JP2018502820A - 紫外線吸収剤 - Google Patents
紫外線吸収剤 Download PDFInfo
- Publication number
- JP2018502820A JP2018502820A JP2017516918A JP2017516918A JP2018502820A JP 2018502820 A JP2018502820 A JP 2018502820A JP 2017516918 A JP2017516918 A JP 2017516918A JP 2017516918 A JP2017516918 A JP 2017516918A JP 2018502820 A JP2018502820 A JP 2018502820A
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- Prior art keywords
- group
- independently
- hydrogen
- substituted
- diyl
- Prior art date
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Links
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Classifications
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- C—CHEMISTRY; METALLURGY
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Abstract
Description
本発明は、紫外線吸収特性を有し、また、メソゲン特性も有することができる化合物に関する。
液晶の分子は、実質的に1つの方向に互いに整列することができ、これは、異方性の光学的、電磁気的および/または機械的特性などの1つまたは複数の異方性の特性を有する液体材料をもたらす。メソゲンは、一般に、液晶(例えば、存在する他の液晶材料)との間(amongst and between)で構造的秩序(order)を誘発しかつ/または誘発されてその構造的秩序に至る液晶材料の一次的または基本的な単位(またはセグメントもしくは基)と記載される。
本明細書で使用される冠詞「a」、「an」および「the」は、1つの指示対象への別段の明示的で明確な限定のない限り、複数の指示対象を含む。
(1)−(CH2)g−、−(CF2)h−、−Si(CH2)g−、−(Si[(CH3)2]O)h−(式中、gは、各出現について、1〜20から独立に選択され;hは1〜16から選択される);
(2)−N(Z)−、−C(Z)=C(Z)−、−C(Z)=N−、−C(Z’)−C(Z’)−(式中、Zは、各出現について、水素、C1〜C6アルキル、シクロアルキルおよびアリールから独立に選択され、Z’は、各出現について、C1〜C6アルキル、シクロアルキルおよびアリールから独立に選択される);および、
(3)−O−、−C(O)−、−C≡C−、−N=N−、−S−、−S(O)−、−S(O)(O)−、直鎖状または分枝状C1〜C24アルキレン残基(該C1〜C24アルキレン残基は、置換されていないか、シアノもしくはハロで一置換されているかまたはハロでポリ置換されている);
から選択されるスペーサー単位から独立に選択される。しかし、S1、S2、S3、S4およびS5の選択は、ヘテロ原子を含む2つのスペーサー単位が互いに連結されている場合、そのスペーサー単位は、ヘテロ原子が互いに直接連結されないように連結され、S1およびS5がそれぞれPCおよびPと連結されている場合、それらは、2個のヘテロ原子が互いに直接連結されないように連結されるという条件に従う。本明細書で使用される「ヘテロ原子」という用語は、炭素または水素以外の原子を意味する。
パートA
(実施例1)
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(実施例2)
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(実施例3)
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(実施例4)
(実施例5)
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(実施例6)
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(実施例7)
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(実施例8)
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(実施例9)
(実施例10)
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(実施例11)
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(実施例12)
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(実施例13)
