JP2013529375A - 有機電子デバイスを作製するための組成物および方法 - Google Patents
有機電子デバイスを作製するための組成物および方法 Download PDFInfo
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- JP2013529375A JP2013529375A JP2013504153A JP2013504153A JP2013529375A JP 2013529375 A JP2013529375 A JP 2013529375A JP 2013504153 A JP2013504153 A JP 2013504153A JP 2013504153 A JP2013504153 A JP 2013504153A JP 2013529375 A JP2013529375 A JP 2013529375A
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Abstract
Description
a)上記および下記の組成物を基板上に堆積させて、膜または層を形成するステップと、
b)溶媒を除去するステップと
を含む方法に関する。
nは、1より大きい整数であり、好ましくは10〜1,000であり、
Rは、出現する毎に、同一または異なり、H、F、Cl、Br、I、CN、1〜40個のC原子を有する直鎖状、分枝状もしくは環状アルキル基(ここで、1個以上のC原子は、O原子および/またはS原子が互いに直接連結されないように、O、S、O−CO、CO−O、O−CO−O、CR0=CR0もしくはC≡Cで任意に置きかえられていてもよい)(また、ここで、1個以上のH原子は、F、Cl、Br、IもしくはCNで任意に置きかえられていてもよい)を示すか、または無置換もしくは1つ以上の非芳香族基Rsで置換されている、4〜20個の環原子を有するアリールもしくはヘテロアリール基を示し、ここで、1つ以上の基Rは、相互におよび/またはそれらが結合する環と共に、単環式または多環式の脂肪族または芳香族環系を形成していてもよく、
Rsは、出現する毎に、同一または異なり、F、Cl、Br、I、CN、Sn(R00)3、Si(R00)3またはB(R00)2、1〜25個のC原子を有する直鎖状、分枝状もしくは環状アルキル基(ここで、1個以上のC原子は、O原子および/またはS原子が互いに直接連結されないように、O、S、O−CO、CO−O、O−CO−O、CR0=CR0、C≡Cで任意に置きかえられていてもよい)(また、ここで、1個以上のH原子は、F、Cl、Br、IもしくはCNで任意に置きかえられていてもよい)を示すか、またはRsは、無置換もしくは1つ以上の非芳香族基Rsで置換されている、4〜20個の環原子を有するアリールもしくはヘテロアリール基を示し、ここで、1つ以上の基Rsは、相互におよび/またはRと共に、環系を形成していてもよく、
R0は、出現する毎に、同一または異なり、H、F、Cl、CN、1〜12個のC原子を有するアルキルまたは4〜10個の環原子を有するアリールもしくはヘテロアリールを示し、
R00は、出現する毎に、同一または異なり、Hまたは1〜20個のC原子を有する脂肪族もしくは芳香族炭化水素基を示し、ここで、2つの基R00は、それらが結合するヘテロ原子(Sn、SiまたはB)と一緒になって環を形成していてもよく、
rは、0、1、2、3または4であり、
sは、0、1、2、3、4または5であり、
式中、式P1〜P5のRは、好ましくは、Hとは異なる。
ここで、R1とR2、R2とR3、R3とR4、R7とR8、R8とR9、R9とR10の各対は独立に、任意に架橋されて、C4〜C40飽和または不飽和環を形成していてもよく、その飽和または不飽和環は、酸素原子、硫黄原子、または式−N(Ra)−の基(ここで、Raは、水素原子または炭化水素基である)が任意に介在していてもよいか、あるいは任意に置換されていてもよく、
ここで、当該ポリアセン骨格の1個以上の炭素原子は、N、P、As、O、S、SeおよびTeから選択されるヘテロ原子によって、任意に置換されていてもよく、
ここで、ポリアセンの隣接する環の位置にある置換基R1〜R12のいずれか2つ以上は、独立に、一緒になって、O、S、または−N(Ra)(ここで、Raは、上に規定した通りである)が任意に介在していてもよいさらなるC4〜C40飽和もしくは不飽和環、またはポリアセンと縮合した芳香族環系を任意に構成していてもよく、
ここで、nは、0、1、2、3または4であり、好ましくは、nは、0、1または2であり、最も好ましくは、nは、0または2であり、これはポリアセン化合物が、ペンタセン化合物(n=2の場合)、または「擬似ペンタセン」化合物(n=0の場合)であることを意味する。
ここで、R1とR2、R2とR3、R3とR4、R7とR8、R8とR9、R9とR10、R15とR16、およびR16とR17の各対は独立に、任意に相互に架橋されて、C4〜C40飽和または不飽和環を形成していてもよく、その飽和または不飽和環は、酸素原子、硫黄原子または式−N(Ra)−の基(ここで、Raは、水素原子または炭化水素基である)が任意に介在しているか、あるいは任意に置換されていてもよく、
ここで、当該ポリアセン骨格の1個以上の炭素原子は、N、P、As、O、S、SeおよびTeから選択されるヘテロ原子で任意に置換されていてもよい。
ここで、R2とR3、R8とR9、R15とR16、およびR16とR17の各対は、独立に、任意に相互に架橋されて、C4〜C40飽和または不飽和環を形成していてもよく、その飽和または不飽和環は、酸素原子、硫黄原子、または式−N(Ra)−の基(ここで、Raは、水素原子または炭化水素基である)が任意に介在し、また、任意に置換されていてもよく、
ここで、ポリアセン骨格の1個以上の炭素原子は、N、P、As、O、S、SeおよびTeから選択されるヘテロ原子によって、任意に置換されていてもよい。
Y1およびY2の一方が、−CH=または=CH−を示し、他方が、−X−を示し、
Y3およびY4の一方が、−CH=または=CH−を示し、他方が、−X−を示し、
Xは、−O−、−S−、−Se−または−NR’’’−であり、
R’は、H、F、Cl、Br、I、CN、1〜20個、好ましくは1〜8個のC原子を有し、任意にフッ素化またはペルフルオロ化されていてもよい直鎖状もしくは分枝状のアルキルもしくはアルコキシ、6〜30個のC原子を有し、任意にフッ素化またはペルフルオロ化されていてもよいアリール、好ましくはC6F5、またはCO2R’’’’(R’’’’は、H、1〜20個のC原子を有する、任意にフッ素化されていてもよいアルキル、または2〜30個、好ましくは5〜20個のC原子を有する、任意にフッ素化されていてもよいアリールである)であり、
R’’は、複数存在する場合、相互に独立に、1〜20個、好ましくは1〜8個のC原子を有する環状、直鎖状、もしくは分枝状のアルキルもしくはアルコキシ、または2〜30個のC原子を有するアリールであり、それらはすべて、任意にフッ素化またはペルフルオロ化されていてもよく、SiR’’3は、好ましくは、トリアルキルシリルであり、
R’’’は、H、または1〜10個のC原子を有する環状、直鎖状、もしくは分枝状のアルキル、好ましくはHであり、
mは、0または1であり、
oは、0または1である。
DCyは、出現する毎に、同一または異なり、少なくとも1つのドナー原子、好ましくは、窒素、カルベンの形態の炭素またはリンを含有する環状基であり、該環状基は前記ドナー原子を介して当該金属に結合し、さらに、1つ以上の置換基R18を有していてもよく;基DCyおよびCCyは、共有結合を介して相互に接続され;
CCyは、出現する毎に、同一または異なり、炭素原子を含有する環状基であり、該環状基は前記炭素原子を介して当該金属に結合し、さらに、1つ以上の置換基R18を有していてもよく;
Aは、出現する毎に、同一または異なり、モノアニオン性二座キレート配位子、好ましくはジケトナート配位子であり;
R18は、各場合において同一または異なり、F、Cl、Br、I、NO2、CN、1〜20個の炭素原子を有する直鎖状、分枝状もしくは環状のアルキルもしくはアルコキシ基(ここで、1つ以上の非隣接CH2基は、−O−、−S−、−NR19−、−CONR19−、−CO−O−、−C=O−、−CH=CH−または−C≡C−で置きかえられていてもよい)(また、ここで、1個以上の水素原子は、Fで置きかえられていてもよい)、または4〜14個の炭素原子を有し、1つ以上の非芳香族R18ラジカルで置換されていてもよいアリールもしくはヘテロアリール基であり、同じ環上または2つの異なる環上の複数の置換基R18は、一緒になって、さらに、単環式または多環式の脂肪族または芳香族環系を形成していてもよく;
R19は、各場合において同一または異なり、1〜20個の炭素原子を有する直鎖状、分枝状もしくは環状のアルキルもしくはアルコキシ基(ここで、1つ以上の非隣接CH2基は、−O−、−S−、−CO−O−、−C=O−、−CH=CH−または−C≡C−で置きかえられていてもよい)(また、ここで、1個以上の水素原子は、Fで置き換えられていてもよい)、または4〜14個の炭素原子を有し、1つ以上の非芳香族R18ラジカルで置換されていてもよいアリールもしくはヘテロアリール基である。
− 任意に、基板(1)と、
− ゲート電極(2)と、
− 誘電材料を含む絶縁層(3)と、
− OSC層(4)と
− ソースおよびドレイン電極(5)と、
