WO2014002061A3 - Substituted terrylene and quaterrylene derivates and use as semiconductors thereof - Google Patents

Substituted terrylene and quaterrylene derivates and use as semiconductors thereof Download PDF

Info

Publication number
WO2014002061A3
WO2014002061A3 PCT/IB2013/055309 IB2013055309W WO2014002061A3 WO 2014002061 A3 WO2014002061 A3 WO 2014002061A3 IB 2013055309 W IB2013055309 W IB 2013055309W WO 2014002061 A3 WO2014002061 A3 WO 2014002061A3
Authority
WO
WIPO (PCT)
Prior art keywords
quaterrylene
derivates
semiconductors
terrylene
substituted
Prior art date
Application number
PCT/IB2013/055309
Other languages
French (fr)
Other versions
WO2014002061A2 (en
Inventor
Thomas Gessner
Helmut Reichelt
Glauco BATTAGLIARIN
Chen Li
Klaus MÜLLEN
Original Assignee
Basf Se
Max-Planck-Gesellschaft zur Förderung der Wissenschaften e. V.
Basf (China) Company Limited
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 Basf Se, Max-Planck-Gesellschaft zur Förderung der Wissenschaften e. V., Basf (China) Company Limited filed Critical Basf Se
Priority to US14/411,184 priority Critical patent/US20150179954A1/en
Priority to EP13810563.0A priority patent/EP2867234A2/en
Publication of WO2014002061A2 publication Critical patent/WO2014002061A2/en
Publication of WO2014002061A3 publication Critical patent/WO2014002061A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B5/00Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/62Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60Organic compounds having low molecular weight
    • H10K85/649Aromatic compounds comprising a hetero atom
    • H10K85/657Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/06Peri-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/06Peri-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/04Esters of boric acids
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60Organic compounds having low molecular weight
    • H10K85/615Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • H10K85/621Aromatic anhydride or imide compounds, e.g. perylene tetra-carboxylic dianhydride or perylene tetracarboxylic di-imide
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K10/00Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
    • H10K10/40Organic transistors
    • H10K10/46Field-effect transistors, e.g. organic thin-film transistors [OTFT]
    • H10K10/462Insulated gate field-effect transistors [IGFETs]
    • H10K10/466Lateral bottom-gate IGFETs comprising only a single gate
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K10/00Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
    • H10K10/40Organic transistors
    • H10K10/46Field-effect transistors, e.g. organic thin-film transistors [OTFT]
    • H10K10/462Insulated gate field-effect transistors [IGFETs]
    • H10K10/484Insulated gate field-effect transistors [IGFETs] characterised by the channel regions
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K10/00Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
    • H10K10/80Constructional details
    • H10K10/82Electrodes
    • H10K10/84Ohmic electrodes, e.g. source or drain electrodes
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K19/00Integrated devices, or assemblies of multiple devices, comprising at least one organic element specially adapted for rectifying, amplifying, oscillating or switching, covered by group H10K10/00
    • H10K19/10Integrated devices, or assemblies of multiple devices, comprising at least one organic element specially adapted for rectifying, amplifying, oscillating or switching, covered by group H10K10/00 comprising field-effect transistors
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/10OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/10OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/17Carrier injection layers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/80Constructional details
    • H10K50/805Electrodes
    • H10K50/82Cathodes
    • H10K50/828Transparent cathodes, e.g. comprising thin metal layers
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Thin Film Transistor (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)

Abstract

Disclosed are terrylene and quaterrylene derivates of general formula (I) and the use thereof as organic semiconductor materials.
PCT/IB2013/055309 2012-06-29 2013-06-28 Substituted terrylene and quaterrylene derivatives and the use as semiconductors WO2014002061A2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US14/411,184 US20150179954A1 (en) 2012-06-29 2013-06-28 Substituted terrylene and quaterrylene derivates and use as semiconductors thereof
EP13810563.0A EP2867234A2 (en) 2012-06-29 2013-06-28 Substituted terrylene and quaterrylene derivatives and the use as semiconductors thereof

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201261665914P 2012-06-29 2012-06-29
US61/665,914 2012-06-29
EP12174337 2012-06-29
EP12174337.1 2012-06-29

Publications (2)

Publication Number Publication Date
WO2014002061A2 WO2014002061A2 (en) 2014-01-03
WO2014002061A3 true WO2014002061A3 (en) 2014-02-27

Family

ID=49783957

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2013/055309 WO2014002061A2 (en) 2012-06-29 2013-06-28 Substituted terrylene and quaterrylene derivatives and the use as semiconductors

Country Status (3)

