te2-Np1-C≡C-Np1-CN, R ¹ -Te2-Np1-C≡C-Np2-CN, R ¹ -Te2-Np1-C≡C-Np3-CN, R ¹ -Te2-Np1-C≡C-Np4-CN,
[0149]
R ¹ -Te1-Np2-Ph1-CN, R ¹ -Te1-Np2-Ph2-CN, R ¹ -Te1-Np2-Ph3-CN, R ¹ -Te1-Np2-Np1-CN, R ¹ -Te1-Np2-Np2-CN, R ¹ -Te1-Np2-Np3-CN, R ¹ -Te1-Np2-Np4-CN, R ¹ -Te2-Np2-Ph1-CN, R ¹ -Te2-Np2-Ph2-CN, R ¹ -Te2-Np2-Ph3-CN, R ¹ -Te2-Np2-Np1-CN, R ¹ -Te2-Np2-Np2-CN, R ¹ -Te2-Np2-Np3-CN, R ¹ -Te2-Np2-Np4-CN, R ¹ -Te1-Np2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Np2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Np2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Np2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-Np2-C≡C-Ph2-CN, R ¹ -Te1-Np2-C≡C-Ph3-CN, R ¹ -Te1-Np2-C≡C-Np1-CN, R ¹ -Te1-Np2-C≡C-Np2-CN, R ¹ -Te1-Np2-C≡C-Np3-CN, R ¹ -Te1-Np2-C≡C-Np4-CN, R ¹ -Te2-Np2-C≡C-Ph1-CN, R ¹ -Te2-Np2-C≡C-Ph2-CN, R ¹ -Te2-Np2-C≡C-Ph3-CN, R ¹ -Te2-Np2-C≡C-Np1-CN, R ¹ -Te2-Np2-C≡C-Np2-CN, R ¹ -Te2-Np2-C≡C-Np3-CN, R ¹ -Te2-Np2-C≡C-Np4-CN,
[0150]
R ¹ -Te1-Np3-Ph1-CN, R ¹ -Te1-Np3-Ph2-CN, R ¹ -Te1-Np3-Ph3-CN, R ¹ -Te1-Np3-Np1-CN, R ¹ -Te1-Np3-Np2-CN, R ¹ -Te1-Np3-Np3-CN, R ¹ -Te1-Np3-Np4-CN, R ¹ -Te2-Np3-Ph1-CN, R ¹ -Te2-Np3-Ph2-CN, R ¹ -Te2-Np3-Ph3-CN, R ¹ -Te2-Np3-Np1-CN, R ¹ -Te2-Np3-Np2-CN, R ¹ -Te2-Np3-Np3-CN, R ¹ -Te2-Np3-Np4-CN, R ¹ -Te1-Np3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Np3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Np3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Np3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-Np3-C≡C-Ph2-CN, R ¹ -Te1-Np3-C≡C-Ph3-CN, R ¹ -Te1-Np3-C≡C-Np1-CN, R ¹ -Te1-Np3-C≡C-Np2-CN, R ¹ -Te1-Np3-C≡C-Np3-CN, R ¹ -Te1-Np3-C≡C-Np4-CN, R ¹ -Te2-Np3-C≡C-Ph1-CN, R ¹ -Te2-Np3-C≡C-Ph2-CN, R ¹ -Te2-Np3-C≡C-Ph3-CN, R ¹ -Te2-Np3-C≡C-Np1-CN, R ¹ -Te2-Np3-C≡C-Np2-CN, R ¹ -Te2-Np3-C≡C-Np3-CN, R ¹ -Te2-Np3-C≡C-Np4-CN,
[0151]
R ¹ -Te1-Np4-Ph1-CN, R ¹ -Te1-Np4-Ph2-CN, R ¹ -Te1-Np4-Ph3-CN, R ¹ -Te1-Np4-Np1-CN, R ¹ -Te1-Np4-Np2-CN, R ¹ -Te1-Np4-Np3-CN, R ¹ -Te1-Np4-Np4-CN, R ¹ -Te2-Np4-Ph1-CN, R ¹ -Te2-Np4-Ph2-CN, R ¹ -Te2-Np4-Ph3-CN, R ¹ -Te2-Np4-Np1-CN, R ¹ -Te2-Np4-Np2-CN, R ¹ -Te2-Np4-Np3-CN, R ¹ -Te2-Np4-Np4-CN, R ¹ -Te1-Np4-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-Np4-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-Np4-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-Np4-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-Np4-C≡C-Ph2-CN, R ¹ -Te1-Np4-C≡C-Ph3-CN, R ¹ -Te1-Np4-C≡C-Np1-CN, R ¹ -Te1-Np4-C≡C-Np2-CN, R ¹ -Te1-Np4-C≡C-Np3-CN, R ¹ -Te1-Np4-C≡C-Np4-CN, R ¹ -Te2-Np4-C≡C-Ph1-CN, R ¹ -Te2-Np4-C≡C-Ph2-CN, R ¹ -Te2-Np4-C≡C-Ph3-CN, R ¹ -Te2-Np4-C≡C-Np1-CN, R ¹ -Te2-Np4-C≡C-Np2-CN, R ¹ -Te2-Np4-C≡C-Np3-CN, R ¹ -Te2-Np4-C≡C-Np4-CN,
[0152]
R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np4-CN,
[0153]
R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np4-CN,
[0154]
R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np4-CN,
[0155]
R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np4-CN,
[0156]
R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np4-CN,
[0157]
R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np4-CN,
[0158]
R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Ph2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Ph3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np1-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np2-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np3-CN, R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np4-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np1-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np2-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np3-CN, R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np4-CN,
[0159]
R ¹ -Te1-C≡C-Ph1-Ph1-CN, R ¹ -Te1-C≡C-Ph1-Ph2-CN, R ¹ -Te1-C≡C-Ph1-Ph3-CN, R ¹ -Te1-C≡C-Ph1-Np1-CN, R ¹ -Te1-C≡C-Ph1-Np2-CN, R ¹ -Te1-C≡C-Ph1-Np3-CN, R ¹ -Te1-C≡C-Ph1-Np4-CN, R ¹ -Te2-C≡C-Ph1-Ph1-CN, R ¹ -Te2-C≡C-Ph1-Ph2-CN, R ¹ -Te2-C≡C-Ph1-Ph3-CN, R ¹ -Te2-C≡C-Ph1-Np1-CN, R ¹ -Te2-C≡C-Ph1-Np2-CN, R ¹ -Te2-C≡C-Ph1-Np3-CN, R ¹ -Te2-C≡C-Ph1-Np4-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Ph2-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Np1-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Np2-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Np3-CN, R ¹ -Te1-C≡C-Ph1-C≡C-Np4-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Ph1-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Ph2-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Np1-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Np2-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Np3-CN, R ¹ -Te2-C≡C-Ph1-C≡C-Np4-CN,
[0160]
R ¹ -Te1-C≡C-Ph2-Ph1-CN, R ¹ -Te1-C≡C-Ph2-Ph2-CN, R ¹ -Te1-C≡C-Ph2-Ph3-CN, R ¹ -Te1-C≡C-Ph2-Np1-CN, R ¹ -Te1-C≡C-Ph2-Np2-CN, R ¹ -Te1-C≡C-Ph2-Np3-CN, R ¹ -Te1-C≡C-Ph2-Np4-CN, R ¹ -Te2-C≡C-Ph2-Ph1-CN, R ¹ -Te2-C≡C-Ph2-Ph2-CN, R ¹ -Te2-C≡C-Ph2-Ph3-CN, R ¹ -Te2-C≡C-Ph2-Np1-CN, R ¹ -Te2-C≡C-Ph2-Np2-CN, R ¹ -Te2-C≡C-Ph2-Np3-CN, R ¹ -Te2-C≡C-Ph2-Np4-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Ph2-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Np1-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Np2-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Np3-CN, R ¹ -Te1-C≡C-Ph2-C≡C-Np4-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Ph1-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Ph2-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Np1-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Np2-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Np3-CN, R ¹ -Te2-C≡C-Ph2-C≡C-Np4-CN,
[0161]
R ¹ -Te1-C≡C-Ph3-Ph1-CN, R ¹ -Te1-C≡C-Ph3-Ph2-CN, R ¹ -Te1-C≡C-Ph3-Ph3-CN, R ¹ -Te1-C≡C-Ph3-Np1-CN, R ¹ -Te1-C≡C-Ph3-Np2-CN, R ¹ -Te1-C≡C-Ph3-Np3-CN, R ¹ -Te1-C≡C-Ph3-Np4-CN, R ¹ -Te2-C≡C-Ph3-Ph1-CN, R ¹ -Te2-C≡C-Ph3-Ph2-CN, R ¹ -Te2-C≡C-Ph3-Ph3-CN, R ¹ -Te2-C≡C-Ph3-Np1-CN, R ¹ -Te2-C≡C-Ph3-Np2-CN, R ¹ -Te2-C≡C-Ph3-Np3-CN, R ¹ -Te2-C≡C-Ph3-Np4-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Ph2-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Np1-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Np2-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Np3-CN, R ¹ -Te1-C≡C-Ph3-C≡C-Np4-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Ph1-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Ph2-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Np1-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Np2-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Np3-CN, R ¹ -Te2-C≡C-Ph3-C≡C-Np4-CN,
[0162]
R ¹ -Te1-C≡C-Np1-Ph1-CN, R ¹ -Te1-C≡C-Np1-Ph2-CN, R ¹ -Te1-C≡C-Np1-Ph3-CN, R ¹ -Te1-C≡C-Np1-Np1-CN, R ¹ -Te1-C≡C-Np1-Np2-CN, R ¹ -Te1-C≡C-Np1-Np3-CN, R ¹ -Te1-C≡C-Np1-Np4-CN, R ¹ -Te2-C≡C-Np1-Ph1-CN, R ¹ -Te2-C≡C-Np1-Ph2-CN, R ¹ -Te2-C≡C-Np1-Ph3-CN, R ¹ -Te2-C≡C-Np1-Np1-CN, R ¹ -Te2-C≡C-Np1-Np2-CN, R ¹ -Te2-C≡C-Np1-Np3-CN, R ¹ -Te2-C≡C-Np1-Np4-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-C≡C-Np1-C≡C-Ph2-CN, R ¹ -Te1-C≡C-Np1-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np1-C≡C-Np1-CN, R ¹ -Te1-C≡C-Np1-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np1-C≡C-Np3-CN, R ¹ -Te1-C≡C-Np1-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np1-C≡C-Ph1-CN, R ¹ -Te2-C≡C-Np1-C≡C-Ph2-CN, R ¹ -Te2-C≡C-Np1-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np1-C≡C-Np1-CN, R ¹ -Te2-C≡C-Np1-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np1-C≡C-Np3-CN, R ¹ -Te2-C≡C-Np1-C≡C-Np4-CN,
[0163]
R ¹ -Te1-C≡C-Np2-Ph1-CN, R ¹ -Te1-C≡C-Np2-Ph2-CN, R ¹ -Te1-C≡C-Np2-Ph3-CN, R ¹ -Te1-C≡C-Np2-Np1-CN, R ¹ -Te1-C≡C-Np2-Np2-CN, R ¹ -Te1-C≡C-Np2-Np3-CN, R ¹ -Te1-C≡C-Np2-Np4-CN, R ¹ -Te2-C≡C-Np2-Ph1-CN, R ¹ -Te2-C≡C-Np2-Ph2-CN, R ¹ -Te2-C≡C-Np2-Ph3-CN, R ¹ -Te2-C≡C-Np2-Np1-CN, R ¹ -Te2-C≡C-Np2-Np2-CN, R ¹ -Te2-C≡C-Np2-Np3-CN, R ¹ -Te2-C≡C-Np2-Np4-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-C≡C-Np2-C≡C-Ph2-CN, R ¹ -Te1-C≡C-Np2-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np2-C≡C-Np1-CN, R ¹ -Te1-C≡C-Np2-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np2-C≡C-Np3-CN, R ¹ -Te1-C≡C-Np2-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np2-C≡C-Ph1-CN, R ¹ -Te2-C≡C-Np2-C≡C-Ph2-CN, R ¹ -Te2-C≡C-Np2-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np2-C≡C-Np1-CN, R ¹ -Te2-C≡C-Np2-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np2-C≡C-Np3-CN, R ¹ -Te2-C≡C-Np2-C≡C-Np4-CN,
[0164]
R ¹ -Te1-C≡C-Np3-Ph1-CN, R ¹ -Te1-C≡C-Np3-Ph2-CN, R ¹ -Te1-C≡C-Np3-Ph3-CN, R ¹ -Te1-C≡C-Np3-Np1-CN, R ¹ -Te1-C≡C-Np3-Np2-CN, R ¹ -Te1-C≡C-Np3-Np3-CN, R ¹ -Te1-C≡C-Np3-Np4-CN, R ¹ -Te2-C≡C-Np3-Ph1-CN, R ¹ -Te2-C≡C-Np3-Ph2-CN, R ¹ -Te2-C≡C-Np3-Ph3-CN, R ¹ -Te2-C≡C-Np3-Np1-CN, R ¹ -Te2-C≡C-Np3-Np2-CN, R ¹ -Te2-C≡C-Np3-Np3-CN, R ¹ -Te2-C≡C-Np3-Np4-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-C≡C-Np3-C≡C-Ph2-CN, R ¹ -Te1-C≡C-Np3-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np3-C≡C-Np1-CN, R ¹ -Te1-C≡C-Np3-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np3-C≡C-Np3-CN, R ¹ -Te1-C≡C-Np3-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np3-C≡C-Ph1-CN, R ¹ -Te2-C≡C-Np3-C≡C-Ph2-CN, R ¹ -Te2-C≡C-Np3-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np3-C≡C-Np1-CN, R ¹ -Te2-C≡C-Np3-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np3-C≡C-Np3-CN, R ¹ -Te2-C≡C-Np3-C≡C-Np4-CN,
[0165]
R ¹ -Te1-C≡C-Np4-Ph1-CN, R ¹ -Te1-C≡C-Np4-Ph2-CN, R ¹ -Te1-C≡C-Np4-Ph3-CN, R ¹ -Te1-C≡C-Np4-Np1-CN, R ¹ -Te1-C≡C-Np4-Np2-CN, R ¹ -Te1-C≡C-Np4-Np3-CN, R ¹ -Te1-C≡C-Np4-Np4-CN, R ¹ -Te2-C≡C-Np4-Ph1-CN, R ¹ -Te2-C≡C-Np4-Ph2-CN, R ¹ -Te2-C≡C-Np4-Ph3-CN, R ¹ -Te2-C≡C-Np4-Np1-CN, R ¹ -Te2-C≡C-Np4-Np2-CN, R ¹ -Te2-C≡C-Np4-Np3-CN, R ¹ -Te2-C≡C-Np4-Np4-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np1-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np3-CN, R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np4-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph1-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph2-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph3-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np1-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np2-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np3-CN, R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np4-CN, R ¹ -Te1-C≡C-Np4-C≡C-Ph2-CN, R ¹ -Te1-C≡C-Np4-C≡C-Ph3-CN, R ¹ -Te1-C≡C-Np4-C≡C-Np1-CN, R ¹ -Te1-C≡C-Np4-C≡C-Np2-CN, R ¹ -Te1-C≡C-Np4-C≡C-Np3-CN, R ¹ -Te1-C≡C-Np4-C≡C-Np4-CN, R ¹ -Te2-C≡C-Np4-C≡C-Ph1-CN, R ¹ -Te2-C≡C-Np4-C≡C-Ph2-CN, R ¹ -Te2-C≡C-Np4-C≡C-Ph3-CN, R ¹ -Te2-C≡C-Np4-C≡C-Np1-CN, R ¹ -Te2-C≡C-Np4-C≡C-Np2-CN, R ¹ -Te2-C≡C-Np4-C≡C-Np3-CN, R ¹ -Te2-C≡C-Np4-C≡C-Np4-CN,
[0166]
When m = 0, n = 1, V is a single bond, and Z is a trifluoromethyl group,
[0167]
R ¹ -Te1-Cy-Ph1-CF _Three , R ¹ -Te1-Cy-Ph2-CF _Three , R ¹ -Te1-Cy-Ph3-CF _Three , R ¹ -Te1-Cy-Np1-CF _Three , R ¹ -Te1-Cy-Np2-CF _Three , R ¹ -Te1-Cy-Np3-CF _Three , R ¹ -Te1-Cy-Np4-CF _Three , R ¹ -Te2-Cy-Ph1-CF _Three , R ¹ -Te2-Cy-Ph2-CF _Three , R ¹ -Te2-Cy-Ph3-CF _Three , R ¹ -Te2-Cy-Np1-CF _Three , R ¹ -Te2-Cy-Np2-CF _Three , R ¹ -Te2-Cy-Np3-CF _Three , R ¹ -Te2-Cy-Np4-CF _Three , R ¹ -Te1-Cy-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Cy-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Cy-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Cy-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Cy-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Cy-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Cy-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Cy-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Cy-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Cy-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Cy-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Cy-CH ₂ CH ₂ -Np4-CF _Three ,
[0168]
R ¹ -Te1-Ph1-Ph1-CF _Three , R ¹ -Te1-Ph1-Ph2-CF _Three , R ¹ -Te1-Ph1-Ph3-CF _Three , R ¹ -Te1-Ph1-Np1-CF _Three , R ¹ -Te1-Ph1-Np2-CF _Three , R ¹ -Te1-Ph1-Np3-CF _Three , R ¹ -Te1-Ph1-Np4-CF _Three , R ¹ -Te2-Ph1-Ph1-CF _Three , R ¹ -Te2-Ph1-Ph2-CF _Three , R ¹ -Te2-Ph1-Ph3-CF _Three , R ¹ -Te2-Ph1-Np1-CF _Three , R ¹ -Te2-Ph1-Np2-CF _Three , R ¹ -Te2-Ph1-Np3-CF _Three , R ¹ -Te2-Ph1-Np4-CF _Three , R ¹ -Te1-Ph1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Ph1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Ph1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Ph1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Ph1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-Ph1-C≡C-Ph2-CF _Three , R ¹ -Te1-Ph1-C≡C-Ph3-CF _Three , R ¹ -Te1-Ph1-C≡C-Np1-CF _Three , R ¹ -Te1-Ph1-C≡C-Np2-CF _Three , R ¹ -Te1-Ph1-C≡C-Np3-CF _Three , R ¹ -Te1-Ph1-C≡C-Np4-CF _Three , R ¹ -Te2-Ph1-C≡C-Ph1-CF _Three , R ¹ -Te2-Ph1-C≡C-Ph2-CF _Three , R ¹ -Te2-Ph1-C≡C-Ph3-CF _Three , R ¹ -Te2-Ph1-C≡C-Np1-CF _Three , R ¹ -Te2-Ph1-C≡C-Np2-CF _Three , R ¹ -Te2-Ph1-C≡C-Np3-CF _Three , R ¹ -Te2-Ph1-C≡C-Np4-CF _Three ,
[0169]
R ¹ -Te1-Ph2-Ph1-CF _Three , R ¹ -Te1-Ph2-Ph2-CF _Three , R ¹ -Te1-Ph2-Ph3-CF _Three , R ¹ -Te1-Ph2-Np1-CF _Three , R ¹ -Te1-Ph2-Np2-CF _Three , R ¹ -Te1-Ph2-Np3-CF _Three , R ¹ -Te1-Ph2-Np4-CF _Three , R ¹ -Te2-Ph2-Ph1-CF _Three , R ¹ -Te2-Ph2-Ph2-CF _Three , R ¹ -Te2-Ph2-Ph3-CF _Three , R ¹ -Te2-Ph2-Np1-CF _Three , R ¹ -Te2-Ph2-Np2-CF _Three , R ¹ -Te2-Ph2-Np3-CF _Three , R ¹ -Te2-Ph2-Np4-CF _Three , R ¹ -Te1-Ph2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Ph2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Ph2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Ph2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Ph2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-Ph2-C≡C-Ph2-CF _Three , R ¹ -Te1-Ph2-C≡C-Ph3-CF _Three , R ¹ -Te1-Ph2-C≡C-Np1-CF _Three , R ¹ -Te1-Ph2-C≡C-Np2-CF _Three , R ¹ -Te1-Ph2-C≡C-Np3-CF _Three , R ¹ -Te1-Ph2-C≡C-Np4-CF _Three , R ¹ -Te2-Ph2-C≡C-Ph1-CF _Three , R ¹ -Te2-Ph2-C≡C-Ph2-CF _Three , R ¹ -Te2-Ph2-C≡C-Ph3-CF _Three , R ¹ -Te2-Ph2-C≡C-Np1-CF _Three , R ¹ -Te2-Ph2-C≡C-Np2-CF _Three , R ¹ -Te2-Ph2-C≡C-Np3-CF _Three , R ¹ -Te2-Ph2-C≡C-Np4-CF _Three ,
[0170]
R ¹ -Te1-Ph3-Ph1-CF _Three , R ¹ -Te1-Ph3-Ph2-CF _Three , R ¹ -Te1-Ph3-Ph3-CF _Three , R ¹ -Te1-Ph3-Np1-CF _Three , R ¹ -Te1-Ph3-Np2-CF _Three , R ¹ -Te1-Ph3-Np3-CF _Three , R ¹ -Te1-Ph3-Np4-CF _Three , R ¹ -Te2-Ph3-Ph1-CF _Three , R ¹ -Te2-Ph3-Ph2-CF _Three , R ¹ -Te2-Ph3-Ph3-CF _Three , R ¹ -Te2-Ph3-Np1-CF _Three , R ¹ -Te2-Ph3-Np2-CF _Three , R ¹ -Te2-Ph3-Np3-CF _Three , R ¹ -Te2-Ph3-Np4-CF _Three , R ¹ -Te1-Ph3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Ph3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Ph3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Ph3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Ph3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-Ph3-C≡C-Ph2-CF _Three , R ¹ -Te1-Ph3-C≡C-Ph3-CF _Three , R ¹ -Te1-Ph3-C≡C-Np1-CF _Three , R ¹ -Te1-Ph3-C≡C-Np2-CF _Three , R ¹ -Te1-Ph3-C≡C-Np3-CF _Three , R ¹ -Te1-Ph3-C≡C-Np4-CF _Three , R ¹ -Te2-Ph3-C≡C-Ph1-CF _Three , R ¹ -Te2-Ph3-C≡C-Ph2-CF _Three , R ¹ -Te2-Ph3-C≡C-Ph3-CF _Three , R ¹ -Te2-Ph3-C≡C-Np1-CF _Three , R ¹ -Te2-Ph3-C≡C-Np2-CF _Three , R ¹ -Te2-Ph3-C≡C-Np3-CF _Three , R ¹ -Te2-Ph3-C≡C-Np4-CF _Three ,
[0171]
