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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...

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Autores principales: Wang, Qingyu, Jia, Hongge, Shi, Yongqiang, Ma, Liqun, Yang, Guoxing, Wang, Yazhen, Xu, Shuangping, Wang, Jianjun, Zang, Yu, Aoki, Toshiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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