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(実施例14)
(実施例15)
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(実施例16)
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(実施例17)
(実施例18)
(実施例19)
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(実施例20)
(実施例21)
(実施例22)
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(実施例23)
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(実施例24)
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(実施例25)
(実施例26)
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(実施例27)
(実施例28)
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(実施例29)
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(実施例30)
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パートB
パート1 − プライマー層配合物(PLF)の調製。
2 Great Lakes Chemical Corp.から入手可能なポリアルキレンカーボネートジオール
3 Covestro AGから入手可能なブロック化脂肪族ポリイソシアネート
4 Baxenden Chemicals, Ltdから入手可能なブロック化三官能性ウレタン架橋剤
5 BYK Chemie、USAから入手可能なポリエーテル改質ポリジメチルシロキサン
6 King Industriesから入手可能なカルボン酸ビスマス触媒
7 BASF Corporationから入手可能なヒンダードアミン光安定剤
8 BASF Corporationから入手可能な酸化防止剤
パート2 − 液晶配列配合物(LCAF)の調製。
パート3 − コーティング層配合物(CLF)の調製。
2 EMD Chemicals, Inc.から市販されている液晶モノマー、4−(3−アクリロイルオキシプロピルオキシ)−安息香酸2−メチル−1,4−フェニレンエステル
3 米国特許第7,910,019B2号に記載されている手順に従って調製された1−(6−(6−(6−(6−(6−(6−(6−(6−(8−(4−(4−((1r,1’s,4R,4’R)−4’−ペンチル−[1,1’−ビ(シクロヘキサン)]−4−カルボニルオキシ)2−または3−メチルフェニルオキシカルボニル)フェノキシ)オクチルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−2−メチルプロパ−2−エン−1−オン
4 米国特許第7,910,019B2号の実施例17に従って調製された1−(6−(6−(6−(6−(6−(6−(6−(6−(8−(4−(4−(4−(6−アクリロイルオキシヘキシルオキシ)ベンゾイルオキシ)フェノキシカルボニル)フェノキシ)オクチルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキシルオキシ)−6−オキソヘキサノール
5 4−(((1s,4r)−r−ペンチルシクロヘキサン−1−カルボニル)オキシ)フェニル4−((6−(アクリロイルオキシ)ヘキシル)オキシ)ベンゾエート
6 BASF Corporationから入手可能な光開始剤
7 米国特許第8,518,546B2号の実施例44の手順に従って調製された、構造3,3−ビス(4−メトキシフェニル)−6−メトキシ−7−(4−(4−(trans,trans−4’−ペンチル−[1,1’−ビ(シクロヘキサン)]−4−カルボニルオキシ)フェニル)ピペラジン−1−イル)−10,12−ジ(トリフルオロメチル)−13,13−ジメチル−3,13−ジヒドロ−インデノ[2’,3’:3,4]ナフト[1,2−b]ピランのフォトクロミック二色性染料
8 米国特許第8,545,984B2号の実施例33に従って調製された、構造3−フェニル−3−(4−モルホリノフェニル)−10−[4−(4−(4−(trans−4−ペンチルシクロヘキシル)フェニル)ベンズアミド)フェニル]−6−トリフルオロメチル−13,13−ジメチル−3,13−ジヒドロ−インデノ[2’,3’:3,4]ナフト[1,2−b]ピランのフォトクロミック二色性染料
2 BASF Corporationから入手可能な光開始剤
3 Momentive Performance Materialsから入手可能なガンマ−アミノプロピルトリエトキシシラン
パート5 − ハードコート配合物(HCF)の調製。
パート6 − 表6にまとめた基材およびコーティングスタックを調製するために使用した手順。
コロナ処理
基材調製
プライマー層のためのコーティング手順
液晶配列層のためのコーティング手順
コーティング層のためのコーティング手順
