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Synthesis of High Molecular Weight Biobased Aliphatic Polyesters Exhibiting Tensile Properties Beyond Polyethylene
[Image: see text] Synthesis of high molecular weight polyesters prepared by acyclic diene metathesis (ADMET) polymerization of bis(undec-10-enoate) with isosorbide (M1), isomannide (M2), and 1,3-propanediol (M3) and the subsequent hydrogenation have been achieved by using a molybdenum-alkylidene cat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586459/ https://www.ncbi.nlm.nih.gov/pubmed/37793171 http://dx.doi.org/10.1021/acsmacrolett.3c00481 |
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author | Kojima, Mika Wang, Xiuxiu Go, Lance O’Hari P. Makino, Ryoji Matsumoto, Yuichi Shimoyama, Daisuke Abdellatif, Mohamed Mehawed Kadota, Joji Higashi, Seiji Hirano, Hiroshi Nomura, Kotohiro |
author_facet | Kojima, Mika Wang, Xiuxiu Go, Lance O’Hari P. Makino, Ryoji Matsumoto, Yuichi Shimoyama, Daisuke Abdellatif, Mohamed Mehawed Kadota, Joji Higashi, Seiji Hirano, Hiroshi Nomura, Kotohiro |
author_sort | Kojima, Mika |
collection | PubMed |
description | [Image: see text] Synthesis of high molecular weight polyesters prepared by acyclic diene metathesis (ADMET) polymerization of bis(undec-10-enoate) with isosorbide (M1), isomannide (M2), and 1,3-propanediol (M3) and the subsequent hydrogenation have been achieved by using a molybdenum-alkylidene catalyst. The resultant polymers (P1) prepared by the ADMET polymerization of M1 (in toluene at 25 °C) possessed high M(n) values (M(n) = 44400–49400 g/mol), and no significant differences in the M(n) values and the PDI (M(w)/M(n)) values were observed in the samples after the hydrogenation. Both the tensile strength and the elongation at break in the hydrogenated polymers from M1 (HP1) increased upon increasing the molar mass, and the sample with an M(n) value of 48200 exhibited better tensile properties (tensile strength of 39.7 MPa, elongation at break of 436%) than conventional polyethylene, polypropylene, as well as polyester containing C(18) alkyl chains. The tensile properties were affected by the diol segment employed, whereas HP2 showed a similar property to HP1. |
format | Online Article Text |
id | pubmed-10586459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105864592023-10-20 Synthesis of High Molecular Weight Biobased Aliphatic Polyesters Exhibiting Tensile Properties Beyond Polyethylene Kojima, Mika Wang, Xiuxiu Go, Lance O’Hari P. Makino, Ryoji Matsumoto, Yuichi Shimoyama, Daisuke Abdellatif, Mohamed Mehawed Kadota, Joji Higashi, Seiji Hirano, Hiroshi Nomura, Kotohiro ACS Macro Lett [Image: see text] Synthesis of high molecular weight polyesters prepared by acyclic diene metathesis (ADMET) polymerization of bis(undec-10-enoate) with isosorbide (M1), isomannide (M2), and 1,3-propanediol (M3) and the subsequent hydrogenation have been achieved by using a molybdenum-alkylidene catalyst. The resultant polymers (P1) prepared by the ADMET polymerization of M1 (in toluene at 25 °C) possessed high M(n) values (M(n) = 44400–49400 g/mol), and no significant differences in the M(n) values and the PDI (M(w)/M(n)) values were observed in the samples after the hydrogenation. Both the tensile strength and the elongation at break in the hydrogenated polymers from M1 (HP1) increased upon increasing the molar mass, and the sample with an M(n) value of 48200 exhibited better tensile properties (tensile strength of 39.7 MPa, elongation at break of 436%) than conventional polyethylene, polypropylene, as well as polyester containing C(18) alkyl chains. The tensile properties were affected by the diol segment employed, whereas HP2 showed a similar property to HP1. American Chemical Society 2023-10-04 /pmc/articles/PMC10586459/ /pubmed/37793171 http://dx.doi.org/10.1021/acsmacrolett.3c00481 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Kojima, Mika Wang, Xiuxiu Go, Lance O’Hari P. Makino, Ryoji Matsumoto, Yuichi Shimoyama, Daisuke Abdellatif, Mohamed Mehawed Kadota, Joji Higashi, Seiji Hirano, Hiroshi Nomura, Kotohiro Synthesis of High Molecular Weight Biobased Aliphatic Polyesters Exhibiting Tensile Properties Beyond Polyethylene |
title | Synthesis of
High Molecular Weight Biobased Aliphatic
Polyesters Exhibiting Tensile Properties Beyond Polyethylene |
title_full | Synthesis of
High Molecular Weight Biobased Aliphatic
Polyesters Exhibiting Tensile Properties Beyond Polyethylene |
title_fullStr | Synthesis of
High Molecular Weight Biobased Aliphatic
Polyesters Exhibiting Tensile Properties Beyond Polyethylene |
title_full_unstemmed | Synthesis of
High Molecular Weight Biobased Aliphatic
Polyesters Exhibiting Tensile Properties Beyond Polyethylene |
title_short | Synthesis of
High Molecular Weight Biobased Aliphatic
Polyesters Exhibiting Tensile Properties Beyond Polyethylene |
title_sort | synthesis of
high molecular weight biobased aliphatic
polyesters exhibiting tensile properties beyond polyethylene |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586459/ https://www.ncbi.nlm.nih.gov/pubmed/37793171 http://dx.doi.org/10.1021/acsmacrolett.3c00481 |
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