− 任意に、1つ以上の保護またはパッシベーション層(6)と
を含む。
− それらのうちの1つが透明である、低仕事関数電極(31)(例えば、アルミニウムなどの金属)および高仕事関数電極(32)(例えば、ITO)と、
− 電極(31、32)の間に配置される、好ましくはOSC材料から選択される正孔輸送材料および電子輸送材料を含む層(33)(「アクティブ層」とも言う)であって、例えば、p型およびn型半導体の二重層もしくは2つの別個の層、またはブレンドもしくは混合物として存在し得る、層(33)と、
− 高仕事関数電極の仕事関数を変更して、正孔のためのオーミック接触を与えるために、アクティブ層(33)と高仕事関数電極(32)の間に配置される、例えば、PEDOT:PSS(ポリ(3,4−エチルレンジオキシチオフェン):ポリ(スチレンスルホネート))のブレンドを含む、任意に導電性ポリマー層(34)と、
− 電子のためのオーミック接触を与えるための、低仕事関数電極(31)のアクティブ層(33)に面している面での、(例えば、LiFの)任意にコーティング(35)と
を好ましくは含む。
− それらのうちの1つが透明である、低仕事関数電極(41)(例えば、金などの金属)および高仕事関数電極(42)(例えば、ITO)と、
− 電極(41、42)の間に配置される、好ましくはOSC材料から選択される正孔輸送材料および電子輸送材料を含む層(43)(「アクティブ層」とも言う)であって、例えば、p型およびn型半導体の二重層もしくは2つの別個の層、またはブレンドまたは混合物として存在し得る、層(43)と、
− 電子のためのオーミック接触を与えるために、アクティブ層(43)と低仕事関数電極(41)の間に配置される、例えば、PEDOT:PSSのブレンドを含む、任意に導電性ポリマー層(44)と、
− 正孔のためのオーミック接触を与えるための、高仕事関数電極(42)のアクティブ層(43)に面している面での、(例えば、TiOxの)任意にコーティング(45)と
を好ましくは含む。
例1
基板(PEDOTでコーティングした2cm2ガラスプレート)を、180℃で10分間加熱することにより活性化させて、直接使用した。
例1を繰り返した。しかし、例1で述べた1%OLEDポリマーを、溶媒を80℃に加熱することにより、2−メチルナフタレン、ペンタメチルベンゼン、および1,5−ジメチルナフタレンそれぞれに溶解した。
例1を繰り返した。しかし、例1で述べた1%OLEDポリマーを、溶媒を85℃に加熱することにより、1,2,4,5−テトラメチルベンゼンに溶解した。
基板(PEDOTでコーティングした2cm2ガラスプレート)を、180℃で10分間加熱することにより活性化させて、直接使用した。
例6で述べた通りの、式107による燐光性化合物と、式147を有するホスト材料とを、1:4の重量比で含む混合物を、高温下(一般に、溶媒の融点を10℃上回る)で、2−メチルナフタレン、1,5−ジメチルナフタレン(1,5−DMN)、5−インダノール、1,2,3,4−テトラヒドロ−1−ナフトール、5,6,7,8−テトラヒドロ−2−ナフトール、2−エトキシナフタレン、2−インダノール、スルホラン、ビフェニル、および1,2,4,5−テトラメチルベンゼンに溶解した。溶媒中の化合物107と147の両方の濃度は、約1重量%であった。
例6で述べた通りの、式107による燐光性化合物と、式147を有するホスト材料とを、1:4の重量比で含む混合物を、高温下(一般に、溶媒の融点を10℃上回る)で、1:1のビフェニル:1,5−DMN、1:1のビフェニル:1,2,4,5−テトラメチルベンゼン、2−メチルナフタレン、および2−エトキシナフタレンに溶解した。溶媒中の化合物107と147の両方の濃度は、約1重量%であった。
Corning Eagle XGガラスを、超音波メタノール浴中で、2分間洗浄し、次いで、メタノールですすいだ。約40nm厚の銀ゲート電極を蒸発させた。誘電材料であるLisicon(商標)D207(Merck KGaAから入手可能)のUV硬化性誘電層を、デバイス上のOSC層の上で回転させ、120℃で、1分間アニーリングすると、約1ミクロン厚の乾燥誘電膜が得られた。次いで、誘電層を、365nm波長で、全UV量2.6Jcm-2下でのUV硬化によって架橋した。
Claims (17)
- 1種以上の有機半導体化合物(OSC)と、1種以上の有機溶媒とを含む組成物であって、前記組成物は、25℃の温度では固体であり、より高い温度、好ましくは200℃では流体であり、前記溶媒の沸点は、400℃以下であることを特徴とする組成物。
- 前記組成物は、最も高い沸点を有する前記溶媒の融点より10℃高い温度で、25mN/m〜45mN/mの範囲の表面張力を構成することを特徴とする、請求項1に記載の組成物。
- 前記組成物は、最も高い沸点を有する前記溶媒の融点より10℃高い温度で、0.25〜100mPasの範囲の粘度を構成することを特徴とする、請求項1または2に記載の組成物。
- 前記有機溶媒は、芳香族および/またはヘテロ芳香族化合物、好ましくは、ナフタレン化合物、ベンゼン化合物、ピリジン化合物、ピラジン化合物または少なくとも120g/molの分子量を有するピラゾール化合物を含むことを特徴とする、請求項1〜3のいずれか1項に記載の組成物。
- 前記溶媒は混合物であり、好ましくは、少なくともベンゼン化合物、ナフタレン化合物、スルホラン化合物、スルホン化合物またはアルコール化合物を含むものであることを特徴とする、請求項1〜4のいずれか1項に記載の組成物。
- 前記組成物は、少なくとも1種の不活性バインダーを含むことを特徴とする請求項1〜5のいずれか1項に記載の組成物。
- 前記有機半導体化合物は、有機発光材料および/または電荷輸送材料であることを特徴とする請求項1〜6のいずれか1項に記載の組成物。
- 前記有機半導体化合物は、下式から選択される化合物であることを特徴とする請求項1〜7のいずれか1項に記載の組成物:
nは、1より大きい整数であり、好ましくは10〜1,000であり、
Rは、出現する毎に、同一または異なり、H、F、Cl、Br、I、CN、1〜40個のC原子を有する直鎖状、分枝状もしくは環状アルキル基(ここで、1個以上のC原子は、O原子および/またはS原子が互いに直接連結されないように、O、S、O−CO、CO−O、O−CO−O、CR0=CR0もしくはC≡Cで任意に置きかえられていてもよい)(また、ここで、1個以上のH原子は、F、Cl、Br、IもしくはCNで任意に置きかえられていてもよい)を示すか、または無置換もしくは1つ以上の非芳香族基Rsで置換されている、4〜20個の環原子を有するアリールもしくはヘテロアリール基を示し、ここで、1つ以上の基Rは、相互におよび/またはそれらが結合する環と共に、単環式または多環式の脂肪族または芳香族環系を形成していてもよく、
Rsは、出現する毎に、同一または異なり、F、Cl、Br、I、CN、Sn(R00)3、Si(R00)3またはB(R00)2、1〜25個のC原子を有する直鎖状、分枝状もしくは環状アルキル基(ここで、1個以上のC原子は、O原子および/またはS原子が互いに直接連結されないように、O、S、O−CO、CO−O、O−CO−O、CR0=CR0、C≡Cで任意に置きかえられていてもよい)(また、ここで、1個以上のH原子は、F、Cl、Br、IもしくはCNで任意に置きかえられていてもよい)を示すか、またはRsは、無置換もしくは1つ以上の非芳香族基Rsで置換されている、4〜20個の環原子を有するアリールもしくはヘテロアリール基を示し、ここで、1つ以上の基Rsは、相互におよび/またはRと共に、環系を形成していてもよく、
R0は、出現する毎に、同一または異なり、H、F、Cl、CN、1〜12個のC原子を有するアルキルまたは4〜10個の環原子を有するアリールもしくはヘテロアリールを示し、
R00は、出現する毎に、同一または異なり、Hまたは1〜20個のC原子を有する脂肪族もしくは芳香族炭化水素基を示し、ここで、2つの基R00は、それらが結合するヘテロ原子(Sn、SiまたはB)と一緒になって環を形成していてもよく、
rは、0、1、2、3または4であり、
sは、0、1、2、3、4または5である。 - 前記有機半導体化合物は、下式の化合物であることを特徴とする、請求項1〜7のいずれか1項に記載の組成物:
ここで、R1とR2、R2とR3、R3とR4、R7とR8、R8とR9、R9とR10、R15とR16、およびR16とR17の各対は独立に、任意に相互に架橋されて、C4〜C40飽和または不飽和環を形成していてもよく、その飽和または不飽和環は、酸素原子、硫黄原子または式−N(Ra)−の基(ここで、Raは、水素原子または炭化水素基である)が任意に介在していてもよいか、あるいは任意に置換されていてもよく、
ここで、当該ポリアセン骨格の1個以上の炭素原子は、N、P、As、O、S、SeおよびTeから選択されるヘテロ原子で任意に置換されていてもよい。 - 前記有機半導体化合物は、発光し、加えて、38より大きい原子番号を有する少なくとも1つの原子を含有する有機燐光性化合物であることを特徴とする、請求項1〜7のいずれか1項に記載の組成物。
- 前記燐光性化合物は、式(1)〜(4)の化合物であることを特徴とする請求項10に記載の組成物:
DCyは、出現する毎に、同一または異なり、少なくとも1つのドナー原子、好ましくは、窒素、カルベンの形態の炭素またはリンを含有する環状基であり、該環状基は前記ドナー原子を介して当該金属に結合し、さらに、1つ以上の置換基R18を有していてもよく;基DCyおよびCCyは、共有結合を介して相互に接続され;
