Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Kazuaki Oniwa"'
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Simple synthetic routes to polyaromatic hydrocarbons are important due to their applications in organic electronics. Here the authors report a straightforward synthesis of a diverse range of polyaromatic hydrocarbons, via a one-pot oxidative cyclisat
Externí odkaz:
https://doaj.org/article/1e63fa2d7f3d4b889832cdf1b7e3d7c7
Publikováno v:
Journal of Chemical Physics; 2015, Vol. 142 Issue 14, p1-10, 10p, 4 Diagrams, 2 Graphs
Autor:
Hiromasa Kikuchi, Kazuaki Oniwa, Yoshinori Yamamoto, Masahiro Terada, Tienan Jin, Zhanqiang Xu, Ming Bao
Publikováno v:
Chemistry - A European Journal. 24:9041-9050
Star-shaped π-extended molecules comprising discotic aromatic cores and peripheral π-conjugated arms have attracted significant attention as diverse optoelectronic materials in terms of their large π-surface, tunable self-assembly, enhanced charge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2998fa60a7872b84a1a3f0df262a865
https://doi.org/10.1002/chem.201801849
https://doi.org/10.1002/chem.201801849
Publikováno v:
Bulletin of the Chemical Society of Japan. 90:789-797
A new series of highly π-extended dicyanomethylene-endcapped quinoidal S,N-heteroacenes (JH-quinoids) fused with thiophene and pyrrole rings have been designed and synthesized. The π-extension of the central S,N-heteroacene cores gives rise to sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65df3b89a0e7ea2543ff5eb4d89cc058
https://doi.org/10.1246/bcsj.20170083
https://doi.org/10.1246/bcsj.20170083
Publikováno v:
Organic Electronics. 34:23-27
A highly emissive red luminescent single crystal which shows aggregation induced emission (AIE) property and optical waveguide edge emission based on small organic functional molecule, cyano-substituted 2,5-di((E)-styryl)thieno[3,2-b]thiophene (CNP2V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e30a0b8645692c39aa9501746ee2372
https://doi.org/10.1016/j.orgel.2016.04.001
https://doi.org/10.1016/j.orgel.2016.04.001
2-Positional pyrene end-capped oligothiophenes for high performance organic field effect transistors
Autor:
Yoshinori Yamamoto, Susumu Ikeda, Hidekazu Shimotani, Kazuaki Oniwa, Naoki Asao, Hiromasa Kikuchi, Katsumi Tanigaki, Tienan Jin
Publikováno v:
Chemical Communications. 52:4800-4803
Three new 2-positional pyrene end-capped oligothiophene co-oligomers, BPynT (n = 1, 2, 3), have been synthesized for application in organic field effect transistors (OFETs). BPy2T showed the highest hole mobility of 3.3 cm(2) V(-1) s(-1) in a single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a80a0c4075725c61132e61af32b1f97a
https://doi.org/10.1039/c6cc00948d
https://doi.org/10.1039/c6cc00948d
Publikováno v:
Angewandte Chemie. 128:267-271
A novel FeCl3-mediated oxidative spirocyclization for construction of a new class of di-spirolinked π-conjugated molecules, dispiro[fluorene-9,5'-indeno[2,1-a]indene-10',9''-fluorene]s (DSFIIFs), has been reported. The combination of FeCl3 with FeO(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b5c49c26afe68419df0546c696a38d2
https://doi.org/10.1002/ange.201507794
https://doi.org/10.1002/ange.201507794
Autor:
Jian Zhao, Yoshinori Yamamoto, Kazuaki Oniwa, Ashraful Islam, Tienan Jin, Naoki Asao, Hua Jiang, Liyuan Han, Ming Bao, Ying Ji Sun
Publikováno v:
Tetrahedron. 71:6534-6540
A new series of donor-p-acceptor organic dyes based on thieno[3,2-a]carbazole as a new donor moiety, designated as JH-dyes, has been synthesized for dye-sensitized solar cells (DSCs). The photophysical properties and DSC performances of JH-dyes have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::412d10a4f56f1dff25de63ab1485fd14
https://doi.org/10.1016/j.tet.2015.04.018
https://doi.org/10.1016/j.tet.2015.04.018
Autor:
Liyuan Han, Jian Zhao, Yoshinori Yamamoto, Tienan Jin, Ashraful Islam, Kazuaki Oniwa, Naoki Asao, Chuanjiang Qin
Publikováno v:
Organic Chemistry Frontiers. 2:253-258
A new series of donor–π-acceptor organic K-dyes based on the thieno[2,3,a]carbazole moiety as a new electron donor, trithiophene as a π-linker and cyanoacrylic acid as an electron acceptor were designed and synthesized for achieving high performa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4899a090169558251eb3013a082b6f7
https://doi.org/10.1039/c4qo00285g
https://doi.org/10.1039/c4qo00285g
Autor:
T. Kanagasekaran, Susumu Ikeda, Hiroyuki Tamura, Hidekazu Shimotani, Yoshinori Yamamoto, Naoki Asao, Tienan Jin, Hui Shang, Katsumi Tanigaki, Masayuki Yoshizawa, Kazuaki Oniwa, Miyuki Kanno, K. Abe
Publikováno v:
The Journal of Physical Chemistry C, Vol. 121, no.4, p. 2364-2368 (2017)
Three organic semiconductors consisting of thiophene, furan, and phenylene groups showed either one or two gain-narrowed emission peaks by excitation with a laser pulse. The two gain-narrowed emission peaks are optically studied and assigned to 0 →
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc44f4c02688be1e74d248dec6f851dd
https://hdl.handle.net/2078.1/226066
https://hdl.handle.net/2078.1/226066