トップコート層のためのコーティング手順
ハードコート層のためのコーティング手順
Claims (24)
- 以下の式(I)、(II)、(III)、(IV)、(V)、(VI)、(VII)、(VIII)および(IX)
R1は各xについて独立に、R2は各yについて独立に、そしてR6は各dについて独立に、いずれの場合にも、水素、ヒドロカルビル、置換ヒドロカルビルおよび−OR7からなる群から独立に選択され、各R7は、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から独立に選択され、R1、R2、R6およびR7の前記ヒドロカルビルおよび置換ヒドロカルビルは、いずれの場合にも、−O−、−S−、−C(O)−、−C(O)O−、−OC(O)O−、−S(O)−、−SO2−、−N(R9)−および−Si(R9)(R10)−の少なくとも1つで独立にかつ任意選択で介在されており、R9およびR10はそれぞれ独立に、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、
各nについて独立にM1、各pについて独立にM2、各fについて独立にM3および各gについて独立にM4は、いずれの場合にも、独立に、以下の式(X)
L1は、いずれの場合にも、単結合;−O−;−S−;−C(O)−;−S(O)−;−SO2−;−N=N−;−N(R11’)−の少なくとも1つからなる群から独立に選択され、R11’は、水素、ヒドロカルビルまたは置換ヒドロカルビル;−Si(OR8’)w(R8’)e−から選択され、wおよびeはそれぞれ独立に0〜2であり、ただし、wとeの合計は2であり、各R8’は、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から独立に選択され;ヒドロカルビルおよび置換ヒドロカルビルはそれぞれ、−O−、−S−、−C(O)−、−C(O)O−、−S(O)−、−SO2−、−N=N−、−N(R11’)−の少なくとも1つで任意選択でかつ独立に介在されており、R11’は、水素、ヒドロカルビルまたは置換ヒドロカルビル、−Si(OR8’)w(R8’)e−からなる群から選択され、wおよびeはそれぞれ独立に0〜2であり、ただし、wとeの合計は2であり、各R8’は、水素、ヒドロカルビルおよび置換ヒドロカルビルならびにそれらの2つまたはそれ超の組合せからなる群から独立に選択され、
tは1〜4であり、
mは、各tについて独立に、0〜8であり、
L2は、各mについて独立に、二価の直鎖状または分枝状C1〜C25アルキル、二価の直鎖状または分枝状C1〜C25ペルハロアルキルおよび二価の直鎖状または分枝状C2〜C25アルケニルからなる群から選択され、いずれの場合にも、−O−、−S−、−C(O)−、−C(O)O−、−OC(O)O−、−S(O)−、−SO2−、−N(R9)−および−Si(R9)(R10)−の少なくとも1つで任意選択で介在されており、R9およびR10はそれぞれ独立に、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、
qは、各tについて独立に、0〜8であり、ただし、mとqの合計は各tについて少なくとも1であり、ただし、qは少なくとも1つのtについて少なくとも1であり、
L3は、各qについて独立に、以下の式(XI−1)
Yは、各qについて独立に、単結合、−O−、−S−、−C(O)−、−C(O)O−、−OC(O)O−、−S(O)−、−SO2−、−N(R9)−、−N(R9)−C(O)−O−、−C(O)−N(R9)−および−Si(R9)(R10)−からなる群から選択される二価連結基であり、R9およびR10はそれぞれ独立に、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、
vおよびuは、各qについてそれぞれ独立に、0〜5から選択され、ただし、vとuの合計は、0より大きい各qについて少なくとも2であり、
Zは、各vについて独立に、単結合、−O−、−S−、−C(O)−、−C(O)O−、−OC(O)O−、−S(O)−、−SO2−、−N(R9)−、−N(R9)−C(O)−O−、−C(O)−N(R9)−および−Si(R9)(R10)−からなる群から選択される二価連結基であり、R9およびR10はそれぞれ独立に、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、
二価の環
E1は、水素、ヒドロカルビル、置換ヒドロカルビルからなる群から選択され、それぞれ、−O−、−S−、−C(O)−、−C(O)O−、−OC(O)O−、−S(O)−、−SO2−、−N(R9)−および−Si(R9)(R10)−の少なくとも1つで任意選択で介在されており、R9およびR10はそれぞれ独立に、水素、ヒドロカルビルおよび置換ヒドロカルビルならびに(メタ)アクリロイルからなる群から選択され、
ただし、L1とL2の間の直接的なL1−L2連結は、互いに連結された2個のヘテロ原子を含まず、L1とL3の間の直接的なL1−L3連結は、互いに連結された2個のヘテロ原子を含まず、それぞれ直接に連結されたL2とL3の間のそれぞれの直接的なL2−L3連結は、互いに連結された2個のヘテロ原子を含まず;
式(I)について、
R3は単結合または−CH2−であり、
xは0〜4であり、
nは0〜4であり、ただし、xとnの合計は4であり、
