Chen et al., 2005 - Google Patents
Synthesis and characterization of n‐type materials for non‐doped organic red‐light‐emitting diodesChen et al., 2005
- Document ID
- 1654617026334968090
- Author
- Chen S
- Xu X
- Liu Y
- Yu G
- Sun X
- Qiu W
- Ma Y
- Zhu D
- Publication year
- Publication venue
- Advanced functional materials
External Links
Snippet
Abstract Two compounds, 2, 3‐dicyano‐5, 6‐di (4′‐diphenylamino‐biphenyl‐4‐yl) pyrazine (CAPP) and 6, 7‐dicyano‐2, 3‐di (4′‐diphenylamino‐biphenyl‐4‐yl) quinoxaline (CAPQ), capable of intramolecular charge transfer, have been designed and synthesized in …
- 239000000463 material 0 title description 26
Classifications
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
- H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
- H01L51/0072—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
- H01L51/0084—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H01L51/0085—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Iridium
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
- H01L51/0079—Metal complexes comprising a IIIB-metal (B, Al, Ga, In or TI), e.g. Tris (8-hydroxyquinoline) gallium (Gaq3)
- H01L51/0081—Metal complexes comprising a IIIB-metal (B, Al, Ga, In or TI), e.g. Tris (8-hydroxyquinoline) gallium (Gaq3) comprising aluminium, e.g. Alq3
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0059—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0052—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/50—Solid 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];
- H01L51/5012—Electroluminescent [EL] layer
- H01L51/5016—Triplet emission
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- 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
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L2251/00—Indexing scheme relating to organic semiconductor devices covered by group H01L51/00
- H01L2251/30—Materials
- H01L2251/301—Inorganic materials
- H01L2251/303—Oxides, e.g. metal oxides
- H01L2251/305—Transparent conductive oxides [TCO]
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- 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
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Chen et al. | Synthesis and characterization of n‐type materials for non‐doped organic red‐light‐emitting diodes | |
Justin Thomas et al. | Color tuning in benzo [1, 2, 5] thiadiazole‐based small molecules by amino conjugation/deconjugation: bright red‐light‐emitting diodes | |
Lyu et al. | Highly efficient red phosphorescent OLEDs based on non‐conjugated silicon‐cored spirobifluorene derivative doped with Ir‐complexes | |
Sun et al. | Novel carbazolyl-substituted spiro [acridine-9, 9′-fluorene] derivatives as deep-blue emitting materials for OLED applications | |
Tang et al. | Novel yellow phosphorescent iridium complexes containing a carbazole–oxadiazole unit used in polymeric light-emitting diodes | |
KR100850886B1 (en) | Organometalic compounds for electroluminescence and organic electroluminescent device using the same | |
EP2145936A2 (en) | Fluorene and pyrene derivatives and organic electroluminescent device using the same | |
KR101807644B1 (en) | Luminescent element material and luminescent element | |
Chen et al. | Synthesis, structure and luminescence properties of zinc (II) complexes with terpyridine derivatives as ligands | |
Cui et al. | A simple systematic design of phenylcarbazole derivatives for host materials to high-efficiency phosphorescent organic light-emitting diodes | |
CN105576138B (en) | Platinum (II) isoquinoline-pyridine-benzene-based complex, preparation method thereof and organic light emitting diode prepared therefrom | |
JP2012507507A (en) | Novel compound for organic electronic material and organic electronic device including the same | |
KR20110041726A (en) | Aromatic compound and organic electroluminescent device using the same | |
KR20130007934A (en) | Organic electroluminescence device using the triphenylene derivative | |
KR20100106014A (en) | Novel organic electroluminescent compounds and organic electroluminescent device using the same | |
Xu et al. | High‐Efficiency Blue Light‐Emitting Diodes Based on a Polyphenylphenyl Compound with Strong Electron‐Accepting Groups | |
KR20170057856A (en) | Compound having spiro structure and organic light emitting device comprising the same | |
US20210249612A1 (en) | Luminescent tetradentate gold(iii) compounds for organic light-emitting devices and their preparation | |
Islam et al. | Efficient non-doped deep blue organic light emitting diodes with high external quantum efficiency and a low efficiency roll-off based on donor-acceptor molecules | |
Li et al. | Synthesis and properties of n-type triphenylpyridine derivatives and applications in deep-blue organic light-emitting devices as electron-transporting layer | |
KR20170057855A (en) | Compound having spiro structure and organic light emitting device comprising the same | |
Zhu et al. | Multifunctional homoleptic iridium (III) dendrimers towards solution-processed nondoped electrophosphorescence with low efficiency roll-off | |
Song et al. | [1, 2, 4] Triazolo [1, 5-a] pyridine based host materials for high-performance red PhOLEDs with external quantum efficiencies over 23% | |
Sun et al. | Aminoborane-based bipolar host material for blue and white-emitting electrophosphorescence devices | |
Zang et al. | Efficient multilayer and single layer phosphorescent organic light-emitting devices using a host with balanced bipolar transporting properties and appropriate energy level |