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Fluorine-substituted quinoidal thiophene with a F-H hydrogen bond locked conformation for high-performance n-channel organic transistors
The novel dicyanomethylene-substituted 1,2-bis(thieno[3,2- b ]thiophene-2-yl)ethene based quinoidal compounds QBTTE and F2-QBTTE are reported. The F H (vinylene) hydrogen bonds lock the backbone conformation and greatly improve the transistor performance of F2-QBTTE . The novel dicyanomethylene-subs...
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Published in: | Chemical communications (Cambridge, England) England), 2019-05, Vol.55 (44), p.6253-6256 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The novel dicyanomethylene-substituted 1,2-bis(thieno[3,2-
b
]thiophene-2-yl)ethene based quinoidal compounds
QBTTE
and
F2-QBTTE
are reported. The F H (vinylene) hydrogen bonds lock the backbone conformation and greatly improve the transistor performance of
F2-QBTTE
.
The novel dicyanomethylene-substituted 1,2-bis(thieno[3,2-
b
]thiophene-2-yl)ethene based quinoidal compounds
QBTTE
and
F2-QBTTE
are reported. |
---|---|
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c9cc02872b |