Country Link
US (1) US20150179954A1 (en)
EP (1) EP2867234A2 (en)
WO (1) WO2014002061A2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9428518B2 (en) 2013-03-18 2016-08-30 Basf Se Perylenemonoimide and naphthalenemonoimide derivatives and their use in dye-sensitized solar cells
JP6433852B2 (en) * 2015-05-28 2018-12-05 株式会社東芝 Compound, organic photoelectric conversion device, and solid-state imaging device
WO2017006703A1 (en) * 2015-07-07 2017-01-12 富士フイルム株式会社 Organic semiconductor element, compound, organic semiconductor composition, and organic semiconductor film and method for producing same
CN109428005B (en) * 2017-08-30 2020-05-08 昆山国显光电有限公司 Organic electroluminescent device
CN116375736A (en) * 2023-03-07 2023-07-04 大连理工大学 Naphthol dioxazine imide compound and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1169155A (en) * 1995-01-20 1997-12-31 巴斯福股份公司 Substituted quaterrylene tetracarboxylic acid diimides
WO2005089094A2 (en) * 2003-11-21 2005-09-29 The Board Of Regents Of The University And Community College System Of Nevada Materials and methods for the preparation of anisotropically-ordered solids
CN101467276A (en) * 2006-04-07 2009-06-24 巴斯夫欧洲公司 Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof
CN101263608B (en) * 2005-09-12 2010-07-21 巴斯夫欧洲公司 Fluorescent solar conversion cells based on fluorescent terylene dyes

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1169155A (en) * 1995-01-20 1997-12-31 巴斯福股份公司 Substituted quaterrylene tetracarboxylic acid diimides
WO2005089094A2 (en) * 2003-11-21 2005-09-29 The Board Of Regents Of The University And Community College System Of Nevada Materials and methods for the preparation of anisotropically-ordered solids
CN101263608B (en) * 2005-09-12 2010-07-21 巴斯夫欧洲公司 Fluorescent solar conversion cells based on fluorescent terylene dyes
CN101467276A (en) * 2006-04-07 2009-06-24 巴斯夫欧洲公司 Liquid crystalline rylene tetracarboxylic acid derivatives and use thereof

Also Published As

Publication number Publication date
WO2014002061A2 (en) 2014-01-03
US20150179954A1 (en) 2015-06-25
EP2867234A2 (en) 2015-05-06

Similar Documents

Publication Publication Date Title
WO2014008967A3 (en) Materials for organic electroluminescent devices
WO2014111269A3 (en) Materials for electronic devices
EP3033767A4 (en) Semiconductor structures and methods of fabrication of same
WO2012143080A3 (en) Materials for organic electroluminescent devices
EP2992562A4 (en) Stress relieving semiconductor layer
EP3145924A4 (en) An organic electroluminescent compound and an organic electroluminescent device comprising the same
EP3058586A4 (en) Integrated circuit package substrate
EP3489990A4 (en) Semiconductor substrate
EP3177628A4 (en) Organic electroluminescent compounds and organic electroluminescent devices comprising the same
EP2622644A4 (en) Semiconductor devices and methods for manufacturing the same
EP3201200A4 (en) Organic electroluminescent compound and organic electroluminescent device comprising the same
EP3270409A4 (en) Compound semiconductor substrate
EP3386987A4 (en) Organic electroluminescent compound and organic electroluminescent device comprising the same
EP3137467A4 (en) Organic electroluminescent compound and organic electroluminescent device comprising the same
GB2514918B (en) Nitride semiconductor substrate
EP2981567A4 (en) Organic phosphor-functionalized nanoparticles and compositions comprising the same
WO2014058232A3 (en) Spiro-type organic material, and organic electroluminescent device using same
EP3442020A4 (en) Power semiconductor module
EP3405511A4 (en) Organic semiconductor formulation and application thereof
EP3210663A4 (en) Organic silicon composition, and preparation and use thereof
EP3061739A4 (en) Silicon nitride substrate and silicon nitride circuit substrate using same
EP3166947A4 (en) An organic electroluminescent compound and an organic electroluminescent device comprising the same
EP3073535A4 (en) Novel compound semiconductor and utilization thereof
EP3087583A4 (en) Heterogeneous semiconductor material integration techniques
EP3135726A4 (en) Composition and polymer compound, and organic semiconductor element containing said composition and said polymer compound

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 14411184

Country of ref document: US

REEP Request for entry into the european phase

Ref document number: 2013810563

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2013810563

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2015519458

Country of ref document: JP

Kind code of ref document: A

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13810563

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: JP