Facile construction of functional poly(monothiocarbonate) copolymers under mild operating conditions. Issue 21 (12th May 2022)
- Record Type:
- Journal Article
- Title:
- Facile construction of functional poly(monothiocarbonate) copolymers under mild operating conditions. Issue 21 (12th May 2022)
- Main Title:
- Facile construction of functional poly(monothiocarbonate) copolymers under mild operating conditions
- Authors:
- Habets, Thomas
Siragusa, Fabiana
Müller, Alejandro J.
Grossman, Quentin
Ruffoni, Davide
Grignard, Bruno
Detrembleur, Christophe - Abstract:
- Abstract : Functional poly(monothiocarbonate)-based copolymers are easily prepared by terpolymerization of a CO2 -sourced bis(cyclic carbonate) with dithiols and diamines under ambient conditions. Abstract : The installation of both oxazolidone and thiocarbonate linkages within a single polymer backbone remains elusive by simple procedures under mild conditions. In this work, we report the construction of copolymers containing these two linkages by the one-pot terpolymerization of diamines, dithiols and a CO2 -sourced activated dicyclic carbonate of the α-alkylidene type. This process is facile and efficient with many commercially available diamine and dithiol comonomers, and occurs at room temperature under catalyst-free conditions. In contrast to polyoxazolidones that are insoluble in many organic solvents, the copolymers are highly soluble, facilitating their processing as adhesives. The polymers present an unusual thermal behavior with the presence of two glass transition temperatures. Importantly, they can undergo facile and quantitative dehydration by a simple thermal treatment at moderate temperature (110–160 °C) without using any catalyst or dehydrating agent, thereby furnishing novel polymers presenting both thiocarbonate and α-alkylidene oxazolidone linkages. The pendant double bonds are exploited for the facile thiol–ene functionalization with a scope of commercially available thiols under mild conditions. This work gives access to functionalAbstract : Functional poly(monothiocarbonate)-based copolymers are easily prepared by terpolymerization of a CO2 -sourced bis(cyclic carbonate) with dithiols and diamines under ambient conditions. Abstract : The installation of both oxazolidone and thiocarbonate linkages within a single polymer backbone remains elusive by simple procedures under mild conditions. In this work, we report the construction of copolymers containing these two linkages by the one-pot terpolymerization of diamines, dithiols and a CO2 -sourced activated dicyclic carbonate of the α-alkylidene type. This process is facile and efficient with many commercially available diamine and dithiol comonomers, and occurs at room temperature under catalyst-free conditions. In contrast to polyoxazolidones that are insoluble in many organic solvents, the copolymers are highly soluble, facilitating their processing as adhesives. The polymers present an unusual thermal behavior with the presence of two glass transition temperatures. Importantly, they can undergo facile and quantitative dehydration by a simple thermal treatment at moderate temperature (110–160 °C) without using any catalyst or dehydrating agent, thereby furnishing novel polymers presenting both thiocarbonate and α-alkylidene oxazolidone linkages. The pendant double bonds are exploited for the facile thiol–ene functionalization with a scope of commercially available thiols under mild conditions. This work gives access to functional poly(monothiocarbonate)-based copolymers under mild operating conditions without requiring specific equipment. … (more)
- Is Part Of:
- Polymer chemistry. Volume 13:Issue 21(2022)
- Journal:
- Polymer chemistry
- Issue:
- Volume 13:Issue 21(2022)
- Issue Display:
- Volume 13, Issue 21 (2022)
- Year:
- 2022
- Volume:
- 13
- Issue:
- 21
- Issue Sort Value:
- 2022-0013-0021-0000
- Page Start:
- 3076
- Page End:
- 3090
- Publication Date:
- 2022-05-12
- Subjects:
- Polymers -- Periodicals
Macromolecules -- Periodicals
Polymerization -- Periodicals
547.705 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/PY/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2py00307d ↗
- Languages:
- English
- ISSNs:
- 1759-9954
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.703400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21732.xml