Hydrogen bond templated synthesis of catenanes and rotaxanes from a single isophthalic acid derivative

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Abstract

Hydrogen bond templated [2]catenanes and [2]rotaxanes have been synthesized using azide precursors derived from a single isophthalic acid derivative precursor. The interlocked molecules were prepared using either stoichiometric or near stoichiometric amounts of macrocycle and CuAAC “click” precursors, with yields of up to 70% for the mechanical bond formation step. Successful preparation of the interlocked structures was confirmed by NMR spectroscopy and mass spectrometry, with detail of co-conformational behaviour being elucidated by a range of 1H NMR spectroscopic experiments.

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Barlow, S. R., Akien, G. R., & Evans, N. H. (2023). Hydrogen bond templated synthesis of catenanes and rotaxanes from a single isophthalic acid derivative. Organic and Biomolecular Chemistry, 21(2), 402–414. https://doi.org/10.1039/d2ob02019j

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