Journal
CHEMICAL COMMUNICATIONS
Volume 51, Issue 9, Pages 1681-1684Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc08451a
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Funding
- National Natural Science Foundation [21102120, J1210014]
- PhD Programs Foundation of Ministry of Education of China [20110121120016, 2012121024, 2011121014]
- NFFTBS [J1310024]
- Program for Changjiang Scholars and Innovative Research Team in University
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For the first time, electron-rich thiophene units were fused into the skeleton of corannulene to extend pi-surfaces and tune arrangement in single crystals. Two isomeric butterfly-like thiophene-fused dibenzo[a, g]corannulenes (3 and 5) were synthesized. Isomer 3 showed p-type transport properties, with a hole mobility of 0.06 cm(2) V-1 s(-1).
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