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Synthesis of nucleobase-calix[4]arenes via click chemistry and evaluation of their complexation with alkali metal ions and molecular assembly
Supramolecular Chemistry
  • Wanbo Liu, University of the Pacific
  • Mikael A. Minier, University of the Pacific
  • Andreas H. Franz, University of the Pacific
  • Matthew Curtis, University of the Pacific
  • Liang Xue, University of the Pacific
Document Type
Article
Department
Chemistry
DOI
10.1080/10610278.2011.632824
Publication Date
11-28-2011
Disciplines
Abstract

In this study, calix[4]arene derivatives (11–14) bearing a single nucleobase (adenine, thymine, cytosine or guanine) were synthesised via click chemistry. The complexation ability of the synthesised derivatives with alkali metal ions was measured using MALDI-TOF mass spectrometry, and their molecular assembly in CDCl3 was determined using 1H NMR. Calix[4]arene derivatives (11–14) formed 1:1 complexes with all alkali metal ions and the rank order for the complexation selectivity was Rb+ > Cs+ > K+ ≅ Na+ > Li+. The attachment of nucleobase at the upper rim of calix[4]arene had little effect on its complexation selectivity for alkali metal ions. Thymine-, adenine- and guanine-calix[4]arenes formed self-assembled structures in CDCl3 via base–base interactions. In addition, adenine-calix[4]arene (11) bound to thymine-calix[4]arene (12) to form a discrete species via Hoogsteen hydrogen bonding.

Citation Information
Wanbo Liu, Mikael A. Minier, Andreas H. Franz, Matthew Curtis, et al.. "Synthesis of nucleobase-calix[4]arenes via click chemistry and evaluation of their complexation with alkali metal ions and molecular assembly" Supramolecular Chemistry Vol. 23 Iss. 12 (2011) p. 806 - 818 ISSN: 1061-0278
Available at: http://works.bepress.com/andreas-franz/73/