Padalkar et al., 2016 - Google Patents

AIE active triphenylamine–benzothiazole based motifs: ESIPT or ICT emission

Padalkar et al., 2016

Document ID
5325380878815301854
Author
Padalkar V
Sakamaki D
Kuwada K
Tohnai N
Akutagawa T
Sakai K
Seki S
Publication year
Publication venue
RSC advances

External Links

Snippet

Two novel donor–π bridge–acceptor compounds containing excited state intramolecular proton transfer (ESIPT) and non-ESIPT units based on triphenylamine–benzothiazole were synthesized via Suzuki coupling reaction. Their photophysical properties were studied in the …
Continue reading at pubs.rsc.org (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1003Carbocyclic compounds
    • C09K2211/1007Non-condensed systems
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • C09K2211/1044Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
    • H01L51/0071Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1003Carbocyclic compounds
    • C09K2211/1011Condensed systems
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/50Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes [OLED] or polymer light emitting devices [PLED];
    • H01L51/5012Electroluminescent [EL] layer
    • H01L51/5016Triplet emission
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • 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

Similar Documents

Publication Publication Date Title
Padalkar et al. AIE active triphenylamine–benzothiazole based motifs: ESIPT or ICT emission
Zhang et al. Synthesis of blue light emitting bis (triphenylethylene) derivatives: a case of aggregation-induced emission enhancement
Liao et al. Quinoxaline based D–A–D molecules: high contrast reversible solid-state mechano-and thermo-responsive fluorescent materials
Li et al. New aggregation-induced emission enhancement materials combined triarylamine and dicarbazolyl triphenylethylene moieties
Tang et al. Efficient near-infrared emission based on donor-acceptor molecular architecture: The role of ancillary acceptor of cyanophenyl
Padalkar et al. Highly emissive excited-state intramolecular proton transfer (ESIPT) inspired 2-(2′-hydroxy) benzothiazole–fluorene motifs: spectroscopic and photophysical properties investigation
Petdee et al. Imidazole-based solid-state fluorophores with combined ESIPT and AIE features as self-absorption-free non-doped emitters for electroluminescent devices
Lee et al. Excimer emission based on the control of molecular structure and intermolecular interactions
TW201425275A (en) Compounds and organic electronic devices
Zhan et al. Phenothiazine substituted phenanthroimidazole derivatives: Synthesis, photophysical properties and efficient piezochromic luminescence
EP3533798B1 (en) Dibenzopyrromethene boron chelate compound, near infrared light absorbing material, thin film, and organic electronic device
TW201307352A (en) Nitrogenated aromatic heterocyclic derivative, and organic electroluminescent element using same
Zhan et al. Aggregation-induced emission and reversible mechanochromic luminescence of carbazole-based triphenylacrylonitrile derivatives
Kanekar et al. Quinoxaline based amines as Blue-orange emitters: Effect of modulating donor system on Optoelectrochemical and theoretical properties
Yan et al. A novel coumarin-based red fluorogen with AIE, self-assembly, and TADF properties
Padalkar et al. π–π Interactions: Influence on Molecular Packing and Solid‐State Emission of ESIPT and non‐ESIPT Motifs
Li et al. Highly efficient deep-red/near-infrared DA chromophores based on naphthothiadiazole for OLEDs applications
Zhang et al. A new series of N-substituted tetraphenylethene-based benzimidazoles: Aggregation-induced emission, fast-reversible mechanochromism and blue electroluminescence
Skardziute et al. Synthesis and optical properties of the isomeric pyrimidine and carbazole derivatives: effects of polar substituents and linking topology
Zhang et al. Synthesis, crystal Structures and aggregation-induced emission enhancement of aryl-substituted cyclopentadiene derivatives
Telore et al. Push–pull fluorophores with viscosity dependent and aggregation induced emissions insensitive to polarity
Yuan et al. Aggregation-induced bathochromic fluorescent enhancement for fluorenone dyes
Maeng et al. Rigid indolocarbazole donor moiety for highly efficient thermally activated delayed fluorescent device
Najare et al. Design, synthesis and characterization of π-conjugated 2, 5-diphenylsubstituted-1, 3, 4-oxadiazole-based D-π-A-π’-D′ form of efficient deep blue functional materials: Photophysical properties and fluorescence “Turn-off” chemsensors approach
Singh et al. Blue-orange emitting carbazole based donor-acceptor derivatives: Synthesis and studies of modulating acceptor unit on opto-electrochemical and theoretical properties