Amine-Activated Ring-Opening Polymerization of 1,2-Dithiolane in a Cascade Fashion and Organocatalyzed Pendant Modification: A Path to Functional Dynamic Covalent Poly(disulfide)-Based Macromolecules

Dynamic covalent poly(disulfide)s are regarded as sustainable intelligent materials for the future because of their dynamicity and recyclability. Consequently, establishing a comprehensive process for the synthesis of poly(disulfide)s with varied structures and functionalities is highly valuable. This work describes a versatile and efficient cascade ring-opening polymerization (ROP) methodology and postpolymerization route for the synthesis of a library of functional poly(disulfide)s with structural diversity. Here, an amine activates a dormant thiolactone ring to produce a thiolate anion initiator, which subsequently opens the pentafluorophenyl ester (PFP-ester)-containing cyclic disulfide (1,2-dithiolane ring) monomer, thereby propagating polymerization at room temperature under open-air conditions. This cascade ring-opening approach facilitates one-step, in situ dual modification at the polymer chain end, thereby enabling pendant modification with both alcohols and amines through organocatalyzed transesterification and amidation, respectively, at room temperature. As a result, the polymerization approach combined with postpolymerization pendant modification allows multifunctionalization at the same polymer chain of poly(disulfide)s. The room-temperature and open-air mild reaction conditions for the polymerization and postpolymerization modification (PPM) protected the integrity of the delicate disulfide bonds. Previously, postpolymerization was largely unexplored for synthesizing a series of pendant ester and amide-functionalized poly(disulfide)s from a common, end-modified precursor poly(disulfide)s. However, this is now established in the current work through a meticulous design of the monomer and polymerization methodology. We anticipate that this versatile and convenient platform will provide access to numerous functional dynamic covalent poly(disulfide)s via minimal synthetic steps.

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Publication Details

Journal
Macromolecules
Published
2026-01-30
DOI
https://doi.org/10.1021/acs.macromol.6c00006
Citations
1
Primary Topic
Advanced Polymer Synthesis and Characterization
Type
article
Field-Weighted Citation Impact
22.95
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article

Amine-Activated Ring-Opening Polymerization of 1,2-Dithiolane in a Cascade Fashion and Organocatalyzed Pendant Modification: A Path to Functional Dynamic Covalent Poly(disulfide)-Based Macromolecules

Aditi Banerjee, Arun Mondal, Soumya Kolay, Dhiman Mondal et al.
1 citations
Macromolecules
Advanced Polymer Synthesis and Characterization
22.95
article

Amine-Activated Ring-Opening Polymerization of 1,2-Dithiolane in a Cascade Fashion and Organocatalyzed Pendant Modification: A Path to Functional Dynamic Covalent Poly(disulfide)-Based Macromolecules

Aditi Banerjee, Arun Mondal, Soumya Kolay, Dhiman Mondal, Mijanur Rahaman Molla
article en
1 citations

Abstract

Dynamic covalent poly(disulfide)s are regarded as sustainable intelligent materials for the future because of their dynamicity and recyclability. Consequently, establishing a comprehensive process for the synthesis of poly(disulfide)s with varied structures and functionalities is highly valuable. This work describes a versatile and efficient cascade ring-opening polymerization (ROP) methodology and postpolymerization route for the synthesis of a library of functional poly(disulfide)s with structural diversity. Here, an amine activates a dormant thiolactone ring to produce a thiolate anion initiator, which subsequently opens the pentafluorophenyl ester (PFP-ester)-containing cyclic disulfide (1,2-dithiolane ring) monomer, thereby propagating polymerization at room temperature under open-air conditions. This cascade ring-opening approach facilitates one-step, in situ dual modification at the polymer chain end, thereby enabling pendant modification with both alcohols and amines through organocatalyzed transesterification and amidation, respectively, at room temperature. As a result, the polymerization approach combined with postpolymerization pendant modification allows multifunctionalization at the same polymer chain of poly(disulfide)s. The room-temperature and open-air mild reaction conditions for the polymerization and postpolymerization modification (PPM) protected the integrity of the delicate disulfide bonds. Previously, postpolymerization was largely unexplored for synthesizing a series of pendant ester and amide-functionalized poly(disulfide)s from a common, end-modified precursor poly(disulfide)s. However, this is now established in the current work through a meticulous design of the monomer and polymerization methodology. We anticipate that this versatile and convenient platform will provide access to numerous functional dynamic covalent poly(disulfide)s via minimal synthetic steps.

MacromoleculesVol. 59(3)
University of Calcutta (IN)
Responsible consumption and production
Openalex Percentile: Top 1%
Advanced Polymer Synthesis and Characterization
22.95
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