折叠动态大环系统以稳定其阳离子激态

IF 4.6 1区 化学 Q1 CHEMISTRY, ORGANIC
Arnab Dutta, Krzysztof Dzieszkowski, Marco Farinone, Łukasz Orzeł, Krzysztof Kruczała, Monika Kijewska, Miłosz Pawlicki
{"title":"折叠动态大环系统以稳定其阳离子激态","authors":"Arnab Dutta, Krzysztof Dzieszkowski, Marco Farinone, Łukasz Orzeł, Krzysztof Kruczała, Monika Kijewska, Miłosz Pawlicki","doi":"10.1039/d4qo01566e","DOIUrl":null,"url":null,"abstract":"A precise design of unsaturated systems remains an important factor that determines the quality of formed products based on a specific spatial orientation, but also defining the available -electron density open for postsynthetic modulation via a redox change. Three strictly defined reagents showing a different degree of flexibility, but also introducing two mutual orientations of reacting ends (parallel and obtuse) determine the quality of formed products obtained via an intramolecular or an intermolecular reaction. The redox activated transformation of mono- and double-looped systems results in a dissimilar oxidation state of a strongly pi-conjugated dication (2 electron process) or a cation-radical (1 electron process) derived from the difference in dynamic of the skeleton documented for monomer and dimer, respectively.","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Folding of a Dynamic Macrocyclic System to Stabilize its Cation Radical State\",\"authors\":\"Arnab Dutta, Krzysztof Dzieszkowski, Marco Farinone, Łukasz Orzeł, Krzysztof Kruczała, Monika Kijewska, Miłosz Pawlicki\",\"doi\":\"10.1039/d4qo01566e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A precise design of unsaturated systems remains an important factor that determines the quality of formed products based on a specific spatial orientation, but also defining the available -electron density open for postsynthetic modulation via a redox change. Three strictly defined reagents showing a different degree of flexibility, but also introducing two mutual orientations of reacting ends (parallel and obtuse) determine the quality of formed products obtained via an intramolecular or an intermolecular reaction. The redox activated transformation of mono- and double-looped systems results in a dissimilar oxidation state of a strongly pi-conjugated dication (2 electron process) or a cation-radical (1 electron process) derived from the difference in dynamic of the skeleton documented for monomer and dimer, respectively.\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-10-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d4qo01566e\",\"RegionNum\":1,\"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":"Organic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4qo01566e","RegionNum":1,"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

不饱和体系的精确设计仍然是一个重要因素,它不仅决定了基于特定空间取向形成的产物的质量,而且还确定了可用的  电子密度,以便通过氧化还原变化进行合成后调节。三种严格定义的试剂显示出不同程度的灵活性,同时也引入了两种反应端的相互取向(平行和钝角),这决定了通过分子内或分子间反应所形成的产物的质量。单环和双环系统的氧化还原活化转化会产生不同的强π-共轭二价氧化态(2 个电子过程)或阳离子-自由基氧化态(1 个电子过程),这分别源于单体和二聚体所记录的骨架动态的不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Folding of a Dynamic Macrocyclic System to Stabilize its Cation Radical State
A precise design of unsaturated systems remains an important factor that determines the quality of formed products based on a specific spatial orientation, but also defining the available -electron density open for postsynthetic modulation via a redox change. Three strictly defined reagents showing a different degree of flexibility, but also introducing two mutual orientations of reacting ends (parallel and obtuse) determine the quality of formed products obtained via an intramolecular or an intermolecular reaction. The redox activated transformation of mono- and double-looped systems results in a dissimilar oxidation state of a strongly pi-conjugated dication (2 electron process) or a cation-radical (1 electron process) derived from the difference in dynamic of the skeleton documented for monomer and dimer, respectively.
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
Organic Chemistry Frontiers
Organic Chemistry Frontiers CHEMISTRY, ORGANIC-
CiteScore
7.90
自引率
11.10%
发文量
686
审稿时长
1 months
期刊介绍: Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.
×
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