RETRACTED: N-Phenylglycine as a Versatile Photoinitiator under Near-UV LED (Retracted article. See vol. 53, pg. 3255, 2020)

被引:36
作者
Zhang, J. [1 ,2 ,3 ,4 ]
Lalevee, J. [2 ,3 ]
Mou, X. [4 ]
Morlet-Savary, F. [2 ,3 ]
Graff, B. [2 ,3 ]
Xiao, P. [1 ,2 ,3 ,4 ]
机构
[1] Australian Natl Univ, Res Sch Chem, Canberra, ACT 2601, Australia
[2] Univ Haute Alsace, CNRS, UMR IS2M 7361, F-68100 Mulhouse, France
[3] Univ Strasbourg, Strasbourg, France
[4] Univ New South Wales, Sch Chem, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
FREE-RADICAL POLYMERIZATION; ACYLGERMANE-BASED PHOTOINITIATOR; PHOTOCLEAVABLE STRUCTURES; CATIONIC-POLYMERIZATION; SYSTEMS; PHOTOPOLYMERIZATION; DERIVATIVES; KINETICS; ELECTRON;
D O I
10.1021/acs.macromol.8b00747
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
N-Phenylglycine is normally used as a co-initiator and can be photodecomposed by different dyes under UV or visible light irradiation to generate radicals for the initiation of free radical photopolymerization. However, the photochemistry and photoinitiation ability of N-phenylglycine alone upon exposure to near-UV light (e.g., UV LED at 392 nm), to the best of our knowledge, have not been investigated. In this research, the photochemistry of N-phenylglycine under the UV LED at 392 nm is studied using various approaches, and it reveals that radicals (PhNHCH2 center dot) can be produced from the direct photodecomposition of N-phenylglycine. In addition, N-phenylglycine can also interact with iodonium salt under the UV LED at 392 nm to generate phenyl radicals and cations. These formed active species exhibit high performance to initiate the free radical photopolymerization of acylates and cationic photopolymerization of epoxides and divinyl ethers.
引用
收藏
页码:3767 / 3773
页数:7
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