se -芳基- n -苯基苯硒肼盐:含有光敏剂单元的芳基自由基前体

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Takuma Kurokawa, Shintaro Takahashi, Naokazu Kano
{"title":"se -芳基- n -苯基苯硒肼盐:含有光敏剂单元的芳基自由基前体","authors":"Takuma Kurokawa, Shintaro Takahashi, Naokazu Kano","doi":"10.1039/d5cc03637b","DOIUrl":null,"url":null,"abstract":"Se-Aryl-N-phenylphenoselenazinium salts were synthesized as triarylselenonium salts incorporating a photosensitizer unit. Under blue-light irradiation, these served as aryl radical precursors, yielding arylphosphonates, phenol, and phenylboronic ester. The reaction mechanism was investigated by spectroscopic methods, which suggests that the aryl radical formation proceeds through intramolecular charge transfer and intermolecular photoredox cycles.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"31 1","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Se-Aryl-N-phenylphenoselenazinium Salts: Aryl Radical Precursors Incorporating a Photosensitizer Unit\",\"authors\":\"Takuma Kurokawa, Shintaro Takahashi, Naokazu Kano\",\"doi\":\"10.1039/d5cc03637b\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Se-Aryl-N-phenylphenoselenazinium salts were synthesized as triarylselenonium salts incorporating a photosensitizer unit. Under blue-light irradiation, these served as aryl radical precursors, yielding arylphosphonates, phenol, and phenylboronic ester. The reaction mechanism was investigated by spectroscopic methods, which suggests that the aryl radical formation proceeds through intramolecular charge transfer and intermolecular photoredox cycles.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"31 1\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5cc03637b\",\"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":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc03637b","RegionNum":2,"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

采用光敏剂合成了se -芳基- n -苯基苯硒鎓盐。在蓝光照射下,它们作为芳基自由基前体,生成芳基膦酸盐、苯酚和苯硼酯。用光谱方法研究了反应机理,表明芳基自由基的形成是通过分子内电荷转移和分子间光氧化还原循环进行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Se-Aryl-N-phenylphenoselenazinium Salts: Aryl Radical Precursors Incorporating a Photosensitizer Unit
Se-Aryl-N-phenylphenoselenazinium salts were synthesized as triarylselenonium salts incorporating a photosensitizer unit. Under blue-light irradiation, these served as aryl radical precursors, yielding arylphosphonates, phenol, and phenylboronic ester. The reaction mechanism was investigated by spectroscopic methods, which suggests that the aryl radical formation proceeds through intramolecular charge transfer and intermolecular photoredox cycles.
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
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信