Jorge Andrés Mora Vargas , Ketan S. Mandrekar , Radell Echemendía , Antonio C. B. Burtoloso
{"title":"Innovations in isocyanate synthesis for a sustainable future","authors":"Jorge Andrés Mora Vargas , Ketan S. Mandrekar , Radell Echemendía , Antonio C. B. Burtoloso","doi":"10.1039/d4ob01598c","DOIUrl":null,"url":null,"abstract":"<div><div>Isocyanates play a crucial role as key building blocks in the production of thermoplastic foams, elastomers, adhesives, agrochemicals, and pharmaceuticals. These compounds are essential in the manufacture of various polymeric products, such as polyurethane foams, synthetic rubbers, and surface coatings. Given their significance, and the fact that many isocyanates are highly reactive and toxic, there is an increasing demand for innovative and sustainable methods for their synthesis and detection that emphasize safety, efficiency, and selectivity. Developing processes for isocyanate production that avoid hazardous reagents like phosgene is particularly critical. While several methods exist for the <em>in situ</em> generation of isocyanates, the search for an eco-friendly and sustainable approach for their direct synthesis and isolation continues. Recent advances in isocyanate synthesis promise innovative and efficient strategies with broad industrial and environmental benefits. This review highlights various methods for synthesizing di- and monoisocyanates, emphasizing their isolation and conversion into ureas and carbamates in line with the principles of sustainable and green chemistry.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 3","pages":"Pages 487-505"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S147705202401036X","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Isocyanates play a crucial role as key building blocks in the production of thermoplastic foams, elastomers, adhesives, agrochemicals, and pharmaceuticals. These compounds are essential in the manufacture of various polymeric products, such as polyurethane foams, synthetic rubbers, and surface coatings. Given their significance, and the fact that many isocyanates are highly reactive and toxic, there is an increasing demand for innovative and sustainable methods for their synthesis and detection that emphasize safety, efficiency, and selectivity. Developing processes for isocyanate production that avoid hazardous reagents like phosgene is particularly critical. While several methods exist for the in situ generation of isocyanates, the search for an eco-friendly and sustainable approach for their direct synthesis and isolation continues. Recent advances in isocyanate synthesis promise innovative and efficient strategies with broad industrial and environmental benefits. This review highlights various methods for synthesizing di- and monoisocyanates, emphasizing their isolation and conversion into ureas and carbamates in line with the principles of sustainable and green chemistry.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.