R ¹ -Te1-Np1-Ph1-CF _Three , R ¹ -Te1-Np1-Ph2-CF _Three , R ¹ -Te1-Np1-Ph3-CF _Three , R ¹ -Te1-Np1-Np1-CF _Three , R ¹ -Te1-Np1-Np2-CF _Three , R ¹ -Te1-Np1-Np3-CF _Three , R ¹ -Te1-Np1-Np4-CF _Three , R ¹ -Te2-Np1-Ph1-CF _Three , R ¹ -Te2-Np1-Ph2-CF _Three , R ¹ -Te2-Np1-Ph3-CF _Three , R ¹ -Te2-Np1-Np1-CF _Three , R ¹ -Te2-Np1-Np2-CF _Three , R ¹ -Te2-Np1-Np3-CF _Three , R ¹ -Te2-Np1-Np4-CF _Three , R ¹ -Te1-Np1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Np1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Np1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Np1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Np1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Np1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Np1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Np1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Np1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Np1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Np1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-Np1-C≡C-Ph2-CF _Three , R ¹ -Te1-Np1-C≡C-Ph3-CF _Three , R ¹ -Te1-Np1-C≡C-Np1-CF _Three , R ¹ -Te1-Np1-C≡C-Np2-CF _Three , R ¹ -Te1-Np1-C≡C-Np3-CF _Three , R ¹ -Te1-Np1-C≡C-Np4-CF _Three , R ¹ -Te2-Np1-C≡C-Ph1-CF _Three , R ¹ -Te2-Np1-C≡C-Ph2-CF _Three , R ¹ -Te2-Np1-C≡C-Ph3-CF _Three , R ¹ -Te2-Np1-C≡C-Np1-CF _Three , R ¹ -Te2-Np1-C≡C-Np2-CF _Three , R ¹ -Te2-Np1-C≡C-Np3-CF _Three , R ¹ -Te2-Np1-C≡C-Np4-CF _Three ,
[0172]
R ¹ -Te1-Np2-Ph1-CF _Three , R ¹ -Te1-Np2-Ph2-CF _Three , R ¹ -Te1-Np2-Ph3-CF _Three , R ¹ -Te1-Np2-Np1-CF _Three , R ¹ -Te1-Np2-Np2-CF _Three , R ¹ -Te1-Np2-Np3-CF _Three , R ¹ -Te1-Np2-Np4-CF _Three , R ¹ -Te2-Np2-Ph1-CF _Three , R ¹ -Te2-Np2-Ph2-CF _Three , R ¹ -Te2-Np2-Ph3-CF _Three , R ¹ -Te2-Np2-Np1-CF _Three , R ¹ -Te2-Np2-Np2-CF _Three , R ¹ -Te2-Np2-Np3-CF _Three , R ¹ -Te2-Np2-Np4-CF _Three , R ¹ -Te1-Np2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Np2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Np2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Np2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Np2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Np2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Np2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Np2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Np2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Np2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Np2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-Np2-C≡C-Ph2-CF _Three , R ¹ -Te1-Np2-C≡C-Ph3-CF _Three , R ¹ -Te1-Np2-C≡C-Np1-CF _Three , R ¹ -Te1-Np2-C≡C-Np2-CF _Three , R ¹ -Te1-Np2-C≡C-Np3-CF _Three , R ¹ -Te1-Np2-C≡C-Np4-CF _Three , R ¹ -Te2-Np2-C≡C-Ph1-CF _Three , R ¹ -Te2-Np2-C≡C-Ph2-CF _Three , R ¹ -Te2-Np2-C≡C-Ph3-CF _Three , R ¹ -Te2-Np2-C≡C-Np1-CF _Three , R ¹ -Te2-Np2-C≡C-Np2-CF _Three , R ¹ -Te2-Np2-C≡C-Np3-CF _Three , R ¹ -Te2-Np2-C≡C-Np4-CF _Three ,
[0173]
R ¹ -Te1-Np3-Ph1-CF _Three , R ¹ -Te1-Np3-Ph2-CF _Three , R ¹ -Te1-Np3-Ph3-CF _Three , R ¹ -Te1-Np3-Np1-CF _Three , R ¹ -Te1-Np3-Np2-CF _Three , R ¹ -Te1-Np3-Np3-CF _Three , R ¹ -Te1-Np3-Np4-CF _Three , R ¹ -Te2-Np3-Ph1-CF _Three , R ¹ -Te2-Np3-Ph2-CF _Three , R ¹ -Te2-Np3-Ph3-CF _Three , R ¹ -Te2-Np3-Np1-CF _Three , R ¹ -Te2-Np3-Np2-CF _Three , R ¹ -Te2-Np3-Np3-CF _Three , R ¹ -Te2-Np3-Np4-CF _Three , R ¹ -Te1-Np3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Np3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Np3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Np3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Np3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Np3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Np3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Np3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Np3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Np3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Np3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-Np3-C≡C-Ph2-CF _Three , R ¹ -Te1-Np3-C≡C-Ph3-CF _Three , R ¹ -Te1-Np3-C≡C-Np1-CF _Three , R ¹ -Te1-Np3-C≡C-Np2-CF _Three , R ¹ -Te1-Np3-C≡C-Np3-CF _Three , R ¹ -Te1-Np3-C≡C-Np4-CF _Three , R ¹ -Te2-Np3-C≡C-Ph1-CF _Three , R ¹ -Te2-Np3-C≡C-Ph2-CF _Three , R ¹ -Te2-Np3-C≡C-Ph3-CF _Three , R ¹ -Te2-Np3-C≡C-Np1-CF _Three , R ¹ -Te2-Np3-C≡C-Np2-CF _Three , R ¹ -Te2-Np3-C≡C-Np3-CF _Three , R ¹ -Te2-Np3-C≡C-Np4-CF _Three ,
[0174]
R ¹ -Te1-Np4-Ph1-CF _Three , R ¹ -Te1-Np4-Ph2-CF _Three , R ¹ -Te1-Np4-Ph3-CF _Three , R ¹ -Te1-Np4-Np1-CF _Three , R ¹ -Te1-Np4-Np2-CF _Three , R ¹ -Te1-Np4-Np3-CF _Three , R ¹ -Te1-Np4-Np4-CF _Three , R ¹ -Te2-Np4-Ph1-CF _Three , R ¹ -Te2-Np4-Ph2-CF _Three , R ¹ -Te2-Np4-Ph3-CF _Three , R ¹ -Te2-Np4-Np1-CF _Three , R ¹ -Te2-Np4-Np2-CF _Three , R ¹ -Te2-Np4-Np3-CF _Three , R ¹ -Te2-Np4-Np4-CF _Three , R ¹ -Te1-Np4-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-Np4-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-Np4-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-Np4-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-Np4-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-Np4-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-Np4-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-Np4-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-Np4-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-Np4-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-Np4-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-Np4-C≡C-Ph2-CF _Three , R ¹ -Te1-Np4-C≡C-Ph3-CF _Three , R ¹ -Te1-Np4-C≡C-Np1-CF _Three , R ¹ -Te1-Np4-C≡C-Np2-CF _Three , R ¹ -Te1-Np4-C≡C-Np3-CF _Three , R ¹ -Te1-Np4-C≡C-Np4-CF _Three , R ¹ -Te2-Np4-C≡C-Ph1-CF _Three , R ¹ -Te2-Np4-C≡C-Ph2-CF _Three , R ¹ -Te2-Np4-C≡C-Ph3-CF _Three , R ¹ -Te2-Np4-C≡C-Np1-CF _Three , R ¹ -Te2-Np4-C≡C-Np2-CF _Three , R ¹ -Te2-Np4-C≡C-Np3-CF _Three , R ¹ -Te2-Np4-C≡C-Np4-CF _Three ,
[0175]
R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph1-C≡C-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph1-C≡C-Np4-CF _Three ,
[0176]
R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph2-C≡C-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph2-C≡C-Np4-CF _Three ,
[0177]
R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Ph3-C≡C-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Ph3-C≡C-Np4-CF _Three ,
[0178]
R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np1-C≡C-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np1-C≡C-Np4-CF _Three ,
[0179]
R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np2-C≡C-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np2-C≡C-Np4-CF _Three ,
[0180]
R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np3-C≡C-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np3-C≡C-Np4-CF _Three ,
[0181]
R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Ph2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Ph3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np1-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np2-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np3-CF _Three , R ¹ -Te1-CH ₂ CH ₂ -Np4-C≡C-Np4-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Ph3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np1-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np2-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np3-CF _Three , R ¹ -Te2-CH ₂ CH ₂ -Np4-C≡C-Np4-CF _Three ,
[0182]
R ¹ -Te1-C≡C-Ph1-Ph1-CF _Three , R ¹ -Te1-C≡C-Ph1-Ph2-CF _Three , R ¹ -Te1-C≡C-Ph1-Ph3-CF _Three , R ¹ -Te1-C≡C-Ph1-Np1-CF _Three , R ¹ -Te1-C≡C-Ph1-Np2-CF _Three , R ¹ -Te1-C≡C-Ph1-Np3-CF _Three , R ¹ -Te1-C≡C-Ph1-Np4-CF _Three , R ¹ -Te2-C≡C-Ph1-Ph1-CF _Three , R ¹ -Te2-C≡C-Ph1-Ph2-CF _Three , R ¹ -Te2-C≡C-Ph1-Ph3-CF _Three , R ¹ -Te2-C≡C-Ph1-Np1-CF _Three , R ¹ -Te2-C≡C-Ph1-Np2-CF _Three , R ¹ -Te2-C≡C-Ph1-Np3-CF _Three , R ¹ -Te2-C≡C-Ph1-Np4-CF _Three , R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-C≡C-Ph1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-C≡C-Ph1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-C≡C-Ph1-C≡C-Ph2-CF _Three , R ¹ -Te1-C≡C-Ph1-C≡C-Ph3-CF _Three , R ¹ -Te1-C≡C-Ph1-C≡C-Np1-CF _Three , R ¹ -Te1-C≡C-Ph1-C≡C-Np2-CF _Three , R ¹ -Te1-C≡C-Ph1-C≡C-Np3-CF _Three , R ¹ -Te1-C≡C-Ph1-C≡C-Np4-CF _Three , R ¹ -Te2-C≡C-Ph1-C≡C-Ph1-CF _Three , R ¹ -Te2-C≡C-Ph1-C≡C-Ph2-CF _Three , R ¹ -Te2-C≡C-Ph1-C≡C-Ph3-CF _Three , R ¹ -Te2-C≡C-Ph1-C≡C-Np1-CF _Three , R ¹ -Te2-C≡C-Ph1-C≡C-Np2-CF _Three , R ¹ -Te2-C≡C-Ph1-C≡C-Np3-CF _Three , R ¹ -Te2-C≡C-Ph1-C≡C-Np4-CF _Three ,
[0183]
R ¹ -Te1-C≡C-Ph2-Ph1-CF _Three , R ¹ -Te1-C≡C-Ph2-Ph2-CF _Three , R ¹ -Te1-C≡C-Ph2-Ph3-CF _Three , R ¹ -Te1-C≡C-Ph2-Np1-CF _Three , R ¹ -Te1-C≡C-Ph2-Np2-CF _Three , R ¹ -Te1-C≡C-Ph2-Np3-CF _Three , R ¹ -Te1-C≡C-Ph2-Np4-CF _Three , R ¹ -Te2-C≡C-Ph2-Ph1-CF _Three , R ¹ -Te2-C≡C-Ph2-Ph2-CF _Three , R ¹ -Te2-C≡C-Ph2-Ph3-CF _Three , R ¹ -Te2-C≡C-Ph2-Np1-CF _Three , R ¹ -Te2-C≡C-Ph2-Np2-CF _Three , R ¹ -Te2-C≡C-Ph2-Np3-CF _Three , R ¹ -Te2-C≡C-Ph2-Np4-CF _Three , R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-C≡C-Ph2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-C≡C-Ph2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-C≡C-Ph2-C≡C-Ph2-CF _Three , R ¹ -Te1-C≡C-Ph2-C≡C-Ph3-CF _Three , R ¹ -Te1-C≡C-Ph2-C≡C-Np1-CF _Three , R ¹ -Te1-C≡C-Ph2-C≡C-Np2-CF _Three , R ¹ -Te1-C≡C-Ph2-C≡C-Np3-CF _Three , R ¹ -Te1-C≡C-Ph2-C≡C-Np4-CF _Three , R ¹ -Te2-C≡C-Ph2-C≡C-Ph1-CF _Three , R ¹ -Te2-C≡C-Ph2-C≡C-Ph2-CF _Three , R ¹ -Te2-C≡C-Ph2-C≡C-Ph3-CF _Three , R ¹ -Te2-C≡C-Ph2-C≡C-Np1-CF _Three , R ¹ -Te2-C≡C-Ph2-C≡C-Np2-CF _Three , R ¹ -Te2-C≡C-Ph2-C≡C-Np3-CF _Three , R ¹ -Te2-C≡C-Ph2-C≡C-Np4-CF _Three ,
[0184]
R ¹ -Te1-C≡C-Ph3-Ph1-CF _Three , R ¹ -Te1-C≡C-Ph3-Ph2-CF _Three , R ¹ -Te1-C≡C-Ph3-Ph3-CF _Three , R ¹ -Te1-C≡C-Ph3-Np1-CF _Three , R ¹ -Te1-C≡C-Ph3-Np2-CF _Three , R ¹ -Te1-C≡C-Ph3-Np3-CF _Three , R ¹ -Te1-C≡C-Ph3-Np4-CF _Three , R ¹ -Te2-C≡C-Ph3-Ph1-CF _Three , R ¹ -Te2-C≡C-Ph3-Ph2-CF _Three , R ¹ -Te2-C≡C-Ph3-Ph3-CF _Three , R ¹ -Te2-C≡C-Ph3-Np1-CF _Three , R ¹ -Te2-C≡C-Ph3-Np2-CF _Three , R ¹ -Te2-C≡C-Ph3-Np3-CF _Three , R ¹ -Te2-C≡C-Ph3-Np4-CF _Three , R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-C≡C-Ph3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-C≡C-Ph3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-C≡C-Ph3-C≡C-Ph2-CF _Three , R ¹ -Te1-C≡C-Ph3-C≡C-Ph3-CF _Three , R ¹ -Te1-C≡C-Ph3-C≡C-Np1-CF _Three , R ¹ -Te1-C≡C-Ph3-C≡C-Np2-CF _Three , R ¹ -Te1-C≡C-Ph3-C≡C-Np3-CF _Three , R ¹ -Te1-C≡C-Ph3-C≡C-Np4-CF _Three , R ¹ -Te2-C≡C-Ph3-C≡C-Ph1-CF _Three , R ¹ -Te2-C≡C-Ph3-C≡C-Ph2-CF _Three , R ¹ -Te2-C≡C-Ph3-C≡C-Ph3-CF _Three , R ¹ -Te2-C≡C-Ph3-C≡C-Np1-CF _Three , R ¹ -Te2-C≡C-Ph3-C≡C-Np2-CF _Three , R ¹ -Te2-C≡C-Ph3-C≡C-Np3-CF _Three , R ¹ -Te2-C≡C-Ph3-C≡C-Np4-CF _Three ,
[0185]
R ¹ -Te1-C≡C-Np1-Ph1-CF _Three , R ¹ -Te1-C≡C-Np1-Ph2-CF _Three , R ¹ -Te1-C≡C-Np1-Ph3-CF _Three , R ¹ -Te1-C≡C-Np1-Np1-CF _Three , R ¹ -Te1-C≡C-Np1-Np2-CF _Three , R ¹ -Te1-C≡C-Np1-Np3-CF _Three , R ¹ -Te1-C≡C-Np1-Np4-CF _Three , R ¹ -Te2-C≡C-Np1-Ph1-CF _Three , R ¹ -Te2-C≡C-Np1-Ph2-CF _Three , R ¹ -Te2-C≡C-Np1-Ph3-CF _Three , R ¹ -Te2-C≡C-Np1-Np1-CF _Three , R ¹ -Te2-C≡C-Np1-Np2-CF _Three , R ¹ -Te2-C≡C-Np1-Np3-CF _Three , R ¹ -Te2-C≡C-Np1-Np4-CF _Three , R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-C≡C-Np1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-C≡C-Np1-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-C≡C-Np1-C≡C-Ph2-CF _Three , R ¹ -Te1-C≡C-Np1-C≡C-Ph3-CF _Three , R ¹ -Te1-C≡C-Np1-C≡C-Np1-CF _Three , R ¹ -Te1-C≡C-Np1-C≡C-Np2-CF _Three , R ¹ -Te1-C≡C-Np1-C≡C-Np3-CF _Three , R ¹ -Te1-C≡C-Np1-C≡C-Np4-CF _Three , R ¹ -Te2-C≡C-Np1-C≡C-Ph1-CF _Three , R ¹ -Te2-C≡C-Np1-C≡C-Ph2-CF _Three , R ¹ -Te2-C≡C-Np1-C≡C-Ph3-CF _Three , R ¹ -Te2-C≡C-Np1-C≡C-Np1-CF _Three , R ¹ -Te2-C≡C-Np1-C≡C-Np2-CF _Three , R ¹ -Te2-C≡C-Np1-C≡C-Np3-CF _Three , R ¹ -Te2-C≡C-Np1-C≡C-Np4-CF _Three ,
[0186]
R ¹ -Te1-C≡C-Np2-Ph1-CF _Three , R ¹ -Te1-C≡C-Np2-Ph2-CF _Three , R ¹ -Te1-C≡C-Np2-Ph3-CF _Three , R ¹ -Te1-C≡C-Np2-Np1-CF _Three , R ¹ -Te1-C≡C-Np2-Np2-CF _Three , R ¹ -Te1-C≡C-Np2-Np3-CF _Three , R ¹ -Te1-C≡C-Np2-Np4-CF _Three , R ¹ -Te2-C≡C-Np2-Ph1-CF _Three , R ¹ -Te2-C≡C-Np2-Ph2-CF _Three , R ¹ -Te2-C≡C-Np2-Ph3-CF _Three , R ¹ -Te2-C≡C-Np2-Np1-CF _Three , R ¹ -Te2-C≡C-Np2-Np2-CF _Three , R ¹ -Te2-C≡C-Np2-Np3-CF _Three , R ¹ -Te2-C≡C-Np2-Np4-CF _Three , R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-C≡C-Np2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-C≡C-Np2-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-C≡C-Np2-C≡C-Ph2-CF _Three , R ¹ -Te1-C≡C-Np2-C≡C-Ph3-CF _Three , R ¹ -Te1-C≡C-Np2-C≡C-Np1-CF _Three , R ¹ -Te1-C≡C-Np2-C≡C-Np2-CF _Three , R ¹ -Te1-C≡C-Np2-C≡C-Np3-CF _Three , R ¹ -Te1-C≡C-Np2-C≡C-Np4-CF _Three , R ¹ -Te2-C≡C-Np2-C≡C-Ph1-CF _Three , R ¹ -Te2-C≡C-Np2-C≡C-Ph2-CF _Three , R ¹ -Te2-C≡C-Np2-C≡C-Ph3-CF _Three , R ¹ -Te2-C≡C-Np2-C≡C-Np1-CF _Three , R ¹ -Te2-C≡C-Np2-C≡C-Np2-CF _Three , R ¹ -Te2-C≡C-Np2-C≡C-Np3-CF _Three , R ¹ -Te2-C≡C-Np2-C≡C-Np4-CF _Three ,
[0187]
R ¹ -Te1-C≡C-Np3-Ph1-CF _Three , R ¹ -Te1-C≡C-Np3-Ph2-CF _Three , R ¹ -Te1-C≡C-Np3-Ph3-CF _Three , R ¹ -Te1-C≡C-Np3-Np1-CF _Three , R ¹ -Te1-C≡C-Np3-Np2-CF _Three , R ¹ -Te1-C≡C-Np3-Np3-CF _Three , R ¹ -Te1-C≡C-Np3-Np4-CF _Three , R ¹ -Te2-C≡C-Np3-Ph1-CF _Three , R ¹ -Te2-C≡C-Np3-Ph2-CF _Three , R ¹ -Te2-C≡C-Np3-Ph3-CF _Three , R ¹ -Te2-C≡C-Np3-Np1-CF _Three , R ¹ -Te2-C≡C-Np3-Np2-CF _Three , R ¹ -Te2-C≡C-Np3-Np3-CF _Three , R ¹ -Te2-C≡C-Np3-Np4-CF _Three , R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-C≡C-Np3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-C≡C-Np3-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-C≡C-Np3-C≡C-Ph2-CF _Three , R ¹ -Te1-C≡C-Np3-C≡C-Ph3-CF _Three , R ¹ -Te1-C≡C-Np3-C≡C-Np1-CF _Three , R ¹ -Te1-C≡C-Np3-C≡C-Np2-CF _Three , R ¹ -Te1-C≡C-Np3-C≡C-Np3-CF _Three , R ¹ -Te1-C≡C-Np3-C≡C-Np4-CF _Three , R ¹ -Te2-C≡C-Np3-C≡C-Ph1-CF _Three , R ¹ -Te2-C≡C-Np3-C≡C-Ph2-CF _Three , R ¹ -Te2-C≡C-Np3-C≡C-Ph3-CF _Three , R ¹ -Te2-C≡C-Np3-C≡C-Np1-CF _Three , R ¹ -Te2-C≡C-Np3-C≡C-Np2-CF _Three , R ¹ -Te2-C≡C-Np3-C≡C-Np3-CF _Three , R ¹ -Te2-C≡C-Np3-C≡C-Np4-CF _Three ,
[0188]
R ¹ -Te1-C≡C-Np4-Ph1-CF _Three , R ¹ -Te1-C≡C-Np4-Ph2-CF _Three , R ¹ -Te1-C≡C-Np4-Ph3-CF _Three , R ¹ -Te1-C≡C-Np4-Np1-CF _Three , R ¹ -Te1-C≡C-Np4-Np2-CF _Three , R ¹ -Te1-C≡C-Np4-Np3-CF _Three , R ¹ -Te1-C≡C-Np4-Np4-CF _Three , R ¹ -Te2-C≡C-Np4-Ph1-CF _Three , R ¹ -Te2-C≡C-Np4-Ph2-CF _Three , R ¹ -Te2-C≡C-Np4-Ph3-CF _Three , R ¹ -Te2-C≡C-Np4-Np1-CF _Three , R ¹ -Te2-C≡C-Np4-Np2-CF _Three , R ¹ -Te2-C≡C-Np4-Np3-CF _Three , R ¹ -Te2-C≡C-Np4-Np4-CF _Three , R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te1-C≡C-Np4-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph1-CF _Three , R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph2-CF _Three , R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Ph3-CF _Three , R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np1-CF _Three , R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np2-CF _Three , R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np3-CF _Three , R ¹ -Te2-C≡C-Np4-CH ₂ CH ₂ -Np4-CF _Three , R ¹ -Te1-C≡C-Np4-C≡C-Ph2-CF _Three , R ¹ -Te1-C≡C-Np4-C≡C-Ph3-CF _Three , R ¹ -Te1-C≡C-Np4-C≡C-Np1-CF _Three , R ¹ -Te1-C≡C-Np4-C≡C-Np2-CF _Three , R ¹ -Te1-C≡C-Np4-C≡C-Np3-CF _Three , R ¹ -Te1-C≡C-Np4-C≡C-Np4-CF _Three , R ¹ -Te2-C≡C-Np4-C≡C-Ph1-CF _Three , R ¹ -Te2-C≡C-Np4-C≡C-Ph2-CF _Three , R ¹ -Te2-C≡C-Np4-C≡C-Ph3-CF _Three , R ¹ -Te2-C≡C-Np4-C≡C-Np1-CF _Three , R ¹ -Te2-C≡C-Np4-C≡C-Np2-CF _Three , R ¹ -Te2-C≡C-Np4-C≡C-Np3-CF _Three , R ¹ -Te2-C≡C-Np4-C≡C-Np4-CF _Three ,
[0189]
The compounds of general formula (I) are m, n, R, V, W, X, Y, Z, Q ¹ , Q ² , Q ^Three Depending on the selection of ring A, ring B and ring C, they can be produced by various synthetic methods, and typical examples are listed below.
[0190]
For example, m = n = 0, Y is a single bond, R is substituted with a fluorine atom having 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms, and may contain a branched chain When 1 to 20 alkyl groups and Z is a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group or a hydrogen atom, they can be produced according to the following formula.
[0191]
[Chemical Formula 10]

