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AbstractIn 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. View Full-Text
Keywords: graphene oxide; graphene azide; Raman; TGA-MSgraphene oxide; graphene azide; Raman; TGA-MS►▼ Figures
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MDPI and ACS Style
Halbig, C.E.; Rietsch, P.; Eigler, S. Towards the Synthesis of Graphene Azide from Graphene Oxide. Molecules2015, 20, 21050-21057.
Halbig CE, Rietsch P, Eigler S. Towards the Synthesis of Graphene Azide from Graphene Oxide. Molecules. 2015; 20(12):21050-21057.Chicago/Turabian Style
Halbig, Christian E.; Rietsch, Philipp; Eigler, Siegfried. 2015. "Towards the Synthesis of Graphene Azide from Graphene Oxide." Molecules 20, no. 12: 21050-21057.
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