{"title":"生物基衣康酸二丁酯与常规和可再生(甲基)丙烯酸酯的反应性比率:退化的影响。","authors":"Jyoti Gupta, Radmila Tomovska, Shaghayegh Hamzehlou, Miren Aguirre","doi":"10.1021/acs.biomac.5c01505","DOIUrl":null,"url":null,"abstract":"<p><p>The global push for sustainability has driven interest in renewable monomers such as dibutyl itaconate (DBI). Despite its potential for biobased high-performance polymers, DBI's copolymerization with (meth)acrylates is challenging due to low propagation rates, depropagation at moderate temperatures, and unfavorable reactivity ratios. This study investigates the solution copolymerization of DBI with both conventional, butyl acrylate (BA) and methyl methacrylate (MMA), and biobased (2-octyl acrylate (2-OA) and isobornyl acrylate (IBOA)) monomers. Using in situ <sup>1</sup>H NMR and nonlinear least-squares fitting, reactivity ratios were determined: BA/DBI (<i>r</i><sub>BA</sub> = 0.68, <i>r</i><sub>DBI</sub> = 0.68), MMA/DBI (<i>r</i><sub>MMA</sub> = 3.53, <i>r</i><sub>DBI</sub> = 0.38), 2-OA/DBI (<i>r</i><sub>2-OA</sub> = 1.64, <i>r</i><sub>DB</sub>I = 1.44), and IBOA/DBI (<i>r</i><sub>IBOA</sub> = 1.87, <i>r</i><sub>DBI</sub> = 2.0). The study also clarifies discrepancies in literature values for BA/DBI due to uncertainties in DBI's depropagation rates. DBI copolymers with BA, 2-OA, and IBOA showed a lower composition drift than MMA/DBI, which showed a greater disparity in reactivity ratios.</p>","PeriodicalId":30,"journal":{"name":"Biomacromolecules","volume":" ","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reactivity Ratios of Biobased Dibutyl Itaconate with Conventional and Renewable (Meth)Acrylates: Influence of Depropagation.\",\"authors\":\"Jyoti Gupta, Radmila Tomovska, Shaghayegh Hamzehlou, Miren Aguirre\",\"doi\":\"10.1021/acs.biomac.5c01505\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The global push for sustainability has driven interest in renewable monomers such as dibutyl itaconate (DBI). Despite its potential for biobased high-performance polymers, DBI's copolymerization with (meth)acrylates is challenging due to low propagation rates, depropagation at moderate temperatures, and unfavorable reactivity ratios. This study investigates the solution copolymerization of DBI with both conventional, butyl acrylate (BA) and methyl methacrylate (MMA), and biobased (2-octyl acrylate (2-OA) and isobornyl acrylate (IBOA)) monomers. Using in situ <sup>1</sup>H NMR and nonlinear least-squares fitting, reactivity ratios were determined: BA/DBI (<i>r</i><sub>BA</sub> = 0.68, <i>r</i><sub>DBI</sub> = 0.68), MMA/DBI (<i>r</i><sub>MMA</sub> = 3.53, <i>r</i><sub>DBI</sub> = 0.38), 2-OA/DBI (<i>r</i><sub>2-OA</sub> = 1.64, <i>r</i><sub>DB</sub>I = 1.44), and IBOA/DBI (<i>r</i><sub>IBOA</sub> = 1.87, <i>r</i><sub>DBI</sub> = 2.0). The study also clarifies discrepancies in literature values for BA/DBI due to uncertainties in DBI's depropagation rates. DBI copolymers with BA, 2-OA, and IBOA showed a lower composition drift than MMA/DBI, which showed a greater disparity in reactivity ratios.</p>\",\"PeriodicalId\":30,\"journal\":{\"name\":\"Biomacromolecules\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomacromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.biomac.5c01505\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomacromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.biomac.5c01505","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Reactivity Ratios of Biobased Dibutyl Itaconate with Conventional and Renewable (Meth)Acrylates: Influence of Depropagation.
The global push for sustainability has driven interest in renewable monomers such as dibutyl itaconate (DBI). Despite its potential for biobased high-performance polymers, DBI's copolymerization with (meth)acrylates is challenging due to low propagation rates, depropagation at moderate temperatures, and unfavorable reactivity ratios. This study investigates the solution copolymerization of DBI with both conventional, butyl acrylate (BA) and methyl methacrylate (MMA), and biobased (2-octyl acrylate (2-OA) and isobornyl acrylate (IBOA)) monomers. Using in situ 1H NMR and nonlinear least-squares fitting, reactivity ratios were determined: BA/DBI (rBA = 0.68, rDBI = 0.68), MMA/DBI (rMMA = 3.53, rDBI = 0.38), 2-OA/DBI (r2-OA = 1.64, rDBI = 1.44), and IBOA/DBI (rIBOA = 1.87, rDBI = 2.0). The study also clarifies discrepancies in literature values for BA/DBI due to uncertainties in DBI's depropagation rates. DBI copolymers with BA, 2-OA, and IBOA showed a lower composition drift than MMA/DBI, which showed a greater disparity in reactivity ratios.
期刊介绍:
Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine.
Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.