TY - JOUR
T1 - 2,6-Diphenylbenzo[1,2-b:4,5-b′]dichalcogenophenes
T2 - A New Class of High-Performance Semiconductors for Organic Field-Effect Transistors
AU - Takimiya, Kazuo
AU - Kunugi, Yoshihito
AU - Konda, Yasushi
AU - Niihara, Naoto
AU - Otsubo, Tetsuo
PY - 2004/4/28
Y1 - 2004/4/28
N2 - 2,6-Diphenylbenzo[1,2-b:4,5-b′]dichalcogenophenes including thiophene, selenophene, and tellurophene analogues as organic semiconductors for field-effect transistors were effectively synthesized in three steps from commercially available 1,4-dibromobenzene. All three benzodichalcogenophenes acted as good p-type semiconductors, and particularly the selenophene analogue, 2,6-diphenylbenzo[1,2-b:4,5-b′]diselenophene, showed high FET mobility of 0.17 cm2 V-1 s-1.
AB - 2,6-Diphenylbenzo[1,2-b:4,5-b′]dichalcogenophenes including thiophene, selenophene, and tellurophene analogues as organic semiconductors for field-effect transistors were effectively synthesized in three steps from commercially available 1,4-dibromobenzene. All three benzodichalcogenophenes acted as good p-type semiconductors, and particularly the selenophene analogue, 2,6-diphenylbenzo[1,2-b:4,5-b′]diselenophene, showed high FET mobility of 0.17 cm2 V-1 s-1.
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U2 - 10.1021/ja0496930
DO - 10.1021/ja0496930
M3 - Article
C2 - 15099088
AN - SCOPUS:1942489279
VL - 126
SP - 5084
EP - 5085
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 0002-7863
IS - 16
ER -