Zobrazeno 1 - 10
of 157
pro vyhledávání: '"Ko Furukawa"'
Autor:
Ayano Nakagawa, Makiko Nishino, Hiroyuki Niwa, Katsuma Ishino, Zhiyong Wang, Haruka Omachi, Ko Furukawa, Takahisa Yamaguchi, Tatsuhisa Kato, Shunji Bandow, Jeremy Rio, Chris Ewels, Shinobu Aoyagi, Hisanori Shinohara
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-9 (2018)
While endohedral metallofullerenes have demonstrated advantageous electronic and magnetic properties, the isolation of monomeric M@C60 remains highly challenging. Here, the authors prepare trifluoromethylated Gd@C60 and La@C60, where the functionaliz
Externí odkaz:
https://doaj.org/article/941fe21500694600a1b74936afb16454
Autor:
Satish Jakkampudi, Manabu Abe, Naomitsu Komori, Ryukichi Takagi, Ko Furukawa, Claudine Katan, Wakako Sawada, Noriko Takahashi, Haruo Kasai
Publikováno v:
ACS Omega, Vol 1, Iss 2, Pp 193-201 (2016)
Externí odkaz:
https://doaj.org/article/029c86a155024abfa3a0bc50dbe750b3
Supramolecular copolymerization of hydrophobic and hydrophilic monomers in liquid crystalline media.
Publikováno v:
Chemical Science; 3/21/2024, Vol. 15 Issue 11, p4068-4074, 7p
Autor:
Keito Shimomura, Yuma Nakamura, Hiroto Kai, Kyosuke Saito, Ko Furukawa, Shigeki Mori, Masatoshi Ishida, Hiroyuki Furuta
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 26:807-814
Novel site-selective hetero-copper(II)/zinc(II) complexes of a cisoid-configured doubly N-confused dioxohexaphyrin analog (c-ZnCu-2 and c-CuZn-2) were synthesized and characterized. The resulting heterometal complexes exhibited a unique near-infrared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87a332ca93f729c6e3eadd2dae738024
https://doi.org/10.1142/s1088424622500456
https://doi.org/10.1142/s1088424622500456
Publikováno v:
Chemistry Letters; Feb2024, Vol. 53 Issue 2, p1-5, 5p
Publikováno v:
Bulletin of the Chemical Society of Japan; Feb2024, Vol. 97 Issue 2, p1-5, 5p
Publikováno v:
Organic Letters. 24:3839-3843
A one-pot synthesis of cobalt(II) complexes of 5,10,15,20-tetraaryl-5,15-diazaporphyrins (CoTADAPs) from the corresponding 5-aryl-1-arylamino-9-chlorodipyrrins and cobalt(II) acetate is reported. The CoTADAPs exhibited characteristic electrochemical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e85467e91b0b0e6906557917a8d33a36
https://doi.org/10.1021/acs.orglett.2c01411
https://doi.org/10.1021/acs.orglett.2c01411
Autor:
Naoya Muramatsu, Ko Furukawa, Yutaro Fujita, Yuna Satoh, Yoshihiro Matano, Mao Minoura, Haruyuki Nakano, Tadaaki Ikoma
Publikováno v:
ChemPlusChem. 86:1476-1486
This work reports a series of covalently linked hybrids comprising 5,10,15,20-tetraaryl-5,15-diazaporphyrinoids (M-TADAP; M = Ni, Zn, Cu) and amines. M-TADAP-amine hybrids were prepared via the metal-templated cyclization of the corresponding metal(I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36ab559e49f0034f25f1478fb4902d67
https://doi.org/10.1002/cplu.202100429
https://doi.org/10.1002/cplu.202100429
Autor:
Ko Furukawa, Masatoshi Ishida, Hajime Kusaba, Shigeki Mori, Kazuhisa Yamasumi, Yongshu Xie, Hiroyuki Furuta, Pingchun Wei, Tatsumi Ishihara, Yogesh Kumar Maurya, Takahide Shimada
Publikováno v:
Chemistry – An Asian Journal. 16:743-747
A facile synthetic strategy towards conformationally stable chiral chromophores based on dimeric porphyrinoids has been established. A peculiar class of face-to-face intramolecularly interlocked corrole dimers were formed by the oxidative C-C couplin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2918316ad19ce700a0d911e7aa4484f
https://doi.org/10.1002/asia.202100083
https://doi.org/10.1002/asia.202100083
Autor:
Jianxin Song, Pingting Liu, Atsuhiro Osuka, Mingbo Zhou, Ko Furukawa, Ling Xu, Fenni Zhang, Takayuki Tanaka, Kaisheng Wang, Kenichi Kato, Akito Nakai
Publikováno v:
Angewandte Chemie. 133:7078-7082
The synthesis of robust high-spin carbon radicals is an important topic in organic chemistry. Toward this end, several porphyrin-stabilized radicals have been systematically explored. A singly naphthalene-fused porphyrin radical was synthesized by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b8b4741781e003684a8bab998cba4a2
https://doi.org/10.1002/ange.202015356
https://doi.org/10.1002/ange.202015356