Beilstein Journal of Organic Chemistry (Jun 2020)

Five-component, one-pot synthesis of an electroactive rotaxane comprising a bisferrocene macrocycle

  • Natalie Lagesse,
  • Luca Pisciottani,
  • Maxime Douarre,
  • Pascale Godard,
  • Brice Kauffmann,
  • Vicente Martí-Centelles,
  • Nathan D. McClenaghan

DOI
https://doi.org/10.3762/bjoc.16.128
Journal volume & issue
Vol. 16, no. 1
pp. 1564 – 1571

Abstract

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The templated clipping of a ferrocene-grafted isophthalic acid derivative to encircle a hydrogen-bonding axle through the reaction with 1,4-bis(aminomethyl)benzene is described. The constituent electroactive macrocycle of the resultant [2]rotaxane is a homologue of the versatile benchmark tetraamide variant developed by Leigh and co-workers. The relative templating effect of different hydrogen-bonding motifs in rotaxane and pseudorotaxane generation is compared, with yields varying from 0 to 41%. The electrochemical properties and single crystal X-ray structure of a doubly ferrocene-decorated [2]rotaxane are further reported.

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