yは0〜5であり、
pは0〜5であり、ただし、yとpの合計は5であり、
ただし、
nとpの合計は少なくとも1であり、
M1およびM2はそれぞれ、L3および/またはE1がヒドロキシル置換アリール基を含む末端−L3−E1基を含まず、
M1およびM2はそれぞれ、E1がヒドロキシル置換アリール基を含む末端−L2−E1基を含まず、
式(II)について、
xは0〜3であり、
nは1〜4であり、ただし、xとnの合計は4であり、
R4は、水素、ヒドロカルビル、置換ヒドロカルビル、ヘテロアリール、置換ヘテロアリール、−OR8およびM2からなる群から選択され、R8は、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、
式(III)について、
xは0〜4であり、
nは0〜4であり、ただし、xとnの合計は4であり、
gは0〜6であり、ただし、nとgの合計は少なくとも1であり、
環Aは、アリール、置換アリール、ヘテロアリールおよび置換ヘテロアリールからなる群から選択され、
式(IV)について、
xは0〜4であり、
nは1〜4であり、ただし、xとnの合計は4であり、
gは0〜6であり、ただし、nとgの合計は少なくとも1であり、
環Bは、アリール、置換アリール、ヘテロアリールおよび置換ヘテロアリールからなる群から選択され、
Dは、O、SおよびN−R2’からなる群から選択され、R2’は、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、それぞれ、−O−、−S−、−C(O)−、−C(O)O−、−S(O)−、−SO2−、−N=N−、−N(R11’)−の少なくとも1つで任意選択でかつ独立に介在されており、R11’は、水素、ヒドロカルビルまたは置換ヒドロカルビル、−Si(OR8’)w(R8’)e−からなる群から選択され、wおよびeはそれぞれ独立に0〜2であり、ただし、wとeの合計は2であり、各R8’は、水素、ヒドロカルビルおよび置換ヒドロカルビルならびにそれらの2つまたはそれ超の組合せからなる群から独立に選択され、
式(V)について、
xは0〜5であり、
nは0〜5であり、ただし、xとnの合計は5であり、
yは0〜5であり、
pは0〜5であり、ただし、yとpの合計は5であり、
ただし、nとpの合計は少なくとも1であり、
式(VI)について、
xは0〜5であり、
nは0〜5であり、ただし、xとnの合計は5であり、
R5は、水素、ヒドロカルビル、置換ヒドロカルビルおよびM2からなる群から選択され、
R11およびR12はそれぞれ独立に、水素、−CN、−C(O)OR13、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、R13は、水素、ヒドロカルビルおよび置換ヒドロカルビルからなる群から選択され、
ただし、nは少なくとも1であり、かつ/またはR5はM2であり、
式(VII)について、
xは0〜4であり、
nは0〜4であり、ただし、xとnの合計は4であり、
yは0〜5であり、
pは0〜5であり、ただし、yとpの合計は5であり、
dは0〜5であり、
fは0〜5であり、ただし、dとfの合計は5であり、
ただし、n、pおよびfの合計は少なくとも1であり、
式(VIII)について、
xは0〜3であり、
nは1〜4であり、ただし、xとnの合計は4であり、
式(IX)について、
xは0〜3であり、
nは1〜4であり、ただし、xとnの合計は4である)
の少なくとも1つで表される化合物。 - 式(I)、(II)、(III)、(IV)、(V)、(VI)、(VII)、(VIII)および(IX)のそれぞれについて独立に、
R1が各xについて独立に、R2が各yについて独立に、そしてR6が各dについて独立に、いずれの場合にも、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニル、C3〜C12シクロアルキル、C3〜C12ヘテロシクロアルキル、アリール、ヘテロアリールおよび−OR7からなる群から独立に選択され、各R7は、水素、C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニル、C3〜C12シクロアルキル、C3〜C12ヘテロシクロアルキル、アリールおよびヘテロアリールからなる群から独立に選択され、
各式(X)について独立に、かつ、各M1について独立に、各M2について独立に、各M3について独立に、そして各M4について独立に、
mが、少なくとも1つのtについて少なくとも1であり、
L2が、各mについて独立に、二価の直鎖状または分枝状C1〜C25アルキルおよび二価の直鎖状または分枝状C1〜C25ペルハロアルキルからなる群から選択され、いずれの場合にも、−O−、−C(O)O−および−OC(O)O−の少なくとも1つで任意選択で介在されており、
L3が、各qについて独立に、以下の式(XI−2)
E1が、いずれの場合にも、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニルからなる群から独立に選択され、それぞれ、−O−および−C(O)O−の少なくとも1つで任意選択で介在されており;
式(II)について、
