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Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes

[Image: see text] A series of dimethylaluminum complexes (L(1a–i))AlMe(2) (2a–i, where HL(1a–i) = 2-(2′-ArNH)phenyl-4-R(1)-oxazoline) bearing chiral, bidentate anilido-oxazolinate ligands have been prepared and characterized. Six of the complexes, in the presence of an alcohol cocatalyst, are shown...

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Autores principales: Bian, Shi, Abbina, Srinivas, Lu, Zhengliang, Kolodka, Edward, Du, Guodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036730/
https://www.ncbi.nlm.nih.gov/pubmed/24891754
http://dx.doi.org/10.1021/om401226j
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author Bian, Shi
Abbina, Srinivas
Lu, Zhengliang
Kolodka, Edward
Du, Guodong
author_facet Bian, Shi
Abbina, Srinivas
Lu, Zhengliang
Kolodka, Edward
Du, Guodong
author_sort Bian, Shi
collection PubMed
description [Image: see text] A series of dimethylaluminum complexes (L(1a–i))AlMe(2) (2a–i, where HL(1a–i) = 2-(2′-ArNH)phenyl-4-R(1)-oxazoline) bearing chiral, bidentate anilido-oxazolinate ligands have been prepared and characterized. Six of the complexes, in the presence of an alcohol cocatalyst, are shown to be active initiators for the stereoselective ring-opening polymerization of rac-lactide in toluene solution and under bulk conditions, yielding polylactides with a range of tacticity from slightly isotactic to moderately heterotactic. The reactivity and selectivity of these catalysts are discussed on the basis of the effect of their substituents.
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spelling pubmed-40367302015-05-09 Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes Bian, Shi Abbina, Srinivas Lu, Zhengliang Kolodka, Edward Du, Guodong Organometallics [Image: see text] A series of dimethylaluminum complexes (L(1a–i))AlMe(2) (2a–i, where HL(1a–i) = 2-(2′-ArNH)phenyl-4-R(1)-oxazoline) bearing chiral, bidentate anilido-oxazolinate ligands have been prepared and characterized. Six of the complexes, in the presence of an alcohol cocatalyst, are shown to be active initiators for the stereoselective ring-opening polymerization of rac-lactide in toluene solution and under bulk conditions, yielding polylactides with a range of tacticity from slightly isotactic to moderately heterotactic. The reactivity and selectivity of these catalysts are discussed on the basis of the effect of their substituents. American Chemical Society 2014-05-09 2014-05-27 /pmc/articles/PMC4036730/ /pubmed/24891754 http://dx.doi.org/10.1021/om401226j Text en Copyright © 2014 American Chemical Society
spellingShingle Bian, Shi
Abbina, Srinivas
Lu, Zhengliang
Kolodka, Edward
Du, Guodong
Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes
title Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes
title_full Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes
title_fullStr Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes
title_full_unstemmed Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes
title_short Ring-Opening Polymerization of rac-Lactide with Aluminum Chiral Anilido-Oxazolinate Complexes
title_sort ring-opening polymerization of rac-lactide with aluminum chiral anilido-oxazolinate complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4036730/
https://www.ncbi.nlm.nih.gov/pubmed/24891754
http://dx.doi.org/10.1021/om401226j
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