Difluorocarbene Generation via a Spin-Forbidden Excitation under Visible Light Irradiation.

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-11-13 Epub Date: 2024-11-04 DOI:10.1021/jacs.4c10939
Shan Liu, Guang-Ning Pan, Yijing Ling, Feng Gao, Yin Yang, Ganglong Cui, Qilong Shen, Tianfei Liu
{"title":"Difluorocarbene Generation via a Spin-Forbidden Excitation under Visible Light Irradiation.","authors":"Shan Liu, Guang-Ning Pan, Yijing Ling, Feng Gao, Yin Yang, Ganglong Cui, Qilong Shen, Tianfei Liu","doi":"10.1021/jacs.4c10939","DOIUrl":null,"url":null,"abstract":"<p><p>The generation of difluorocarbene from difluoromethane bis(sulfonium ylide) <b>1</b> through spin-forbidden excitation under irradiation with 450 nm blue light was reported. The formation of difluorocarbene was confirmed by its reaction with styrene derivatives for the generation of difluorocyclopropanation and insertion into RX-H bonds (X = O, S) for the generation of RXCF<sub>2</sub>H. The spin-forbidden excitation mechanism for the formation of difluorocarbene from difluoromethane bis(sulfonium ylide) was supported by spectroscopic and kinetic studies as well as computational chemistry. The homolytic cleavage of two S-C bonds in compound <b>1</b> under irradiation was confirmed by time-resolved EPR spectroscopic studies of the precursor's free-radical-capturing reaction, as well as the isolation of the dimer of dimethyl (phenylthiol)malonyl radical. Further studies showed that the homolytic cleavage process occurred asynchronously in the solvent cage based on the isotope-labeled scrambling experiments and DFT calculations.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":" ","pages":"31094-31105"},"PeriodicalIF":14.4000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c10939","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/4 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The generation of difluorocarbene from difluoromethane bis(sulfonium ylide) 1 through spin-forbidden excitation under irradiation with 450 nm blue light was reported. The formation of difluorocarbene was confirmed by its reaction with styrene derivatives for the generation of difluorocyclopropanation and insertion into RX-H bonds (X = O, S) for the generation of RXCF2H. The spin-forbidden excitation mechanism for the formation of difluorocarbene from difluoromethane bis(sulfonium ylide) was supported by spectroscopic and kinetic studies as well as computational chemistry. The homolytic cleavage of two S-C bonds in compound 1 under irradiation was confirmed by time-resolved EPR spectroscopic studies of the precursor's free-radical-capturing reaction, as well as the isolation of the dimer of dimethyl (phenylthiol)malonyl radical. Further studies showed that the homolytic cleavage process occurred asynchronously in the solvent cage based on the isotope-labeled scrambling experiments and DFT calculations.

Abstract Image

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
在可见光照射下通过自旋禁激生成二氟碳。
在 450 nm 蓝光照射下,二氟甲烷双(亚砜)1 通过自旋禁止激发生成了二氟碳。通过与苯乙烯衍生物反应生成二氟环丙烷和插入 RX-H 键(X = O、S)生成 RXCF2H,证实了二氟碳的形成。光谱和动力学研究以及计算化学支持了二氟甲烷双(亚磺酰基)形成二氟碳的自旋禁激机制。通过对前体自由基捕获反应的时间分辨 EPR 光谱研究,以及二甲基(苯硫醇)丙二酰自由基的二聚物的分离,证实了化合物 1 中的两个 S-C 键在辐照下发生了同解裂解。进一步的研究表明,根据同位素标记的扰乱实验和 DFT 计算,同源裂解过程是在溶剂笼中异步发生的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
期刊最新文献
Geminal Synergy in Pt–Co Dual-Atom Catalysts: From Synthesis to Photocatalytic Hydrogen Production Performance Descriptor of Subsurface Metal-Promoted Boron Catalysts for Low-Temperature Propane Oxidative Dehydrogenation to Propylene Remote-Contact Catalysis for Target-Diameter Semiconducting Carbon Nanotube Arrays DNA-Regulated Multi-Protein Complement Control Issue Publication Information
×
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