CCyは、出現する毎に、同一または異なり、炭素原子を含有する環状基であり、該環状基は前記炭素原子を介して当該金属に結合し、さらに、1つ以上の置換基R18を有していてもよく;
Aは、出現する毎に、同一または異なり、モノアニオン性二座キレート配位子、好ましくはジケトナート配位子であり;
R18は、各場合において同一または異なり、F、Cl、Br、I、NO2、CN、1〜20個の炭素原子を有する直鎖状、分枝状もしくは環状のアルキルもしくはアルコキシ基(ここで、1つ以上の非隣接CH2基は、−O−、−S−、−NR19−、−CONR19−、−CO−O−、−C=O−、−CH=CH−または−C≡C−で置きかえられていてもよい)(また、ここで、1個以上の水素原子は、Fで置きかえられていてもよい)、または4〜14個の炭素原子を有し、1つ以上の非芳香族R18ラジカルで置換されていてもよいアリールもしくはヘテロアリール基であり、同じ環上または2つの異なる環上の複数の置換基R18は、一緒になって、さらに、単環式または多環式の脂肪族または芳香族環系を形成していてもよく;
R19は、各場合において同一または異なり、1〜20個の炭素原子を有する直鎖状、分枝状もしくは環状のアルキルもしくはアルコキシ基(ここで、1つ以上の非隣接CH2基は、−O−、−S−、−CO−O−、−C=O−、−CH=CH−または−C≡C−で置きかえられていてもよい)(また、ここで、1個以上の水素原子は、Fで置き換えられていてもよい)、または4〜14個の炭素原子を有し、1つ以上の非芳香族R18ラジカルで置換されていてもよいアリールもしくはヘテロアリール基である。 - 前記組成物は、ホスト材料を含むことを特徴とする請求項1〜11のいずれか1項に記載の組成物。
- 前記組成物は、少なくとも1種の湿潤剤を含むことを特徴とする請求項1〜12のいずれか1項に記載の組成物。
- OEデバイスの作製のためのコーティング用または印刷用インクとしての、請求項1〜13のいずれか1項に記載の組成物の使用。
- 有機電子(OE)デバイスを作製する方法であって、
a)請求項1〜13のいずれか1項に記載の組成物を基板上に堆積させて、膜または層を形成するステップと、
b)前記溶媒を除去するステップと
を含む方法。 - 請求項1〜13のいずれか1項に記載の組成物から、または請求項15に記載の方法によって作製されるOEデバイス。
- 前記OEデバイスは、有機発光ダイオード(OLED)、有機電界効果トランジスタ(OFET)または有機光電変換(OPV)デバイスであることを特徴とする、請求項16に記載のOEデバイス。
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018519616A (ja) * | 2015-03-30 | 2018-07-19 | メルク パテント ゲーエムベーハー | シロキサン溶媒を含む有機機能性材料の調合物 |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20170091788A (ko) * | 2009-12-23 | 2017-08-09 | 메르크 파텐트 게엠베하 | 중합체성 결합제를 포함하는 조성물 |
WO2011128034A1 (en) * | 2010-04-12 | 2011-10-20 | Merck Patent Gmbh | Composition having improved performance |
EP2576724B1 (en) * | 2010-05-27 | 2019-04-24 | Merck Patent GmbH | Method for preparation of organic electronic devices |
US8906752B2 (en) | 2011-09-16 | 2014-12-09 | Kateeva, Inc. | Polythiophene-containing ink compositions for inkjet printing |
US20150155494A1 (en) * | 2012-07-13 | 2015-06-04 | Merck Patent Gmbh | Organic electronic device comprising an organic semiconductors formulation |
JP6225413B2 (ja) * | 2012-11-16 | 2017-11-08 | セイコーエプソン株式会社 | 機能層形成用インク、インク容器、吐出装置、機能層の形成方法、有機el素子の製造方法 |
WO2014101981A1 (en) * | 2012-12-28 | 2014-07-03 | Merck Patent Gmbh | Composition comprising polymeric organic semiconducting compounds |
CN104282834B (zh) * | 2013-07-07 | 2019-06-14 | 潘才法 | 一种组合物及其在有机电子器件中的应用 |
WO2015023302A1 (en) | 2013-08-12 | 2015-02-19 | Kateeva, Inc. | Ester-based solvent systems for printable organic light-emitting diode ink formulations |
EP3183757B1 (en) * | 2014-08-18 | 2022-05-04 | CLAP Co., Ltd. | Organic semiconductor composition comprising liquid medium |
WO2016076213A1 (ja) * | 2014-11-13 | 2016-05-19 | 住友化学株式会社 | インク組成物およびそれを用いて製造した光電変換素子 |
CN105038408B (zh) * | 2015-08-14 | 2020-01-07 | 广州华睿光电材料有限公司 | 印刷油墨及应用其印刷而成的电子器件 |
US10875957B2 (en) * | 2015-11-11 | 2020-12-29 | The Regents Of The University Of California | Fluorine substitution influence on benzo[2,1,3]thiodiazole based polymers for field-effect transistor applications |
EP3390549B1 (en) * | 2015-12-16 | 2022-06-29 | Merck Patent GmbH | Formulations containing a solid solvent |
KR102685722B1 (ko) * | 2015-12-16 | 2024-07-16 | 메르크 파텐트 게엠베하 | 유기 기능성 재료의 잉크 조성물 |
US11473929B2 (en) * | 2017-03-16 | 2022-10-18 | Ford Global Technologies, Llc | Vehicle event identification |
EP3454373A1 (en) | 2017-09-11 | 2019-03-13 | Siemens Healthcare GmbH | Optoelectronic device with spray coated organic semiconductor based photoactive layer with reduced defective pixels and improved morphology |
CN112662287B (zh) * | 2020-12-24 | 2021-11-30 | 湖南梵鑫科技有限公司 | 一种附着力好的电子披覆胶及其制备方法 |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000059267A1 (fr) * | 1999-03-29 | 2000-10-05 | Seiko Epson Corporation | Composition, procede de preparation d'un film, et element fonctionnel et son procede de preparation |
JP2006128256A (ja) * | 2004-10-27 | 2006-05-18 | Konica Minolta Holdings Inc | 有機薄膜トランジスタの製造方法及び該製造方法で作製した有機薄膜トランジスタ |
JP2006156824A (ja) * | 2004-11-30 | 2006-06-15 | Seiko Epson Corp | 発光材料及び有機el装置とその製造方法 |
JP2006523740A (ja) * | 2003-04-15 | 2006-10-19 | メルク・オーエルイーディー・マテリアルス・ゲーエムベーハー | 発光可能な、マトリックス材料と有機半導体との混合物、その使用、ならびに前記混合物を含む電子部品 |
