{"title":"非均相铜聚合物催化芳基卤化物与亚硫酸钠的光磺化反应","authors":"Lijie Chen , Zhengbin Yun , Weiwei Fang","doi":"10.1002/ajoc.202500534","DOIUrl":null,"url":null,"abstract":"<div><div>A general method for photosulfonylation of aryl halides with sodium sulfinates was successfully developed by using reusable copper‐containing hyper‐cross‐linked polymers (HCPs‐Cu). These heterogeneous catalysts were easily prepared from molecular BINAP/Cu(MeCN)<sub>4</sub>PF<sub>6</sub> complex (BINAP‐Cu) with different amounts of benzene and formaldehyde dimethyl acetal (FDA) via direct knitting strategy, and the Cu center was uniformly dispersed in the matrices of HCPs‐Cu, featuring the same coordination environment to that of molecular BINAP‐Cu. This photosulfonylation system not only tolerates a wide range of substrates to furnish aryl sulfones, showing a potential in the synthesis of several drugs, but also highlights a moderate recyclability of 10 runs with minimal loss of catalytic activity.</div></div>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"14 10","pages":"Article e00534"},"PeriodicalIF":2.7000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photosulfonylation of Aryl Halides with Sodium Sulfinates Catalyzed by Heterogeneous Copper Polymers\",\"authors\":\"Lijie Chen , Zhengbin Yun , Weiwei Fang\",\"doi\":\"10.1002/ajoc.202500534\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A general method for photosulfonylation of aryl halides with sodium sulfinates was successfully developed by using reusable copper‐containing hyper‐cross‐linked polymers (HCPs‐Cu). These heterogeneous catalysts were easily prepared from molecular BINAP/Cu(MeCN)<sub>4</sub>PF<sub>6</sub> complex (BINAP‐Cu) with different amounts of benzene and formaldehyde dimethyl acetal (FDA) via direct knitting strategy, and the Cu center was uniformly dispersed in the matrices of HCPs‐Cu, featuring the same coordination environment to that of molecular BINAP‐Cu. This photosulfonylation system not only tolerates a wide range of substrates to furnish aryl sulfones, showing a potential in the synthesis of several drugs, but also highlights a moderate recyclability of 10 runs with minimal loss of catalytic activity.</div></div>\",\"PeriodicalId\":130,\"journal\":{\"name\":\"Asian Journal of Organic Chemistry\",\"volume\":\"14 10\",\"pages\":\"Article e00534\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2193580725003988\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2193580725003988","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Photosulfonylation of Aryl Halides with Sodium Sulfinates Catalyzed by Heterogeneous Copper Polymers
A general method for photosulfonylation of aryl halides with sodium sulfinates was successfully developed by using reusable copper‐containing hyper‐cross‐linked polymers (HCPs‐Cu). These heterogeneous catalysts were easily prepared from molecular BINAP/Cu(MeCN)4PF6 complex (BINAP‐Cu) with different amounts of benzene and formaldehyde dimethyl acetal (FDA) via direct knitting strategy, and the Cu center was uniformly dispersed in the matrices of HCPs‐Cu, featuring the same coordination environment to that of molecular BINAP‐Cu. This photosulfonylation system not only tolerates a wide range of substrates to furnish aryl sulfones, showing a potential in the synthesis of several drugs, but also highlights a moderate recyclability of 10 runs with minimal loss of catalytic activity.
期刊介绍:
Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC)
The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.