1.
Chem Commun (Camb)
; 51(9): 1681-4, 2015 Jan 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25512949
RESUMO
For the first time, electron-rich thiophene units were fused into the skeleton of corannulene to extend π-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).