JP2007258724A (ja) * | 2006-03-24 | 2007-10-04 | Merck Patent Gmbh | 有機半導性配合体 |
JP2008303365A (ja) * | 2007-06-11 | 2008-12-18 | Toppan Printing Co Ltd | 蛍光材料、発光インク組成物および有機el素子 |
WO2009109273A1 (en) * | 2008-03-06 | 2009-09-11 | Merck Patent Gmbh | Organic semiconductor formulation |
WO2009122870A1 (ja) * | 2008-03-31 | 2009-10-08 | 住友化学株式会社 | 有機エレクトロルミネッセンス素子の製造方法、有機エレクトロルミネッセンス素子および表示装置 |
JP2009536981A (ja) * | 2006-05-12 | 2009-10-22 | メルク パテント ゲーエムベーハー | インデノフルオレンポリマー系有機半導体材料 |
Family Cites Families (141)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4780536A (en) | 1986-09-05 | 1988-10-25 | The Ohio State University Research Foundation | Hexaazatriphenylene hexanitrile and its derivatives and their preparations |
EP0443861B2 (en) | 1990-02-23 | 2008-05-28 | Sumitomo Chemical Company, Limited | Organic electroluminescence device |
US5061569A (en) | 1990-07-26 | 1991-10-29 | Eastman Kodak Company | Electroluminescent device with organic electroluminescent medium |
US5679757A (en) | 1990-12-12 | 1997-10-21 | The Regents Of The University Of California | Highly organic solvent soluble, water insoluble electroluminescent polyphenylene vinylenes having pendant steroid groups and products and uses thereof |
DE4111878A1 (de) | 1991-04-11 | 1992-10-15 | Wacker Chemie Gmbh | Leiterpolymere mit konjugierten doppelbindungen |
JPH061973A (ja) | 1992-06-18 | 1994-01-11 | Konica Corp | 有機エレクトロルミネッセンス素子 |
US5331183A (en) | 1992-08-17 | 1994-07-19 | The Regents Of The University Of California | Conjugated polymer - acceptor heterojunctions; diodes, photodiodes, and photovoltaic cells |
US5965241A (en) | 1993-08-25 | 1999-10-12 | Polaroid Corp | Electroluminescent devices and processes using polythiophenes |
DE4331401A1 (de) | 1993-09-15 | 1995-03-16 | Hoechst Ag | Verwendung von Polymeren mit isolierten Chromophoren als Elektrolumineszenzmaterialen |
DE69432054T2 (de) | 1993-09-29 | 2003-10-09 | Idemitsu Kosan Co | Organische elektrolumineszenzelemente und arylendiaminderivate |
DE69412567T2 (de) | 1993-11-01 | 1999-02-04 | Hodogaya Chemical Co., Ltd., Tokio/Tokyo | Aminverbindung und sie enthaltende Elektrolumineszenzvorrichtung |
EP0676461B1 (de) | 1994-04-07 | 2002-08-14 | Covion Organic Semiconductors GmbH | Spiroverbindungen und ihre Verwendung als Elektrolumineszenzmaterialien |
EP0681019B1 (en) | 1994-04-26 | 1999-09-01 | TDK Corporation | Phenylanthracene derivative and organic EL element |
DE4422670A1 (de) | 1994-06-30 | 1996-01-04 | Hoechst Ag | Konjugierte Polymere mit Ansateilstrukturen und ihre Verwendung als Elektrolumineszenzmaterialien |
DE4431039A1 (de) | 1994-09-01 | 1996-03-07 | Hoechst Ag | Poly(4,5,9,10-tetrahydropyren-2,7-diyl)-Derivate und ihre Verwendung als Elektrolumineszenzmaterialien |
DE4436773A1 (de) | 1994-10-14 | 1996-04-18 | Hoechst Ag | Konjugierte Polymere mit Spirozentren und ihre Verwendung als Elektrolumineszenzmaterialien |
DE4442052A1 (de) | 1994-11-25 | 1996-05-30 | Hoechst Ag | Konjugierte Polymere mit Hetero-Spiroatomen und ihre Verwendung als Elektrolumineszenzmaterialien |
WO1997005184A1 (en) | 1995-07-28 | 1997-02-13 | The Dow Chemical Company | 2,7-aryl-9-substituted fluorenes and 9-substituted fluorene oligomers and polymers |
DE19614971A1 (de) | 1996-04-17 | 1997-10-23 | Hoechst Ag | Polymere mit Spiroatomen und ihre Verwendung als Elektrolumineszenzmaterialien |
PL326841A1 (en) | 1995-12-01 | 1998-10-26 | Ciba Geigy Ag | Poly (9,9'-spirodiffluorenes), their production and application |
DE19606511A1 (de) | 1996-02-22 | 1997-09-04 | Hoechst Ag | Teilkonjugierte Polymere mit Spirozentren und ihre Verwendung als Elektrolumineszenzmaterialien |
DE19652261A1 (de) | 1996-12-16 | 1998-06-18 | Hoechst Ag | Arylsubstituierte Poly(p-arylenvinylene), Verfahren zur Herstellung und deren Verwendung in Elektroluminszenzbauelementen |
EP0891121B8 (en) | 1996-12-28 | 2013-01-02 | Futaba Corporation | Organic electroluminescent elements |
US6309763B1 (en) | 1997-05-21 | 2001-10-30 | The Dow Chemical Company | Fluorene-containing polymers and electroluminescent devices therefrom |
