Molecules (Nov 2015)

Towards the Synthesis of Graphene Azide from Graphene Oxide

  • Christian E. Halbig,
  • Philipp Rietsch,
  • Siegfried Eigler

DOI
https://doi.org/10.3390/molecules201219747
Journal volume & issue
Vol. 20, no. 12
pp. 21050 – 21057

Abstract

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In the last decades, organic azides haven proven to be very useful precursors in organic chemistry, for example in 1,3-dipolar cycloaddition reactions (click-chemistry). Likewise, azides can be introduced into graphene oxide with an almost intact carbon framework, namely oxo-functionalized graphene (oxo-G1), which is a highly oxidized graphene derivative and a powerful precursor for graphene that is suitable for electronic devices. The synthesis of a graphene derivative with exclusively azide groups (graphene azide) is however still a challenge. In comparison also hydrogenated graphene, called graphene or halogenated graphene remain challenging to synthesize. A route to graphene azide would be the desoxygenation of azide functionalized oxo-G1. Here we show how treatment of azide functionalized oxo-G1 with HCl enlarges the π-system and removes strongly adsorbed water and some oxo-functional groups. This development reflects one step towards graphene azide.

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