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[Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes
The [Rh(L-alaninate)(cod)] (cod = 1,5-Cyclooctadiene) complex was synthesized and characterized. Asymmetric polymerizations of achiral phenylacetylene with two hydroxyl groups and a dodecyl group (DoDHPA) were performed by using the rhodium complex as the catalyst to provide polymers with a higher m...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290612/ https://www.ncbi.nlm.nih.gov/pubmed/30961148 http://dx.doi.org/10.3390/polym10111223 |
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author | Wang, Qingyu Jia, Hongge Shi, Yongqiang Ma, Liqun Yang, Guoxing Wang, Yazhen Xu, Shuangping Wang, Jianjun Zang, Yu Aoki, Toshiki |
author_facet | Wang, Qingyu Jia, Hongge Shi, Yongqiang Ma, Liqun Yang, Guoxing Wang, Yazhen Xu, Shuangping Wang, Jianjun Zang, Yu Aoki, Toshiki |
author_sort | Wang, Qingyu |
collection | PubMed |
description | The [Rh(L-alaninate)(cod)] (cod = 1,5-Cyclooctadiene) complex was synthesized and characterized. Asymmetric polymerizations of achiral phenylacetylene with two hydroxyl groups and a dodecyl group (DoDHPA) were performed by using the rhodium complex as the catalyst to provide polymers with a higher molecular weight (>10(5)) than the polymers obtained using the [Rh(cod)Cl](2) initiator systems. The resulting polymers showed circular dichroism (CD) signals at approximately 310 and 470 nm, indicating that they have a preferential one-handed helical structure. The helix sense in the polymer main chain was controlled by the sign of the catalyst chirality. These findings suggest that the rhodium complex with a chiral amine is the true active species for the helix-sense-selective polymerization of DoDHPA. The [Rh(L-alaninate)(cod)] complex also exhibits high catalytic activity in the polymerization of phenylacetylene (PA) to give a high yield and molecular weight. All these results demonstrate that this Rh complex is an excellent catalyst for the polymerization of phenylacetylene monomers. |
format | Online Article Text |
id | pubmed-6290612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62906122019-04-02 [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes Wang, Qingyu Jia, Hongge Shi, Yongqiang Ma, Liqun Yang, Guoxing Wang, Yazhen Xu, Shuangping Wang, Jianjun Zang, Yu Aoki, Toshiki Polymers (Basel) Article The [Rh(L-alaninate)(cod)] (cod = 1,5-Cyclooctadiene) complex was synthesized and characterized. Asymmetric polymerizations of achiral phenylacetylene with two hydroxyl groups and a dodecyl group (DoDHPA) were performed by using the rhodium complex as the catalyst to provide polymers with a higher molecular weight (>10(5)) than the polymers obtained using the [Rh(cod)Cl](2) initiator systems. The resulting polymers showed circular dichroism (CD) signals at approximately 310 and 470 nm, indicating that they have a preferential one-handed helical structure. The helix sense in the polymer main chain was controlled by the sign of the catalyst chirality. These findings suggest that the rhodium complex with a chiral amine is the true active species for the helix-sense-selective polymerization of DoDHPA. The [Rh(L-alaninate)(cod)] complex also exhibits high catalytic activity in the polymerization of phenylacetylene (PA) to give a high yield and molecular weight. All these results demonstrate that this Rh complex is an excellent catalyst for the polymerization of phenylacetylene monomers. MDPI 2018-11-03 /pmc/articles/PMC6290612/ /pubmed/30961148 http://dx.doi.org/10.3390/polym10111223 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Qingyu Jia, Hongge Shi, Yongqiang Ma, Liqun Yang, Guoxing Wang, Yazhen Xu, Shuangping Wang, Jianjun Zang, Yu Aoki, Toshiki [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes |
title | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes |
title_full | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes |
title_fullStr | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes |
title_full_unstemmed | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes |
title_short | [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes |
title_sort | [rh(l-alaninate)(1,5-cyclooctadiene)] catalyzed helix-sense-selective polymerizations of achiral phenylacetylenes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290612/ https://www.ncbi.nlm.nih.gov/pubmed/30961148 http://dx.doi.org/10.3390/polym10111223 |
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