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Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes

[Image: see text] Meldrum’s acid (MA) is utilized as a monomer to polymerize with diisocyanates to result in polyamides, containing MA moieties at polymer chains. This reaction is also employed to prepare isocyanate-terminated polyamide segments which are utilized as a precursor for preparation of M...

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Autores principales: Chen, Ying-Chen, Huang, Chien-Ho, Liu, Ying-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648850/
https://www.ncbi.nlm.nih.gov/pubmed/31459875
http://dx.doi.org/10.1021/acsomega.9b00777
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author Chen, Ying-Chen
Huang, Chien-Ho
Liu, Ying-Ling
author_facet Chen, Ying-Chen
Huang, Chien-Ho
Liu, Ying-Ling
author_sort Chen, Ying-Chen
collection PubMed
description [Image: see text] Meldrum’s acid (MA) is utilized as a monomer to polymerize with diisocyanates to result in polyamides, containing MA moieties at polymer chains. This reaction is also employed to prepare isocyanate-terminated polyamide segments which are utilized as a precursor for preparation of MA-containing polyurethanes. Based on the thermolysis reaction of MA groups, followed by ketene dimerization reaction, the reactive polyamides and polyurethanes show self-cross-linkable features. The cross-linked polyurethanes exhibit good film formability, thermal stability, and mechanical properties. A new MA-based polymerization method and a novel synthesis route for preparation of reactive polyamides and polyurethanes are demonstrated.
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spelling pubmed-66488502019-08-27 Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes Chen, Ying-Chen Huang, Chien-Ho Liu, Ying-Ling ACS Omega [Image: see text] Meldrum’s acid (MA) is utilized as a monomer to polymerize with diisocyanates to result in polyamides, containing MA moieties at polymer chains. This reaction is also employed to prepare isocyanate-terminated polyamide segments which are utilized as a precursor for preparation of MA-containing polyurethanes. Based on the thermolysis reaction of MA groups, followed by ketene dimerization reaction, the reactive polyamides and polyurethanes show self-cross-linkable features. The cross-linked polyurethanes exhibit good film formability, thermal stability, and mechanical properties. A new MA-based polymerization method and a novel synthesis route for preparation of reactive polyamides and polyurethanes are demonstrated. American Chemical Society 2019-04-30 /pmc/articles/PMC6648850/ /pubmed/31459875 http://dx.doi.org/10.1021/acsomega.9b00777 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Chen, Ying-Chen
Huang, Chien-Ho
Liu, Ying-Ling
Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes
title Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes
title_full Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes
title_fullStr Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes
title_full_unstemmed Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes
title_short Polymerization of Meldrum’s Acid and Diisocyanate: An Effective Approach for Preparation of Reactive Polyamides and Polyurethanes
title_sort polymerization of meldrum’s acid and diisocyanate: an effective approach for preparation of reactive polyamides and polyurethanes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648850/
https://www.ncbi.nlm.nih.gov/pubmed/31459875
http://dx.doi.org/10.1021/acsomega.9b00777
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