Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kanako Ogasawara"'
Autor:
Shigeaki Nakazawa, Takeji Takui, Yasushi Morita, Tomoaki Ise, Tomohiro Yoshino, Kanako Ogasawara, Kazuhiro Nakasuji, Kazunobu Sato, Akira Ueda, Shinsuke Nishida
Publikováno v:
Angewandte Chemie. 122:6477-6481
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50a597df541b1599da9b09d6cf763ec5
https://doi.org/10.1002/ange.201002626
https://doi.org/10.1002/ange.201002626
Autor:
Yasushi Morita, Kazunobu Sato, Tadahiro Kobayashi, Shinsuke Nishida, Kozo Fukui, Akira Ueda, Kazuhiro Nakasuji, Takeji Takui, Kanako Ogasawara
Publikováno v:
Journal of the American Chemical Society. 130:14954-14955
We have demonstrated the features of curve-structured phenalenyl chemistry, for the first time. A phenalenyl-fused corannulene anion has been designed by the annelation of a six-memberd ring across peri-positions of corannulene and generated as a sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6136f9369772e52de29bb19d0b5c15aa
https://doi.org/10.1021/ja806708j
https://doi.org/10.1021/ja806708j
Autor:
Kanako Ogasawara, Akira Ueda, Yasushi Morita, Kozo Fukui, Kazunobu Sato, Takeji Takui, Kazuhiro Nakasuji, Shinsuke Nishida
Publikováno v:
Australian Journal of Chemistry. 63:1627
A new corannulene-based curved neutral π-radical bearing a tert-butylnitroxide moiety has been synthesized and isolated as an air-stable solid. Direct attachment of the spin centre to the corannulene skeleton gives rise to an extensive spin-delocali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c95afc34170e0d0ac0d118dea11ad92
https://doi.org/10.1071/ch10280
https://doi.org/10.1071/ch10280
Autor:
Akira Ueda, Kanako Ogasawara, Shinsuke Nishida, Kozo Fukui, Kazunobu Sato, Takeji Takui, Kazuhiro Nakasuji, Yasushi Morita
Publikováno v:
Australian Journal of Chemistry; Dec2010, Vol. 63 Issue 12, p1627-1633, 7p