{"title":"基于功能化橄榄石的新型氧化铜(I)生物催化剂在非常温和的条件下合成 1,4-二取代的-1,2,3-三唑","authors":"Arantxa Forte-Castro , Juana M. Pérez , Celia García-Mañas , Gracia García-García , Pedro Urquiza , Tania Romacho , Ignacio Fernández","doi":"10.1016/j.scp.2024.101832","DOIUrl":null,"url":null,"abstract":"<div><div>An efficient methodology for coating silanized olive stone with copper(I) oxide has been described and fully characterized using various techniques, including X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR-ATR), X-ray fluorescence (XRF), electronic microscopy, thermogravimetric analysis (TGA), moisture content, electrophoretic mobility and particle size distribution. The applicability of this new biocatalyst in the 1,3-dipolar cycloaddition click reaction between alkynes and azides has been demonstrated leading to the obtention of a great variety of 1,4-disubstituted-1,2,3-triazoles with good to excellent conversions. The new biocatalyst showed promising features in terms of recyclability and industrial or biomedical application. It could be recycled up to five times with minimal loss of catalytic activity when synthezing compound <strong>3a</strong>-<strong>3n</strong>. Additionally, it was effective in the multi-gram scale synthesis of compounds <strong>3b</strong> and <strong>3e</strong>, which were tested for the first time in cells, specifically on the human fibroblast-derived M1 cell line, demonstrating that these compounds are non-cytotoxic and thus suitable for potential uses in biomedicine.</div></div>","PeriodicalId":22138,"journal":{"name":"Sustainable Chemistry and Pharmacy","volume":null,"pages":null},"PeriodicalIF":5.5000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New Copper(I) oxide biocatalyst based on functionalized olive stone for the synthesis of 1,4-disubstituted-1,2,3-triazoles under very mild conditions\",\"authors\":\"Arantxa Forte-Castro , Juana M. Pérez , Celia García-Mañas , Gracia García-García , Pedro Urquiza , Tania Romacho , Ignacio Fernández\",\"doi\":\"10.1016/j.scp.2024.101832\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>An efficient methodology for coating silanized olive stone with copper(I) oxide has been described and fully characterized using various techniques, including X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR-ATR), X-ray fluorescence (XRF), electronic microscopy, thermogravimetric analysis (TGA), moisture content, electrophoretic mobility and particle size distribution. The applicability of this new biocatalyst in the 1,3-dipolar cycloaddition click reaction between alkynes and azides has been demonstrated leading to the obtention of a great variety of 1,4-disubstituted-1,2,3-triazoles with good to excellent conversions. The new biocatalyst showed promising features in terms of recyclability and industrial or biomedical application. It could be recycled up to five times with minimal loss of catalytic activity when synthezing compound <strong>3a</strong>-<strong>3n</strong>. Additionally, it was effective in the multi-gram scale synthesis of compounds <strong>3b</strong> and <strong>3e</strong>, which were tested for the first time in cells, specifically on the human fibroblast-derived M1 cell line, demonstrating that these compounds are non-cytotoxic and thus suitable for potential uses in biomedicine.</div></div>\",\"PeriodicalId\":22138,\"journal\":{\"name\":\"Sustainable Chemistry and Pharmacy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2024-11-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sustainable Chemistry and Pharmacy\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2352554124004078\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sustainable Chemistry and Pharmacy","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2352554124004078","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
New Copper(I) oxide biocatalyst based on functionalized olive stone for the synthesis of 1,4-disubstituted-1,2,3-triazoles under very mild conditions
An efficient methodology for coating silanized olive stone with copper(I) oxide has been described and fully characterized using various techniques, including X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR-ATR), X-ray fluorescence (XRF), electronic microscopy, thermogravimetric analysis (TGA), moisture content, electrophoretic mobility and particle size distribution. The applicability of this new biocatalyst in the 1,3-dipolar cycloaddition click reaction between alkynes and azides has been demonstrated leading to the obtention of a great variety of 1,4-disubstituted-1,2,3-triazoles with good to excellent conversions. The new biocatalyst showed promising features in terms of recyclability and industrial or biomedical application. It could be recycled up to five times with minimal loss of catalytic activity when synthezing compound 3a-3n. Additionally, it was effective in the multi-gram scale synthesis of compounds 3b and 3e, which were tested for the first time in cells, specifically on the human fibroblast-derived M1 cell line, demonstrating that these compounds are non-cytotoxic and thus suitable for potential uses in biomedicine.
期刊介绍:
Sustainable Chemistry and Pharmacy publishes research that is related to chemistry, pharmacy and sustainability science in a forward oriented manner. It provides a unique forum for the publication of innovative research on the intersection and overlap of chemistry and pharmacy on the one hand and sustainability on the other hand. This includes contributions related to increasing sustainability of chemistry and pharmaceutical science and industries itself as well as their products in relation to the contribution of these to sustainability itself. As an interdisciplinary and transdisciplinary journal it addresses all sustainability related issues along the life cycle of chemical and pharmaceutical products form resource related topics until the end of life of products. This includes not only natural science based approaches and issues but also from humanities, social science and economics as far as they are dealing with sustainability related to chemistry and pharmacy. Sustainable Chemistry and Pharmacy aims at bridging between disciplines as well as developing and developed countries.