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Photoreactions of Endohedral Metallofullerene with Siliranes: Electronic Properties of Carbosilylated Lu?N@Ih-C80.


ABSTRACT: Photochemical carbosilylation of Lu?N@Ih-C80 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 Lu?N@Ih-C80 was verified on the basis of density functional theory calculations.

SUBMITTER: Kako M 

PROVIDER: S-EPMC6154294 | biostudies-literature | 2017 May

REPOSITORIES: biostudies-literature

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Photoreactions of Endohedral Metallofullerene with Siliranes: Electronic Properties of Carbosilylated Lu₃N@I<sub>h</sub>-C<sub>80</sub>.

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]

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