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ABSTRACT:
SUBMITTER: Kako M
PROVIDER: S-EPMC6154294 | biostudies-literature | 2017 May
REPOSITORIES: biostudies-literature
Kako Masahiro M Minami Kazuya K Kuroiwa Taiki T Fukazawa Shinpei S Arikawa Yuki Y Yamada Michio M Maeda Yutaka Y Li Qiao-Zhi QZ Nagase Shigeru S Akasaka Takeshi T
Molecules (Basel, Switzerland) 20170520 5
Photochemical carbosilylation of Lu₃N@<i>I<sub>h</sub></i>-C<sub>80</sub> was performed using siliranes (silacyclopropanes) to afford the corresponding [5,6]- and [6,6]-adducts. Electrochemical studies indicated that the redox potentials of the carbosilylated derivatives were shifted cathodically in comparison with those of the [5,6]-pyrrolidino adducts. The electronic effect of the silirane addends on Lu₃N@<i>I<sub>h</sub></i>-C<sub>80</sub> was verified on the basis of density functional theor ...[more]