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WO2010123266A3 - 여기 상태 분자내 양성자 이동 특성을 이용한 백색 발광 단분자 화합물, 이를 포함하는 유기 전계 발광 소자 및 레이저 소자 - Google Patents

여기 상태 분자내 양성자 이동 특성을 이용한 백색 발광 단분자 화합물, 이를 포함하는 유기 전계 발광 소자 및 레이저 소자 Download PDF

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Publication number
WO2010123266A3
WO2010123266A3 PCT/KR2010/002482 KR2010002482W WO2010123266A3 WO 2010123266 A3 WO2010123266 A3 WO 2010123266A3 KR 2010002482 W KR2010002482 W KR 2010002482W WO 2010123266 A3 WO2010123266 A3 WO 2010123266A3
Authority
WO
WIPO (PCT)
Prior art keywords
white
light emission
excited
organic electroluminescence
monomolecular compound
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/KR2010/002482
Other languages
English (en)
French (fr)
Other versions
WO2010123266A2 (ko
Inventor
박수영
박상혁
권지언
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dongwoo Fine Chem Co Ltd
SNU R&DB Foundation
Original Assignee
Dongwoo Fine Chem Co Ltd
SNU R&DB Foundation
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
Priority claimed from KR1020100035707A external-priority patent/KR101763424B1/ko
Application filed by Dongwoo Fine Chem Co Ltd, SNU R&DB Foundation filed Critical Dongwoo Fine Chem Co Ltd
Priority to CN201080016641.6A priority Critical patent/CN102395647B/zh
Priority to US13/264,968 priority patent/US8569510B2/en
Priority to JP2012505832A priority patent/JP5509468B2/ja
Publication of WO2010123266A2 publication Critical patent/WO2010123266A2/ko
Publication of WO2010123266A3 publication Critical patent/WO2010123266A3/ko
Anticipated expiration legal-status Critical
Priority to US14/025,161 priority patent/US9024036B2/en
Priority to US14/025,150 priority patent/US9077155B2/en
Priority to US14/025,166 priority patent/US9106057B2/en
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/12—Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1007—Non-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1011—Condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
    • C09K2211/1033—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with oxygen
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • C09K2211/1048—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms with oxygen
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/14—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range characterised by the material used as the active medium
    • H01S3/16—Solid materials
    • H01S3/17—Solid materials amorphous, e.g. glass
    • H01S3/178—Solid materials amorphous, e.g. glass plastic
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
    • Y02B20/00—Energy efficient lighting technologies, e.g. halogen lamps or gas discharge lamps

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Electroluminescent Light Sources (AREA)
  • Luminescent Compositions (AREA)

Abstract

본 발명은 여기 상태 분자내 양성자 이동 특성을 이용한 백색 발광 단분자 화합물, 이를 포함하는 유기 전계 발광 소자 및 레이저 소자에 관한 것으로서, 본 발명에 따른 백색 발광 단분자 화합물은 서로 다른 발색을 나타내는 적어도 두 종의 여기 상태 분자내 양성자 이동(excited-state intramolecular proton transfer, ESIPT) 특성을 갖는 분자들을 서로 공유 결합시켜서 된 것이다. 상기한 본 발명에 따른 백색 발광 단분자 화합물은 농도 및 물질의 상태에 관계 없이 백색 발광을 구현시킬 수 있는 특성을 가지며, 그에 따라 유기 전계 발광 소자 및 레이저 소자를 포함하여 다양한 분야에서 응용이 가능하다는 이점이 있다.
PCT/KR2010/002482 2009-04-21 2010-04-21 여기 상태 분자내 양성자 이동 특성을 이용한 백색 발광 단분자 화합물, 이를 포함하는 유기 전계 발광 소자 및 레이저 소자 Ceased WO2010123266A2 (ko)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CN201080016641.6A CN102395647B (zh) 2009-04-21 2010-04-21 利用激发态分子内质子转移特性的白色发光单分子化合物、及包含该化合物的有机电致发光元件及激光元件
US13/264,968 US8569510B2 (en) 2009-04-21 2010-04-21 White-emitting compounds using excited-state intramolecular proton transfer, organic electroluminescent element and laser material using the same
JP2012505832A JP5509468B2 (ja) 2009-04-21 2010-04-21 励起状態分子内プロトン移動特性を利用した白色発光単分子化合物、これを含む有機電界発光素子及びレーザ素子
US14/025,161 US9024036B2 (en) 2009-04-21 2013-09-12 White-emitting monomolecular compound using excited-state intramolecular proton transfer, organic electroluminescent element and laser device using the same
US14/025,150 US9077155B2 (en) 2009-04-21 2013-09-12 White-emitting monomolecular compound using excited-state intramolecular proton transfer, organic electroluminescent element and laser device using the same
US14/025,166 US9106057B2 (en) 2009-04-21 2013-09-12 White-emitting monomolecular compound using excited-state intramolecular proton transfer, organic electroluminescent element and laser device using the same

