1994Angewandte Chemie International Edition in EnglishRequires access

Functionalization of C60 Buckminsterfullerene by [8 + 2] Cycloaddition: Spectroscopic and Electron‐Transfer Properties of a Tetrahydroazulenofullerene

Ernst Beer, Michaela Feuerer, Andreas Knorr, A. Mirlach, Jörg Daub

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Abstract

The novel C60 cycloadduct 1 is formed in the reaction of 8-methoxyheptafulvene with buckminster-fullerene C60. Compound 1 can be reduced to its tetraanion in four reversible steps; the spectral properties of the radical anion, dianion, and trianion were examined by UV/VIS/NIR spectroelectro-chemistry. Adduct 1 may lead to other functional-ized fullerenes having substructures with electron-transfer properties.

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What this paper is about

The novel C60 cycloadduct 1 is formed in the reaction of 8-methoxyheptafulvene with buckminster-fullerene C60. Compound 1 can be reduced to its tetraanion in four reversible steps; the spectral properties of the radical anion, dianion, and trianion were examined by UV/VIS/NIR spectroelectro-chemistry. Adduct 1 may lead to other functional-ized fullerenes having substructures with electron-transfer properties.

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Available abstract

The novel C60 cycloadduct 1 is formed in the reaction of 8-methoxyheptafulvene with buckminster-fullerene C60. Compound 1 can be reduced to its tetraanion in four reversible steps; the spectral properties of the radical anion, dianion, and trianion were examined by UV/VIS/NIR spectroelectro-chemistry. Adduct 1 may lead to other functional-ized fullerenes having substructures with electron-transfer properties.

Key concepts: Buckminsterfullerene, Fullerene, Cycloaddition, Electron transfer, Surface modification, Chemistry, Adduct, Photochemistry

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Functionalization of C60 Buckminsterfullerene by [8 + 2] Cycloaddition: Spectroscopic and Electron‐Transfer Properties of a Tetrahydroazulenofullerene — Research Paper | ScholarLens