[0192]
(Where V, Q ¹ , Q ² , Q ^Three And ring C have the same meaning as in general formula (I), and R ² Represents a saturated alkyl group having 1 to 20 carbon atoms which may be substituted with 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms and may contain a branched chain; ¹ Represents a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group or a hydrogen atom, and Mtl ¹ Represents a metal ion such as Li, BrMg, or IMg. )
That is, the aryllithium or magnesium reactant represented by the general formula (III-a) is added to the ketone represented by the general formula (II-a) in the presence of a metal salt such as cerium chloride or manganese chloride or a Lewis acid. Alternatively, the alcohol represented by the general formula (IV-a) is obtained by reacting in the absence of coexistence, and then heated in the presence of an acid catalyst such as p-toluenesulfonic acid to represent the general formula (Va). Dihydronaphthalene compound, which is converted into Pd-C, Rh-C, Pt-C, Pd (OH) ₂ The target compound represented by the general formula (Ia) can be obtained by hydrogenation in the presence of a metal catalyst such as
[0193]
The aryllithium or magnesium reactant represented by the general formula (III-a) used here is often used in the production of liquid crystals and can be easily prepared from a corresponding halide or the like.
[0194]
The compound represented by the general formula (II-a) can be produced by several methods. As a typical method, as shown in the following formula, phenylacetic acid represented by the general formula (VI-a) There is a method in which a derivative is converted into an acid chloride and then reacted with ethylene in the presence of aluminum chloride.
[0195]
Embedded image

