TY - JOUR
T1 - Phenanthro[1,2-b:8,7-b']dithiophene
T2 - A new picene-type molecule for transistor applications
AU - Nishihara, Yasushi
AU - Kinoshita, Megumi
AU - Hyodo, Keita
AU - Okuda, Yasuhiro
AU - Eguchi, Ritsuko
AU - Goto, Hidenori
AU - Hamao, Shino
AU - Takabayashi, Yasuhiro
AU - Kubozono, Yoshihiro
PY - 2013/11/14
Y1 - 2013/11/14
N2 - A new picene-type molecule, phenanthro[1,2-b:8,7-b']dithiophene, has been synthesized for use in organic field-effect transistors (OFETs). The molecule consists of a phenanthrene core with two thiophene rings fused on the ends. This molecule can be recognized as a picene analogue. The electronic structure of the molecule was determined by its optical absorption spectrum together with a theoretical calculation based on density functional theory (DFT). The topological and electronic structures of thin films produced by direct thermal evaporation of the compounds and by deposition from a solution were characterized by optical imaging, X-ray diffraction, and atomic force microscopy. FET devices were fabricated with these thin films, and showed field-effect mobility as high as 10-1 cm2 V-1 s-1.
AB - A new picene-type molecule, phenanthro[1,2-b:8,7-b']dithiophene, has been synthesized for use in organic field-effect transistors (OFETs). The molecule consists of a phenanthrene core with two thiophene rings fused on the ends. This molecule can be recognized as a picene analogue. The electronic structure of the molecule was determined by its optical absorption spectrum together with a theoretical calculation based on density functional theory (DFT). The topological and electronic structures of thin films produced by direct thermal evaporation of the compounds and by deposition from a solution were characterized by optical imaging, X-ray diffraction, and atomic force microscopy. FET devices were fabricated with these thin films, and showed field-effect mobility as high as 10-1 cm2 V-1 s-1.
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U2 - 10.1039/c3ra44050h
DO - 10.1039/c3ra44050h
M3 - Article
AN - SCOPUS:84885404106
SN - 2046-2069
VL - 3
SP - 19341
EP - 19347
JO - RSC Advances
JF - RSC Advances
IS - 42
ER -