Polymers 2012, 4(2), 1125-1156; doi:10.3390/polym4021125
Review

Controlled Photoradical Polymerization Mediated by 2,2,6,6-Tetramethylpiperidine-1-Oxyl

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Received: 1 March 2012; in revised form: 13 April 2012 / Accepted: 19 April 2012 / Published: 2 May 2012
(This article belongs to the Special Issue Living Polymerization Techniques)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: In recent years, controlled photoradical polymerization has been established using 2,2,6,6-tetramethylpiperidine-1-oxyl as a mediator. This review article will describe the molecular weight control, polymerization mechanism, influence of initiator structure, effect of substituents supported on photo-acid generator, stability of the propagating chain end, photo-latency of the polymerization, molecular design, and an application to heterogeneous polymerization in an alcoholic medium.
Keywords: controlled photoradical polymerization; 2,2,6,6-tetramethylpiperidine-1-oxyl; azoinitiators; photo-acid generators; methyl methacrylate
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MDPI and ACS Style

Yoshida, E. Controlled Photoradical Polymerization Mediated by 2,2,6,6-Tetramethylpiperidine-1-Oxyl. Polymers 2012, 4, 1125-1156.

AMA Style

Yoshida E. Controlled Photoradical Polymerization Mediated by 2,2,6,6-Tetramethylpiperidine-1-Oxyl. Polymers. 2012; 4(2):1125-1156.

Chicago/Turabian Style

Yoshida, Eri. 2012. "Controlled Photoradical Polymerization Mediated by 2,2,6,6-Tetramethylpiperidine-1-Oxyl." Polymers 4, no. 2: 1125-1156.

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