[0196]
(Where R ² , V, Q ¹ , Q ² And Q ^Three Is the same as above. )
Q ¹ , Q ² , And Q ^Three Are all hydrogen, the compound represented by the general formula (II-a ′) is a naphthol derivative represented by the general formula (VII-a) such as palladium, rhodium, platinum, ruthenium, etc. It can be synthesized by hydrogenating in the presence of a transition metal catalyst and further oxidizing if necessary.
[0197]
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[0198]
(Where R ² And V are the same as above. )
In addition, as shown in the following formula, octahydronaphthalenedione monoacetal which can be synthesized by reacting 1,4-cyclohexadione monoacetal with an amine such as pyrrolidine and further reacting with methyl vinyl ketone, R ² -Mtl ¹ In addition, octahydronaphthalenone acetal is obtained by a dehydration reaction. Using a metal catalyst such as palladium, rhodium, ruthenium or platinum as a dehydrogenation catalyst, or allowing an oxidizing agent such as 2,3-dichloro-5,6-dicyano-1,4-benzoquinone to act on this, or After aromatizing with sulfur, bromine, iodine or the like, the compound represented by the general formula (II-a ″) can be synthesized by converting the acetal into a ketone.
[0199]
Embedded image

[0200]
(Where R ² Is the same as above. )
m = n = 0, Y is -CH ₂ CH ₂ -, R is a saturated alkyl group having 1 to 20 carbon atoms which may be substituted by 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms and may contain a branched chain, and Z is fluorine When it is an atom, chlorine atom, trifluoromethyl group, trifluoromethoxy group, difluoromethoxy group or hydrogen atom, it can be produced according to the following formula.
[0201]
Embedded image

