中性杯[4]间苯二酚中的阳离子-π相互作用

Jerry L Atwood, Agnieszka Szumna
{"title":"中性杯[4]间苯二酚中的阳离子-π相互作用","authors":"Jerry L Atwood,&nbsp;Agnieszka Szumna","doi":"10.1016/S1472-7862(03)00068-6","DOIUrl":null,"url":null,"abstract":"<div><p>The interaction of the neutral form of resorcin[4]arene <strong>1</strong> (R=<em>i-</em>Bu) with tetraalkylammonium cations (Me<sub>4</sub>N<sup>+</sup>, Et<sub>4</sub>N<sup>+</sup>, Pr<sub>4</sub>N<sup>+</sup>and Bu<sub>4</sub>N<sup>+</sup>) was analyzed in the solid state and in methanol solutions. In methanol, NMR titration results indicate almost no differentiation between Me<sub>4</sub>N<sup>+</sup> and Et<sub>4</sub>N<sup>+</sup> cations (K<sub>ass</sub>(Me<sub>4</sub>N<sup>+</sup>)=93<!--> <!-->M<sup>−1</sup> and K<sub>ass</sub>(Et<sub>4</sub>N<sup>+</sup>)=81<!--> <!-->M<sup>−1</sup>) and a relatively low association constant for Pr<sub>4</sub>N<sup>+</sup>( K<sub>ass</sub>(Pr<sub>4</sub>N<sup>+</sup>)=25<!--> <!-->M<sup>−1</sup>). In the solid state, for the Me<sub>4</sub>NCl complex, the resorcinarene assumes the C<sub>2v</sub> boat conformation and is surrounded by as many as four Me<sub>4</sub>NCl moieties. The structure of the Et<sub>4</sub><span>NCl complex indicates that ethyl group can be conveniently placed in the resocin[4]arene cavity. The larger Bu</span><sub>4</sub>N<sup>+</sup> cation was found completely external to the cavity.</p></div>","PeriodicalId":100833,"journal":{"name":"Journal of Supramolecular Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2002-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1472-7862(03)00068-6","citationCount":"36","resultStr":"{\"title\":\"Cation–pi interactions in neutral calix[4]resorcinarenes\",\"authors\":\"Jerry L Atwood,&nbsp;Agnieszka Szumna\",\"doi\":\"10.1016/S1472-7862(03)00068-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The interaction of the neutral form of resorcin[4]arene <strong>1</strong> (R=<em>i-</em>Bu) with tetraalkylammonium cations (Me<sub>4</sub>N<sup>+</sup>, Et<sub>4</sub>N<sup>+</sup>, Pr<sub>4</sub>N<sup>+</sup>and Bu<sub>4</sub>N<sup>+</sup>) was analyzed in the solid state and in methanol solutions. In methanol, NMR titration results indicate almost no differentiation between Me<sub>4</sub>N<sup>+</sup> and Et<sub>4</sub>N<sup>+</sup> cations (K<sub>ass</sub>(Me<sub>4</sub>N<sup>+</sup>)=93<!--> <!-->M<sup>−1</sup> and K<sub>ass</sub>(Et<sub>4</sub>N<sup>+</sup>)=81<!--> <!-->M<sup>−1</sup>) and a relatively low association constant for Pr<sub>4</sub>N<sup>+</sup>( K<sub>ass</sub>(Pr<sub>4</sub>N<sup>+</sup>)=25<!--> <!-->M<sup>−1</sup>). In the solid state, for the Me<sub>4</sub>NCl complex, the resorcinarene assumes the C<sub>2v</sub> boat conformation and is surrounded by as many as four Me<sub>4</sub>NCl moieties. The structure of the Et<sub>4</sub><span>NCl complex indicates that ethyl group can be conveniently placed in the resocin[4]arene cavity. The larger Bu</span><sub>4</sub>N<sup>+</sup> cation was found completely external to the cavity.</p></div>\",\"PeriodicalId\":100833,\"journal\":{\"name\":\"Journal of Supramolecular Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1472-7862(03)00068-6\",\"citationCount\":\"36\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Supramolecular Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1472786203000686\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Supramolecular Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1472786203000686","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 36

摘要

分析了中性形式的间苯二酚[4]芳烃1(R=i-Bu)与四烷基铵阳离子(Me4N+,Et4N+、Pr4N+和Bu4N+)在固态和甲醇溶液中的相互作用。在甲醇中,NMR滴定结果表明Me4N+和Et4N+阳离子之间几乎没有差异(Kass(Me4N+)=93 M−1和Kass(Et4N+)=81 M−1),Pr4N+的缔合常数相对较低(Kass。在固态中,对于Me4NCl络合物,间苯二酚烯呈现C2v舟皿构象,并被多达四个Me4NCl部分包围。Et4NCl配合物的结构表明,乙基可以方便地放置在resocin[4]芳烃腔中。发现较大的Bu4N+阳离子完全在空腔外部。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cation–pi interactions in neutral calix[4]resorcinarenes

The interaction of the neutral form of resorcin[4]arene 1 (R=i-Bu) with tetraalkylammonium cations (Me4N+, Et4N+, Pr4N+and Bu4N+) was analyzed in the solid state and in methanol solutions. In methanol, NMR titration results indicate almost no differentiation between Me4N+ and Et4N+ cations (Kass(Me4N+)=93 M−1 and Kass(Et4N+)=81 M−1) and a relatively low association constant for Pr4N+( Kass(Pr4N+)=25 M−1). In the solid state, for the Me4NCl complex, the resorcinarene assumes the C2v boat conformation and is surrounded by as many as four Me4NCl moieties. The structure of the Et4NCl complex indicates that ethyl group can be conveniently placed in the resocin[4]arene cavity. The larger Bu4N+ cation was found completely external to the cavity.

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
自引率
0.00%
发文量
0
×
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