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
KR20090034806 2009-04-21
KR10-2009-0034806 2009-04-21
KR1020100035707A KR101763424B1 (ko) 2009-04-21 2010-04-19 여기 상태 분자내 양성자 이동 특성을 이용한 백색 발광 단분자 화합물, 이를 포함하는 유기 전계 발광 소자 및 레이저 소자
KR10-2010-0035707 2010-04-19

Related Child Applications (4)

Application Number Title Priority Date Filing Date
US13/264,968 A-371-Of-International US8569510B2 (en) 2009-04-21 2010-04-21 White-emitting compounds using excited-state intramolecular proton transfer, organic electroluminescent element and laser material using the same
US14/025,161 Division US9024036B2 (en) 2009-04-21 2013-09-12 White-emitting monomolecular compound using excited-state intramolecular proton transfer, organic electroluminescent element and laser device using the same
US14/025,150 Division US9077155B2 (en) 2009-04-21 2013-09-12 White-emitting monomolecular compound using excited-state intramolecular proton transfer, organic electroluminescent element and laser device using the same
US14/025,166 Division US9106057B2 (en) 2009-04-21 2013-09-12 White-emitting monomolecular compound using excited-state intramolecular proton transfer, organic electroluminescent element and laser device using the same

Publications (2)

Publication Number Publication Date
WO2010123266A2 WO2010123266A2 (ko) 2010-10-28
WO2010123266A3 true WO2010123266A3 (ko) 2011-02-24

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2010/002482 Ceased WO2010123266A2 (ko) 2009-04-21 2010-04-21 여기 상태 분자내 양성자 이동 특성을 이용한 백색 발광 단분자 화합물, 이를 포함하는 유기 전계 발광 소자 및 레이저 소자

Country Status (1)

Country Link
WO (1) WO2010123266A2 (ko)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI465441B (zh) * 2011-08-12 2014-12-21 Ind Tech Res Inst 含乙烯官能基之咪唑衍生物及其用於電致發光元件之用途
BR102018016840B1 (pt) * 2018-08-17 2023-02-14 Universidade Estadual De Campinas - Unicamp Síntese de um composto da classe de fluoróforos, composto obtido e seu uso, processo de obtenção de diodos orgânicos emissores de luz branca e diodos obtidos

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5587112A (en) * 1994-09-02 1996-12-24 Philadelphia College Of Pharmacy And Science Benzazole compounds with ESIPT fluorescence
US7262301B1 (en) * 2003-07-08 2007-08-28 Northwestern University Zinc-chelating ratiometric fluorescent probes and related methods

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5587112A (en) * 1994-09-02 1996-12-24 Philadelphia College Of Pharmacy And Science Benzazole compounds with ESIPT fluorescence
US7262301B1 (en) * 2003-07-08 2007-08-28 Northwestern University Zinc-chelating ratiometric fluorescent probes and related methods

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
JANGWON SEO ET AL.: "Highly fluorescent columnar liquid crystals with elliptical molecular shape: oblique molecular stacking and excited-state intramolecular proton- transfer fluorescece", JOURNAL OF MATERIALS CHEMISTRY, vol. 17, 2007, pages 5052 - 5057 *
MARCELO DOMINGUES KUPLICH: "Master's Dissertation", 2007, UNIVERSIDADE FEDERAL DO RIO GRANDE DO SUL (UFRGS)., article "Synthesis of New Heterocycles Benzazoles Fluores cence and its incorporation into cellulose matrix" *
SEHOON KIM ET AL.: "White Luminescence from Polymer Thin Films Containing Excited- State Intramolecular Proton-Transfer Dyes", ADVANCED MATERIALS, vol. 17, 2005, pages 2077 - 2082 *

Also Published As

Publication number Publication date
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