膦酸盐取代的吡嗪卟啉--一种用于高效硫氧化的通用光催化剂

IF 3 4区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY ChemPlusChem Pub Date : 2024-09-11 DOI:10.1002/cplu.202400469
Kirill P. Birin, Daria A. Polivanovskaia, Inna A. Abdulaeva, Yulia G. Gorbunova, Aslan Yu. Tsivadze
{"title":"膦酸盐取代的吡嗪卟啉--一种用于高效硫氧化的通用光催化剂","authors":"Kirill P. Birin, Daria A. Polivanovskaia, Inna A. Abdulaeva, Yulia G. Gorbunova, Aslan Yu. Tsivadze","doi":"10.1002/cplu.202400469","DOIUrl":null,"url":null,"abstract":"An exceptional efficiency of pyrazine‐annelated porphyrin as a general photocatalyst for the oxidation of organic sulfides is demonstrated. It is shown that phosphonate‐substituted pyrazinoporphyrin 2H‐1 brings together sufficient photostability and high efficiency in the aerobic photooxidation of a series of various sulfides. The influence of the reaction conditions onto the efficiency of homogeneous sulfide photooxidation in the presence of the PS was investigated and strong dependence on the solvent system was observed. The use of methanol is required for the photocatalytic sulfoxidation and the ratio of the alcohol/other solvent can significantly affect the conversion and selectivity of the reaction. The application of the prepared photosensitizer (PS) in 0.001 mol% loading allowed achieving complete conversion (97‐100%, turnover number up to 100000, turnover frequency up to 6250 h‐1) of substrates bearing substituents of different nature, namely aromatic and aliphatic sulfides with donor or acceptor substituents and substituents prone to oxidation, as well as cyclic sulfides. The selectivity of the of the corresponding sulfoxides formation of 96‐100% was revealed. Finally, a gram‐scale synthesis of several sulfoxides was successfully performed with the PS under investigation, providing desired products in 66‐96% yield with over 98% purity.","PeriodicalId":148,"journal":{"name":"ChemPlusChem","volume":"22 1","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phosphonate‐substituted Pyrazinoporphyrin – a General Photocatalyst for Efficient Sulfoxidation\",\"authors\":\"Kirill P. Birin, Daria A. Polivanovskaia, Inna A. Abdulaeva, Yulia G. Gorbunova, Aslan Yu. Tsivadze\",\"doi\":\"10.1002/cplu.202400469\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An exceptional efficiency of pyrazine‐annelated porphyrin as a general photocatalyst for the oxidation of organic sulfides is demonstrated. It is shown that phosphonate‐substituted pyrazinoporphyrin 2H‐1 brings together sufficient photostability and high efficiency in the aerobic photooxidation of a series of various sulfides. The influence of the reaction conditions onto the efficiency of homogeneous sulfide photooxidation in the presence of the PS was investigated and strong dependence on the solvent system was observed. The use of methanol is required for the photocatalytic sulfoxidation and the ratio of the alcohol/other solvent can significantly affect the conversion and selectivity of the reaction. The application of the prepared photosensitizer (PS) in 0.001 mol% loading allowed achieving complete conversion (97‐100%, turnover number up to 100000, turnover frequency up to 6250 h‐1) of substrates bearing substituents of different nature, namely aromatic and aliphatic sulfides with donor or acceptor substituents and substituents prone to oxidation, as well as cyclic sulfides. The selectivity of the of the corresponding sulfoxides formation of 96‐100% was revealed. Finally, a gram‐scale synthesis of several sulfoxides was successfully performed with the PS under investigation, providing desired products in 66‐96% yield with over 98% purity.\",\"PeriodicalId\":148,\"journal\":{\"name\":\"ChemPlusChem\",\"volume\":\"22 1\",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemPlusChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/cplu.202400469\",\"RegionNum\":4,\"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":"ChemPlusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cplu.202400469","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

研究表明,吡嗪沟道化卟啉作为一种普通光催化剂,在氧化有机硫化物方面具有非凡的效率。研究表明,膦酸盐取代的吡嗪卟啉 2H-1 在一系列各种硫化物的有氧光氧化反应中具有足够的光稳定性和高效率。研究人员考察了反应条件对 PS 存在下均相硫化物光氧化效率的影响,并观察到这种影响与溶剂系统有很大关系。光催化硫氧化反应需要使用甲醇,而醇/其他溶剂的比例会显著影响反应的转化率和选择性。所制备的光敏剂(PS)以 0.001 mol%的负载量应用于带有不同性质取代基(即带有供体或受体取代基和易氧化取代基的芳香族和脂肪族硫化物以及环状硫化物)的底物,可实现完全转化(97%-100%,周转次数高达 100000,周转频率高达 6250 h-1)。结果表明,形成相应硫化物的选择性为 96%-100%。最后,利用所研究的 PS 成功地进行了几种硫化物的克级合成,提供了所需的产品,收率为 66-96%,纯度超过 98%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Phosphonate‐substituted Pyrazinoporphyrin – a General Photocatalyst for Efficient Sulfoxidation
An exceptional efficiency of pyrazine‐annelated porphyrin as a general photocatalyst for the oxidation of organic sulfides is demonstrated. It is shown that phosphonate‐substituted pyrazinoporphyrin 2H‐1 brings together sufficient photostability and high efficiency in the aerobic photooxidation of a series of various sulfides. The influence of the reaction conditions onto the efficiency of homogeneous sulfide photooxidation in the presence of the PS was investigated and strong dependence on the solvent system was observed. The use of methanol is required for the photocatalytic sulfoxidation and the ratio of the alcohol/other solvent can significantly affect the conversion and selectivity of the reaction. The application of the prepared photosensitizer (PS) in 0.001 mol% loading allowed achieving complete conversion (97‐100%, turnover number up to 100000, turnover frequency up to 6250 h‐1) of substrates bearing substituents of different nature, namely aromatic and aliphatic sulfides with donor or acceptor substituents and substituents prone to oxidation, as well as cyclic sulfides. The selectivity of the of the corresponding sulfoxides formation of 96‐100% was revealed. Finally, a gram‐scale synthesis of several sulfoxides was successfully performed with the PS under investigation, providing desired products in 66‐96% yield with over 98% purity.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ChemPlusChem
ChemPlusChem CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
5.90
自引率
0.00%
发文量
200
审稿时长
1 months
期刊介绍: ChemPlusChem is a peer-reviewed, general chemistry journal that brings readers the very best in multidisciplinary research centering on chemistry. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies. Fully comprehensive in its scope, ChemPlusChem publishes articles covering new results from at least two different aspects (subfields) of chemistry or one of chemistry and one of another scientific discipline (one chemistry topic plus another one, hence the title ChemPlusChem). All suitable submissions undergo balanced peer review by experts in the field to ensure the highest quality, originality, relevance, significance, and validity.
期刊最新文献
Localized Light-Induced Precipitation of Inorganic Materials. Multicolor, Non-Traditional Intrinsically Luminescent Polymers: Recent Advances. Origin of Regioselectivity Inversion Tuned by Substrate Electronic Properties in Co(III)-Catalyzed Annulation of N-Chlorobenzamide with Alkenes. The Dual-Role of Benzothiadiazole Fluorophores for Enabling Electrofluorochromic and Electrochromic Devices. Modelling Lithium-ion Transport Properties in Sulfoxides and Sulfones with Polarizable Molecular Dynamics and NMR Spectroscopy.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1