[0202]
(Where V, Q ¹ , Q ² , Q ^Three And ring C have the same meaning as in general formula (I), and R ² Represents a saturated alkyl group having 1 to 20 carbon atoms which may be substituted with 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms and may contain a branched chain; ¹ Represents a fluorine atom, a chlorine atom, a trifluoromethyl group, a trifluoromethoxy group, a difluoromethoxy group or a hydrogen atom, and Mtl ¹ Represents a metal ion such as Li, BrMg, or IMg. )
That is, the aryllithium or magnesium reactant represented by the general formula (III-b) is added to the ketone represented by the general formula (II-a) in the presence of a metal salt such as cerium chloride or manganese chloride or a Lewis acid. Alternatively, the alcohol represented by the general formula (IV-b) is obtained by reacting in the absence of coexistence, and then heated in the presence of an acid catalyst such as p-toluenesulfonic acid to represent the general formula (Vb). Dihydronaphthalene compound, which is converted into Pd-C, Rh-C, Pt-C, Pd (OH) ₂ The target compound represented by the general formula (Ib) can be obtained by hydrogenation in the presence of a metal catalyst such as
[0203]
The ethynyllithium or magnesium reactant represented by the general formula (III-b) used here is often used in the production of liquid crystals, and can be easily obtained by allowing alkyllithium or alkylmagnesium halide to act on the corresponding acetylene compound. Can be prepared.
[0204]
Further, when (III-c) and (III-d) are used instead of (III-a) and (III-b) in the above formulas, the compounds represented by the general formulas (Ic) and (Id) are produced. can do.
[0205]
Embedded image

[0206]
(Where V, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), R ² , Z ¹ And Mtl ¹ Means the same as above, Y ¹ Is a single bond or -CH ₂ CH ₂ -Represents. In addition to this, as shown in the following formula, the compound represented by the general formula (II-a) is reacted with an ylide compound represented by the general formula (VIII-a), etc. A compound represented by the general formula (Ib) can be produced by hydrogenating IX-a).
[0207]
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[0208]
(Where V, Z, Q ¹ , Q ² , Q ^Three And ring C have the same meaning as in general formula (I), and R ² And Y ¹ Represents the same meaning as above. )
Similarly, the compound represented by the general formula (Id) can be produced by using (VIII-b) instead of (VIII-a).
[0209]
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[0210]
(Where V, Z, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), R ² And Y ¹ Represents the same meaning as above. )
Further, as shown in the following formula, the tetrahydronaphthalenone represented by (II-a) is reacted with an ylide compound represented by (VIII-c) and treated with an acid to give a general formula (Xa) The aldehyde represented can be obtained. By reacting this with an ylide compound represented by (VIII-d) and hydrogenating the resulting olefin (XI-a), a compound represented by the general formula (Ib) can be produced.
[0211]
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[0212]
(Where V, Z, Q ¹ , Q ² , Q ^Three And ring C have the same meaning as in general formula (I), and R ² And Y ¹ Represents the same meaning as above. )
Similarly, the compound represented by the general formula (Id) can be produced by using (VIII-e) instead of (VIII-d).
[0213]
Embedded image

[0214]
(Where V, Z, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), R ² , Y ¹ Represents the same meaning as above. )
In the above method, when (II-b) is used instead of (II-a), a compound represented by the general formula (XII-a) can be produced.
[0215]
Embedded image

