{"title":"反应性可降解线性聚(氨基酰胺):合成、聚合后改性和逐层涂层","authors":"Sulbha Kumari and Subrata Chattopadhyay","doi":"10.1039/D4ME00003J","DOIUrl":null,"url":null,"abstract":"<p >The design of reactive biodegradable polymers and materials is an extremely important topic of research. This work presents the synthesis of a highly reactive and degradable poly(aminoamide) containing indole functional group in each repeating unit. The presence of indole functional groups allows for easy post-modification of such poly(aminoamide), enabling the synthesis of a library of functional poly(aminoamide)s <em>via</em> triazolinedione (TAD)–indole click reactions. Furthermore, the use of bifunctional TAD molecules facilitates the crosslinking of such poly(aminoamide), where the degree of crosslinking directly influencing the surface area of the resulting materials. The thermoreversible characteristics of such crosslinked material was also investigated. Additionally, such indole decorated poly(aminoamide) was used as an excellent platform for layer-by-layer coatings and surface functionalization. Degradation studies reveals that both the linear and crosslinked poly(aminoamide)s can be degraded in alkaline solution, where the crosslinked materials degrade faster compared to the linear analogues.</p>","PeriodicalId":91,"journal":{"name":"Molecular Systems Design & Engineering","volume":" 5","pages":" 490-499"},"PeriodicalIF":3.2000,"publicationDate":"2024-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reactive degradable linear poly(aminoamide)s: synthesis, post-polymerization modifications and layer-by-layer coating†\",\"authors\":\"Sulbha Kumari and Subrata Chattopadhyay\",\"doi\":\"10.1039/D4ME00003J\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The design of reactive biodegradable polymers and materials is an extremely important topic of research. This work presents the synthesis of a highly reactive and degradable poly(aminoamide) containing indole functional group in each repeating unit. The presence of indole functional groups allows for easy post-modification of such poly(aminoamide), enabling the synthesis of a library of functional poly(aminoamide)s <em>via</em> triazolinedione (TAD)–indole click reactions. Furthermore, the use of bifunctional TAD molecules facilitates the crosslinking of such poly(aminoamide), where the degree of crosslinking directly influencing the surface area of the resulting materials. The thermoreversible characteristics of such crosslinked material was also investigated. Additionally, such indole decorated poly(aminoamide) was used as an excellent platform for layer-by-layer coatings and surface functionalization. Degradation studies reveals that both the linear and crosslinked poly(aminoamide)s can be degraded in alkaline solution, where the crosslinked materials degrade faster compared to the linear analogues.</p>\",\"PeriodicalId\":91,\"journal\":{\"name\":\"Molecular Systems Design & Engineering\",\"volume\":\" 5\",\"pages\":\" 490-499\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Systems Design & Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/me/d4me00003j\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Systems Design & Engineering","FirstCategoryId":"5","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/me/d4me00003j","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
摘要-- 设计活性生物可降解聚合物和材料是极其重要的研究课题。本研究提出了一种高活性、可降解的聚酰胺,其每个重复单元中都含有吲哚官能团。由于吲哚官能团的存在,这种聚(氨基酰胺)可以很容易地进行后修饰,通过三唑二酮(TAD)-吲哚点击反应制备功能性聚(氨基酰胺)库。此外,使用双官能 TAD 分子可使这种聚(氨基酰胺)发生交联,而交联度会影响交联材料的表面积。此外,还研究了这种交联材料的热可逆特性。此外,这种吲哚装饰聚(氨基酰胺)被用作逐层涂层和表面功能化的绝佳平台。降解研究表明,线性和交联聚(氨基酰胺)都能在碱性溶液中降解,其中交联材料比线性类似物降解得更快。
Reactive degradable linear poly(aminoamide)s: synthesis, post-polymerization modifications and layer-by-layer coating†
The design of reactive biodegradable polymers and materials is an extremely important topic of research. This work presents the synthesis of a highly reactive and degradable poly(aminoamide) containing indole functional group in each repeating unit. The presence of indole functional groups allows for easy post-modification of such poly(aminoamide), enabling the synthesis of a library of functional poly(aminoamide)s via triazolinedione (TAD)–indole click reactions. Furthermore, the use of bifunctional TAD molecules facilitates the crosslinking of such poly(aminoamide), where the degree of crosslinking directly influencing the surface area of the resulting materials. The thermoreversible characteristics of such crosslinked material was also investigated. Additionally, such indole decorated poly(aminoamide) was used as an excellent platform for layer-by-layer coatings and surface functionalization. Degradation studies reveals that both the linear and crosslinked poly(aminoamide)s can be degraded in alkaline solution, where the crosslinked materials degrade faster compared to the linear analogues.
期刊介绍:
Molecular Systems Design & Engineering provides a hub for cutting-edge research into how understanding of molecular properties, behaviour and interactions can be used to design and assemble better materials, systems, and processes to achieve specific functions. These may have applications of technological significance and help address global challenges.