Loading…

Unique Method for Facile Postsynthetic Modification of Nonisocyanate Polyurethanes

Nonisocyanate polyurethanes (NIPUs) are broadly investigated as a potential replacement for conventional polyurethanes (PUs) to eliminate the use of toxic isocyanates and reduce occupational hazards. One of the most popular approaches to NIPU synthesis is the polyaddition of cyclic bis­(carbonate)­s...

Full description

Saved in:
Bibliographic Details
Published in:Macromolecules 2024-03, Vol.57 (5), p.2385-2393
Main Authors: Zubkevich, Sergei V., Makarov, Maksim, Dieden, Reiner, Puchot, Laura, Berthé, Vincent, Westermann, Stephan, Shaplov, Alexander S., Schmidt, Daniel F.
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-a450t-8772a45db952e05788860bfecaaf4f44ff33d024dc4a6a7c8d630b007c0ec2ea3
cites cdi_FETCH-LOGICAL-a450t-8772a45db952e05788860bfecaaf4f44ff33d024dc4a6a7c8d630b007c0ec2ea3
container_end_page 2393
container_issue 5
container_start_page 2385
container_title Macromolecules
container_volume 57
creator Zubkevich, Sergei V.
Makarov, Maksim
Dieden, Reiner
Puchot, Laura
Berthé, Vincent
Westermann, Stephan
Shaplov, Alexander S.
Schmidt, Daniel F.
description Nonisocyanate polyurethanes (NIPUs) are broadly investigated as a potential replacement for conventional polyurethanes (PUs) to eliminate the use of toxic isocyanates and reduce occupational hazards. One of the most popular approaches to NIPU synthesis is the polyaddition of cyclic bis­(carbonate)­s and diamines to form poly­(hydroxyurethane)­s (PHUs). However, such PHUs are highly hydrophilic due to the presence of two hydroxyl groups per repeat unit, and the resulting moisture absorption significantly degrades their thermomechanical performance and physical stability upon exposure to humidity, thus limiting their utility. Here, we introduce a simple and scalable approach for the modification of PHUs to increase hydrophobicity and adjust their properties. The proposed reaction between aldehydes and appropriately spaced hydroxyl groups in the polymer backbone resulted in high degrees of modification (up to 84%) and up to 3-fold reductions in water uptake at 85% RH. Furthermore, the use of aromatic aldehydes in particular enabled the retention of mechanical properties over a wide range of humidity levels, resulting in performance comparable to conventional PUs. Finally, we note that this approach is not limited to reducing moisture sensitivity alone and provides ample opportunities for imparting a broad range of novel properties to PHUs through an appropriate selection of functional aldehydes.
doi_str_mv 10.1021/acs.macromol.3c02232
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10938877</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2967057755</sourcerecordid><originalsourceid>FETCH-LOGICAL-a450t-8772a45db952e05788860bfecaaf4f44ff33d024dc4a6a7c8d630b007c0ec2ea3</originalsourceid><addsrcrecordid>eNp9UctOHDEQtKKgsJD8AUJzzGWWHj92PCcUIV4SkAjB2er12KzRjE1sD9L-fbzaBcElp26pq6q7qwg5amDeAG1OUKf5iDqGMQxzpoFSRr-QWSMo1EIy8ZXMACivO9q1--QgpWeAphGcfSP7TPJOMNnNyP2jd38nU92avAp9ZUOsLlC7wVR_Qspp7fPKZKer29A76zRmF3wVbHUXvEtBr9Fj3mCH9RSLBHqTvpM9i0MyP3b1kDxenD-cXdU3vy-vz37d1MgF5Fq2LS1dv-wENSBaKeUCltZoRMst59Yy1pcHes1xga2W_YLBEqDVYDQ1yA7J6Vb3ZVqOptfG54iDeoluxLhWAZ36PPFupZ7Cq2qgY7KsLwo_dwoxFBNSVqNL2gxDeSNMSdFu0ZbLWiEKlG-hxfCUorHvexpQmzxUyUO95aF2eRTa8ccb30lvARQAbAEb-nOYoi-W_V_zH7j_nYc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2967057755</pqid></control><display><type>article</type><title>Unique Method for Facile Postsynthetic Modification of Nonisocyanate Polyurethanes</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Zubkevich, Sergei V. ; Makarov, Maksim ; Dieden, Reiner ; Puchot, Laura ; Berthé, Vincent ; Westermann, Stephan ; Shaplov, Alexander S. ; Schmidt, Daniel F.</creator><creatorcontrib>Zubkevich, Sergei V. ; Makarov, Maksim ; Dieden, Reiner ; Puchot, Laura ; Berthé, Vincent ; Westermann, Stephan ; Shaplov, Alexander S. ; Schmidt, Daniel F.