R4が、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニル、C3〜C12シクロアルキル、C3〜C12ヘテロシクロアルキル、アリール、ヘテロアリール、−OR8およびM2からなる群から選択され、R8は、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニル、C3〜C12シクロアルキル、C3〜C12ヘテロシクロアルキル、アリールおよびヘテロアリールからなる群から選択され、
式(III)について、
環Aがアリールまたは置換アリールであり、
式(IV)について、
環Bがアリールまたは置換アリールであり、
DのR2’が、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニル、C3〜C12シクロアルキル、C3〜C12ヘテロシクロアルキル、アリールおよびヘテロアリールからなる群から選択され、
式(VI)について、
R5が、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニル、C3〜C12シクロアルキル、C3〜C12ヘテロシクロアルキル、アリール、ヘテロアリールおよびM2からなる群から選択され、
R11が、水素、−CN、−C(O)OR13、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニルおよびC3〜C12シクロアルキルからなる群から選択され、R13は、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニルおよびC3〜C12シクロアルキルからなる群から選択され、
R12が、水素、直鎖状または分枝状C1〜C25アルキル、直鎖状または分枝状C2〜C25アルケニルおよびC3〜C12シクロアルキルからなる群から選択される、請求項1に記載の化合物。 - 式(I)、(II)、(III)、(IV)、(V)、(VI)、(VII)、(VIII)および(IX)のそれぞれについて独立に、
R1が各xについて独立に、R2が各yについて独立に、そしてR6が各dについて独立に、いずれの場合にも、水素、直鎖状または分枝状C1〜C10アルキルおよび−OR7からなる群から独立に選択され、各R7は、水素および直鎖状または分枝状C1〜C10アルキルからなる群から独立に選択され、
各式(X)について独立に、かつ、各M1について独立に、各M2について独立に、各M3について独立に、そして各M4について独立に、
L2が、各mについて独立に、二価の直鎖状または分枝状C1〜C10アルキルおよび二価の直鎖状または分枝状C1〜C10ペルフルオロアルキルからなる群から選択され、いずれの場合にも、−O−、−C(O)O−および−OC(O)O−の少なくとも1つで任意選択で介在されており、
各L3について独立に、
Zが、各vについて独立に、単結合、−O−および−C(O)O−からなる群から選択され、
二価の環
E1が、いずれの場合にも、水素、ならびに−O−および−C(O)O−の少なくとも1つで任意選択で介在されている直鎖状または分枝状C1〜C10アルキルからなる群から独立に選択され;
式(II)について、
R4が、水素、直鎖状または分枝状C1〜C10アルキル、−OR8およびM2からなる群から選択され、R8は、水素および直鎖状または分枝状C1〜C10アルキルからなる群から選択され、
式(III)について、
環Aがフェニルであり、
gが0〜4であり、ただし、nとgの合計は少なくとも1であり、
式(IV)について、
環Bがフェニルであり、
DのR2’が、水素および直鎖状または分枝状C1〜C10アルキルからなる群から選択され、
gが0〜4であり、ただし、nとgの合計は少なくとも1であり、
式(VI)について、
R5が、水素、直鎖状または分枝状C1〜C10アルキルおよびM2からなる群から選択され、
R11が、水素、−CN、−C(O)OR13および直鎖状または分枝状C1〜C10アルキルからなる群から選択され、R13は、水素および直鎖状または分枝状C1〜C10アルキルからなる群から選択され、
R12が、水素および直鎖状または分枝状C1〜C10アルキルからなる群から選択される、請求項2に記載の化合物。 - 二価の環(C)および二価の環(D)の少なくとも1つが、それぞれ独立に、二価アリール、置換二価アリール、二価ヘテロアリールおよび置換二価ヘテロアリールからなる群から選択される、請求項1に記載の化合物。
- 二価の環(C)および二価の環(D)の少なくとも1つが、それぞれ独立に、フェニレン−1,4−ジイル、置換フェニレン−1,4−ジイル、ピリミジン−2,5−ジイル、置換ピリミジン−2,5−ジイル、ピリジン−2,5−ジイル、置換ピリジン−2,5−ジイル、ナフタレン−2,6−ジイル、置換ナフタレン−2,6−ジイルおよびフェナントレン−2,7−ジイルからなる群から選択される、請求項2に記載の化合物。
- 少なくとも1つの二価の環(C)および少なくとも1つの二価の環(D)が、それぞれ独立に、フェニレン−1,4−ジイルおよび置換フェニレン−1,4−ジイルからなる群から選択される、請求項3に記載の化合物。
- 式(I)について、
nとpの合計が1であり、
式(II)について、
nが1であり、
R4が、水素、直鎖状または分枝状C1〜C10アルキルおよび−OR8からなる群から選択され、R8は、水素および直鎖状または分枝状C1〜C10アルキルからなる群から選択され、
式(III)について、
nとgの合計が1であり、
