Synthesis and 13C NMR features of N-substituted aziridino[60]fullerenes View Full Text


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Article Info

DATE

2015-11

AUTHORS

M. Khalilov, A. R. Tulyabaev, A. R. Akhmetov, A. R. Tuktarov

ABSTRACT

An effective cycloaddition of organic azides to fullerene C60 in the presence stoichiometric amounts of Cu(OTf)2 to form individual aziridino[60]fullerenes was developed. Considering the 13C NMR data, it was ascertained that among the synthesized aziridinofullerenes only the compound with the adamantane substituent possessed the local C2v symmetry of the fullerene core. In the 13C NMR spectra of the other compounds, 11 resonances were unexpectedly observed for the fullerene carbon atoms instead of probable 16 signals. The 13C NMR chemical shifts were computed with the high level GIAO-PBE/3ζ technique and the possible reasons of the signal overlap in the 13C NMR spectra were discussed. More... »

PAGES

2725-2730

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-015-1214-x

DOI

http://dx.doi.org/10.1007/s11172-015-1214-x

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1025482724


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