[0216]
(Where n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), R ² , Z ¹ , Y ¹ Means the same as above, X ¹ Is a single bond or -CH ₂ CH ₂ -Represents. )
By substituting bromine of this compound (XII-a), many of the compounds of the general formula (I) can be produced.
For example, an acetylene compound represented by (XIII-a) is converted to PdCl ₂ (PPh _Three ) ₂ Or Pd (PPh _Three ) _Four Is reacted with (XII-a) in the presence of an amine such as triethylamine, a compound represented by the general formula (Ie) can be obtained. Further, hydrogenation was performed in the presence of a metal catalyst, and the acetylenediyl group (-C≡C-) was converted to an ethylene group (-CH ₂ CH ₂ It can also be converted to-).
[0217]
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[0218]
(Where n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), and Z ¹ , Y ¹ And X ¹ Means the same as above, R ² R represents a saturated or unsaturated alkyl group having 1 to 18 carbon atoms which may be substituted with 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms and may contain a branched chain. )
Furthermore, a compound represented by the general formula (If) can be obtained by replacing (XIII-a) with (XIII-b). Further, this was hydrogenated in the presence of a metal catalyst, and the acetylenediyl group (-C≡C-) was converted to an ethylene group (-CH ₂ CH ₂ It can also be converted to-).
[0219]
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[0220]
(Where R, V, n, Q ¹ , Q ² , Q ^Three , Ring A, ring B and ring C have the same meaning as in general formula (I), and Z ¹ , Y ¹ And X ¹ Represents the same meaning as above. )
R-Mtl in the presence of nickel or palladium catalyst ¹ The compound represented by the general formula (Ig) can be produced by reacting (XII-a) with an organolithium or organomagnesium reactant represented by
[0221]
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[0222]
(Where R, n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), and Z ¹ , Y ¹ , X ¹ And Mtl ¹ Represents the same meaning as above. )
In addition, by reacting an organolithium or organomagnesium reagent represented by (XIV-a) with (XII-a) in the presence of a nickel or palladium catalyst, or an organolithium represented by (XIV-a) A compound represented by the general formula (Ih) can be produced by converting an organomagnesium reactant into a boron, tin, or silicon compound and then reacting with (XII-a) in the presence of nickel or a palladium catalyst.
[0223]
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[0224]
(Where R, n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), and Z ¹ , Y ¹ , X ¹ And Mtl ¹ Means the same as above, V ¹ Represents a single bond or an oxygen atom, and ring A ¹ Represents a 1,4-phenylene group which may be substituted with one or two fluorine atoms or a naphthalene-2,6-diyl group which may be substituted with two fluorine atoms. In addition, (XII-a) is reacted with magnesium, lithium, alkyllithium, etc., converted to (XV-a), and then reacted with the halide represented by (XVI-a) in the presence of nickel or palladium catalyst. Or by converting (XIV-a) into a boron, tin, or silicon compound, and then reacting with a halide represented by (XVI-a) in the presence of a nickel or palladium catalyst. The compound represented by these can be manufactured.
[0225]
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[0226]
(Where R, V, n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), and Z ¹ , Y ¹ , X ¹ And Mtl ¹ Represents the same meaning as above, and ring A ² Is a 1,4-phenylene group, pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, pyrazine-2,5-diyl group, pyridazine- which may be substituted with one or two fluorine atoms A 3,6-diyl group and a naphthalene-2,6-diyl group which may be substituted with one or two fluorine atoms, Hal represents a chlorine atom, a bromine atom or an iodine atom. )
The compound represented by (XV-a) is reacted with a cyclohexane derivative represented by (XVII-a) to give an alcohol (XVII-a). This can be dehydrated by heating in the presence of an acid catalyst to obtain compound (XVIII-a). Furthermore, hydrogenation can be performed in the presence of a transition metal catalyst to obtain a compound represented by (Ij).
[0227]
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[0228]
(Where V, n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), R ² , Z ¹ , Y ¹ , X ¹ And Mtl ¹ Represents the same meaning as above. )
In the above method, when (II-c) is used instead of (II-a), a compound represented by the general formula (Ik) can be produced.
[0229]
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[0230]
(Where n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), R ² , Z ¹ , X ¹ , Y ¹ Represents the same meaning as above. )
When the compound represented by (Ik) is demethylated by the action of hydrobromic acid, boron tribromide, aluminum chloride or the like, (XIX-a)
[0231]
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[0232]
(Where n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), and Z ¹ , X ¹ , Y ¹ Represents the same meaning as above. ) Is obtained. This is represented by the general formulas (XX-a) and (XX-b)
[0233]
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[0234]
(Wherein R, V and ring A have the same meaning as in general formula (I)), or a reaction with a dehydrating condensing agent such as dicyclohexylcarbodiimide, or (XX-a) and ( XX-b) is converted to an acid halide using thionyl chloride and the like, and then reacted in the presence of an amine to give a general formula (Il) and (Im)
[0235]
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[0236]
(Where R, n, Q ¹ , Q ² , Q ^Three , Ring A, ring B and ring C have the same meaning as in general formula (I), and Z ¹ , X ¹ , Y ¹ Represents the same meaning as above. ) Can be obtained.
[0237]
(XIX-a) is converted to general formulas (XXI-a) and (XXI-b)
[0238]
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[0239]
(Wherein R, V and ring A represent the same meaning as in general formula (I), and R ^Three Is a saturated or unsaturated carbon which may be substituted by 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms, and may contain a branched chain, except when the 1,2-position is unsaturated The alkyl group of number 1-20 is represented. ) And a halide represented by general formulas (In) and (Io) by reacting in the presence of a base such as sodium hydride or sodium hydroxide.
[0240]
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[0241]
(Where R, n, Q ¹ , Q ² , Q ^Three , Ring A, ring B and ring C have the same meaning as in general formula (I), R ^Three , Z ¹ , X ¹ , Y ¹ Represents the same meaning as above. ) Can be obtained.
[0242]
Further, (XIX-a) is obtained by reacting trifluoromethanesulfonate chloride or anhydride with a base, and is represented by the general formula (XXII-a)
[0243]
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[0244]
(Where n, Q ¹ , Q ² , Q ^Three , Ring B and ring C have the same meaning as in general formula (I), and Z ¹ , X ¹ , Y ¹ Represents the same meaning as above. ) Is represented by (XIII-a), (XIII-b), R-Mtl ¹ When (XIV-a) and (XII-a) are reacted under the same conditions, (Ie), (If), (Ig) and (Ih) can be obtained.
[0245]
As shown in the following formula, an octahydronaphthalenone derivative, which can be synthesized by reacting a cyclohexanone derivative represented by the general formula (XXIII-a) with an amine such as pyrrolidine and further reacting with methyl vinyl ketone, R ² -Mtl ¹ In addition, an octahydronaphthalenone derivative is obtained by dehydration reaction. Using a metal catalyst such as palladium, rhodium, ruthenium or platinum as a dehydrogenation catalyst, or allowing an oxidizing agent such as 2,3-dichloro-5,6-dicyano-1,4-benzoquinone to act on this, or The compound represented by the general formula (Ip) can be synthesized by aromatization using sulfur, bromine, iodine or the like.
[0246]
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[0247]
Wherein n, X, Y, Z, ring B and ring C have the same meaning as in general formula (I), and R ² And Mtl ¹ Represents the same meaning as above. )
Here, the cyclohexanone derivative represented by the general formula (XXIII-a) is often used in the production of liquid crystals and is easily available.
[0248]
In addition, R ² -Mtl ¹ Instead of (XIV-a), (XIV-b) and (XIV-c)
[0249]
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[0250]
(Wherein R represents the same meaning as in general formula (I), and V ¹ , Ring A ¹ And Mtl ¹ Represents the same meaning as above. ), The general formula (Iq)
[0251]
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[0252]
Wherein R, n, X, Y, Z, ring B and ring C have the same meaning as in general formula (I) and V ¹ , R ² And ring A ¹ Means the same as above, W ¹ Is a single bond, -C≡C- or -CH ₂ CH ₂ -Represents. ) Can be manufactured.
[0253]
In the compound represented by the general formula (I), Z is a chlorine atom (Ir)
[0254]
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[0255]
(Where m, n, R, V, W, X, Y, Q ¹ , Q ² , Q ^Three , Ring A, ring B and ring C have the same meaning as in general formula (I). ) With copper cyanide, the general formula (Is)
[0256]
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[0257]
(Where m, n, R, V, W, X, Y, Q ¹ , Q ² , Q ^Three , Ring A, ring B and ring C have the same meaning as in general formula (I). ) Can be obtained.
[0258]
Typical examples of the compound represented by the general formula (I) thus produced are listed below.
[0259]
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[0260]
The present invention also provides a liquid crystal composition containing at least one compound represented by the general formula (I) as a constituent component.
[0261]
In the liquid crystal composition containing at least one compound represented by the general formula (I) as a constituent component, in addition to the compound represented by the general formula (I), as long as the composition exhibits liquid crystallinity. Any compound may be contained, but the first component contains at least one compound represented by the general formula (I), but as other components, at least from the following second to fourth components. It is preferable to contain 1 type.
[0262]
That is, the second component is a so-called fluorine-based (halogen-based) p-type liquid crystal compound, and is composed of compounds represented by the following general formulas (A1) to (A3).
[0263]
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[0264]
In the above formula, Alk ^a Represents an alkyl group having 1 to 12 carbon atoms, which may be linear or methyl or ethyl branched, and may have a 3 to 6-membered ring structure, Any -CH present in the group ₂ -May be replaced by -O-, -CH = CH-, -CH = CF-, -CF = CH-, -CF = CF-, or -C≡C-, and any group present in the group The hydrogen atom may be substituted by a fluorine atom or a trifluoromethoxy group, but a linear alkyl group having 2 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms, and the number of carbon atoms A linear 3-alkenyl group having 4 to 7 carbon atoms and an alkyl group having 1 to 5 carbon atoms substituted with an alkoxyl group having 1 to 3 carbon atoms at the end are preferable. Further, when asymmetric carbon is generated by branching, the compound may be optically active or racemic.
[0265]
Ring Fa, Ring Fb and Ring Fc may each independently be substituted with a trans-1,4-cyclohexylene group, a transdecahydronaphthalene-trans-2,6-diyl group, or one or more fluorine atoms. 1,4-phenylene group, naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, tetrahydronaphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms Group, 1,4-cyclohexenylene group optionally substituted by a fluorine atom, 1,3-dioxane-trans-2,5-diyl group, pyrimidine-2,5-diyl group or pyridine-2,5- Represents a diyl group, trans-1,4-cyclohexylene group, transdecahydronaphthalene-trans-2,6-diyl group, naphthalene-2,6-diyl group optionally substituted by a fluorine atom, or 1 to Optionally substituted by two fluorine atoms A 1,4-phenylene group is preferred. In particular, when the ring Fb is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group, the ring Fa is preferably a trans-1,4-cyclohexylene group, When the ring Fc is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group, the ring Fb and the ring Fa are preferably a trans-1,4-cyclohexylene group. . In (A3), ring Fa is preferably a trans-1,4-cyclohexylene group. L ^a , L ^b And L ^c Are linking groups, each independently a single bond, ethylene group (-CH ₂ CH ₂ -), 1,2-propylene group (-CH (CH _Three ) CH ₂ -And-CH ₂ CH (CH _Three )-), 1,4-butylene group, -COO-, -OCO-, -OCF ₂ -, -CF ₂ O-, -CH = CH-, -CH = CF-, -CF = CH-, -CF = CF-, -C≡C- or -CH = NN = CH- represents a single bond, ethylene group, 1,4-butylene group, -COO-, -OCF ₂ -, -CF ₂ O—, —CF═CF— or —C≡C— is preferred, and a single bond or an ethylene group is particularly preferred. In addition, it is preferable that at least one of (A2) represents a single bond and at least two of (A3) represent a single bond.
[0266]
Ring Fz is an aromatic ring and can be represented by the following general formulas (Ga) to (Gc).
[0267]
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[0268]
Where J ^a ~ J ^j Each independently represents a hydrogen atom or a fluorine atom, but in (Ga), J ^a And J ^b Is preferably a fluorine atom, and in (Gb), J ^d ~ J ^f Is preferably a fluorine atom, particularly J ^d Is more preferably a fluorine atom.
[0269]
Terminal group P ^a Is a fluorine atom, a chlorine atom, a trifluoromethoxy group, a difluoromethoxy group, a trifluoromethyl group, a difluoromethyl group, or an alkoxyl group having 2 or 3 carbon atoms substituted by two or more fluorine atoms, an alkyl group, an alkenyl group Or an alkenyloxy group, preferably a fluorine atom, a trifluoromethoxy group or a difluoromethoxy group, and particularly preferably a fluorine atom.
[0270]
In (A1) to (A3), the compound of the general formula (I) of the present invention is excluded.
[0271]
The third component is a so-called cyano p-type liquid crystal compound, which is composed of compounds represented by the following general formulas (B1) to (B3).
[0272]
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[0273]
In the above formula, Alk ^b Represents an alkyl group having 1 to 12 carbon atoms, which may be linear or methyl or ethyl branched, and may have a 3 to 6-membered ring structure, Any -CH present in the group ₂ -May be replaced by -O-, -CH = CH-, -CH = CF-, -CF = CH-, -CF = CF-, or -C≡C-, and any group present in the group The hydrogen atom may be substituted by a fluorine atom or a trifluoromethoxy group, but a linear alkyl group having 2 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms, and the number of carbon atoms A linear 3-alkenyl group having 4 to 7 carbon atoms and an alkyl group having 1 to 5 carbon atoms substituted with an alkoxyl group having 1 to 3 carbon atoms at the end are preferable. Further, when asymmetric carbon is generated by branching, the compound may be optically active or racemic.
[0274]
Ring Fd, Ring Fe and Ring Ff may each independently be substituted with a trans-1,4-cyclohexylene group, a transdecahydronaphthalene-trans-2,6-diyl group, or one or more fluorine atoms. 1,4-phenylene group, naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, tetrahydronaphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms Group, 1,4-cyclohexenylene group optionally substituted by a fluorine atom, 1,3-dioxane-trans-2,5-diyl group, pyrimidine-2,5-diyl group or pyridine-2,5- Represents a diyl group, trans-1,4-cyclohexylene group, transdecahydronaphthalene-trans-2,6-diyl group, naphthalene-2,6-diyl group optionally substituted by a fluorine atom, or 1 to Optionally substituted by two fluorine atoms A 1,4-phenylene group is preferred. In particular, when the ring Fe is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group, the ring Fd is preferably a trans-1,4-cyclohexylene group, When the ring Ff is a trans-1,4-cyclohexylene group or a transdecahydronaphthalene-trans-2,6-diyl group, the ring Fd and the ring Fe are preferably a trans-1,4-cyclohexylene group. . In (B3), ring Fd is preferably a trans-1,4-cyclohexylene group.
[0275]
L ^d , L ^e And L ^f Are linking groups, each independently a single bond, ethylene group (-CH ₂ CH ₂ -), 1,2-propylene group (-CH (CH _Three ) CH ₂ -And-CH ₂ CH (CH _Three )-), 1,4-butylene group, -COO-, -OCO-, -OCF ₂ -, -CF ₂ O-, -CH = CH-, -CH = CF-, -CF = CH-, -CF = CF-, -C≡C-, -OCH ₂ -, -CH ₂ O- or -CH = NN = CH- represents a single bond, ethylene group, -COO-, -OCF ₂ -, -CF ₂ O—, —CF═CF— or —C≡C— is preferred, and a single bond, ethylene group or —COO— is particularly preferred. In addition, it is preferable that at least one of them in (B2) represents a single bond in (B3).
[0276]
Ring Fy is an aromatic ring and can be represented by the following general formulas (Gd) to (Gf).
[0277]
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[0278]
Where J ^k ~ J ^q Each independently represents a hydrogen atom or a fluorine atom, but in (Ge), J ⁿ And J ^o Is preferably a hydrogen atom.
Terminal group P ^a Represents a cyano group (—CN), a cyanate group (—OCN) or —C≡CCN, with a cyano group being preferred.
[0279]
In (B1) to (B3), the compound of the general formula (I) of the present invention is excluded.
[0280]
The fourth component is a so-called n-type liquid crystal having a dielectric anisotropy of about 0 or less, and is composed of compounds represented by the following general formulas (C1) to (C3).
[0281]
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[0282]
In the above formula, Alk ^c And Alk ^d Each independently represents an alkyl group having 1 to 12 carbon atoms, which may be linear or have a methyl or ethyl branch, and have a 3- to 6-membered cyclic structure. Any --CH present in the group ₂ -May be replaced by -O-, -CH = CH-, -CH = CF-, -CF = CH-, -CF = CF-, or -C≡C-, and any group present in the group The hydrogen atom may be substituted by a fluorine atom or a trifluoromethoxy group, but a linear alkyl group having 1 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms, and the number of carbon atoms A linear 3-alkenyl group having 4 to 7 carbon atoms, a linear alkoxyl group having 1 to 3 carbon atoms, or a linear chain having 1 to 5 carbon atoms substituted with an alkoxyl group having 1 to 3 carbon atoms at the end An alkyl group is preferred, and at least one of them is a linear alkyl group having 1 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms, or a linear 3-alkenyl group having 4 to 7 carbon atoms. Particularly preferred is a group.
[0283]
Ring Fg, Ring Fh, Ring Fi and Ring Fj are each independently a trans-1,4-cyclohexylene group, a transdecahydronaphthalene-trans-2,6-diyl group, 1 to 2 fluorine atoms or methyl 1,4-phenylene group optionally substituted by a group, naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, may be substituted by 1 to 2 fluorine atoms Good tetrahydronaphthalene-2,6-diyl group, 1,4-cyclohexenylene group optionally substituted by 1 to 2 fluorine atoms, 1,3-dioxane-trans-2,5-diyl group, pyrimidine -2,5-diyl group or pyridine-2,5-diyl group, each compound may be substituted with transdecahydronaphthalene-trans-2,6-diyl group, one or more fluorine atoms A good naphthalene-2,6-diyl group, with one or two fluorine atoms Optionally substituted tetrahydronaphthalene-2,6-diyl group, 1,4-cyclohexenylene group optionally substituted by a fluorine atom, 1,3-dioxane-trans-2,5-diyl group, pyrimidine -2,5-diyl group or pyridine-2,5-diyl group is preferably 1 or less, and the other ring is trans-1,4-cyclohexylene group or 1 to 2 fluorine atoms or methyl group A 1,4-phenylene group which may be substituted with is preferable.