式(IV)について、
nとgの合計が1であり、
式(V)について、
nとpの合計が1であり、
式(VI)について、
nが1であり、
R5が、水素および直鎖状または分枝状C1〜C10アルキルからなる群から選択され、
式(VII)について、
n、pおよびfの合計が1であり、
式(VIII)について、
nが1であり、
式(IX)について、
nが1である、
請求項3に記載の化合物。 - 少なくとも1つのL3が独立にメソゲン基であり、前記化合物がメソゲン化合物である、請求項1に記載の化合物。
- 前記化合物がメソゲン紫外線吸収性化合物である、請求項9に記載の化合物。
- 請求項1に記載の化合物を含む組成物。
- (i)フォトクロミック化合物、(ii)二色性化合物、(iii)フォトクロミック−二色性化合物および(iv)固定ティントの少なくとも1つをさらに含む、請求項11に記載の組成物。
- 液晶材料をさらに含む、請求項11に記載の組成物。
- 請求項1に記載の化合物を含む製造物品。
- 前記製造物品が、
光学的基材;および
前記光学的基材の表面の少なくとも一部の上にある層
を含む光学素子であり、前記層が請求項1に記載の化合物を含む、請求項14に記載の製造物品。 - 前記層が、前記層の少なくとも一部を、磁場、電場、直線偏光した放射線およびせん断力の少なくとも1つに曝露することによって少なくとも部分的に配列されている、請求項15に記載の光学素子。
- 前記層が、ネマチック相、スメクチック相およびキラルネマチック相の少なくとも1つを有する液晶相を含む、請求項15に記載の光学素子。
- 前記層が、プライマー層、保護層、フォトクロミック層、配列層および反射防止層から選択される、請求項15に記載の光学素子。
- 少なくとも1つのさらなる層をさらに含み、さらなる層が各々、プライマー層、保護層、フォトクロミック層、配列層および反射防止層から独立に選択される、請求項15に記載の光学素子。
- 前記光学素子が眼用素子、表示素子、ウィンドウ、ミラーおよび液晶セル素子からなる群から選択される、請求項15に記載の光学素子。
- 前記眼用素子が、矯正レンズ、非矯正レンズ、コンタクトレンズ、眼内レンズ、拡大レンズ、保護レンズおよびバイザーからなる群から選択される、請求項20に記載の光学素子。
- 前記層がフォトクロミック−二色性化合物をさらに含み、前記層がフォトクロミック層である、請求項15に記載の光学素子。
- 前記フォトクロミック−二色性化合物がフォトクロミック化合物の残基を含み、
前記フォトクロミック化合物が、インデノ縮合ナフトピラン、ナフト[1,2−b]ピラン、ナフト[2,1−b]ピラン、スピロフルオロエノ[1,2−b]ピラン、フェナントロピラン、キノリノピラン、フルオロアンテノピラン、スピロピラン、ベンゾオキサジン、ナフトオキサジン、スピロ(インドリン)ナフトオキサジン、スピロ(インドリン)ピリドベンゾオキサジン、スピロ(インドリン)フルオランテノオキサジン、スピロ(インドリン)キノキサジン、フルジド、フルジミド、ジアリールエテン、ジアリールアルキルエテン、ジアリールアルケニルエテン、熱的に可逆性のフォトクロミック化合物および非熱的に可逆性のフォトクロミック化合物からなる群から選択される、請求項22に記載の光学素子。 - 前記層が固定ティントをさらに含み、前記層が二色性層である、請求項15に記載の光学素子。
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JP6935462B2 (ja) | 2021-09-15 |
EP3201292A1 (en) | 2017-08-09 |
MX368296B (es) | 2019-09-27 |
EP3201292B1 (en) | 2018-08-01 |
KR102563675B1 (ko) | 2023-08-04 |
KR102474637B1 (ko) | 2022-12-05 |
CA2962919C (en) | 2024-01-02 |
JP2019194260A (ja) | 2019-11-07 |
CN107109227A (zh) | 2017-08-29 |
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AU2015324313A1 (en) | 2017-04-13 |
BR112017006502B1 (pt) | 2022-10-11 |
AU2015324313B2 (en) | 2018-11-15 |
KR20220108826A (ko) | 2022-08-03 |
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US20170275534A1 (en) | 2017-09-28 |
KR20220108825A (ko) | 2022-08-03 |
JP2019194259A (ja) | 2019-11-07 |
CA2962919A1 (en) | 2016-04-07 |
MX2017004136A (es) | 2017-09-07 |
CN107109227B (zh) | 2021-05-04 |
US10619098B2 (en) | 2020-04-14 |
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