Issue 79, 2019

Self-sorting in dynamic disulfide assembly: new biphenyl-bridged “nanohoops” and unsymmetrical cyclophanes

Abstract

We expand on our approach combining dynamic covalent self-assembly and sulfur extrusion to synthesize new biphenyl-linked disulfide and thioether macrocycles, which are variants of the venerable phenyl-bridged paracyclophanes. We then advance this strategy further to use two different thiols in tandem to provide new, elusive unsymmetrical disulfides which can also be trapped as unsymmetrical thioether “nanohoops”. This approach enables substantial amplification of two unsymmetrical trimers out of a library of at least 21 possible macrocycles of various sizes.

Graphical abstract: Self-sorting in dynamic disulfide assembly: new biphenyl-bridged “nanohoops” and unsymmetrical cyclophanes

Supplementary files

Article information

Article type
Communication
Submitted
22 Aug 2019
Accepted
05 Sep 2019
First published
13 Sep 2019

Chem. Commun., 2019,55, 11840-11843

Author version available

Self-sorting in dynamic disulfide assembly: new biphenyl-bridged “nanohoops” and unsymmetrical cyclophanes

N. Phan, E. P. K. L. Choy, L. N. Zakharov and D. W. Johnson, Chem. Commun., 2019, 55, 11840 DOI: 10.1039/C9CC06503B

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