</creatorcontrib><description>Nonisocyanate polyurethanes (NIPUs) are broadly investigated as a potential replacement for conventional polyurethanes (PUs) to eliminate the use of toxic isocyanates and reduce occupational hazards. One of the most popular approaches to NIPU synthesis is the polyaddition of cyclic bis­(carbonate)­s and diamines to form poly­(hydroxyurethane)­s (PHUs). However, such PHUs are highly hydrophilic due to the presence of two hydroxyl groups per repeat unit, and the resulting moisture absorption significantly degrades their thermomechanical performance and physical stability upon exposure to humidity, thus limiting their utility. Here, we introduce a simple and scalable approach for the modification of PHUs to increase hydrophobicity and adjust their properties. The proposed reaction between aldehydes and appropriately spaced hydroxyl groups in the polymer backbone resulted in high degrees of modification (up to 84%) and up to 3-fold reductions in water uptake at 85% RH. Furthermore, the use of aromatic aldehydes in particular enabled the retention of mechanical properties over a wide range of humidity levels, resulting in performance comparable to conventional PUs. Finally, we note that this approach is not limited to reducing moisture sensitivity alone and provides ample opportunities for imparting a broad range of novel properties to PHUs through an appropriate selection of functional aldehydes.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/acs.macromol.3c02232</identifier><identifier>PMID: 38495389</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Macromolecules, 2024-03, Vol.57 (5), p.2385-2393</ispartof><rights>2024 The Authors. Published by American Chemical Society</rights><rights>2024 The Authors. Published by American Chemical Society.</rights><rights>2024 The Authors. Published by American Chemical Society 2024 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a450t-8772a45db952e05788860bfecaaf4f44ff33d024dc4a6a7c8d630b007c0ec2ea3</citedby><cites>FETCH-LOGICAL-a450t-8772a45db952e05788860bfecaaf4f44ff33d024dc4a6a7c8d630b007c0ec2ea3</cites><orcidid>0000-0001-5371-0901 ; 0000-0001-5116-1742 ; 0000-0002-7789-2663 ; 0000-0003-2511-1906</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38495389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zubkevich, Sergei V.</creatorcontrib><creatorcontrib>Makarov, Maksim</creatorcontrib><creatorcontrib>Dieden, Reiner</creatorcontrib><creatorcontrib>Puchot, Laura</creatorcontrib><creatorcontrib>Berthé, Vincent</creatorcontrib><creatorcontrib>Westermann, Stephan</creatorcontrib><creatorcontrib>Shaplov, Alexander S.</creatorcontrib><creatorcontrib>Schmidt, Daniel F.</creatorcontrib><title>Unique Method for Facile Postsynthetic Modification of Nonisocyanate Polyurethanes</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>Nonisocyanate polyurethanes (NIPUs) are broadly investigated as a potential replacement for conventional polyurethanes (PUs) to eliminate the use of toxic isocyanates and reduce occupational hazards. One of the most popular approaches to NIPU synthesis is the polyaddition of cyclic bis­(carbonate)­s and diamines to form poly­(hydroxyurethane)­s (PHUs). However, such PHUs are highly hydrophilic due to the presence of two hydroxyl groups per repeat unit, and the resulting moisture absorption significantly degrades their thermomechanical performance and physical stability upon exposure to humidity, thus limiting their utility. Here, we introduce a simple and scalable approach for the modification of PHUs to increase hydrophobicity and adjust their properties. The proposed reaction between aldehydes and appropriately spaced hydroxyl groups in the polymer backbone resulted in high degrees of modification (up to 84%) and up to 3-fold reductions in water uptake at 85% RH. Furthermore, the use of aromatic aldehydes in particular enabled the retention of mechanical properties over a wide range of humidity levels, resulting in performance comparable to conventional PUs. Finally, we note that this approach is not limited to reducing moisture sensitivity alone and provides ample opportunities for imparting a broad range of novel properties to PHUs through an appropriate selection of functional aldehydes.</description><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9UctOHDEQtKKgsJD8AUJzzGWWHj92PCcUIV4SkAjB2er12KzRjE1sD9L-fbzaBcElp26pq6q7qwg5amDeAG1OUKf5iDqGMQxzpoFSRr-QWSMo1EIy8ZXMACivO9q1--QgpWeAphGcfSP7TPJOMNnNyP2jd38nU92avAp9ZUOsLlC7wVR_Qspp7fPKZKer29A76zRmF3wVbHUXvEtBr9Fj3mCH9RSLBHqTvpM9i0MyP3b1kDxenD-cXdU3vy-vz37d1MgF5Fq2LS1dv-wENSBaKeUCltZoRMst59Yy1pcHes1xga2W_YLBEqDVYDQ1yA7J6Vb3ZVqOptfG54iDeoluxLhWAZ36PPFupZ7Cq2qgY7KsLwo_dwoxFBNSVqNL2gxDeSNMSdFu0ZbLWiEKlG-hxfCUorHvexpQmzxUyUO95aF2eRTa8ccb30lvARQAbAEb-nOYoi-W_V_zH7j_nYc</recordid><startdate>20240312</startdate><enddate>20240312</enddate><creator>Zubkevich, Sergei V.</creator><creator>Makarov, Maksim</creator><creator>Dieden, Reiner</creator><creator>Puchot, Laura</creator><creator>Berthé, Vincent</creator><creator>Westermann, Stephan</creator><creator>Shaplov, Alexander S.</creator><creator>Schmidt, Daniel F.