Issue 7, 2012

Topochemical photo-reversible polymerization of a bioinspired monomer and its recovery and repolymerization after photo-depolymerization

Abstract

Solid-state topochemical polymerization is one way to synthesize novel macromolecular architectures with stereoregular chain structures. Topochemical reactions are attractive, “green” synthetic pathways in material design, since they occur in solvent-free conditions and in response to external stimuli, such as heat and light. For the first time, we have used the reversible [2π + 2π]-cycloaddition of a bioinspired bis-thymine monomer to topochemically synthesize a polymer. The polymer can be fully photo-depolymerized to the monomer and then reversibly and repeatedly photo-polymerized and photo-depolymerized. This is the first demonstration of complete photo-depolymerization and subsequent monomer recycling using this mechanism.

Graphical abstract: Topochemical photo-reversible polymerization of a bioinspired monomer and its recovery and repolymerization after photo-depolymerization

Supplementary files

Article information

Article type
Edge Article
Submitted
28 Mar 2012
Accepted
18 Apr 2012
First published
18 Apr 2012

Chem. Sci., 2012,3, 2301-2306

Topochemical photo-reversible polymerization of a bioinspired monomer and its recovery and repolymerization after photo-depolymerization

P. Johnston, C. Braybrook and K. Saito, Chem. Sci., 2012, 3, 2301 DOI: 10.1039/C2SC20380D

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