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Fluorine-substituted quinoidal thiophene with a F–H hydrogen bond locked conformation for high-performance n-channel organic transistors†
Deliang Wang,Xiaolan Qiao,Guangcheng Ouyang,Hongzhuo Wu,Hongxiang Li
Chemical Communications Pub Date : 05/07/2019 00:00:00 , DOI:10.1039/C9CC02872B
Abstract

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.

Graphical abstract: Fluorine-substituted quinoidal thiophene with a F–H hydrogen bond locked conformation for high-performance n-channel organic transistors
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