Hangman Fe(IV)助剂在bayer - villiger氧化反应中的应用

IF 2.7 4区 化学 Q1 CHEMISTRY, ORGANIC
Yi-Feng Qiu, Xu-You Cao, Feng Li, Guo-Chao Liang, Dr. Hao Zhang, Prof. Fu-Rong Wang, Prof. Hai Yang Liu
{"title":"Hangman Fe(IV)助剂在bayer - villiger氧化反应中的应用","authors":"Yi-Feng Qiu,&nbsp;Xu-You Cao,&nbsp;Feng Li,&nbsp;Guo-Chao Liang,&nbsp;Dr. Hao Zhang,&nbsp;Prof. Fu-Rong Wang,&nbsp;Prof. Hai Yang Liu","doi":"10.1002/ajoc.202500030","DOIUrl":null,"url":null,"abstract":"<p>A series of new hangman iron corroles with different electronic structure and pending aldehyde group were prepared and used as catalyst in Baeyer–Villiger (B–V) oxidation reactions. The results show that hangman iron corroles exhibit faster reaction rates and higher ε-caprolactone yields as compared to triaryl iron 5,10,15-tri(pentafluorophenyl) corrole (Fe(tpfc)Cl). With the increase in the electron-withdrawing ability of the meso-position substituents of hangman iron corrole, the yield of caprolactone also increases. Under optimal conditions, the best hangman iron corrole bearing two pentafluorophenyl groups (FePXC) may give a yield of 97% at only 0.07 mol% catalyst loading. The turnover number (TON) of the FePXC catalyst could be up to 2100 in a gram-scale test of oxidation of cyclohexanone. This work demonstrates the good potential of hangman corroles in B–V oxidation.</p>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"14 8","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction\",\"authors\":\"Yi-Feng Qiu,&nbsp;Xu-You Cao,&nbsp;Feng Li,&nbsp;Guo-Chao Liang,&nbsp;Dr. Hao Zhang,&nbsp;Prof. Fu-Rong Wang,&nbsp;Prof. Hai Yang Liu\",\"doi\":\"10.1002/ajoc.202500030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A series of new hangman iron corroles with different electronic structure and pending aldehyde group were prepared and used as catalyst in Baeyer–Villiger (B–V) oxidation reactions. The results show that hangman iron corroles exhibit faster reaction rates and higher ε-caprolactone yields as compared to triaryl iron 5,10,15-tri(pentafluorophenyl) corrole (Fe(tpfc)Cl). With the increase in the electron-withdrawing ability of the meso-position substituents of hangman iron corrole, the yield of caprolactone also increases. Under optimal conditions, the best hangman iron corrole bearing two pentafluorophenyl groups (FePXC) may give a yield of 97% at only 0.07 mol% catalyst loading. The turnover number (TON) of the FePXC catalyst could be up to 2100 in a gram-scale test of oxidation of cyclohexanone. This work demonstrates the good potential of hangman corroles in B–V oxidation.</p>\",\"PeriodicalId\":130,\"journal\":{\"name\":\"Asian Journal of Organic Chemistry\",\"volume\":\"14 8\",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-06-07\",\"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://aces.onlinelibrary.wiley.com/doi/10.1002/ajoc.202500030\",\"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://aces.onlinelibrary.wiley.com/doi/10.1002/ajoc.202500030","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

制备了一系列具有不同电子结构和醛基的新型hangman铁催化剂,并将其用作Baeyer-Villiger (B-V)氧化反应的催化剂。结果表明,与三芳基铁5,10,15-三(五氟苯基)铁(Fe(tpfc)Cl)相比,hangman铁衍生物具有更快的反应速率和更高的ε-己内酯产率。随着hangman - iron - corrole中位取代基吸电子能力的增强,己内酯的产率也随之提高。在最佳条件下,含两个五氟苯基(FePXC)的最佳hangman铁催化剂在0.07 mol%的催化剂负载下收率可达97%。FePXC催化剂在克级环己酮氧化试验中,周转数(TON)可达2100。这项工作证明了hangman催化剂在B-V氧化中的良好潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction

The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction

The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction

The Application of Hangman Fe(IV) Corrole in the Baeyer–Villiger Oxidation Reaction

A series of new hangman iron corroles with different electronic structure and pending aldehyde group were prepared and used as catalyst in Baeyer–Villiger (B–V) oxidation reactions. The results show that hangman iron corroles exhibit faster reaction rates and higher ε-caprolactone yields as compared to triaryl iron 5,10,15-tri(pentafluorophenyl) corrole (Fe(tpfc)Cl). With the increase in the electron-withdrawing ability of the meso-position substituents of hangman iron corrole, the yield of caprolactone also increases. Under optimal conditions, the best hangman iron corrole bearing two pentafluorophenyl groups (FePXC) may give a yield of 97% at only 0.07 mol% catalyst loading. The turnover number (TON) of the FePXC catalyst could be up to 2100 in a gram-scale test of oxidation of cyclohexanone. This work demonstrates the good potential of hangman corroles in B–V oxidation.

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
CiteScore
4.70
自引率
3.70%
发文量
372
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.
×
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