DE69833013T2 (de) | 1997-10-21 | 2006-08-24 | Cambridge Display Technology Ltd. | Polymere materialien für elektrolumineszente vorrichtung |
DE19748814A1 (de) | 1997-11-05 | 1999-05-06 | Hoechst Ag | Substituierte Poly(arylenvinylene), Verfahren zur Herstellung und deren Verwendung in Elektrolumineszenz |
KR100697861B1 (ko) | 1998-03-13 | 2007-03-22 | 캠브리지 디스플레이 테크놀로지 리미티드 | 전장 발광 디바이스들 |
US5935721A (en) | 1998-03-20 | 1999-08-10 | Eastman Kodak Company | Organic electroluminescent elements for stable electroluminescent |
US6403237B1 (en) | 1998-06-10 | 2002-06-11 | Sumitomo Chemical Co., Ltd. | Polymeric fluorescent substance and organic electroluminescence device |
JP3302945B2 (ja) | 1998-06-23 | 2002-07-15 | ネースディスプレイ・カンパニー・リミテッド | 新規な有機金属発光物質およびそれを含む有機電気発光素子 |
JP2000072722A (ja) | 1998-08-26 | 2000-03-07 | Yanai Kagaku Kogyo Kk | 3級アリールアミン重合物の製造法 |
DE19846767A1 (de) | 1998-10-10 | 2000-04-20 | Aventis Res & Tech Gmbh & Co | Konjugierte Polymere, enthaltend Fluorbausteine mit verbesserten Eigenschaften |
DE19846766A1 (de) | 1998-10-10 | 2000-04-20 | Aventis Res & Tech Gmbh & Co | Konjugierte Polymere, enthaltend spezielle Fluorenbausteine mit verbesserten Eigenschaften |
DE19846768A1 (de) | 1998-10-10 | 2000-04-20 | Aventis Res & Tech Gmbh & Co | Konjugierte Polymere enthaltend 2,7-Fluorenyleinheiten mit verbesserten Eigenschaften |
JP4429438B2 (ja) | 1999-01-19 | 2010-03-10 | 出光興産株式会社 | アミノ化合物及びそれを用いた有機エレクトロルミネッセンス素子 |
KR100663052B1 (ko) | 1999-02-04 | 2007-01-02 | 다우 글로벌 테크놀로지스 인크. | 플루오렌 공중합체 및 이로부터 제조된 디바이스 |
US6166172A (en) | 1999-02-10 | 2000-12-26 | Carnegie Mellon University | Method of forming poly-(3-substituted) thiophenes |
DE60031729T2 (de) | 1999-05-13 | 2007-09-06 | The Trustees Of Princeton University | Lichtemittierende, organische, auf elektrophosphoreszenz basierende anordnung mit sehr hoher quantenausbeute |
DE19953806A1 (de) | 1999-11-09 | 2001-05-10 | Covion Organic Semiconductors | Substituierte Poly(arylenvinylene), Verfahren zur Herstellung und deren Verwendung in Elektrolumineszenzvorrichtungen |
KR100794975B1 (ko) | 1999-12-01 | 2008-01-16 | 더 트러스티즈 오브 프린스턴 유니버시티 | 유기 led용 인광성 도펀트로서 l2mx 형태의 착물 |
KR100377321B1 (ko) | 1999-12-31 | 2003-03-26 | 주식회사 엘지화학 | 피-형 반도체 성질을 갖는 유기 화합물을 포함하는 전기소자 |
JP4220644B2 (ja) | 2000-02-14 | 2009-02-04 | 三井化学株式会社 | アミン化合物および該化合物を含有する有機電界発光素子 |
TW532048B (en) | 2000-03-27 | 2003-05-11 | Idemitsu Kosan Co | Organic electroluminescence element |
JP2001288416A (ja) | 2000-04-07 | 2001-10-16 | Seiko Epson Corp | 塗布液組成物、薄膜形成方法および薄膜 |
US20020121638A1 (en) | 2000-06-30 | 2002-09-05 | Vladimir Grushin | Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds |
CN100505375C (zh) | 2000-08-11 | 2009-06-24 | 普林斯顿大学理事会 | 有机金属化合物和发射转换有机电致磷光 |
JP4154138B2 (ja) | 2000-09-26 | 2008-09-24 | キヤノン株式会社 | 発光素子、表示装置及び金属配位化合物 |
JP4154139B2 (ja) | 2000-09-26 | 2008-09-24 | キヤノン株式会社 | 発光素子 |
JP4154140B2 (ja) | 2000-09-26 | 2008-09-24 | キヤノン株式会社 | 金属配位化合物 |
EP1381639B1 (de) | 2001-03-24 | 2004-09-08 | Covion Organic Semiconductors GmbH | Konjugierte polymere enthaltend spirobifluoren-einheiten und fluoren-einheiten und deren verwendung |
SG92833A1 (en) | 2001-03-27 | 2002-11-19 | Sumitomo Chemical Co | Polymeric light emitting substance and polymer light emitting device using the same |
WO2003001616A2 (en) | 2001-06-20 | 2003-01-03 | Showa Denko K.K. | Light emitting material and organic light-emitting device |
ITMI20011554A1 (it) | 2001-07-20 | 2003-01-20 | Enichem Spa | Composizione attivante per la (co) polimerizzazione delle alfa-olefine comprendete composti ciclopentadienilici fluorurati |
US6690029B1 (en) | 2001-08-24 | 2004-02-10 | University Of Kentucky Research Foundation | Substituted pentacenes and electronic devices made with substituted pentacenes |
JP4574936B2 (ja) | 2001-08-31 | 2010-11-04 | 日本放送協会 | 燐光発光性化合物及び燐光発光性組成物 |
KR100543837B1 (ko) | 2001-09-04 | 2006-01-23 | 캐논 가부시끼가이샤 | 고분자 화합물 및 유기 발광 소자 |
TW200300154A (en) | 2001-11-09 | 2003-05-16 | Jsr Corp | Light emitting polymer composition, and organic electroluminescene device and production process thereof |
KR100691543B1 (ko) | 2002-01-18 | 2007-03-09 | 주식회사 엘지화학 | 새로운 전자 수송용 물질 및 이를 이용한 유기 발광 소자 |