[0284]
L ^g , L ^h And L ⁱ Are linking groups, each independently a single bond, ethylene group (-CH ₂ CH ₂ -), 1,2-propylene group (-CH (CH _Three ) CH ₂ -And-CH ₂ CH (CH _Three )-), 1,4-butylene group, -COO-, -OCO-, -OCF ₂ -, -CF ₂ O-, -CH = CH-, -CH = CF-, -CF = CH-, -CF = CF-, -C≡C- or -CH = NN = CH- represents a single bond, ethylene group, 1,4-butylene group, -COO-, -OCO-, -OCF ₂ -, -CF ₂ O-, -CF = CF-, -C≡C- or -CH = NN = CH- are preferred, at least one of them represents a single bond in (C2) and at least two of them in (C3) It is preferable.
[0285]
More preferable forms in (C1) can be represented by the following general formulas (C1a) to (C1h).
[0286]
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[0287]
In the above formulas, Alk ^e And Alk ^f Are each independently a linear alkyl group having 1 to 7 carbon atoms, a linear 1-alkenyl group having 2 to 7 carbon atoms, a linear 3-alkenyl group having 4 to 7 carbon atoms, or a carbon atom. Represents a linear alkoxyl group having 1 to 3 carbon atoms or a linear alkyl group having 1 to 5 carbon atoms, the terminal of which is substituted with an alkoxyl group having 1 to 3 carbon atoms, at least one of which has 1 to 7 represents a linear alkyl group, a linear 1-alkenyl group having 2 to 7 carbon atoms, or a linear 3-alkenyl group having 4 to 7 carbon atoms. However, when ring Fg1 to ring Fg3 are aromatic rings, the corresponding Alk ^e Except for 1-alkenyl group and alkoxyl group, when ring Fh1 to ring Fh3 are aromatic rings, the corresponding Alk ^f Excludes 1-alkenyl and alkoxyl groups.
[0288]
Ring Fg1 and Ring Fh1 may be each independently substituted with a trans-1,4-cyclohexylene group, a transdecahydronaphthalene-trans-2,6-diyl group, 1 to 2 fluorine atoms or a methyl group. 1,4-phenylene group, naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, tetrahydronaphthalene-2,6 optionally substituted by 1 to 2 fluorine atoms -Diyl group, 1,4-cyclohexenylene group optionally substituted by 1 to 2 fluorine atoms, 1,3-dioxane-trans-2,5-diyl group, pyrimidine-2,5-diyl group Or a pyridine-2,5-diyl group, but in each compound, a transdecahydronaphthalene-trans-2,6-diyl group, naphthalene-2,6-optionally substituted by one or more fluorine atoms Diyl group, substituted by 1 to 2 fluorine atoms Tetrahydronaphthalene-2,6-diyl group, 1,4-cyclohexenylene group optionally substituted by a fluorine atom, 1,3-dioxane-trans-2,5-diyl group, pyrimidine-2, The number of 5-diyl groups or pyridine-2,5-diyl groups is preferably no more than one, in which case the other ring is a trans-1,4-cyclohexylene group or 1 to 2 fluorine atoms or a methyl group 1,4-phenylene group which may be substituted by Ring Fg2 and Ring Fh2 may be each independently substituted with a trans-1,4-cyclohexylene group, a transdecahydronaphthalene-trans-2,6-diyl group, 1 to 2 fluorine atoms or a methyl group. 1,4-phenylene group, naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, tetrahydronaphthalene-2,6 optionally substituted by 1 to 2 fluorine atoms -Represents a diyl group, but in each compound, transdecahydronaphthalene-trans-2,6-diyl group, naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, 1-2 It is preferable that the number of tetrahydronaphthalene-2,6-diyl groups optionally substituted by one fluorine atom is 1 or less, in which case the other ring is a trans-1,4-cyclohexylene group or 1 to 2 Fluorine atoms or The methyl group may be substituted 1,4-phenylene group. Ring Fg3 and Ring Fh3 are each independently 1,4-phenylene group optionally substituted by 1 to 2 fluorine atoms or methyl group, naphthalene-2 optionally substituted by one or more fluorine atoms , 6-diyl group, tetrahydronaphthalene-2,6-diyl group optionally substituted by 1 to 2 fluorine atoms, but naphthalene optionally substituted by one or more fluorine atoms in each compound It is preferable that the number of -2,6-diyl groups and tetrahydronaphthalene-2,6-diyl groups optionally substituted by 1 to 2 fluorine atoms is 1 or less.
[0289]
More preferable forms in (C2) can be represented by the following general formulas (C2a) to (C2m).
[0290]
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[0291]
In the above formula, ring Fg1, ring Fg2, ring Fg3, ring Fh1, ring Fh2 and ring Fh3 represent the above-mentioned meanings, ring Fi1 is the same as ring Fg1, ring Fi2 is ring Fg2, and ring Fi3 is the same as ring Fg3. Represents meaning.
In each of the above compounds, a transdecahydronaphthalene-trans-2,6-diyl group, a naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, and 1 to 2 fluorine atoms A tetrahydronaphthalene-2,6-diyl group optionally substituted by a 1,4-cyclohexenylene group optionally substituted by a fluorine atom, a 1,3-dioxane-trans-2,5-diyl group, The number of pyrimidine-2,5-diyl groups or pyridine-2,5-diyl groups is preferably one or less, and in this case, the other ring is a trans-1,4-cyclohexylene group or 1 to 2 fluorine atoms. A 1,4-phenylene group which may be substituted by an atom or a methyl group.
[0292]
Next, more preferable forms in (C3) can be represented by the following general formulas (C3a) to (C3f).
[0293]
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[0294]
In the above formula, ring Fg1, ring Fg2, ring Fh1, ring Fh2, ring Fi1 and ring Fi2 represent the above-mentioned meanings, ring Fj1 represents ring Fg1 and ring Fj2 represents the same meaning as ring Fg2. In each of the above compounds, a transdecahydronaphthalene-trans-2,6-diyl group, a naphthalene-2,6-diyl group optionally substituted by one or more fluorine atoms, and 1 to 2 fluorine atoms A tetrahydronaphthalene-2,6-diyl group optionally substituted by a 1,4-cyclohexenylene group optionally substituted by a fluorine atom, a 1,3-dioxane-trans-2,5-diyl group, The number of pyrimidine-2,5-diyl groups or pyridine-2,5-diyl groups is preferably one or less, and in this case, the other ring is a trans-1,4-cyclohexylene group or 1 to 2 fluorine atoms. A 1,4-phenylene group which may be substituted by an atom or a methyl group.
[0295]
Actually, using the above compound, a liquid crystal composition having a maximum temperature of the nematic phase of 117 ° C. was prepared, and when 20% by weight of the compound represented by (I-2) was added thereto, the maximum temperature of the nematic phase was It was 74 ° C. and did not precipitate even when stored at 0 ° C. for 1 week. As a compound having a similar structure, the upper limit temperature of the nematic phase when trans-4-propyl- (3,4,5-trifluorophenyl) cyclohexane is added is 70 ° C. It can be seen that the compound represented has excellent solubility in the host liquid crystal composition and can exhibit a liquid crystal phase in a very wide temperature range.
[0296]
Further, when the voltage holding ratio of this composition was measured, it showed a sufficiently high value in the same manner as the host liquid crystal composition both during preparation, after heating and after ultraviolet irradiation.
[0297]
Thus, the compound of the present invention has excellent liquid crystallinity and excellent compatibility with currently used liquid crystal compounds and liquid crystal compositions. In addition, it can be seen that the liquid crystal composition has an effect superior to conventional compounds in preparing a liquid crystal composition having a wide temperature range showing a liquid crystal phase, a low threshold voltage, and capable of high-speed response.
[0298]
Therefore, the compound of the general formula (I) is a liquid crystal that can be driven at a low voltage with a wide temperature range, particularly for a field effect display cell such as a TN type or STN type in a mixture with other nematic liquid crystal compounds. It can be suitably used as a material. Among the compounds of (I), those that do not contain a cyano group or an ester bond can easily obtain a large specific resistance and a high voltage holding ratio, and can also be used as a component of liquid crystal materials for active matrix driving. Is possible. Furthermore, not only nematic liquid crystals but also ferroelectric liquid crystals and antiferroelectric liquid crystals can be expected to be used as a low-viscosity agent indispensable for realizing a high-speed response.
[0299]
【Example】
Specific examples will be given below to describe the tetrahydronaphthalene derivative of the present invention and the production method thereof, and the advantages in the liquid crystal composition obtained by using the tetrahydronaphthalene derivative of the present invention as a constituent component, but of course, the gist of the present invention, The scope of application is not limited by these examples.
[0300]
(Example 1)
Synthesis of 6-propyl-2- (3,4,5-trifluorophenyl) -1,2,3,4-tetrahydronaphthalene (I-2)
[0301]
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[0302]
A solution of 3,4,5-trifluorobromobenzene (30 g) in tetrahydrofuran (100 ml) was added dropwise to magnesium (4.0 g) to prepare a Grignard reactant. Toluene (150 ml) was added thereto, and about 100 ml of the solvent was distilled off at room temperature under reduced pressure. This was heated to 60 ° C., and a solution of 6-propyl-1,2,3,4-tetrahydronaphthalen-2-one (25 g) in toluene (50 ml) was added dropwise over 20 minutes. After further stirring for 30 minutes, the temperature was returned to room temperature, and the reaction solution was poured into 10% hydrochloric acid. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane: ethyl acetate = 6: 1) to give 2-hydroxy-6-propyl-2- (3,4,5-trifluorophenyl) -1,2,3,4- Tetrahydronaphthalene (29 g) was obtained. Toluene (100 ml) and p-toluenesulfonic acid (3 g) were added thereto, and the mixture was stirred with heating for 1 hour. The reaction mixture was cooled and concentrated, and the residue was purified by silica gel column chromatography (hexane) to give 6-propyl-2- (3,4,5-trifluorophenyl) -3,4-dihydronaphthalene (26 g). Got. Ethanol (50 ml), ethyl acetate (50 ml) and 5% palladium-carbon (3 g) were added thereto, and the mixture was stirred at room temperature for 2 hours under a hydrogen atmosphere. The reaction solution was filtered through celite, and the furnace solution was concentrated. The residue was purified by silica gel column chromatography (hexane) to obtain 6-propyl-2- (3,4,5-trifluorophenyl) -1,2,3,4-tetrahydronaphthalene (26 g). This compound had a purity of 99% by gas chromatography and a molecular weight of 304 by mass spectrometry.
[0303]
Example 2 Synthesis of 2- (3,4-difluorophenyl) -6-propyl-1,2,3,4-tetrahydronaphthalene (I-1)
Under the same conditions as in Example 1, using 3,4-difluorobromobenzene instead of 3,4,5-trifluorobromobenzene, 2- (3,4-difluorophenyl) -6-propyl-1, 2,3,4-Tetrahydronaphthalene was synthesized. Purity 99%, molecular weight 286.
[0304]
Example 3 Synthesis of 6-propyl-2- (4-trifluoromethoxyphenyl) -1,2,3,4-tetrahydronaphthalene (I-3)
Under the same conditions as in Example 1, using 4-trifluoromethoxybromobenzene instead of 3,4,5-trifluorobromobenzene, 6-propyl-2- (4-trifluoromethoxyphenyl) -1, 2,3,4-Tetrahydronaphthalene was synthesized. Purity 99%, molecular weight 334.
[0305]
Example 4 Synthesis of 2- (3,4-difluorophenyl) -6- (trans-4-propylcyclohexyl) -1,2,3,4-tetrahydronaphthalene (I-4)
[0306]
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[0307]
A solution of 3,4-difluorobromobenzene (25 g) in tetrahydrofuran (100 ml) was added dropwise to magnesium (3.5 g) to prepare a Grignard reactant. This was filtered through a glass filter, toluene (150 ml) was added to the filtrate, and then about 100 ml of the solvent was distilled off at room temperature under reduced pressure. This was heated to 60 ° C., and a toluene (50 ml) solution of 6-bromo-1,2,3,4-tetrahydronaphthalen-2-one (27 g) was added dropwise over 20 minutes. After further stirring for 30 minutes, the temperature was returned to room temperature, and the reaction solution was poured into 10% hydrochloric acid. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane: ethyl acetate = 6: 1) to give 6-bromo-2- (3,4-difluorophenyl) -2-hydroxy-1,2,3,4-tetrahydronaphthalene ( 29 g) was obtained. Toluene (100 ml) and p-toluenesulfonic acid (3 g) were added thereto, and the mixture was stirred with heating for 1 hour. The reaction mixture was cooled and concentrated, and the residue was purified by silica gel column chromatography (hexane) to give 6-bromo-2- (3,4-difluorophenyl) -3,4-dihydronaphthalene (26 g). . Ethanol (50 ml), ethyl acetate (50 ml) and 5% rhodium-carbon (3 g) were added thereto, and the mixture was stirred at room temperature for 2 hours under a hydrogen atmosphere. The reaction solution was filtered through celite, and the furnace solution was concentrated. The residue was purified by silica gel column chromatography (hexane) to obtain 6-bromo-2- (3,4-difluorophenyl) -1,2,3,4-tetrahydronaphthalene (26 g). A solution of 6-bromo-2- (3,4-difluorophenyl) -1,2,3,4-tetrahydronaphthalene (26 g) in tetrahydrofuran (70 ml) was added dropwise to magnesium (2.3 g) to give a Grignard reagent. Was prepared. To this was added dropwise a solution of 4-propylcyclohexanone (13.5 g) in tetrahydrofuran (30 ml). After stirring for another 30 minutes, the reaction solution was poured into 10% hydrochloric acid. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane: ethyl acetate = 6: 1) to give 2- (3,4-difluorophenyl) -2-hydroxy-6- (trans-4-propylcyclohexyl) -1,2, 3,4-Tetrahydronaphthalene (23 g) was obtained. Toluene (80 ml) and p-toluenesulfonic acid (2 g) were added thereto, and the mixture was stirred with heating for 1 hour. The reaction mixture is cooled and concentrated, and the residue is purified by silica gel column chromatography (hexane) to give 2- (3,4-difluorophenyl) -6- (trans-4-propylcyclohexyl) -3,4-dihydronaphthalene. (26 g) was obtained. Ethanol (30 ml), ethyl acetate (50 ml) and 5% palladium-carbon (2 g) were added thereto, and the mixture was stirred at room temperature for 2 hours under a hydrogen atmosphere. The reaction solution was filtered through celite, and the furnace solution was concentrated. Dimethylformamide (50 ml) and t-butoxypotassium (5.5 g) were added to the residue, and the mixture was stirred at 70 ° C. for 2 hours. 10% Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with toluene. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane), recrystallized with ethanol, and 2- (3,4-difluorophenyl) -6- (trans-4-propylcyclohexyl) -1,2,3,4- Tetrahydronaphthalene (20 g) was obtained. This compound had a purity of 99.8% by gas chromatography and a molecular weight of 368 by mass spectrometry.
[0308]
Example 5 Synthesis of 2- (3,4-difluorophenyl) -6- (4-propylphenyl) -1,2,3,4-tetrahydronaphthalene (I-5)
[0309]
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[0310]
4-Propylphenylboric acid (4.5 g) obtained by reacting trimethylboric acid with a Grignard reagent prepared from 4-propylbromobenzene and magnesium and then hydrolyzing with dilute hydrochloric acid, synthesized in Example 4 6-bromo-2- (3,4-difluorophenyl) -1,2,3,4-tetrahydronaphthalene (5.0 g), tetrakis (triphenylphosphine) palladium (0) (0.3 g) and potassium phosphate ( 3.0 g) was stirred in dimethylformamide (30 ml) at 80 ° C. for 8 hours. The reaction solution was cooled to room temperature, water was added, and the mixture was extracted with toluene. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (hexane), recrystallized with ethanol, and 2- (3,4-difluorophenyl) -6- (4-propylphenyl) -1,2,3,4-tetrahydronaphthalene. (4 g) was obtained. This compound had a purity of 99.7% by gas chromatography and a molecular weight of 362 by mass spectrometry.
[0311]
(Example 6) Preparation of liquid crystal composition
A general-purpose host liquid crystal (H) with a wide temperature range and low viscosity, which can also be used for active matrix drive, was prepared. This (H) shows a nematic phase at 116.7 ° C. or lower, and its melting point is 11 ° C. The physical properties of this composition and the measured values at 20 ° C. of the threshold voltage (Vth) of a TN cell (cell thickness 4.5 μm) prepared using the composition were as follows.
[0312]
Nematic phase upper limit temperature (T _NI ) 116.7 ℃
Dielectric Anisotropy (Δε) 4.80
Threshold voltage (Vth) 1.88 V
Response time (τ) 21.5 ms
Next, a liquid crystal composition (M-1) comprising 80% of the host liquid crystal (H) and 20% of the compound of the present invention obtained in Example 1 (I-2) was prepared. Temperature (T _NI ) Was 74 ° C. After this (M-1) was left at 150 ° C for 20 hours, its T _NI Was measured, but no change was observed before heating. In addition, ultraviolet rays were irradiated for 20 hours. _NI There was no change. Next, when the voltage holding ratio of this composition was measured, it showed a sufficiently high value in the same manner as the host liquid crystal (H) during preparation, after heating and after ultraviolet irradiation.
[0313]
Next, (M-1) was filled in a TN cell having a cell thickness of 4.5 μm to produce a liquid crystal element, and the electro-optical characteristics were measured. The results were as follows.
[0314]
Nematic phase upper limit temperature (T _NI ) 74.0 ℃
Dielectric Anisotropy (Δε) 5.50
Threshold voltage (Vth) 1.55 V
Response time (τ) 30.5 msec
Therefore, by adding 20% of (I-2), the nematic phase upper limit temperature (T _NI ), The threshold voltage (Vth) could be reduced by 0.33 V. Furthermore, the response time could be suppressed to 9 ms. In addition, no crystals were deposited even after standing at 0 ° C. for 1 week. It was further cooled and crystallized, and its melting point (T _CN ) Shows almost no change from the host liquid crystal (H) at 12 ° C, indicating that (I-2) is well dissolved in the host liquid crystal.
[0315]
Next, the voltage holding ratio at room temperature and 80 ° C. of this device was measured, and it was found that both were very good and could be used sufficiently for active matrix driving.
[0316]
(Comparative Example 1)
In Example 6, instead of (I-2), trans-4-propyl- (3,4,5-trifluorophenyl) cyclohexane was added to the host liquid crystal (H) in the same amount (20%) to obtain a liquid crystal composition A product (M-2) was prepared. The nematic phase upper limit temperature (T _NI ) Is 70 ° C., indicating that the liquid crystallinity is lower than that of (I-2).
[0317]
Other physical property values of this composition and electro-optical property values of devices prepared in the same manner are as follows.
[0318]
Nematic phase upper limit temperature (T _NI ) 70.0 ℃
Dielectric Anisotropy (Δε) 5.60
Threshold voltage (Vth) 1.58 V
Response time (τ) 30.0 msec
Refractive index anisotropy (Δn): 0.080
Therefore, the nematic phase upper limit temperature (T _NI ) Drops by 4 °, the threshold voltage (Vth) hardly changes and the response time hardly changes.
[0319]
【The invention's effect】
The tetrahydronaphthalene derivative provided by the present invention is excellent in liquid crystallinity and compatibility with currently used liquid crystal compounds or compositions. In addition, the addition can greatly reduce the threshold voltage with almost no deterioration in responsiveness. Furthermore, it is easy to manufacture industrially, and is colorless and chemically stable. Accordingly, a liquid crystal composition containing the same is extremely useful as a practical liquid crystal, particularly for a liquid crystal display having a wide temperature range and requiring low voltage driving and high-speed response.

