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Synthesis and Properties of 2,3,6,7-Tetraarylbenzo[1,2-b:4,5-b‘]difurans as Hole-Transporting Material
A new zinc-based annulation method produced regioselectively a variety of 2,3,6,7-tetraarylbenzo[1,2-b:4,5-b‘]difurans in good yields. The organic electroluminescent devices using these tetraarylbenzodifurans as hole-transporting materials showed better performance than those using α-NPD, the curren...
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Published in: | Journal of the American Chemical Society 2007-10, Vol.129 (39), p.11902-11903 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A new zinc-based annulation method produced regioselectively a variety of 2,3,6,7-tetraarylbenzo[1,2-b:4,5-b‘]difurans in good yields. The organic electroluminescent devices using these tetraarylbenzodifurans as hole-transporting materials showed better performance than those using α-NPD, the current standard HTM. The hole drift mobility and the glass-transition temperatures of the tetraarylbenzodifurans were also found to be better than those of α-NPD. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja074365w |