Surprises, Serendipity, and Symmetry in Fullerene Chemistry

Roger Taylor

doi:10.1055/s-2000-6688

Synlett 2000; 2000(6): 0776-0793
DOI: 10.1055/s-2000-6688

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Surprises, Serendipity, and Symmetry in Fullerene Chemistry

Roger Taylor^*

^*The Chemistry Laboratory, CPES School, Sussex University, Brighton BN1 9QJ, UK; E-mail: R.Taylor@sussex.ac.uk

Abstract

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Fullerene chemistry studies often reveal unexpected phenomena, produce the occasional success, and require greater familiarity with symmetry than is customary in organic chemistry. These aspects are encountered in our studies of the formation of fullerene hydrides, hydroxides, halides, oxides, arylfullerenes, and cycloadducts.

fullerenes - reduction - fluorination

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