Parker T. Morris, Kodai Watanabe, Kaitlin R. Albanese, Greggory T. Kent, Rohini Gupta, Matthias Gerst, Javier Read de Alaniz*, Craig J. Hawker* and Christopher M. Bates*,
{"title":"通过微型乳液聚合技术规模化合成含α-硫辛酸的可降解共聚物","authors":"Parker T. Morris, Kodai Watanabe, Kaitlin R. Albanese, Greggory T. Kent, Rohini Gupta, Matthias Gerst, Javier Read de Alaniz*, Craig J. Hawker* and Christopher M. Bates*, ","doi":"10.1021/jacs.4c1243810.1021/jacs.4c12438","DOIUrl":null,"url":null,"abstract":"<p >A robust method is described to synthesize degradable copolymers under aqueous miniemulsion conditions using α-lipoic acid as a cheap and scalable building block. Simple formulations of α-lipoic acid (up to 10 mol %), <i>n</i>-butyl acrylate, a surfactant, and a costabilizer generate stable micelles in water with particle sizes <200 nm. The ready availability of these starting materials facilitated performing polymerization reactions at large scales (4 L), yielding 600 g of poly(<i>n</i>-butyl acrylate-<i>stat</i>-α-lipoic acid) latexes that degrade under reducing conditions (250 kg mol<sup>–1</sup> → 20 kg mol<sup>–1</sup>). Substitution of α-lipoic acid with ethyl lipoate further improves the solubility of dithiolane derivatives in <i>n</i>-butyl acrylate, resulting in copolymers that degrade to even lower molecular weights after polymerization and reduction. In summary, this convenient and scalable strategy provides access to large quantities of degradable copolymers and particles using cheap and commercially available starting materials.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"146 44","pages":"30662–30667 30662–30667"},"PeriodicalIF":14.4000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Scalable Synthesis of Degradable Copolymers Containing α-Lipoic Acid via Miniemulsion Polymerization\",\"authors\":\"Parker T. Morris, Kodai Watanabe, Kaitlin R. Albanese, Greggory T. Kent, Rohini Gupta, Matthias Gerst, Javier Read de Alaniz*, Craig J. Hawker* and Christopher M. Bates*, \",\"doi\":\"10.1021/jacs.4c1243810.1021/jacs.4c12438\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >A robust method is described to synthesize degradable copolymers under aqueous miniemulsion conditions using α-lipoic acid as a cheap and scalable building block. Simple formulations of α-lipoic acid (up to 10 mol %), <i>n</i>-butyl acrylate, a surfactant, and a costabilizer generate stable micelles in water with particle sizes <200 nm. The ready availability of these starting materials facilitated performing polymerization reactions at large scales (4 L), yielding 600 g of poly(<i>n</i>-butyl acrylate-<i>stat</i>-α-lipoic acid) latexes that degrade under reducing conditions (250 kg mol<sup>–1</sup> → 20 kg mol<sup>–1</sup>). Substitution of α-lipoic acid with ethyl lipoate further improves the solubility of dithiolane derivatives in <i>n</i>-butyl acrylate, resulting in copolymers that degrade to even lower molecular weights after polymerization and reduction. In summary, this convenient and scalable strategy provides access to large quantities of degradable copolymers and particles using cheap and commercially available starting materials.</p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"146 44\",\"pages\":\"30662–30667 30662–30667\"},\"PeriodicalIF\":14.4000,\"publicationDate\":\"2024-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/jacs.4c12438\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.4c12438","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
本研究介绍了一种在水性微型乳液条件下合成可降解共聚物的可靠方法,该方法使用α-硫辛酸作为廉价且可扩展的结构单元。α-硫辛酸(最多 10 摩尔%)、丙烯酸正丁酯、表面活性剂和成本稳定剂的简单配方可在水中生成粒径为 200 纳米的稳定胶束。这些起始材料的现成可用性促进了大规模聚合反应的进行(4 升),产生了 600 克在还原条件下降解的聚(丙烯酸正丁酯-stat-α-硫辛酸)胶乳(250 kg mol-1 → 20 kg mol-1)。用硫辛酸乙酯取代α-硫辛酸可进一步提高二硫环戊烷衍生物在丙烯酸正丁酯中的溶解度,从而产生在聚合和还原后降解到更低分子量的共聚物。总之,这种方便且可扩展的策略可以利用廉价的市售起始材料获得大量可降解共聚物和微粒。
Scalable Synthesis of Degradable Copolymers Containing α-Lipoic Acid via Miniemulsion Polymerization
A robust method is described to synthesize degradable copolymers under aqueous miniemulsion conditions using α-lipoic acid as a cheap and scalable building block. Simple formulations of α-lipoic acid (up to 10 mol %), n-butyl acrylate, a surfactant, and a costabilizer generate stable micelles in water with particle sizes <200 nm. The ready availability of these starting materials facilitated performing polymerization reactions at large scales (4 L), yielding 600 g of poly(n-butyl acrylate-stat-α-lipoic acid) latexes that degrade under reducing conditions (250 kg mol–1 → 20 kg mol–1). Substitution of α-lipoic acid with ethyl lipoate further improves the solubility of dithiolane derivatives in n-butyl acrylate, resulting in copolymers that degrade to even lower molecular weights after polymerization and reduction. In summary, this convenient and scalable strategy provides access to large quantities of degradable copolymers and particles using cheap and commercially available starting materials.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.