Oligothiophene-Functionalized Benzene and Tetrathienoanthracene: Effect of Enhanced -Conjugation on Optoelectronic Properties, Self-Assembly and Device Performance

被引:14
作者
Leitch, Alicea A. [1 ,2 ]
Stobo, Kimberly A. [1 ,2 ]
Hussain, Bashir [1 ,2 ]
Ghoussoub, Mireille [3 ]
Ebrahimi-Takalloo, Saeedeh [3 ]
Servati, Peyman [3 ]
Korobkov, Ilia [1 ]
Brusso, Jaclyn L. [1 ,2 ]
机构
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Ctr Catalysis Res & Innovat, Ottawa, ON K1N 6N5, Canada
[3] Univ British Columbia, Dept Elect & Comp Engn, Vancouver, BC V6T 1Z4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Semiconductors; Pi interactions; Substituent effects; Molecular devices; Conducting materials; CHARGE-TRANSPORT; ELECTRONIC-PROPERTIES; CRYSTAL-STRUCTURES; TRANSISTORS; SEMICONDUCTORS; SYSTEMS; DESIGN; ACENES;
D O I
10.1002/ejoc.201300731
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The versatility of fourfold Stille coupling to afford oligothiophene-functionalized tetrathienoanthracene (TTA) and benzene derivatives is described. The influence of the larger, more rigid TTA core on the electronic and structural properties was investigated. Comparative optical and electrochemical studies demonstrate a diminishing HOMO-LUMO gap as the length of the oligothiophene chain increases, with the rigid TTA compounds exhibiting lower energy gaps than the more flexible benzene analogues. X-ray crystallography studies reveal that the thiophene-substituted TTA structure consists of slipped -stacks with several close intrastack - interactions; no close contacts are observed for the benzene derivative due to twisting of the thiophene ligands out of plane. Consequently, the molecules in the benzene analogue are isolated from their neighbours. The thiophene and bithiophene functionalised TTA compounds were fabricated into OTFT devices in bottom-contact configuration and exhibited mobilities of ca. 10(-4) cm(2)V(-1)s(-1) and on/off ratios of more than four orders of magnitude.
引用
收藏
页码:5854 / 5863
页数:10
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