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A Sunlight‐Induced Click Reaction as an Efficient Route to Cyclic Aliphatic Polyesters
Author(s) -
Josse Thomas,
De Winter Julien,
Altintas Ozcan,
Dubois Philippe,
BarnerKowollik Christopher,
Gerbaux Pascal,
Coulembier Olivier
Publication year - 2015
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201500054
Subject(s) - polyester , sunlight , polymer chemistry , chemistry , photochemistry , click chemistry , materials science , organic chemistry , physics , optics
To date, the controlled preparation of cyclic polymers is mainly achieved using click ligation strategies. The light‐induced Diels–Alder click coupling has recently been shown to function as an attractive catalyst‐free alternative to the copper‐catalyzed alkyne–azide cycloaddition. However, the need for a light emitting system limits its applicability. To overcome this drawback, a sunlight‐induced Diels–Alder reaction as an efficient route for the preparation of cyclic aliphatic polyesters in high yields and purity based on the same chemistry is demonstrated in the present contribution. The versatility and robustness of the proposed strategy against divergent atmospheric conditions is demonstrated. In light of the simplicity of the strategy presented here, it is suggested that the sunlight‐induced Diels–Alder click‐cyclization is a world‐wide transposable process.