[2+1] Cycloaddition of Nitrene onto C₆₀ Revisited: Interconversion between an Aziridinofullerene and an Azafulleroid
An open and closed case: The reversible interconversion of a [1,2]aziridinofullerene and a [1,6]azafulleroid represents the first such example for a monosubstituted fullerene. While the [1,2]aziridinofullerene rearranges thermally to the [1,6]azafulleroid, the [1,6]azafulleroid rearranges photochemi...
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Veröffentlicht in: | Angewandte Chemie (International ed.) 2008-02, Vol.47 (7), p.1298-1300 |
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container_title | Angewandte Chemie (International ed.) |
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creator | Nakahodo, Tsukasa Okada, Mitsunori Morita, Hiroyuki Yoshimura, Toshiaki Ishitsuka, Midori O Tsuchiya, Takahiro Maeda, Yutaka Fujihara, Hisashi Akasaka, Takeshi Gao, Xingfa Nagase, Shigeru |
description | An open and closed case: The reversible interconversion of a [1,2]aziridinofullerene and a [1,6]azafulleroid represents the first such example for a monosubstituted fullerene. While the [1,2]aziridinofullerene rearranges thermally to the [1,6]azafulleroid, the [1,6]azafulleroid rearranges photochemically to the [1,2]aziridinofullerene in high yield (see picture). |
doi_str_mv | 10.1002/anie.200704410 |
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While the [1,2]aziridinofullerene rearranges thermally to the [1,6]azafulleroid, the [1,6]azafulleroid rearranges photochemically to the [1,2]aziridinofullerene in high yield (see picture).</abstract><cop>Weinheim</cop><pub>Wiley-VCH Verlag</pub><pmid>18183559</pmid><doi>10.1002/anie.200704410</doi><tpages>3</tpages></addata></record> |
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subjects | azafulleroids fullerenes photochemistry rearrangement structural determination |
title | [2+1] Cycloaddition of Nitrene onto C₆₀ Revisited: Interconversion between an Aziridinofullerene and an Azafulleroid |
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