JP2003229256A (ja) * | 2002-02-04 | 2003-08-15 | Seiko Epson Corp | 有機el装置の製造方法及び有機el装置用インク組成物 |
DE10207859A1 (de) | 2002-02-20 | 2003-09-04 | Univ Dresden Tech | Dotiertes organisches Halbleitermaterial sowie Verfahren zu dessen Herstellung |
JP3890242B2 (ja) | 2002-03-26 | 2007-03-07 | キヤノン株式会社 | 高分子化合物及び電界発光素子 |
WO2003099901A1 (fr) | 2002-05-28 | 2003-12-04 | Sumitomo Chemical Company, Limited | Polymere et element luminescent polymere contenant ce polymere |
DE60323490D1 (de) | 2002-06-03 | 2008-10-23 | Toyo Boseki | Polyesterzusammensetzung und diese enthaltendes verpackungsmaterial |
JP2004027088A (ja) | 2002-06-27 | 2004-01-29 | Jsr Corp | 燐光発光剤およびその製造方法並びに発光性組成物 |
US7090929B2 (en) | 2002-07-30 | 2006-08-15 | E.I. Du Pont De Nemours And Company | Metallic complexes covalently bound to conjugated polymers and electronic devices containing such compositions |
ITRM20020411A1 (it) | 2002-08-01 | 2004-02-02 | Univ Roma La Sapienza | Derivati dello spirobifluorene, loro preparazione e loro uso. |
ATE452954T1 (de) | 2002-08-23 | 2010-01-15 | Idemitsu Kosan Co | Organische elektrolumineszenzvorrichtung und anthracenderivat |
TWI276369B (en) | 2002-09-20 | 2007-03-11 | Idemitsu Kosan Co | Organic electroluminescent device |
GB0226010D0 (en) | 2002-11-08 | 2002-12-18 | Cambridge Display Tech Ltd | Polymers for use in organic electroluminescent devices |
JP4287198B2 (ja) | 2002-11-18 | 2009-07-01 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
US20060063027A1 (en) | 2002-12-23 | 2006-03-23 | Covion Organic Semiconductors Gmbh | Organic electroluminescent element |
DE10310887A1 (de) | 2003-03-11 | 2004-09-30 | Covion Organic Semiconductors Gmbh | Matallkomplexe |
KR101036391B1 (ko) | 2003-03-13 | 2011-05-23 | 이데미쓰 고산 가부시키가이샤 | 신규한 질소 함유 헤테로환 유도체 및 이를 이용한 유기 전기발광 소자 |
JP4411851B2 (ja) | 2003-03-19 | 2010-02-10 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子 |
CN1768029B (zh) | 2003-04-10 | 2012-02-08 | 出光兴产株式会社 | 芳香族胺衍生物和采用该衍生物的有机场致发光元件 |
EP1617710B1 (en) | 2003-04-23 | 2015-05-20 | Konica Minolta Holdings, Inc. | Material for organic electroluminescent device, organic electroluminescent device, illuminating device and display |
DE10324533A1 (de) * | 2003-05-28 | 2004-12-16 | H.C. Starck Gmbh | Stabile Lösungen von organischen halbleitenden Verbindungen |
TWI224473B (en) | 2003-06-03 | 2004-11-21 | Chin-Hsin Chen | Doped co-host emitter system in organic electroluminescent devices |
EP1491568A1 (en) | 2003-06-23 | 2004-12-29 | Covion Organic Semiconductors GmbH | Semiconductive Polymers |
DE112004001446T5 (de) * | 2003-08-04 | 2006-11-02 | Sumitomo Chemical Co. Ltd. | Aromatische Monomer- und konjugierte Polymer-Metallkomplexe |
DE10337346A1 (de) | 2003-08-12 | 2005-03-31 | Covion Organic Semiconductors Gmbh | Konjugierte Polymere enthaltend Dihydrophenanthren-Einheiten und deren Verwendung |
DE10345572A1 (de) | 2003-09-29 | 2005-05-19 | Covion Organic Semiconductors Gmbh | Metallkomplexe |
US7795801B2 (en) | 2003-09-30 | 2010-09-14 | Konica Minolta Holdings, Inc. | Organic electroluminescent element, illuminator, display and compound |
US20050079278A1 (en) * | 2003-10-14 | 2005-04-14 | Burrows Paul E. | Method and apparatus for coating an organic thin film on a substrate from a fluid source with continuous feed capability |
DE10350722A1 (de) | 2003-10-30 | 2005-05-25 | Covion Organic Semiconductors Gmbh | Metallkomplexe |
EP1783781A3 (en) | 2003-11-28 | 2007-10-03 | Merck Patent GmbH | Organic semiconducting layer formulations comprising polyacenes and organic binder polymers |
DE10357044A1 (de) | 2003-12-04 | 2005-07-14 | Novaled Gmbh | Verfahren zur Dotierung von organischen Halbleitern mit Chinondiiminderivaten |
US7252893B2 (en) | 2004-02-17 | 2007-08-07 | Eastman Kodak Company | Anthracene derivative host having ranges of dopants |
DE102004008304A1 (de) | 2004-02-20 | 2005-09-08 | Covion Organic Semiconductors Gmbh | Organische elektronische Vorrichtungen |
WO2005082969A1 (ja) * | 2004-02-26 | 2005-09-09 | Sumitomo Chemical Company, Limited | 高分子化合物およびそれを用いた高分子発光素子 |
