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Design and synthesis of a photoswitchable guanidine catalyst
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 ring-opening polymerization (ROP) of rac-...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511018/ https://www.ncbi.nlm.nih.gov/pubmed/23209518 http://dx.doi.org/10.3762/bjoc.8.209 |
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author | Viehmann, Philipp Hecht, Stefan |
author_facet | Viehmann, Philipp Hecht, Stefan |
author_sort | Viehmann, Philipp |
collection | PubMed |
description | 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 ring-opening 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. |
format | Online Article Text |
id | pubmed-3511018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-35110182012-12-03 Design and synthesis of a photoswitchable guanidine catalyst Viehmann, Philipp Hecht, Stefan Beilstein J Org Chem Full Research Paper 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 ring-opening 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. Beilstein-Institut 2012-10-24 /pmc/articles/PMC3511018/ /pubmed/23209518 http://dx.doi.org/10.3762/bjoc.8.209 Text en Copyright © 2012, Viehmann and Hecht https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Viehmann, Philipp Hecht, Stefan Design and synthesis of a photoswitchable guanidine catalyst |
title | Design and synthesis of a photoswitchable guanidine catalyst |
title_full | Design and synthesis of a photoswitchable guanidine catalyst |
title_fullStr | Design and synthesis of a photoswitchable guanidine catalyst |
title_full_unstemmed | Design and synthesis of a photoswitchable guanidine catalyst |
title_short | Design and synthesis of a photoswitchable guanidine catalyst |
title_sort | design and synthesis of a photoswitchable guanidine catalyst |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511018/ https://www.ncbi.nlm.nih.gov/pubmed/23209518 http://dx.doi.org/10.3762/bjoc.8.209 |
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