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3,9'-Bicarbazole-Based Compounds with Reactive Functional Groups as Potential Cross-Linkable High Triplet Energy Hole-Transporting Materials
New oxiranyl-substituted derivatives of 3,9'-bicarbazole were synthesized by synthetic route involving Ullmann coupling, Vilsmeier formylation, reduction with sodium borohydride and the interaction of hydroxymethyl derivatives with 2-(chloromethyl)oxirane. The optical, photophysical and photoel...
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Published in: | Molecular Crystals and Liquid Crystals 2011-02, Vol.536, p.432 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | New oxiranyl-substituted derivatives of 3,9'-bicarbazole were synthesized by synthetic route involving Ullmann coupling, Vilsmeier formylation, reduction with sodium borohydride and the interaction of hydroxymethyl derivatives with 2-(chloromethyl)oxirane. The optical, photophysical and photoelectrical properties of the newly synthesized materials were studied. The electron photoemission spectra of the materials revealed the ionization potentials ranging range from 5.55 to 5.70 eV. Time-of-flight hole drift mobilities of bisphenol Z polycarbonate doped with 50 wt.% 3,9'-bicarbazole -based compounds exceed 10... cm.../V - s. (ProQuest: ... denotes formulae/symbols omitted.) |
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ISSN: | 1542-1406 1527-1943 |