Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry

Two series of aluminum alkyl complexes supported by pyrrolylaldiminate ligands, LAlMe2(1a-7a) and L2AlMe (1b-7b), were successfully synthesized and characterized by NMR spectroscopy and elemental analysis. Reactions of trimethylaluminum with the corresponding pyrrolylaldiminate ligands in the molar...

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Main Authors: Sittichoke Tabthong, Tanin Nanok, Palangpon Kongsaeree, Samran Prabpai, Pimpa Hormnirun
Other Authors: Kasetsart University
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/33637
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spelling th-mahidol.336372018-11-09T09:06:38Z Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry Sittichoke Tabthong Tanin Nanok Palangpon Kongsaeree Samran Prabpai Pimpa Hormnirun Kasetsart University Mahidol University Chemistry Two series of aluminum alkyl complexes supported by pyrrolylaldiminate ligands, LAlMe2(1a-7a) and L2AlMe (1b-7b), were successfully synthesized and characterized by NMR spectroscopy and elemental analysis. Reactions of trimethylaluminum with the corresponding pyrrolylaldiminate ligands in the molar ratios of 1:1 and 1:2 yielded dimethylaluminum pyrrolylaldiminates (1a-7a) and monomethylaluminum pyrrolylaldiminates (1b-7b), respectively, in good yields. The structure of 3b, determined by single-crystal X-ray diffraction, displayed a distorted trigonal bipyramidal geometry with the τ value of 0.65. Upon addition of 1 equivalent of benzyl alcohol, all complexes promoted the living ring-opening polymerization of rac-lactide with a good control over molecular weights and polydispersities. Complexes 6a and 7a were found to efficiently mediate the immortal polymerization in the presence of excess equivalents of benzyl alcohol (up to 5 equivalents), as evidenced by the narrow PDI values and the good agreement between the experimental Mnvalues and monomer/benzyl alcohol ratios. The steric and electronic effects of the imine nitrogen substituents had a strong influence on the polymerization activities both in catalytic activity and polymer microstructure. The catalytic activity decreased as follows: 4-Me-C6H4(3) > C6H5(1) ≈ 4-F-C6H4(2) ≈ 2-Me-C6H4(5) > 4-OMe-C6H4(4) ≫ 2-tBu-C6H4(6) > adamantyl (7). In comparison, the catalytic activity of the monomethylaluminum complex is slightly higher than that of the dimethylaluminum counterpart. The polymerization of rac-lactide by 6b yielded heterotactically enriched polylactide (Pr= 0.60) whereas the isotactic-enriched polymer (Pm= 0.74) was obtained from 7b. © The Royal Society of Chemistry 2014. 2018-11-09T02:06:38Z 2018-11-09T02:06:38Z 2014-01-21 Article Dalton Transactions. Vol.43, No.3 (2014), 1348-1359 10.1039/c3dt52455h 14779234 14779226 2-s2.0-84890503394 https://repository.li.mahidol.ac.th/handle/123456789/33637 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84890503394&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Chemistry
spellingShingle Chemistry
Sittichoke Tabthong
Tanin Nanok
Palangpon Kongsaeree
Samran Prabpai
Pimpa Hormnirun
Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry
description Two series of aluminum alkyl complexes supported by pyrrolylaldiminate ligands, LAlMe2(1a-7a) and L2AlMe (1b-7b), were successfully synthesized and characterized by NMR spectroscopy and elemental analysis. Reactions of trimethylaluminum with the corresponding pyrrolylaldiminate ligands in the molar ratios of 1:1 and 1:2 yielded dimethylaluminum pyrrolylaldiminates (1a-7a) and monomethylaluminum pyrrolylaldiminates (1b-7b), respectively, in good yields. The structure of 3b, determined by single-crystal X-ray diffraction, displayed a distorted trigonal bipyramidal geometry with the τ value of 0.65. Upon addition of 1 equivalent of benzyl alcohol, all complexes promoted the living ring-opening polymerization of rac-lactide with a good control over molecular weights and polydispersities. Complexes 6a and 7a were found to efficiently mediate the immortal polymerization in the presence of excess equivalents of benzyl alcohol (up to 5 equivalents), as evidenced by the narrow PDI values and the good agreement between the experimental Mnvalues and monomer/benzyl alcohol ratios. The steric and electronic effects of the imine nitrogen substituents had a strong influence on the polymerization activities both in catalytic activity and polymer microstructure. The catalytic activity decreased as follows: 4-Me-C6H4(3) > C6H5(1) ≈ 4-F-C6H4(2) ≈ 2-Me-C6H4(5) > 4-OMe-C6H4(4) ≫ 2-tBu-C6H4(6) > adamantyl (7). In comparison, the catalytic activity of the monomethylaluminum complex is slightly higher than that of the dimethylaluminum counterpart. The polymerization of rac-lactide by 6b yielded heterotactically enriched polylactide (Pr= 0.60) whereas the isotactic-enriched polymer (Pm= 0.74) was obtained from 7b. © The Royal Society of Chemistry 2014.
author2 Kasetsart University
author_facet Kasetsart University
Sittichoke Tabthong
Tanin Nanok
Palangpon Kongsaeree
Samran Prabpai
Pimpa Hormnirun
format Article
author Sittichoke Tabthong
Tanin Nanok
Palangpon Kongsaeree
Samran Prabpai
Pimpa Hormnirun
author_sort Sittichoke Tabthong
title Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry
title_short Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry
title_full Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry
title_fullStr Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry
title_full_unstemmed Monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: Effects of ligand structure and coordination geometry
title_sort monomethylaluminum and dimethylaluminum pyrrolylaldiminates for the ring-opening polymerization of rac-lactide: effects of ligand structure and coordination geometry
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/33637
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