含三卤化物(I2, Br2和IBrCl−)的竹[6]尾尾在卤化和碘催化反应中的作用

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Renato Salviato Cicolani, Antonio Gustavo Sampaio de Oliveira-Filho, Ana Paula de Lima Batista, Grégoire Jean-François Demets
{"title":"含三卤化物(I2, Br2和IBrCl−)的竹[6]尾尾在卤化和碘催化反应中的作用","authors":"Renato Salviato Cicolani,&nbsp;Antonio Gustavo Sampaio de Oliveira-Filho,&nbsp;Ana Paula de Lima Batista,&nbsp;Grégoire Jean-François Demets","doi":"10.1007/s10847-023-01179-0","DOIUrl":null,"url":null,"abstract":"<div><p>We have prepared two new heterotrihalides inside methyl-bambus[6]uril, [Br<sub>2</sub>Cl]<sup>−</sup>@<b>MeBU[6]</b> and [BrICl]<sup>−</sup>@<b>MeBU[6]</b>, both in solution and in the solid state. These heterotrihalides were used alongside with the first one our group has produced, [I<sub>2</sub>Cl]<sup>−</sup>@<b>MeBU[6]</b>, as halogenation agents in classical halogenation and iodine-based catalysts for organic reactions, with comparable yields to those obtained with pure dihalogens.</p></div>","PeriodicalId":54324,"journal":{"name":"Journal of Inclusion Phenomena and Macrocyclic Chemistry","volume":"103 1-2","pages":"81 - 87"},"PeriodicalIF":1.7000,"publicationDate":"2023-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10847-023-01179-0.pdf","citationCount":"0","resultStr":"{\"title\":\"Trihalide-included (I2, Br2 and IBrCl−) bambus[6]urils in halogenation and iodine-catalysed reactions\",\"authors\":\"Renato Salviato Cicolani,&nbsp;Antonio Gustavo Sampaio de Oliveira-Filho,&nbsp;Ana Paula de Lima Batista,&nbsp;Grégoire Jean-François Demets\",\"doi\":\"10.1007/s10847-023-01179-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We have prepared two new heterotrihalides inside methyl-bambus[6]uril, [Br<sub>2</sub>Cl]<sup>−</sup>@<b>MeBU[6]</b> and [BrICl]<sup>−</sup>@<b>MeBU[6]</b>, both in solution and in the solid state. These heterotrihalides were used alongside with the first one our group has produced, [I<sub>2</sub>Cl]<sup>−</sup>@<b>MeBU[6]</b>, as halogenation agents in classical halogenation and iodine-based catalysts for organic reactions, with comparable yields to those obtained with pure dihalogens.</p></div>\",\"PeriodicalId\":54324,\"journal\":{\"name\":\"Journal of Inclusion Phenomena and Macrocyclic Chemistry\",\"volume\":\"103 1-2\",\"pages\":\"81 - 87\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2023-02-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s10847-023-01179-0.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Inclusion Phenomena and Macrocyclic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10847-023-01179-0\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inclusion Phenomena and Macrocyclic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10847-023-01179-0","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

我们在甲基竹[6]脲中制备了两种新的异三卤化物,[Br2Cl]−@MeBU[6]和[Br2Cl]−@MeBU[6],分别是溶液和固态。这些异三卤化物与我们小组生产的第一个异三卤化物[I2Cl]−@MeBU[6]一起用作经典卤化剂和有机反应的碘基催化剂,其产率与纯二卤素的产率相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Trihalide-included (I2, Br2 and IBrCl−) bambus[6]urils in halogenation and iodine-catalysed reactions

Trihalide-included (I2, Br2 and IBrCl−) bambus[6]urils in halogenation and iodine-catalysed reactions

We have prepared two new heterotrihalides inside methyl-bambus[6]uril, [Br2Cl]@MeBU[6] and [BrICl]@MeBU[6], both in solution and in the solid state. These heterotrihalides were used alongside with the first one our group has produced, [I2Cl]@MeBU[6], as halogenation agents in classical halogenation and iodine-based catalysts for organic reactions, with comparable yields to those obtained with pure dihalogens.

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
Journal of Inclusion Phenomena and Macrocyclic Chemistry
Journal of Inclusion Phenomena and Macrocyclic Chemistry Agricultural and Biological Sciences-Food Science
CiteScore
4.10
自引率
8.70%
发文量
54
期刊介绍: The Journal of Inclusion Phenomena and Macrocyclic Chemistry is the premier interdisciplinary publication reporting on original research into all aspects of host-guest systems. Examples of specific areas of interest are: the preparation and characterization of new hosts and new host-guest systems, especially those involving macrocyclic ligands; crystallographic, spectroscopic, thermodynamic and theoretical studies; applications in chromatography and inclusion polymerization; enzyme modelling; molecular recognition and catalysis by inclusion compounds; intercalates in biological and non-biological systems, cyclodextrin complexes and their applications in the agriculture, flavoring, food and pharmaceutical industries; synthesis, characterization and applications of zeolites. The journal publishes primarily reports of original research and preliminary communications, provided the latter represent a significant advance in the understanding of inclusion science. Critical reviews dealing with recent advances in the field are a periodic feature of the journal.
×
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:481959085
Book学术官方微信