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Synthesis of Cleavable Polymers via Oxidation of Thioether Moieties and Thiol Click Reactions: A Click‐Declick Strategy

Lun Wang, Li Liu, Hanying Zhao

2023Angewandte Chemie International Edition21 citationsDOIOpen Access PDF

Abstract

In the past decades click chemistries including thiol chemistries have found wide applications in the synthesis of well-defined polymers. In this research, a click-declick strategy based on the oxidation of heteroaromatic thioethers and the substitution reactions between the oxidized groups and thiols, is proposed for the synthesis of the cleavable polymers. In proof-of-concept experiments, block copolymers (BCPs) and star-like polymers are synthesized by thiol-phenylsulfone substitution reactions, and heteroaromatic thioethers are produced at the junction points of the BCP chains or on the crosslinking sites of the star-like polymer. The thioethers can be oxidized to heteroaromatic sulfoxides or sulfones, depending on the oxidization condition. It is demonstrated that both sulfoxides or sulfones can have base catalyzed nucleophilic substitution reactions with thiols, leading to the cleavage of the polymers.

Topics & Concepts

ThioetherClick chemistryCopolymerPolymerThiolNucleophilic substitutionChemistryNucleophilePolymer chemistryCombinatorial chemistryCatalysisOrganic chemistryAdvanced Polymer Synthesis and CharacterizationClick Chemistry and ApplicationsChemical Synthesis and Reactions
Synthesis of Cleavable Polymers via Oxidation of Thioether Moieties and Thiol Click Reactions: A Click‐Declick Strategy | Litcius