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Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand

[Image: see text] Redox-switching of a formazanate zinc catalyst in ring-opening polymerization (ROP) of lactide is described. Using a redox-active ligand bound to an inert metal ion (Zn(2+)) allows modulation of the catalytic activity by reversible reduction/oxidation chemistry at a purely organic...

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Autores principales: de Vries, Folkert, Otten, Edwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981207/
https://www.ncbi.nlm.nih.gov/pubmed/35391903
http://dx.doi.org/10.1021/acscatal.1c05689
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author de Vries, Folkert
Otten, Edwin
author_facet de Vries, Folkert
Otten, Edwin
author_sort de Vries, Folkert
collection PubMed
description [Image: see text] Redox-switching of a formazanate zinc catalyst in ring-opening polymerization (ROP) of lactide is described. Using a redox-active ligand bound to an inert metal ion (Zn(2+)) allows modulation of the catalytic activity by reversible reduction/oxidation chemistry at a purely organic fragment. A combination of kinetic and spectroscopic studies, together with mass spectrometry of the catalysis mixture, provides insight in the nature of the active species and the initiation of lactide ring-opening polymerization. The mechanistic data highlight the key role of the redox-active ligand and provide a rationale for the formation of cyclic polymer.
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spelling pubmed-89812072022-04-05 Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand de Vries, Folkert Otten, Edwin ACS Catal [Image: see text] Redox-switching of a formazanate zinc catalyst in ring-opening polymerization (ROP) of lactide is described. Using a redox-active ligand bound to an inert metal ion (Zn(2+)) allows modulation of the catalytic activity by reversible reduction/oxidation chemistry at a purely organic fragment. A combination of kinetic and spectroscopic studies, together with mass spectrometry of the catalysis mixture, provides insight in the nature of the active species and the initiation of lactide ring-opening polymerization. The mechanistic data highlight the key role of the redox-active ligand and provide a rationale for the formation of cyclic polymer. American Chemical Society 2022-03-21 2022-04-01 /pmc/articles/PMC8981207/ /pubmed/35391903 http://dx.doi.org/10.1021/acscatal.1c05689 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle de Vries, Folkert
Otten, Edwin
Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand
title Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand
title_full Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand
title_fullStr Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand
title_full_unstemmed Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand
title_short Reversible On/Off Switching of Lactide Cyclopolymerization with a Redox-Active Formazanate Ligand
title_sort reversible on/off switching of lactide cyclopolymerization with a redox-active formazanate ligand
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981207/
https://www.ncbi.nlm.nih.gov/pubmed/35391903
http://dx.doi.org/10.1021/acscatal.1c05689
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