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1.
Chem Commun (Camb) ; 52(2): 339-42, 2016 Jan 07.
Artigo em Inglês | MEDLINE | ID: mdl-26515454

RESUMO

High efficiency and color tuning of thermally activated delayed fluorescent emitters were achieved at the same time by designing emitters with a twin emitter molecular design. The control of the interconnect position between two emitters could manage the emission spectrum of the thermally activated delayed fluorescent emitters without affecting the quantum efficiency.

2.
Angew Chem Int Ed Engl ; 54(17): 5201-4, 2015 Apr 20.
Artigo em Inglês | MEDLINE | ID: mdl-25727757

RESUMO

Dual emitting cores for thermally activated delayed fluorescent (TADF) emitters were developed. Relative to the corresponding TADF emitter with a single emitting core the TADF emitter with a dual emitting core, 3,3',5,5'-tetra(carbazol-9-yl)-[1,1'-biphenyl]-2,2',6,6'-tetracarbonitrile, showed enhanced light absorption accompanied by a high photoluminescence quantum yield. The quantum and power efficiencies of the TADF devices were enhanced by the dual emitting cores.

3.
J Nanosci Nanotechnol ; 12(2): 1361-4, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22629957

RESUMO

We report narrow band gap bipolar host materials, CbPr-3 (9,9'-[(3,3'-Biphenyl-3.3'-yl-bipyridine)-1,3-biphenyl]bis-9H-carbazole) and Bim-4 (9,9'-[5-(1-phenyl-1H-benzimadazol-2yl)-1,3-phenylene] bis-9H-carbazole), for blue phosphorescent OLEDs application. These two bipolar hosts have high triplet energy of > 2.9 eV, capable of reducing the driving voltages and improving efficiencies. Significant low driving voltages of 7.4 and 6.6 V were obtained for CbPr-3 and Bim-4 hosts, compared with 9.0 V of the commonly used host, mCP (1,3-bis(9-carbazolyl)benzene). At a given constant luminance of 1000 cd/m2, the power efficiency of both the bipolar host devices was enhanced by 2.5 times.

4.
Org Lett ; 6(22): 3881-4, 2004 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-15496054

RESUMO

[reaction: see text] The total synthesis of (+/-)-dibromophakellstatin is described. The molecule is constructed from a key syn-diazide, formed by a hypervalent iodine-mediated diazidation of a dihydrodipyrrolopyrazinone ring structure.

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