Four isomeric structures of decachloro[70]fullerene are compatible with the 13C NMR spectrum and qualitative stability rules; explicit calculation at the semi-empirical level shows the most stable isomer to be that which maximises the number of 1,4-chlorine additions whilst excluding double bonds from pentagons.
S. J. Austin, P. W. Fowler, J. P. B. Sandall, P. R. Birkett, A. G. Avent, A. D. Darwish, H. W. Kroto, R. Taylor and D. R. M. Walton, J. Chem. Soc., Perkin Trans. 2, 1995, 1027 DOI: 10.1039/P29950001027
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