US7326371B2 (en) | 2004-03-25 | 2008-02-05 | Eastman Kodak Company | Electroluminescent device with anthracene derivative host |
US7790890B2 (en) | 2004-03-31 | 2010-09-07 | Konica Minolta Holdings, Inc. | Organic electroluminescence element material, organic electroluminescence element, display device and illumination device |
KR100787425B1 (ko) | 2004-11-29 | 2007-12-26 | 삼성에스디아이 주식회사 | 페닐카바졸계 화합물 및 이를 이용한 유기 전계 발광 소자 |
DE102004020298A1 (de) | 2004-04-26 | 2005-11-10 | Covion Organic Semiconductors Gmbh | Elektrolumineszierende Polymere und deren Verwendung |
DE102004023277A1 (de) | 2004-05-11 | 2005-12-01 | Covion Organic Semiconductors Gmbh | Neue Materialmischungen für die Elektrolumineszenz |
US7825249B2 (en) | 2004-05-19 | 2010-11-02 | Merck Patent Gmbh | Metal complexes |
TWI327563B (en) | 2004-05-24 | 2010-07-21 | Au Optronics Corp | Anthracene compound and organic electroluminescent device including the anthracene compound |
JP4862248B2 (ja) | 2004-06-04 | 2012-01-25 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子、照明装置及び表示装置 |
TW200613515A (en) | 2004-06-26 | 2006-05-01 | Merck Patent Gmbh | Compounds for organic electronic devices |
DE102004031000A1 (de) | 2004-06-26 | 2006-01-12 | Covion Organic Semiconductors Gmbh | Organische Elektrolumineszenzvorrichtungen |
DE102004032527A1 (de) | 2004-07-06 | 2006-02-02 | Covion Organic Semiconductors Gmbh | Elektrolumineszierende Polymere |
ITRM20040352A1 (it) | 2004-07-15 | 2004-10-15 | Univ Roma La Sapienza | Derivati oligomerici dello spirobifluorene, loro preparazione e loro uso. |
DE102004034517A1 (de) | 2004-07-16 | 2006-02-16 | Covion Organic Semiconductors Gmbh | Metallkomplexe |
EP1655359A1 (de) | 2004-11-06 | 2006-05-10 | Covion Organic Semiconductors GmbH | Organische Elektrolumineszenzvorrichtung |
TW200639140A (en) | 2004-12-01 | 2006-11-16 | Merck Patent Gmbh | Compounds for organic electronic devices |
TW200634020A (en) | 2004-12-09 | 2006-10-01 | Merck Patent Gmbh | Metal complexes |
US20080303417A1 (en) | 2005-01-05 | 2008-12-11 | Idemitsu Kosan Co., Ltd. | Aromatic Amine Derivative and Organic Electroluminescent Device Using Same |
EP1844060B1 (de) | 2005-02-03 | 2010-11-17 | Merck Patent GmbH | Metallkomplexe |
US7385221B1 (en) | 2005-03-08 | 2008-06-10 | University Of Kentucky Research Foundation | Silylethynylated heteroacenes and electronic devices made therewith |
JP2006253445A (ja) | 2005-03-11 | 2006-09-21 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子 |
JP4263700B2 (ja) | 2005-03-15 | 2009-05-13 | 出光興産株式会社 | 芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
KR100949214B1 (ko) | 2005-03-18 | 2010-03-24 | 이데미쓰 고산 가부시키가이샤 | 방향족 아민 유도체 및 그것을 사용한 유기 전기발광 소자 |
CN101171320B (zh) | 2005-05-03 | 2013-04-10 | 默克专利有限公司 | 有机电致发光器件 |
WO2006119853A1 (en) * | 2005-05-12 | 2006-11-16 | Merck Patent Gmbh | Polyacene and semiconductor formulation |
DE102005023437A1 (de) | 2005-05-20 | 2006-11-30 | Merck Patent Gmbh | Verbindungen für organische elektronische Vorrichtungen |
CN101218278B (zh) * | 2005-06-10 | 2011-11-30 | 住友化学株式会社 | 芳族接枝聚合物 |
JP5401791B2 (ja) | 2005-10-28 | 2014-01-29 | 日産化学工業株式会社 | スプレー又はインクジェット塗布用電荷輸送性ワニス |
KR101082258B1 (ko) | 2005-12-01 | 2011-11-09 | 신닛테츠가가쿠 가부시키가이샤 | 유기 전계 발광소자용 화합물 및 유기 전계 발광소자 |
DE102005058543A1 (de) | 2005-12-08 | 2007-06-14 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
DE102005058557A1 (de) | 2005-12-08 | 2007-06-14 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
US20070153371A1 (en) * | 2005-12-30 | 2007-07-05 | Samsung Electronics Co., Ltd. | Display device, method of manufacturing the same, and composition for use in manufacturing the same |
DE102006015183A1 (de) | 2006-04-01 | 2007-10-04 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
US7582508B2 (en) * | 2006-05-31 | 2009-09-01 | Byoung-Choo Park | Method for manufacturing an organic semiconductor device that utilizes ionic salt |
DE102006025777A1 (de) | 2006-05-31 | 2007-12-06 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
DE102006025846A1 (de) | 2006-06-02 | 2007-12-06 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
DE102006031990A1 (de) | 2006-07-11 | 2008-01-17 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
