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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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