</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5371-0901</orcidid><orcidid>https://orcid.org/0000-0001-5116-1742</orcidid><orcidid>https://orcid.org/0000-0002-7789-2663</orcidid><orcidid>https://orcid.org/0000-0003-2511-1906</orcidid></search><sort><creationdate>20240312</creationdate><title>Unique Method for Facile Postsynthetic Modification of Nonisocyanate Polyurethanes</title><author>Zubkevich, Sergei V. ; Makarov, Maksim ; Dieden, Reiner ; Puchot, Laura ; Berthé, Vincent ; Westermann, Stephan ; Shaplov, Alexander S. ; Schmidt, Daniel F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a450t-8772a45db952e05788860bfecaaf4f44ff33d024dc4a6a7c8d630b007c0ec2ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zubkevich, Sergei V.</creatorcontrib><creatorcontrib>Makarov, Maksim</creatorcontrib><creatorcontrib>Dieden, Reiner</creatorcontrib><creatorcontrib>Puchot, Laura</creatorcontrib><creatorcontrib>Berthé, Vincent</creatorcontrib><creatorcontrib>Westermann, Stephan</creatorcontrib><creatorcontrib>Shaplov, Alexander S.</creatorcontrib><creatorcontrib>Schmidt, Daniel F.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zubkevich, Sergei V.</au><au>Makarov, Maksim</au><au>Dieden, Reiner</au><au>Puchot, Laura</au><au>Berthé, Vincent</au><au>Westermann, Stephan</au><au>Shaplov, Alexander S.</au><au>Schmidt, Daniel F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unique Method for Facile Postsynthetic Modification of Nonisocyanate Polyurethanes</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2024-03-12</date><risdate>2024</risdate><volume>57</volume><issue>5</issue><spage>2385</spage><epage>2393</epage><pages>2385-2393</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><abstract>Nonisocyanate polyurethanes (NIPUs) are broadly investigated as a potential replacement for conventional polyurethanes (PUs) to eliminate the use of toxic isocyanates and reduce occupational hazards. One of the most popular approaches to NIPU synthesis is the polyaddition of cyclic bis­(carbonate)­s and diamines to form poly­(hydroxyurethane)­s (PHUs). However, such PHUs are highly hydrophilic due to the presence of two hydroxyl groups per repeat unit, and the resulting moisture absorption significantly degrades their thermomechanical performance and physical stability upon exposure to humidity, thus limiting their utility. Here, we introduce a simple and scalable approach for the modification of PHUs to increase hydrophobicity and adjust their properties. The proposed reaction between aldehydes and appropriately spaced hydroxyl groups in the polymer backbone resulted in high degrees of modification (up to 84%) and up to 3-fold reductions in water uptake at 85% RH. Furthermore, the use of aromatic aldehydes in particular enabled the retention of mechanical properties over a wide range of humidity levels, resulting in performance comparable to conventional PUs. Finally, we note that this approach is not limited to reducing moisture sensitivity alone and provides ample opportunities for imparting a broad range of novel properties to PHUs through an appropriate selection of functional aldehydes.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>38495389</pmid><doi>10.1021/acs.macromol.3c02232</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5371-0901</orcidid><orcidid>https://orcid.org/0000-0001-5116-1742</orcidid><orcidid>https://orcid.org/0000-0002-7789-2663</orcidid><orcidid>https://orcid.org/0000-0003-2511-1906</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0024-9297
ispartof Macromolecules, 2024-03, Vol.57 (5), p.2385-2393
issn 0024-9297
1520-5835
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10938877
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
title Unique Method for Facile Postsynthetic Modification of Nonisocyanate Polyurethanes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T23%3A10%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Unique%20Method%20for%20Facile%20Postsynthetic%20Modification%20of%20Nonisocyanate%20Polyurethanes&rft.jtitle=Macromolecules&rft.au=Zubkevich,%20Sergei%20V.&rft.date=2024-03-12&rft.volume=57&rft.issue=5&rft.spage=2385&rft.epage=2393&rft.pages=2385-2393&rft.issn=0024-9297&rft.eissn=1520-5835&rft_id=info:doi/10.1021/acs.macromol.3c02232&rft_dat=%3Cproquest_pubme%3E2967057755%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a450t-8772a45db952e05788860bfecaaf4f44ff33d024dc4a6a7c8d630b007c0ec2ea3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2967057755&rft_id=info:pmid/38495389&rfr_iscdi=true