Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tomoya Kashiki"'
Publikováno v:
The Journal of Organic Chemistry. 76:4061-4070
Two dimers (2 and 3), dendritic tetramer (4), hexamer (5), and decamer (6) of benzo[1,2-b:3,4-b':5,6-b'']trithiophene (BTT), a potential π-core unit with C(3h) symmetry, were synthesized, characterized, and evaluated for possible use as organic semi
Publikováno v:
SPIE Proceedings.
The mechanism of high field-effect mobility observed recently in transistors with donor-acceptor alternating polymers was experimentally and numerically examined. It was revealed that the trapped electrons injected from the drain electrode into the l
Autor:
Naoyuki Yanai, Itaru Osaka, Ryusuke Sugimoto, Kazuo Takimiya, Eigo Miyazaki, Noriko Takemura, Tomoya Kashiki, Shoji Shinamura
Publikováno v:
Organic letters. 14(18)
Selective functionalization protocols of naphtho[1,2-b;5,6-b′]dithiophene (NDT3) by combining protection of the thiophene α-positions and direct borylation on the naphthalene core are described, which allows synthesizing a number of new NDT3-based
Publikováno v:
ChemInform. 40
New solution-prosessable n-channel organic semiconductors were developed based on a 2,6-bis(dicyanomethylene)-2,6-dihydrobenzo[1,2-b:4,5-b′]dithiophene core. The OFETs showed n-channel transistor c...
Autor:
Hirokazu Kuwabara, Masahiro Kohara, Shoji Shinamura, Eigo Miyazaki, Masaaki Ikeda, Tomoya Kashiki, Kazuo Takimiya
Publikováno v:
ChemInform. 40
A convenient one-pot procedure for the synthesis of benzo[b]thiophenes and selenophenes from readily available o-halo-ethynylbenzene precursors is described. Regardless of the substituent on the acetylene terminus or the number of cyclization moietie
Autor:
Shoji Shinamura, Eigo Miyazaki, Masahiro Kohara, Masaaki Ikeda, Kazuo Takimiya, Hirokazu Kuwabara, Tomoya Kashiki
Publikováno v:
Organic letters. 11(11)
A convenient one-pot procedure for the synthesis of benzo[b]thiophenes and selenophenes from readily available o-halo-ethynylbenzene precursors is described. Regardless of the substituent on the acetylene terminus or the number of cyclization moietie
Publikováno v:
Chemistry Letters. 38:568-569
New solution-prosessable n-channel organic semiconductors were developed based on a 2,6-bis(dicyanomethylene)-2,6-dihydrobenzo[1,2-b:4,5-b′]dithiophene core. The OFETs showed n-channel transistor c...
Publikováno v:
Chemistry Letters. 38:352-353
2,6-Dialkylbenzo[1,2-b:4,5-b′]diselenophenes developed as soluble organic semiconductors gave a unique molecular arrangement in bulk single crystals, where π-stacking dimeric pairs and monomeric mo...
Publikováno v:
Chemistry Letters. 37:284-285
2,6-Dialkyl[1,2-b:4,5-b′]dithiophenes were synthesized as novel solution-processible organic semiconductors. Thin films of the organic semiconductors deposited on Si/SiO2 substrates by spin coating...
Autor:
Tomoya Kashiki, Shoji Shinamura, Masahiro Kohara, Eigo Miyazaki, Kazuo Takimiya, Masaaki Ikeda, Hirokazu Kuwabara
Publikováno v:
Organic Letters; Jun2009, Vol. 11 Issue 11, p2473-2475, 3p