![]() Bis[2-(diphenylphosphino)phenyl] ether oxide structure
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Common Name | Bis[2-(diphenylphosphino)phenyl] ether oxide | ||
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CAS Number | 808142-23-6 | Molecular Weight | 570.553 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 753.3±60.0 °C at 760 mmHg | |
Molecular Formula | C36H28O3P2 | Melting Point | 280℃ | |
MSDS | Chinese USA | Flash Point | 421.5±53.2 °C |
Pt(II) metal complexes tailored with a newly designed spiro-arranged tetradentate ligand; harnessing of charge-transfer phosphorescence and fabrication of sky blue and white OLEDs.
Inorg. Chem. 54(8) , 4029-38, (2015) Tetradentate bis(pyridyl azolate) chelates are assembled by connecting two bidentate 3-trifluoromethyl-5-(2-pyridyl)azoles at the six position of pyridyl fragment with the tailored spiro-arranged fluorene and/or acridine functionalities. These new chelates we... |
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Stable blue thermally activated delayed fluorescent organic light-emitting diodes with three times longer lifetime than phosphorescent organic light-emitting diodes.
Adv. Mater. 27(15) , 2515-20, (2015) High quantum efficiency above 18% and extended lifetime three times longer than that of phosphorescent organic light-emitting diodes (OLEDs) are demonstrated in blue thermally activated delayed fluorescent OLEDs. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinh... |
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Design of efficient thermally activated delayed fluorescence materials for pure blue organic light emitting diodes.
J. Am. Chem. Soc. 134(36) , 14706-9, (2012) Efficient thermally activated delayed fluorescence (TADF) has been characterized for a carbazole/sulfone derivative in both solutions and doped films. A pure blue organic light emitting diode (OLED) based on this compound demonstrates a very high external qua... |
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Efficient blue organic light-emitting diodes employing thermally activated delayed fluorescence Zhang et al.
Nature Photon. 8(4) , 326-332, (2014)
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Effect of Atom Substitution in Chalcogenodiazole-Containing Thermally Activated Delayed Fluorescence Emitters on Radiationless Transition Tanaka et al.
J. Phys. Chem. C Nanomater. Interfaces 119(6) , 2948-2955, (2015)
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