Claims

Formula (I)

(In the formula, R represents a saturated or unsaturated alkyl group having 1 to 20 carbon atoms which may be substituted by 1 to 7 fluorine atoms or an alkoxyl group having 1 to 7 carbon atoms and may contain a branched chain. The linking group V represents a single bond or an oxygen atom, and the linking groups W, X and Y are each independently a single bond, —CH ₂ CH ₂ —, —CH═CH—, —CF ₂ CF ₂ —, — _{CF = CF -, - CH 2} O -, - OCH 2 -, - C≡C -, - CF 2 O- or -OCF ₂ - represents, Z is a fluorine atom, a chlorine atom, a trifluoromethyl group, tri Represents a fluoromethoxy group or a difluoromethoxy group, Q ¹ and Q ² represent a hydrogen atom, Q ³ represents a hydrogen atom or a fluorine atom, and ring A and ring B are each independently trans-1,4-cyclohexyl. cyclohexylene, trans - decahydronaphthalene-2,6-diyl group, trans-1,3-dioxane-2,5-diyl group, optionally substituted with one or two fluorine atoms Represents have 1,4-phenylene group or one or two good naphthalene-2,6-diyl group which may be substituted with a fluorine atom, ring C may be substituted with one or two fluorine atoms 1, Tetrahydronaphthalene represented by 4-phenylene group or naphthalene-2,6-diyl group which may be substituted with one or two fluorine atoms, m and n each independently represents 0 or 1 Derivative.

2. The compound according to claim 1, wherein m is 0 in the general formula (I).

2. The compound according to claim 1, wherein n is 0 in the general formula (I).

Q ³ is A compound according to claim 1 to 3, wherein where a hydrogen atom in the general formula (I).

5. The compound according to claim 1, wherein in the general formula (I), the linking groups W, X and Y are each independently selected from a single bond or —CH ₂ CH ₂ —.

In general formula (I), ring A and ring B are each independently substituted with a trans-1,4-cyclohexylene group, a trans-decahydronaphthalene-2,6-diyl group, or one or two fluorine atoms. 6. The compound according to claim 1, which is selected from 1,4-phenylene group and naphthalene-2,6-diyl group.

7. The compound according to claims 1 to 6, wherein the ring C in the general formula (I) is selected from a 1,4-phenylene group or a naphthalene-2,6-diyl group substituted with one or two fluorine atoms.

8. The compound according to claim 1, wherein Z in the general formula (I) is selected from a fluorine atom or a trifluoromethoxy group.

9. The compound according to claim 1 , wherein V represents a single bond in the general formula (I).

10. The compound according to claim 1, wherein R in the general formula (I) is selected from linear alkyl groups having 1 to 10 carbon atoms.

11. A liquid crystal composition comprising one or more compounds of general formula (I) according to claim 1-10 .

12. The liquid crystal composition according to claim 11, which is used for driving an active matrix.

12. A liquid crystal device using the liquid crystal composition according to claim 11 .

13. An active matrix driving liquid crystal display device using the liquid crystal composition according to claim 12 .