Controlled-Radical Polymerization of α‑Lipoic Acid: A General Route to Degradable Vinyl Copolymers

83Citations
Citations of this article
95Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Here, we present the synthesis and characterization of statistical and block copolymers containing α-lipoic acid (LA) using reversible addition−fragmentation chain-transfer (RAFT) polymerization. LA, a readily available nutritional supplement, undergoes efficient radical ring-opening copolymerization with vinyl monomers in a controlled manner with predictable molecular weights and low molar-mass dispersities. Because lipoic acid diads present in the resulting copolymers include disulfide bonds, these materials efficiently and rapidly degrade when exposed to mild reducing agents such as tris(2-carboxyethyl)phosphine (Mn = 56 → 3.6 kg mol−1). This scalable and versatile polymerization method affords a facile way to synthesize degradable polymers with controlled architectures, molecular weights, and molar-mass dispersities from α-lipoic acid, a commercially available and renewable monomer.

Cite

CITATION STYLE

APA

Albanese, K. R., Morris, P. T., de Alaniz, J. R., Bates, C. M., & Hawker, C. J. (2023). Controlled-Radical Polymerization of α‑Lipoic Acid: A General Route to Degradable Vinyl Copolymers. Journal of the American Chemical Society, 145(41), 22728–22734. https://doi.org/10.1021/jacs.3c08248

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free