Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper Catalysts

Photochemically mediated reversible-deactivation radical polymerization of methyl methacrylate was successfully performed using 50–400 ppm of various copper compounds such as CuSO4·5H2O, copper acetate, copper triflate and copper acetylacetonate as catalysts. The copper catalysts were reduced in sit...

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Main Authors: Jaroslav Mosnáček, Anna Kundys, Anita Andicsová
Format: Article
Language:English
Published: MDPI AG 2014-11-01
Series:Polymers
Subjects:
Online Access:http://www.mdpi.com/2073-4360/6/11/2862
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spelling doaj-24fce92a6ee24a238dca92ef6b9822d42020-11-25T00:16:53ZengMDPI AGPolymers2073-43602014-11-016112862287410.3390/polym6112862polym6112862Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper CatalystsJaroslav Mosnáček0Anna Kundys1Anita Andicsová2Polymer Institute, Slovak Academy of Sciences, Dubravska cesta 9, 845 41 Bratislava, SlovakiaPolymer Institute, Slovak Academy of Sciences, Dubravska cesta 9, 845 41 Bratislava, SlovakiaPolymer Institute, Slovak Academy of Sciences, Dubravska cesta 9, 845 41 Bratislava, SlovakiaPhotochemically mediated reversible-deactivation radical polymerization of methyl methacrylate was successfully performed using 50–400 ppm of various copper compounds such as CuSO4·5H2O, copper acetate, copper triflate and copper acetylacetonate as catalysts. The copper catalysts were reduced in situ by irradiation at wavelengths of 366–546 nm, without using any additional reducing agent. Bromopropionitrile was used as an initiator. The effects of various solvents and the concentration and structure of ligands were investigated. Well-defined polymers were obtained when at least 100 or 200 ppm of any catalyst complexed with excess tris(2-pyridylmethyl)amine as a ligand was used in dimethyl sulfoxide as a solvent.http://www.mdpi.com/2073-4360/6/11/2862atom transfer radical polymerizationphotopolymerizationmethyl methacrylateUV lightvisible lightliving/controlled polymerization
collection DOAJ
language English
format Article
sources DOAJ
author Jaroslav Mosnáček
Anna Kundys
Anita Andicsová
spellingShingle Jaroslav Mosnáček
Anna Kundys
Anita Andicsová
Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper Catalysts
Polymers
atom transfer radical polymerization
photopolymerization
methyl methacrylate
UV light
visible light
living/controlled polymerization
author_facet Jaroslav Mosnáček
Anna Kundys
Anita Andicsová
author_sort Jaroslav Mosnáček
title Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper Catalysts
title_short Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper Catalysts
title_full Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper Catalysts
title_fullStr Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper Catalysts
title_full_unstemmed Reversible-Deactivation Radical Polymerization of Methyl Methacrylate Induced by Photochemical Reduction of Various Copper Catalysts
title_sort reversible-deactivation radical polymerization of methyl methacrylate induced by photochemical reduction of various copper catalysts
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2014-11-01
description Photochemically mediated reversible-deactivation radical polymerization of methyl methacrylate was successfully performed using 50–400 ppm of various copper compounds such as CuSO4·5H2O, copper acetate, copper triflate and copper acetylacetonate as catalysts. The copper catalysts were reduced in situ by irradiation at wavelengths of 366–546 nm, without using any additional reducing agent. Bromopropionitrile was used as an initiator. The effects of various solvents and the concentration and structure of ligands were investigated. Well-defined polymers were obtained when at least 100 or 200 ppm of any catalyst complexed with excess tris(2-pyridylmethyl)amine as a ligand was used in dimethyl sulfoxide as a solvent.
topic atom transfer radical polymerization
photopolymerization
methyl methacrylate
UV light
visible light
living/controlled polymerization
url http://www.mdpi.com/2073-4360/6/11/2862
work_keys_str_mv AT jaroslavmosnacek reversibledeactivationradicalpolymerizationofmethylmethacrylateinducedbyphotochemicalreductionofvariouscoppercatalysts
AT annakundys reversibledeactivationradicalpolymerizationofmethylmethacrylateinducedbyphotochemicalreductionofvariouscoppercatalysts
AT anitaandicsova reversibledeactivationradicalpolymerizationofmethylmethacrylateinducedbyphotochemicalreductionofvariouscoppercatalysts
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