KR20070026599A - 선형 폴리실록산, 실리콘 조성물 및 유기 발광 다이오드 - Google Patents

선형 폴리실록산, 실리콘 조성물 및 유기 발광 다이오드 Download PDF

Info

Publication number
KR20070026599A
KR20070026599A KR1020067026509A KR20067026509A KR20070026599A KR 20070026599 A KR20070026599 A KR 20070026599A KR 1020067026509 A KR1020067026509 A KR 1020067026509A KR 20067026509 A KR20067026509 A KR 20067026509A KR 20070026599 A KR20070026599 A KR 20070026599A
Authority
KR
South Korea
Prior art keywords
formula
units
mol
iii
transport layer
Prior art date
Application number
KR1020067026509A
Other languages
English (en)
Korean (ko)
Inventor
오마 파루크
폴 샤크
도시오 스즈키
스허 쉬
Original Assignee
다우 코닝 코포레이션
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 다우 코닝 코포레이션 filed Critical 다우 코닝 코포레이션
Publication of KR20070026599A publication Critical patent/KR20070026599A/ko

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04—Polysiloxanes
    • C08G77/38—Polysiloxanes modified by chemical after-treatment
    • C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
    • C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04—Polysiloxanes
    • C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
    • G—PHYSICS
    • G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09G—ARRANGEMENTS OR CIRCUITS FOR CONTROL OF INDICATING DEVICES USING STATIC MEANS TO PRESENT VARIABLE INFORMATION
    • G09G3/00—Control arrangements or circuits, of interest only in connection with visual indicators other than cathode-ray tubes
    • G09G3/20—Control arrangements or circuits, of interest only in connection with visual indicators other than cathode-ray tubes for presentation of an assembly of a number of characters, e.g. a page, by composing the assembly by combination of individual elements arranged in a matrix no fixed position being assigned to or needed to be assigned to the individual characters or partial characters
    • G09G3/22—Control arrangements or circuits, of interest only in connection with visual indicators other than cathode-ray tubes for presentation of an assembly of a number of characters, e.g. a page, by composing the assembly by combination of individual elements arranged in a matrix no fixed position being assigned to or needed to be assigned to the individual characters or partial characters using controlled light sources
    • G09G3/30—Control arrangements or circuits, of interest only in connection with visual indicators other than cathode-ray tubes for presentation of an assembly of a number of characters, e.g. a page, by composing the assembly by combination of individual elements arranged in a matrix no fixed position being assigned to or needed to be assigned to the individual characters or partial characters using controlled light sources using electroluminescent panels
    • G09G3/32—Control arrangements or circuits, of interest only in connection with visual indicators other than cathode-ray tubes for presentation of an assembly of a number of characters, e.g. a page, by composing the assembly by combination of individual elements arranged in a matrix no fixed position being assigned to or needed to be assigned to the individual characters or partial characters using controlled light sources using electroluminescent panels semiconductive, e.g. using light-emitting diodes [LED]
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L27/00—Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/40—Organosilicon compounds, e.g. TIPS pentacene
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K2102/00—Constructional details relating to the organic devices covered by this subclass
    • H10K2102/10—Transparent electrodes, e.g. using graphene
    • H10K2102/101—Transparent electrodes, e.g. using graphene comprising transparent conductive oxides [TCO]
    • H10K2102/103—Transparent electrodes, e.g. using graphene comprising transparent conductive oxides [TCO] comprising indium oxides, e.g. ITO

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Power Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Chemistry (AREA)
  • Computer Hardware Design (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Theoretical Computer Science (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Silicon Polymers (AREA)
  • Electroluminescent Light Sources (AREA)
KR1020067026509A 2004-06-15 2005-04-08 선형 폴리실록산, 실리콘 조성물 및 유기 발광 다이오드 KR20070026599A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US57964004P 2004-06-15 2004-06-15
US60/579,640 2004-06-15

Publications (1)

Publication Number Publication Date
KR20070026599A true KR20070026599A (ko) 2007-03-08

Family

ID=34965776

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020067026509A KR20070026599A (ko) 2004-06-15 2005-04-08 선형 폴리실록산, 실리콘 조성물 및 유기 발광 다이오드