WO2008056746A1 (fr) | 2006-11-09 | 2008-05-15 | Nippon Steel Chemical Co., Ltd. | Composé pour un dispositif électroluminescent organique et dispositif électroluminescent organique |
DE102007002714A1 (de) | 2007-01-18 | 2008-07-31 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
TW200902677A (en) | 2007-02-28 | 2009-01-16 | Idemitsu Kosan Co | Organic-electroluminescence-material-containing solution, method for forming organic electroluminescence thin film and organic electroluminescence device |
WO2008107089A1 (en) | 2007-03-07 | 2008-09-12 | University Of Kentucky Research Foundation | Silylethynylated heteroacenes and electronic devices made therewith |
WO2008117633A1 (en) * | 2007-03-23 | 2008-10-02 | Semiconductor Energy Laboratory Co., Ltd. | Composition, method for fabricating light-emitting element, light-emitting element, light-emitting device, and electronic device |
EP2147006B1 (en) * | 2007-05-18 | 2015-10-28 | Semiconductor Energy Laboratory Co, Ltd. | Organometallic complex, composition and light emitting element including the organometallic complex |
DE102007024850A1 (de) | 2007-05-29 | 2008-12-04 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
JP2011504650A (ja) | 2007-10-18 | 2011-02-10 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 導電性調合物 |
DE102007053771A1 (de) | 2007-11-12 | 2009-05-14 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
US20100243960A1 (en) | 2007-11-16 | 2010-09-30 | Sumitomo Chemical Company, Limited | Coating solution for application method of discharging coating solution through slit-like discharge port |
DE102008027005A1 (de) | 2008-06-05 | 2009-12-10 | Merck Patent Gmbh | Organische elektronische Vorrichtung enthaltend Metallkomplexe |
DE102008033943A1 (de) | 2008-07-18 | 2010-01-21 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
DE102008035413A1 (de) | 2008-07-29 | 2010-02-04 | Merck Patent Gmbh | Verbindungen für organische elektronische Vorrichtungen |
DE102008036982A1 (de) | 2008-08-08 | 2010-02-11 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
US8174000B2 (en) * | 2009-02-11 | 2012-05-08 | Universal Display Corporation | Liquid compositions for inkjet printing of organic layers or other uses |
-
2011
- 2011-04-05 KR KR1020127029207A patent/KR101896723B1/ko active IP Right Grant
- 2011-04-05 US US13/640,408 patent/US20130026421A1/en not_active Abandoned
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Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000059267A1 (fr) * | 1999-03-29 | 2000-10-05 | Seiko Epson Corporation | Composition, procede de preparation d'un film, et element fonctionnel et son procede de preparation |
JP2006523740A (ja) * | 2003-04-15 | 2006-10-19 | メルク・オーエルイーディー・マテリアルス・ゲーエムベーハー | 発光可能な、マトリックス材料と有機半導体との混合物、その使用、ならびに前記混合物を含む電子部品 |
JP2006128256A (ja) * | 2004-10-27 | 2006-05-18 | Konica Minolta Holdings Inc | 有機薄膜トランジスタの製造方法及び該製造方法で作製した有機薄膜トランジスタ |
JP2006156824A (ja) * | 2004-11-30 | 2006-06-15 | Seiko Epson Corp | 発光材料及び有機el装置とその製造方法 |
JP2007258724A (ja) * | 2006-03-24 | 2007-10-04 | Merck Patent Gmbh | 有機半導性配合体 |
JP2009536981A (ja) * | 2006-05-12 | 2009-10-22 | メルク パテント ゲーエムベーハー | インデノフルオレンポリマー系有機半導体材料 |
JP2008303365A (ja) * | 2007-06-11 | 2008-12-18 | Toppan Printing Co Ltd | 蛍光材料、発光インク組成物および有機el素子 |
WO2009109273A1 (en) * | 2008-03-06 | 2009-09-11 | Merck Patent Gmbh | Organic semiconductor formulation |
WO2009122870A1 (ja) * | 2008-03-31 | 2009-10-08 | 住友化学株式会社 | 有機エレクトロルミネッセンス素子の製造方法、有機エレクトロルミネッセンス素子および表示装置 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2018519616A (ja) * | 2015-03-30 | 2018-07-19 | メルク パテント ゲーエムベーハー | シロキサン溶媒を含む有機機能性材料の調合物 |
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KR20130043631A (ko) | 2013-04-30 |
CN102844902B (zh) | 2016-06-08 |
CN102844902A (zh) | 2012-12-26 |
US10256408B2 (en) | 2019-04-09 |
US20130026421A1 (en) | 2013-01-31 |
US20170062725A1 (en) | 2017-03-02 |
EP2559079A1 (en) | 2013-02-20 |
JP6073216B2 (ja) | 2017-02-01 |
KR101896723B1 (ko) | 2018-09-07 |
WO2011128035A1 (en) | 2011-10-20 |
EP2559079B1 (en) | 2020-04-01 |
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