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Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters

A family of aluminium complexes supported by mono-anionic indolyl-phenolate ligands are described. Reactions of indolyl-phenolate based ligand precursors, IndHPh(R)OH, with 1.0 or 0.5 equivalents of AlMe(2)Cl in toluene afforded aluminium indolyl-phenolate complexes 1–4 and aluminium bis-indolyl-phe...

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Detalles Bibliográficos
Autores principales: Chen, Chi-Tien, Lai, Zi-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527570/
https://www.ncbi.nlm.nih.gov/pubmed/36320241
http://dx.doi.org/10.1039/d2ra05112e
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author Chen, Chi-Tien
Lai, Zi-Ling
author_facet Chen, Chi-Tien
Lai, Zi-Ling
author_sort Chen, Chi-Tien
collection PubMed
description A family of aluminium complexes supported by mono-anionic indolyl-phenolate ligands are described. Reactions of indolyl-phenolate based ligand precursors, IndHPh(R)OH, with 1.0 or 0.5 equivalents of AlMe(2)Cl in toluene afforded aluminium indolyl-phenolate complexes 1–4 and aluminium bis-indolyl-phenolate complexes 5–8 respectively. The molecular structure is reported for 5. Based on the NMR spectroscopic and X-ray crystallographic studies, a 1,3-hydrogen shift could happen from nitrogen to carbon on the five-membered ring of the indolyl group upon reacting with aluminium reagents. These novel aluminium complexes demonstrate catalytic activities toward the ring-opening polymerization of cyclic esters in the presence of alcohol.
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spelling pubmed-95275702022-10-31 Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters Chen, Chi-Tien Lai, Zi-Ling RSC Adv Chemistry A family of aluminium complexes supported by mono-anionic indolyl-phenolate ligands are described. Reactions of indolyl-phenolate based ligand precursors, IndHPh(R)OH, with 1.0 or 0.5 equivalents of AlMe(2)Cl in toluene afforded aluminium indolyl-phenolate complexes 1–4 and aluminium bis-indolyl-phenolate complexes 5–8 respectively. The molecular structure is reported for 5. Based on the NMR spectroscopic and X-ray crystallographic studies, a 1,3-hydrogen shift could happen from nitrogen to carbon on the five-membered ring of the indolyl group upon reacting with aluminium reagents. These novel aluminium complexes demonstrate catalytic activities toward the ring-opening polymerization of cyclic esters in the presence of alcohol. The Royal Society of Chemistry 2022-10-03 /pmc/articles/PMC9527570/ /pubmed/36320241 http://dx.doi.org/10.1039/d2ra05112e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Chen, Chi-Tien
Lai, Zi-Ling
Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters
title Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters
title_full Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters
title_fullStr Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters
title_full_unstemmed Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters
title_short Aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters
title_sort aluminium complexes containing indolyl-phenolate ligands as catalysts for ring-opening polymerization of cyclic esters
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527570/
https://www.ncbi.nlm.nih.gov/pubmed/36320241
http://dx.doi.org/10.1039/d2ra05112e
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