Syntheses, photoluminescence, and electroluminescence of a series of iridium complexes with trifluoromethyl-substituted 2-phenylpyridine as the main ligands and tetraphenylimidodiphosphinate as the ancillary ligand.
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Novel Design of Iridium Phosphors with Pyridinylphosphinate Ligands for High-Efficiency Blue Organic Light-emitting Diodes.Functionalization of phosphorescent emitters and their host materials by main-group elements for phosphorescent organic light-emitting devices.Regioisomerism in cationic sulfonyl-substituted [Ir(C^N)2(N^N)](+) complexes: its influence on photophysical properties and LEC performance.Microwave-assisted one-pot synthesis of new ionic iridium complexes of [Ir(bzq)2(N^N)]+A- type and their selected electroluminescent properties.Rationally Designed Blue Triplet Emitting Gold(III) Complexes Based on a Phenylpyridine-Derived Framework.Syntheses, photoluminescence and electroluminescence of two novel platinum(ii) complexes.Crystal structure, photoluminescence and electroluminescence of three bluish green light-emitting iridium complexes.Iridium(iii) phosphorescent complexes with dual stereogenic centers: single crystal, electronic circular dichroism evidence and circularly polarized luminescence properties.Manipulation of phosphorescence efficiency of cyclometalated iridium complexes by substituted o-carboranes.A platinum(II) complex bearing deprotonated 2-(diphenylphosphino)benzoic acid for superior phosphorescence of monomers.A facile color-tuning strategy for constructing a library of Ir(iii) complexes with fine-tuned phosphorescence from bluish green to red using a synergetic substituent effect of –OCH3 and –CN at only the C-ring of C^N ligandNovel phosphorescent iridium(iii) complexes containing 2-thienyl quinazoline ligands: synthesis, photophysical properties and theoretical calculations
P2860
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P2860
Syntheses, photoluminescence, and electroluminescence of a series of iridium complexes with trifluoromethyl-substituted 2-phenylpyridine as the main ligands and tetraphenylimidodiphosphinate as the ancillary ligand.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Syntheses, photoluminescence, ...... inate as the ancillary ligand.
@en
Syntheses, photoluminescence, ...... inate as the ancillary ligand.
@nl
type
label
Syntheses, photoluminescence, ...... inate as the ancillary ligand.
@en
Syntheses, photoluminescence, ...... inate as the ancillary ligand.
@nl
prefLabel
Syntheses, photoluminescence, ...... inate as the ancillary ligand.
@en
Syntheses, photoluminescence, ...... inate as the ancillary ligand.
@nl
P2093
P356
P1433
P1476
Syntheses, photoluminescence, ...... inate as the ancillary ligand.
@en
P2093
Cheng-Cheng Wang
Jing-Lin Zuo
Ming-Yu Teng
Qiu-Lei Xu
Song Zhang
Tian-Yi Li
Wei-Nan Li
Xiao-Zeng You
P304
P356
10.1021/IC302510P
P407
P577
2013-04-15T00:00:00Z