Lactide-derived monomers for radical thiocarbonyl addition ring-opening copolymerisation-Reference-Cited by-同舟云学术

Lactide-derived monomers for radical thiocarbonyl addition ring-opening copolymerisation

Published:2022 Issue:39 Volume:13 Page:5525-5529
ISSN:1759-9954
Container-title:Polymer Chemistry
language:en
Short-container-title:Polym. Chem.

Author:

Ivanchenko Oleksandr¹,Mazières Stéphane¹,Harrisson Simon²^ORCID,Destarac Mathias¹^ORCID

Affiliation:

1. Laboratoire des IMRCP, Université Paul Sabatier, CNRS UMR 5623, 118 Route de Narbonne, 31062 Toulouse, France

2. LCPO, Université de Bordeaux/ENSCBP/CNRS UMR 5623, 16 Avenue Pey Berland, 33607 Pessac, France

Abstract

The six-membered dl-thionolactide and dl-dithionolactide are reactive in radical ring-opening copolymerisation with a series of vinyl monomers to yield chemically degradable polymers.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Polymers and Plastics,Biochemistry,Bioengineering

Link

http://pubs.rsc.org/en/content/articlepdf/2022/PY/D2PY00893A

Reference22 articles.

1. Free radical ring-opening polymerization of 4,7-dimethyl-2-methylene-1,3-dioxepane and 5,6-benzo-2-methylene-1,3-dioxepane

2. Synthesis of poly-ε-caprolactone via a free radical mechanism. Free radical ring-opening polymerization of 2-methylene-1,3-dioxepane

3. Controlling the synthesis of degradable vinyl polymers by xanthate-mediated polymerization

4. Degradable vinyl polymers for biomedical applications

5. Radical Ring-Opening Polymerization: Scope, Limitations, and Application to (Bio)Degradable Materials

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