Issue 66, 2024

Sequential nucleophilic substitution of pseudorotaxanes forms rotaxanes with various linking functionalities and recycling of the surrogate stopper

Abstract

A sequential nucleophilic substitution method produces rotaxanes from anion-sensitive pseudorotaxanes. First, a nucleophilic bulky tertiary aniline interlocks a pseudorotaxane to form a surrogate rotaxane; this unit then functions as a leaving group for a set of bulky nucleophiles, affording rotaxanes with various linking functionalities, along with the bulky aniline recovered in its original form.

Graphical abstract: Sequential nucleophilic substitution of pseudorotaxanes forms rotaxanes with various linking functionalities and recycling of the surrogate stopper

Supplementary files

Article information

Article type
Communication
Submitted
19 jun 2024
Accepted
19 jul 2024
First published
26 jul 2024

Chem. Commun., 2024,60, 8704-8707

Sequential nucleophilic substitution of pseudorotaxanes forms rotaxanes with various linking functionalities and recycling of the surrogate stopper

C. Chang and S. Chiu, Chem. Commun., 2024, 60, 8704 DOI: 10.1039/D4CC02975E

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