Issue 2, 2023

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

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
04 Nov 2022
Accepted
05 Dec 2022
First published
07 Dec 2022
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2023,21, 402-414

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

S. R. Barlow, G. R. Akien and N. H. Evans, Org. Biomol. Chem., 2023, 21, 402 DOI: 10.1039/D2OB02019J

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