Visible-light induced controlled radical polymerization of methacrylates with Cu(dap)2Cl as a photoredox catalyst

2016 ◽  
Vol 7 (25) ◽  
pp. 4226-4236 ◽  
Author(s):  
Wenchao Ma ◽  
Dong Chen ◽  
Yuhong Ma ◽  
Li Wang ◽  
Changwen Zhao ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Block Copolymers ◽  
Visible Light ◽  
Radical Polymerization ◽  
Visible Light Irradiation ◽  
Controlled Radical Polymerization ◽  
Molecular Weights ◽  
Molecular Weight Distributions ◽  
System P ◽  
Weight Distributions

Under visible light irradiation, block copolymers of PPEGMA-b-PMMA with high molecular weights and narrow molecular weight distributions are obtained starting from a PPEGMA macroinitiator in the presence of the Cu(dap)2Cl/Me6TREN catalytic system.

Reversible-deactivation radical polymerization of chloroprene and the synthesis of novel polychloroprene-based block copolymers by the RAFT approach

RSC Advances ◽  
2014 ◽  
Vol 4 (98) ◽  
pp. 55529-55538 ◽  
Author(s):  
Jia Hui ◽  
Zhijiao Dong ◽  
Yan Shi ◽  
Zhifeng Fu ◽  
Wantai Yang
Keyword(s):  
Molecular Weight ◽  
Block Copolymers ◽  
Radical Polymerization ◽  
Molecular Weights ◽  
Molecular Weight Distributions ◽  
Weight Distributions ◽  
Reversible Deactivation ◽  
Raft Agent ◽  
Reversible Deactivation Radical Polymerization

Novel, well-defined PCP-based block copolymers (PSt-b-PCP and PMMA-b-PCP) with controlled number averaged molecular weights and molecular weight distributions can be prepared, employing EPDTB and CPDB, respectively, as the initial RAFT agent.

Tertiary amine catalyzed photo-induced controlled radical polymerization of methacrylates

2015 ◽  
Vol 6 (30) ◽  
pp. 5362-5368 ◽  
Author(s):  
Qiang Fu ◽  
Thomas G. McKenzie ◽  
Shereen Tan ◽  
Eunhyung Nam ◽  
Greg G. Qiao
Keyword(s):  
Molecular Weight ◽  
Radical Polymerization ◽  
Uv Irradiation ◽  
Tertiary Amine ◽  
Controlled Radical Polymerization ◽  
Low Molecular Weight ◽  
Molecular Weight Distributions ◽  
Weight Distributions ◽  
End Group

A novel tertiary amine catalyst and trithiocarbonate synergistic photo-induced controlled radical polymerization of methacrylates has been realized under mild UV irradiation, yielding polymethacrylates with low molecular weight distributions and excellent end-group fidelity.

scholarly journals Aqueous Photo-Living Radical Polymerization of Sodium Methacrylate Using a Water-Soluble Nitroxide Mediator

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Eri Yoshida
Keyword(s):  
Molecular Weight ◽  
Radical Polymerization ◽  
Linear Correlation ◽  
Linear Increase ◽  
Living Radical Polymerization ◽  
Water Soluble ◽  
Molecular Weights ◽  
Molecular Weight Distributions ◽  
Weight Distributions ◽  
Sodium Methacrylate

The aqueous photo-living radical polymerization of sodium methacrylate (NaMA) was attained using 2,2′-azobis2-methyl-N-[1,1-bis(hydroxymethyl)-2-hydroxyethyl]-propionamide (V-80) as the initiator and 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (HTEMPO) as the mediator in the presence of (4-fluorophenyl)diphenylsulfonium triflate (FS). The polymerization was carried out in water at room temperature by irradiation using a high-pressure mercury lamp. Whereas the polymerization by V-80 and/or FS in the absence of HTEMPO produced polymers with very high molecular weights and broad molecular weight distributions, the HTEMPO-mediated polymerization provided still lower-molecular-weight distributions using both V-80 and FS. The first-order time-conversion plots had an induction period up to 2.5 h; however, they thereafter showed a linear increase. The conversion-molecular weight plots also exhibited a linear correlation. A linear correlation was also obtained for the plots of the molecular weights versus the reciprocal of the initiator concentration. Based on these three correlations, it was found that the HTEMPO-mediated photopolymerization proceeded by a living mechanism.