Country Status (5)

Country Link
EP (1) EP1789474A1 (fr)
JP (1) JP2008502770A (fr)
KR (1) KR20070026599A (fr)
CN (1) CN1968993A (fr)
WO (1) WO2006001874A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8455605B2 (en) 2009-12-31 2013-06-04 Cheil Industries, Inc. Resin composition for transparent encapsulation material and electronic device formed using the same
KR101539486B1 (ko) * 2011-01-06 2015-07-24 주식회사 엘지화학 경화성 조성물

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5476234B2 (ja) * 2010-06-30 2014-04-23 ユー・ディー・シー アイルランド リミテッド 有機電界発光素子用材料、有機電界発光素子、及び有機電界発光素子の製造方法
JP5557624B2 (ja) * 2010-06-30 2014-07-23 富士フイルム株式会社 組成物、並びに、該組成物を用いた膜、電荷輸送層、有機電界発光素子、及び電荷輸送層の形成方法
JP2012015337A (ja) 2010-06-30 2012-01-19 Fujifilm Corp 有機電界発光素子用材料、有機電界発光素子、及び有機電界発光素子の製造方法
WO2012093907A2 (fr) * 2011-01-06 2012-07-12 주식회사 엘지화학 Composition durcissable
KR101641404B1 (ko) * 2013-12-17 2016-07-20 주식회사 두산 유기 화합물 및 이를 포함하는 유기 전계 발광 소자
DE112017003257T5 (de) 2016-06-30 2019-04-18 Osram Opto Semiconductors Gmbh Wellenlängenkonverter mit einem polysiloxanmaterial, herstellungsverfahren und ihn enthaltende festkörperbeleuchtungsvorrichtung

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3541161A1 (de) * 1985-11-21 1987-05-27 Basf Ag Carbazolsubstituierte polysiloxane und deren verwendung

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8455605B2 (en) 2009-12-31 2013-06-04 Cheil Industries, Inc. Resin composition for transparent encapsulation material and electronic device formed using the same
KR101539486B1 (ko) * 2011-01-06 2015-07-24 주식회사 엘지화학 경화성 조성물

Also Published As

Publication number Publication date
EP1789474A1 (fr) 2007-05-30
CN1968993A (zh) 2007-05-23
JP2008502770A (ja) 2008-01-31
WO2006001874A1 (fr) 2006-01-05

Similar Documents

Publication Publication Date Title
US7880164B2 (en) Conducting polymer composition and electronic device including layer obtained using the conducting polymer composition
US20070131925A1 (en) Organic light-emitting diode
KR20070026599A (ko) 선형 폴리실록산, 실리콘 조성물 및 유기 발광 다이오드
KR20060065700A (ko) 카바졸릴-관능성 직쇄 폴리실록산, 실리콘 조성물 및 유기발광 다이오드
US20080007158A1 (en) Linear Polysiloxanes, Silicone Composition, and Organic Light-Emitting Diode
US20070090359A1 (en) Organic light-emitting diode
KR101451607B1 (ko) 실리콘 조성물 및 유기 발광 다이오드
JP5377836B2 (ja) ジアリールエテン系誘導体、これを使用して製造された有機電界発光素子及び該有機電界発光素子の製造方法
TW201245196A (en) Curable composition, cured product and organic electroluminescent element using the same
US7135242B2 (en) Electroluminescent polymer, bisfluorenylsilane compound and organic electroluminescent element
WO2012002399A1 (fr) Matière d'élément électroluminescent organique, élément électroluminescent organique et procédé de production pour un élément électroluminescent organique
US20080061679A1 (en) Carbazolyl-Functional Polysiloxane Resins, Silicone Composition, and Organic Light-Emitting Diode
US20060232201A1 (en) Carbazolyl-functional cyclosiloxane silicone composition and organic light-emitting diode
WO2005035632A1 (fr) Polysiloxanes hyperramifies a fonctionnalite carbazolyle, composition de silicone et diode electroluminescente organique

Legal Events

Date Code Title Description
WITN Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid