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WO2010123266A3 - White-light emission monomolecular compound using excited-state intramolecular proton transfer characteristics, and organic electroluminescence device and laser device comprising same - Google Patents

White-light emission monomolecular compound using excited-state intramolecular proton transfer characteristics, and organic electroluminescence device and laser device comprising same 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
Application number
PCT/KR2010/002482
Other languages
French (fr)
Korean (ko)
Other versions
WO2010123266A2 (en
Inventor
박수영
박상혁
권지언
Original Assignee
동우화인켐 주식회사
서울대학교 산학협력단
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/en
Application filed by 동우화인켐 주식회사, 서울대학교 산학협력단 filed Critical 동우화인켐 주식회사
Priority to US13/264,968 priority Critical patent/US8569510B2/en
Priority to CN201080016641.6A priority patent/CN102395647B/en
Priority to JP2012505832A priority patent/JP5509468B2/en
Publication of WO2010123266A2 publication Critical patent/WO2010123266A2/en
Publication of WO2010123266A3 publication Critical patent/WO2010123266A3/en
Priority to US14/025,166 priority patent/US9106057B2/en
Priority to US14/025,161 priority patent/US9024036B2/en
Priority to US14/025,150 priority patent/US9077155B2/en

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

The present invention relates to a white-light emission monomolecular compound using excited-state intramolecular proton transfer (ESIPT) characteristics, and to an organic electroluminescence device and laser device comprising same. The white-light emission monomolecular compound according to the present invention is prepared by covalently bonding at least two types of molecules which produce different colors and have excited-state intramolecular proton transfer (ESIPT) characteristics. The white-light emission monomolecular compound according to the present invention achieves white-light emission irrespective of the concentration thereof and of the state of the materials thereof, and therefore can be used in a variety of fields including an organic electroluminescence device and a laser device.
PCT/KR2010/002482 2009-04-21 2010-04-21 White-light emission monomolecular compound using excited-state intramolecular proton transfer characteristics, and organic electroluminescence device and laser device comprising same WO2010123266A2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
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
CN201080016641.6A CN102395647B (en) 2009-04-21 2010-04-21 White-light emission monomolecular compound using excited-state intramolecular proton transfer characteristics, and organic electroluminescence device and laser device comprising same
JP2012505832A JP5509468B2 (en) 2009-04-21 2010-04-21 White light emitting monomolecular compound utilizing proton transfer characteristics in excited state of molecule, organic electroluminescent device and laser device containing 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
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

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
KR10-2009-0034806 2009-04-21
KR20090034806 2009-04-21
KR10-2010-0035707 2010-04-19
KR1020100035707A KR101763424B1 (en) 2009-04-21 2010-04-19 White-emitting compounds using excited-state intramolecular proton transfer, organinc electroluminescent element and laser material using the same

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
US14/025,166 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
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

Publications (2)

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

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2010/002482 WO2010123266A2 (en) 2009-04-21 2010-04-21 White-light emission monomolecular compound using excited-state intramolecular proton transfer characteristics, and organic electroluminescence device and laser device comprising same

Country Status (1)

Country Link
WO (1) WO2010123266A2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI465441B (en) * 2011-08-12 2014-12-21 Ind Tech Res Inst Imidazole derivatives having vinyl group and its use in electroluminescent element
BR102018016840B1 (en) * 2018-08-17 2023-02-14 Universidade Estadual De Campinas - Unicamp SYNTHESIS OF A COMPOUND OF THE FLUOROPHOR CLASS, COMPOUND OBTAINED AND ITS USE, PROCESS FOR OBTAINING ORGANIC WHITE LIGHT-EMITTING DIODES AND OBTAINED DIODES

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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