Structural Determination and Characterization of Electronic Properties of Photosilylated Derivatives of C<sub>70</sub>

The photoreactions of C 70 and mesityl‐substituted disilirane (disilacyclopropane) 1a afforded the corresponding adducts 2a and 3a , the former of which was reported previously. The structures of 2a and 3a are unequivocally established respectively as a 1,4‐adduct at the [ d , d' ] site and as a 1,2‐adduct at the [ a , b ] bond, respectively, using single‐crystal X‐ray crystallographic analyses. The latter structure represents the first example of crystallographic study of 1,3‐disilolane (1,3‐disilacyclopentane) derivatives of fullerenes. The electronic properties of these products are characterized based on electrochemical and theoretical studies elucidating the electron‐donating effects of silyl groups.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-04-09
DOI
https://doi.org/10.1002/ejoc.202500153
Primary Topic
Fullerene Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Structural Determination and Characterization of Electronic Properties of Photosilylated Derivatives of C70

Masanori Yasui, Keiko Kamioka, Takeshi Akasaka, Michio Yamada et al.
European Journal of Organic Chemistry
Fullerene Chemistry and Applications
article

Structural Determination and Characterization of Electronic Properties of Photosilylated Derivatives of C70

Masanori Yasui, Keiko Kamioka, Takeshi Akasaka, Michio Yamada, Shun Yamazaki, Yutaka Maeda, Masahiro Kako, S. NISHIDA
article en

Abstract

The photoreactions of C 70 and mesityl‐substituted disilirane (disilacyclopropane) 1a afforded the corresponding adducts 2a and 3a , the former of which was reported previously. The structures of 2a and 3a are unequivocally established respectively as a 1,4‐adduct at the [ d , d' ] site and as a 1,2‐adduct at the [ a , b ] bond, respectively, using single‐crystal X‐ray crystallographic analyses. The latter structure represents the first example of crystallographic study of 1,3‐disilolane (1,3‐disilacyclopentane) derivatives of fullerenes. The electronic properties of these products are characterized based on electrochemical and theoretical studies elucidating the electron‐donating effects of silyl groups.

European Journal of Organic ChemistryVol. 28(21)
University of Tsukuba (JP), Tokyo Gakugei University (JP), University of Electro-Communications (JP), Tsukuba University of Technology (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 95%
Fullerene Chemistry and Applications
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