Beilstein Journal of Organic Chemistry (Jan 2020)

Halogen-bonding-induced diverse aggregation of 4,5-diiodo-1,2,3-triazolium salts with different anions

  • Xingyu Xu,
  • Shiqing Huang,
  • Zengyu Zhang,
  • Lei Cao,
  • Xiaoyu Yan

DOI
https://doi.org/10.3762/bjoc.16.10
Journal volume & issue
Vol. 16, no. 1
pp. 78 – 87

Abstract

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The synthesis of 4,5-diiodo-1,3-dimesityl-1,2,3-triazolium salts with different anions have been developed. These triazolium salts show diverse aggregation via halogen bonding between C–I bonds and anions. Triazolium with halide anions exists as a tetramer with saddle conformation. Triazolium tetrafluoroborate exists as a trimer with Chinese lantern shape conformation. Triazolium trifluoroacetate and acetate exist as dimers, respectively, while the former shows boat conformation and the latter forms rectangle conformation. Triazolium salts form a linear polymer with polyiodide.

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