Abstract
A novel design as well as a straight-forward synthesis for a photoswitchable guanidine catalyst is reported. Intense studies of the photochromic properties demonstrated the reversible switchability of its photosensitive azobenzene moiety. Its activity in the ringopening polymerization (ROP) of rac-lactide was investigated as well. The obtained results are discussed, and an additional guanidine was synthesized and utilized in the ROP of rac-lactide in order to explain the findings. © 2012 Viehmann and Hecht; licensee Beilstein-Institut.
Author supplied keywords
Cite
CITATION STYLE
Viehmann, P., & Hecht, S. (2012). Design and synthesis of a photoswitchable guanidine catalyst. Beilstein Journal of Organic Chemistry, 8, 1825–1830. https://doi.org/10.3762/bjoc.8.209
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.