双氨基杯[4]芳烃†与双羧酸盐结合的固溶研究

S. Camiolo, Philip A. Gale, M. Ogden, B. Skelton, Allan H. White
{"title":"双氨基杯[4]芳烃†与双羧酸盐结合的固溶研究","authors":"S. Camiolo, Philip A. Gale, M. Ogden, B. Skelton, Allan H. White","doi":"10.1039/B102831F","DOIUrl":null,"url":null,"abstract":"Bis-amidinium calix[4]arene receptors were shown to coordinate bis-carboxylate anions in DMSO solution; the crystal structure of the malonate salt of one of the receptors revealed a number of different amidinium–carboxylate interactions, demonstrating the propensity of these species to form complex hydrogen bonding networks.","PeriodicalId":17260,"journal":{"name":"Journal of the Chemical Society, Perkin Transactions 2","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"16","resultStr":"{\"title\":\"Solid-state and solution studies of bis-carboxylate binding by bis-amidinium calix[4]arenes†\",\"authors\":\"S. Camiolo, Philip A. Gale, M. Ogden, B. Skelton, Allan H. White\",\"doi\":\"10.1039/B102831F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Bis-amidinium calix[4]arene receptors were shown to coordinate bis-carboxylate anions in DMSO solution; the crystal structure of the malonate salt of one of the receptors revealed a number of different amidinium–carboxylate interactions, demonstrating the propensity of these species to form complex hydrogen bonding networks.\",\"PeriodicalId\":17260,\"journal\":{\"name\":\"Journal of the Chemical Society, Perkin Transactions 2\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"16\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Chemical Society, Perkin Transactions 2\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/B102831F\",\"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 the Chemical Society, Perkin Transactions 2","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/B102831F","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 16

摘要

双氨基杯[4]芳烃受体在DMSO溶液中与双羧酸阴离子配位;其中一种受体的丙二酸盐的晶体结构揭示了许多不同的脒-羧酸盐相互作用,证明了这些物种形成复杂氢键网络的倾向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Solid-state and solution studies of bis-carboxylate binding by bis-amidinium calix[4]arenes†
Bis-amidinium calix[4]arene receptors were shown to coordinate bis-carboxylate anions in DMSO solution; the crystal structure of the malonate salt of one of the receptors revealed a number of different amidinium–carboxylate interactions, demonstrating the propensity of these species to form complex hydrogen bonding networks.
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
期刊最新文献
The effect of oxygen on the regioselectivity in the rhodium catalysed hydrosilylation of 1,3-dienes Screening of yeast species for the stereo-selective reduction of bicyclo[2.2.2]octane-2,6-dione Solid-state and solution studies of bis-carboxylate binding by bis-amidinium calix[4]arenes† The acid-catalysed rearrangements of 4,5-bis(2-thienylhydroxymethyl)-1,3-dithiole-2-thione The crystal structures of a ketone and related acetal macrocycle containing 2,6-pyridino and polyether subunits
×
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