Thiophene-based twisted bistricyclic aromatic ene with tricoordinate boron: a new n-type semiconductor

被引:19
|
作者
Adachi, Yohei [1 ]
Nomura, Takanori [1 ]
Tazuhara, Shion [2 ]
Naito, Hiroyoshi [2 ]
Ohshita, Joji [1 ,3 ]
机构
[1] Hiroshima Univ, Appl Chem Program, Grad Sch Adv Sci & Engn, Higashihiroshima 7398527, Japan
[2] Osaka Prefecture Univ, Dept Phys & Elect, Grad Sch Engn, Naka Ku, 1-1 Gakuen Cho, Sakai, Osaka 5998531, Japan
[3] Hiroshima Univ, Digital Monozukuri Mfg Educ & Res Ctr, Div Mat Model Based Res, Higashihiroshima 7390046, Japan
关键词
DYNAMIC STEREOCHEMISTRY; OVERCROWDED ETHYLENE; OPTICAL-PROPERTIES; THERMOCHROMISM; TRIARYLBORANE; INTERPLAY; ACCEPTOR; COLOR;
D O I
10.1039/d0cc07952a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The incorporation of tricoordinate boron into conjugated systems is of current interest in the field of organic electronics. In this study, a tricoordinate boron-embedded thiophene-based bistricyclic aromatic ene (BAE) was synthesized as a new boron-containing conjugated system. The combination of tricoordinate boron and fused thiophene rings imposed the twisted conformation in the BAE structure, resulting in the narrow energy absorption with the low-lying LUMO. Preliminary studies on the application of the highly electron-deficient boron-embedded BAE to organic field-effect transistors (OFETs) were also performed, revealing its moderately high electron mobility.
引用
收藏
页码:1316 / 1319
页数:5
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