Precise synthesis of poly(N-acryloyl amino acid) through photoinduced living polymerization

2018 ◽  
Vol 9 (20) ◽  
pp. 2733-2745 ◽  
Author(s):  
Guofeng Li ◽  
Wenli Feng ◽  
Nathaniel Corrigan ◽  
Cyrille Boyer ◽  
Xing Wang ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Amino Acid ◽  
Radical Polymerization ◽  
Living Polymerization ◽  
Living Radical Polymerization ◽  
Molecular Weights ◽  
Molecular Weight Distributions ◽  
Weight Distributions

A library of N-acryloylamino acid polymers with controlled molecular weights and narrow molecular weight distributions (Mw/Mn < 1.20) was created by a universal and versatile photoinduced living radical polymerization technique.

Environmentally Benign Adhesive Synthesized by Dispersion Copolymerization of Styrene and Butyl Acrylate

2006 ◽  
Vol 11-12 ◽  
pp. 757-760
Author(s):  
Jun Ying Zhang ◽  
Peng Dou
Keyword(s):  
Molecular Weight ◽  
Butyl Acrylate ◽  
Monomer Concentration ◽  
Environmentally Benign ◽  
Functional Monomer ◽  
Molecular Weights ◽  
Molecular Weight Distributions ◽  
Stabilizer Concentration ◽  
Ethanol Medium ◽  
Weight Distributions

Environmentally benign adhesive was synthesized by dispersion copolymerization of styrene(St) and butyl acrylate (BA) in an ethanol medium with benzoyl peroxide (BPO) as the initiator and poly(vinylpyrrolidone) as the stabilizer in the presence of acrylic acid(AA) as the functional monomer. The effect of the concentration of stabilizer, initiator and functional monomer on the conversions, molecular weights and molecular weight distributions was investigated. The results show that the conversions almost keep invariable with the increasing of stabilizer concentration, but the molecular weights increase and molecular weight distributions decrease. Conversions increase with the increasing of initiator concentration, but the molecular weights and molecular weight distributions decrease. However with the increasing of functional monomer concentration, conversions and molecular weight distributions increase but the molecular weights decrease.

Photoinduced controlled radical polymerization of methacrylates with benzaldehyde derivatives as organic catalysts

2017 ◽  
Vol 8 (23) ◽  
pp. 3574-3585 ◽  
Author(s):  
Wenchao Ma ◽  
Xianhong Zhang ◽  
Yuhong Ma ◽  
Dong Chen ◽  
Li Wang ◽  
...  
Keyword(s):  
Block Copolymers ◽  
Radical Polymerization ◽  
Catalytic System ◽  
Controlled Radical Polymerization ◽  
System P ◽  
Benzaldehyde Derivatives ◽  
Organic Catalysts

Under 23 W CFL irradiation, block copolymers are obtained starting from a Pn-I macroinitiator in the presence of a benzaldehydic molecule-based catalytic system.

scholarly journals Naturally-Derived Amphiphilic Polystyrenes Prepared by Aqueous Controlled/Living Cationic Polymerization and Copolymerization of Vinylguaiacol with R–OH/BF3·OEt2

Polymers ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 1404 ◽  
Author(s):  
Hisaaki Takeshima ◽  
Kotaro Satoh ◽  
Masami Kamigaito
Keyword(s):  
Molecular Weight ◽  
Ferulic Acid ◽  
Cationic Polymerization ◽  
Living Polymerization ◽  
Block Copolymerization ◽  
Molecular Weights ◽  
Molecular Weight Distributions ◽  
Living Cationic Polymerization ◽  
Naturally Occurring ◽  
Weight Distributions

In this study, we investigated direct-controlled/living cationic polymerization and copolymerization of 4-vinylguaiacol (4VG), i.e., 4-hydroxy-3-methoxystyrene, which can be derived from naturally-occurring ferulic acid, to develop novel bio-based amphiphilic polystyrenes with phenol functions. The controlled/living cationic polymerization of 4VG was achieved using the R–OH/BF3·OEt2 initiating system, which is effective for the controlled/living polymerization of petroleum-derived 4-vinylphenol in the presence of a large amount of water via reversible activation of terminal C–OH bond catalyzed by BF3·OEt2, to result in the polymers with controlled molecular weights and narrow molecular weight distributions. The random or block copolymerization of 4VG was also examined using p-methoxystyrene (pMOS) as a comonomer with an aqueous initiating system to tune the amphiphilic nature of the 4VG-derived phenolic polymers. The obtained polymer can be expected not only to be used as a novel styrenic bio-based polymer but also as a material with amphiphilic nature for some applications.

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