Light-mediated controlled and classical polymerizations of less-activated monomers under high-pressure conditions

The innovative combination of light and high pressure allowed us to effectively polymerize for the first time challenging ionic 1,2,4-triazolium-based ionic liquids (ILs) with fluorinate anions (MetTRI/NTF) and non-ionic vinyl acetate (VAc), both classified as less-activated monomers (LAMs). Three d...

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Veröffentlicht in:Polymer chemistry 2021-08, Vol.12 (3), p.4418-4427
Hauptverfasser: Maksym, Paulina, Tarnacka, Magdalena, Bernat, Roksana, Dzienia, Andrzej, Szelwicka, Anna, Hachu a, Barbara, Chrobok, Anna, Paluch, Marian, Kami ski, Kamil
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container_end_page 4427
container_issue 3
container_start_page 4418
container_title Polymer chemistry
container_volume 12
creator Maksym, Paulina
Tarnacka, Magdalena
Bernat, Roksana
Dzienia, Andrzej
Szelwicka, Anna
Hachu a, Barbara
Chrobok, Anna
Paluch, Marian
Kami ski, Kamil
description The innovative combination of light and high pressure allowed us to effectively polymerize for the first time challenging ionic 1,2,4-triazolium-based ionic liquids (ILs) with fluorinate anions (MetTRI/NTF) and non-ionic vinyl acetate (VAc), both classified as less-activated monomers (LAMs). Three different synthetic photo-induced protocols comprising controlled metal-free organocatalyzed Atom Transfer Radical Polymerization ( O -ATRP), chain transfer to solvent free-radical polymerization (CT-FRP), and classical free-radical polymerization (FRP) were investigated. As a result, well-defined polymers with a wide range of molecular weights M n and different concentrations of OH domains incorporated into their polymer backbones in a very short time frame (5-120 min) were produced. Having a series of 1,2,4-triazolium-based poly(ionic liquid)s (PILs), a unique opportunity appeared to study the relationship between their molecular weights, glass transition temperature, and dc conductivity, undoubtedly enriching the library of tailored PILs of enhanced conductivity, a critical parameter determining their serviceability. An entirely new robust setup combining light and high pressure was applied to polymerize less-activated monomers via three different "green" polymerization protocols.
doi_str_mv 10.1039/d1py00738f
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Three different synthetic photo-induced protocols comprising controlled metal-free organocatalyzed Atom Transfer Radical Polymerization ( O -ATRP), chain transfer to solvent free-radical polymerization (CT-FRP), and classical free-radical polymerization (FRP) were investigated. As a result, well-defined polymers with a wide range of molecular weights M n and different concentrations of OH domains incorporated into their polymer backbones in a very short time frame (5-120 min) were produced. Having a series of 1,2,4-triazolium-based poly(ionic liquid)s (PILs), a unique opportunity appeared to study the relationship between their molecular weights, glass transition temperature, and dc conductivity, undoubtedly enriching the library of tailored PILs of enhanced conductivity, a critical parameter determining their serviceability. 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source Royal Society Of Chemistry Journals 2008-
subjects Chain transfer
Free radical polymerization
Free radicals
Glass transition temperature
Ionic liquids
Ions
Molecular weight
Monomers
Polymer chemistry
Polymerization
Radicals
Vinyl acetate
title Light-mediated controlled and classical polymerizations of less-activated monomers under high-pressure conditions
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