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ARGET ATRP of styrene in EtOAc/EtOH using only Na2CO3 to promote the copper catalyst regeneration.

Authors :
Braidi, Niccolò
Buffagni, Mirko
Ghelfi, Franco
Parenti, Francesca
Gennaro, Armando
Isse, Abdirisak A.
Bedogni, Elena
Bonifaci, Luisa
Cavalca, Gianfranco
Ferrando, Angelo
Longo, Aldo
Morandini, Ida
Source :
Journal of Macromolecular Science: Pure & Applied Chemistry. 2021, Vol. 58 Issue 6, p376-386. 11p.
Publication Year :
2021

Abstract

"Activator regenerated by electron transfer" "atom transfer radical polymerization" (ARGET ATRP) process catalyzed by CuCl2/tris(2-pyridylmethyl)amine (TPMA) (1/1) in ethyl acetate/ethanol (EtOAc/EtOH) for the polymerization of styrene from ethyl 2,2-dichloropropanoate (EDCP) is described. The (re)generation of the activating CuI complex is accomplished by Na2CO3 without the addition of any explicit reducing agent. Differently from the analogous process operating in the presence of ascorbic acid/carbonate as the reducing system, branching is not present and control over polymerization is improved. The activation mechanism should follow a composite route, where both EtOH and TPMA contribute to the regeneration of the catalyst. The oxidation of TPMA is suggested by the absence of the ligand in the final reaction mixture and by the reduction of CuII even in t-BuOAc/t-BuOH, notwithstanding the very poor ability of t-BuOH as a reducing agent. Oxidative degradation of TPMA causes a progressive malfunctioning of the redox catalyst. Consequently, the polymerization rate, after a prompt start, becomes slower and slower, fixing conversions at around 50% (4.5 h). This means a gradual decrease of the free radical concentration, which develops unfavorable conditions for the reductive coupling (termination) between the bifunctional growing chains, preserving a controlled growth of the polymer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10601325
Volume :
58
Issue :
6
Database :
Academic Search Index
Journal :
Journal of Macromolecular Science: Pure & Applied Chemistry
Publication Type :
Academic Journal
Accession number :
150145984
Full Text :
https://doi.org/10.1080/10601325.2020.1866434