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. 2017 Jan 30;8:14281. doi: 10.1038/ncomms14281

Figure 1. One-pot functionalization of carbon nanotubes by heterocyclic [2+1] cycloaddition reaction.

Figure 1

(a) After establishment of the heterocyclic bridge between azidodichloro-triazine 1 and SWNTs, (b) the cycloaddition product (2) undergoes ring opening and rehybridization of the C atoms underlying the bridge and is converted into the form (3) with regenerated π-conjugation. (c) Quantum chemically optimized molecular configuration of the triazine on an (8,0) nanotube.