Atom Transfer Radical Polymerization Enabled by Sonochemically Labile Cu-carbonate Species
Atom transfer radical polymerization (ATRP) has been previously mediated by ultrasound using a low concentration of copper complex in water (sono-ATRP) or by addition of piezoelectric materials in organic solvents (mechano-ATRP). However, these procedures proceeded slowly and yielded polymers contam...
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Published in | ACS macro letters Vol. 8; no. 2; pp. 161 - 165 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Chemical Society
19.02.2019
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Abstract | Atom transfer radical polymerization (ATRP) has been previously mediated by ultrasound using a low concentration of copper complex in water (sono-ATRP) or by addition of piezoelectric materials in organic solvents (mechano-ATRP). However, these procedures proceeded slowly and yielded polymers contaminated by new chains initiated by hydroxyl radicals or by residual piezoelectrics. Unexpectedly, in the presence of sodium carbonate, rapid sono-ATRP of methyl acrylate in DMSO was achieved (80% conversion in <2 h) with excellent control of molecular weights and low dispersities (M w/M n < 1.2). The in situ formed CuII/L-CO3 complex in the the presence of ultrasound generated CuI/L species as activators for ATRP and carbonate radical anions. The latter were scavenged by DMSO that was oxidized to dimethyl sulfone. This simple and robust process employs low-intensity ultrasound, air-stable CuII/L catalysts, and carbonate or bicarbonate salts (washing soda or baking soda) to prepare well-defined polyacrylates. |
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AbstractList | Atom transfer radical polymerization (ATRP) has been previously mediated by ultrasound using a low concentration of copper complex in water (sono-ATRP) or by addition of piezoelectric materials in organic solvents (mechano-ATRP). However, these procedures proceeded slowly and yielded polymers contaminated by new chains initiated by hydroxyl radicals or by residual piezoelectrics. Unexpectedly, in the presence of sodium carbonate, rapid sono-ATRP of methyl acrylate in DMSO was achieved (80% conversion in <2 h) with excellent control of molecular weights and low dispersities (Mw/Mn < 1.2). The in situ formed CuII/L-CO3 complex in the the presence of ultrasound generated CuI/L species as activators for ATRP and carbonate radical anions. The latter were scavenged by DMSO that was oxidized to dimethyl sulfone. This simple and robust process employs low-intensity ultrasound, air-stable CuII/L catalysts, and carbonate or bicarbonate salts (washing soda or baking soda) to prepare well-defined polyacrylates.Atom transfer radical polymerization (ATRP) has been previously mediated by ultrasound using a low concentration of copper complex in water (sono-ATRP) or by addition of piezoelectric materials in organic solvents (mechano-ATRP). However, these procedures proceeded slowly and yielded polymers contaminated by new chains initiated by hydroxyl radicals or by residual piezoelectrics. Unexpectedly, in the presence of sodium carbonate, rapid sono-ATRP of methyl acrylate in DMSO was achieved (80% conversion in <2 h) with excellent control of molecular weights and low dispersities (Mw/Mn < 1.2). The in situ formed CuII/L-CO3 complex in the the presence of ultrasound generated CuI/L species as activators for ATRP and carbonate radical anions. The latter were scavenged by DMSO that was oxidized to dimethyl sulfone. This simple and robust process employs low-intensity ultrasound, air-stable CuII/L catalysts, and carbonate or bicarbonate salts (washing soda or baking soda) to prepare well-defined polyacrylates. Atom transfer radical polymerization (ATRP) has been previously mediated by ultrasound using a low concentration of copper complex in water (sono-ATRP) or by addition of piezoelectric materials in organic solvents (mechano-ATRP). However, these procedures proceeded slowly and yielded polymers contaminated by new chains initiated by hydroxyl radicals or by residual piezoelectrics. Unexpectedly, in the presence of sodium carbonate, rapid sono-ATRP of methyl acrylate in DMSO was achieved (80% conversion in <2 h) with excellent control of molecular weights and low dispersities (M w/M n < 1.2). The in situ formed CuII/L-CO3 complex in the the presence of ultrasound generated CuI/L species as activators for ATRP and carbonate radical anions. The latter were scavenged by DMSO that was oxidized to dimethyl sulfone. This simple and robust process employs low-intensity ultrasound, air-stable CuII/L catalysts, and carbonate or bicarbonate salts (washing soda or baking soda) to prepare well-defined polyacrylates. Atom transfer radical polymerization (ATRP) has been previously mediated by ultrasound using a low concentration of copper complex in water (sono-ATRP) or by addition of piezoelectric materials in organic solvents (mechano-ATRP). However, these procedures proceeded slowly and yielded polymers contaminated by new chains initiated by hydroxyl radicals or by residual piezoelectrics. Unexpectedly, in the presence of sodium carbonate, rapid sono-ATRP of methyl acrylate in DMSO was achieved (80% conversion in <2 h) with excellent control of molecular weights and low dispersities ( / < 1.2). The formed Cu /L-CO complex in the the presence of ultrasound generated Cu /L species as activators for ATRP and carbonate radical anions. The latter were scavenged by DMSO that was oxidized to dimethyl sulfone. This simple and robust process employs low-intensity ultrasound, air-stable Cu /L catalysts, and carbonate or bicarbonate salts (washing soda or baking soda) to prepare well-defined polyacrylates. |
Author | Matyjaszewski, Krzysztof Lorandi, Francesca Xia, Hesheng Wang, Zhanhua Wang, Zhenhua Fantin, Marco Wang, Zongyu Yan, Jiajun |
AuthorAffiliation | Department of Chemistry The State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute |
AuthorAffiliation_xml | – name: The State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute – name: Department of Chemistry |
Author_xml | – sequence: 1 givenname: Zhenhua orcidid: 0000-0002-9028-6799 surname: Wang fullname: Wang, Zhenhua organization: Department of Chemistry – sequence: 2 givenname: Francesca surname: Lorandi fullname: Lorandi, Francesca organization: Department of Chemistry – sequence: 3 givenname: Marco surname: Fantin fullname: Fantin, Marco organization: Department of Chemistry – sequence: 4 givenname: Zongyu surname: Wang fullname: Wang, Zongyu organization: Department of Chemistry – sequence: 5 givenname: Jiajun orcidid: 0000-0003-3286-3268 surname: Yan fullname: Yan, Jiajun organization: Department of Chemistry – sequence: 6 givenname: Zhanhua orcidid: 0000-0003-0493-1905 surname: Wang fullname: Wang, Zhanhua organization: The State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute – sequence: 7 givenname: Hesheng surname: Xia fullname: Xia, Hesheng email: xiahs@scu.edu.cn organization: The State Key Laboratory of Polymer Materials Engineering, Polymer Research Institute – sequence: 8 givenname: Krzysztof orcidid: 0000-0003-1960-3402 surname: Matyjaszewski fullname: Matyjaszewski, Krzysztof email: km3b@andrew.cmu.edu organization: Department of Chemistry |
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Title | Atom Transfer Radical Polymerization Enabled by Sonochemically Labile Cu-carbonate Species |
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