基于不同硫脲桥接单官能化双柱[5]芳烃的双-[1]轮烷自组装

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Lu Yang, Cui-Yun Nie, Ying Han, Jing Sun, Chao-Guo Yan
{"title":"基于不同硫脲桥接单官能化双柱[5]芳烃的双-[1]轮烷自组装","authors":"Lu Yang,&nbsp;Cui-Yun Nie,&nbsp;Ying Han,&nbsp;Jing Sun,&nbsp;Chao-Guo Yan","doi":"10.1007/s10847-021-01103-4","DOIUrl":null,"url":null,"abstract":"<div><p>The condensation reaction of mono-amido-functionalized pillar[5]arenes with <i>tere</i>- and <i>iso</i>-phthaloyl diisothiocyanates in acetone under ultrasonic irradiation afforded <i>tere</i>- and <i>iso</i>-phthaloylthiourea-bridged dipillar[5]arenes. The similar reaction of mono-amido-functionalized pillar[5]arenes with 1,ω-bis(4-isothiocyanatophenoxy)alkanes also afforded diphenoxyalkylene thiourea-bridged dipillar[5]arenes. <sup>1</sup>H NMR and NOESY spectra clearly indicated that bis-[1]rotaxanes were formed by insertion of longer alkylene chains into the cavities of two pillar[5]arenes. On the other hand, the free-forms of dipillar[5]arenes were obtained with the shorter ethylene chains existing on the outside of the cavities of two pillar[5]arenes.</p><h3>Graphic abstract</h3>\n <figure><div><div><div><picture><source><img></source></picture></div></div></div></figure>\n </div>","PeriodicalId":54324,"journal":{"name":"Journal of Inclusion Phenomena and Macrocyclic Chemistry","volume":"102 1-2","pages":"89 - 97"},"PeriodicalIF":1.7000,"publicationDate":"2021-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10847-021-01103-4.pdf","citationCount":"3","resultStr":"{\"title\":\"Self-assembly of bis-[1]rotaxanes based on diverse thiourea-bridged mono-functionalized dipillar[5]arenes\",\"authors\":\"Lu Yang,&nbsp;Cui-Yun Nie,&nbsp;Ying Han,&nbsp;Jing Sun,&nbsp;Chao-Guo Yan\",\"doi\":\"10.1007/s10847-021-01103-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The condensation reaction of mono-amido-functionalized pillar[5]arenes with <i>tere</i>- and <i>iso</i>-phthaloyl diisothiocyanates in acetone under ultrasonic irradiation afforded <i>tere</i>- and <i>iso</i>-phthaloylthiourea-bridged dipillar[5]arenes. The similar reaction of mono-amido-functionalized pillar[5]arenes with 1,ω-bis(4-isothiocyanatophenoxy)alkanes also afforded diphenoxyalkylene thiourea-bridged dipillar[5]arenes. <sup>1</sup>H NMR and NOESY spectra clearly indicated that bis-[1]rotaxanes were formed by insertion of longer alkylene chains into the cavities of two pillar[5]arenes. On the other hand, the free-forms of dipillar[5]arenes were obtained with the shorter ethylene chains existing on the outside of the cavities of two pillar[5]arenes.</p><h3>Graphic abstract</h3>\\n <figure><div><div><div><picture><source><img></source></picture></div></div></div></figure>\\n </div>\",\"PeriodicalId\":54324,\"journal\":{\"name\":\"Journal of Inclusion Phenomena and Macrocyclic Chemistry\",\"volume\":\"102 1-2\",\"pages\":\"89 - 97\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2021-09-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://link.springer.com/content/pdf/10.1007/s10847-021-01103-4.pdf\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Inclusion Phenomena and Macrocyclic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10847-021-01103-4\",\"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/s10847-021-01103-4","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: 3

摘要

超声辐照下,单酰胺功能化柱[5]芳烃与邻苯二甲酰二异硫氰酸酯和异邻苯二甲酰二异硫氰酸酯在丙酮中的缩合反应得到了邻苯二甲酰硫脲桥接双柱[5]芳烃。单酰胺功能化柱[5]芳烃与1,ω-双(4-异硫氰酸atophoxy)烷烃的类似反应也得到了二苯氧亚烷基硫脲桥接双柱[5]芳烃。1H NMR和noesi光谱清楚地表明,双-[1]轮烷是通过在两柱[5]芳烃的空腔中插入较长的烷基链而形成的。另一方面,双柱[5]芳烃的自由形式是两柱[5]芳烃的空腔外侧存在较短的乙烯链。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Self-assembly of bis-[1]rotaxanes based on diverse thiourea-bridged mono-functionalized dipillar[5]arenes

Self-assembly of bis-[1]rotaxanes based on diverse thiourea-bridged mono-functionalized dipillar[5]arenes

The condensation reaction of mono-amido-functionalized pillar[5]arenes with tere- and iso-phthaloyl diisothiocyanates in acetone under ultrasonic irradiation afforded tere- and iso-phthaloylthiourea-bridged dipillar[5]arenes. The similar reaction of mono-amido-functionalized pillar[5]arenes with 1,ω-bis(4-isothiocyanatophenoxy)alkanes also afforded diphenoxyalkylene thiourea-bridged dipillar[5]arenes. 1H NMR and NOESY spectra clearly indicated that bis-[1]rotaxanes were formed by insertion of longer alkylene chains into the cavities of two pillar[5]arenes. On the other hand, the free-forms of dipillar[5]arenes were obtained with the shorter ethylene chains existing on the outside of the cavities of two pillar[5]arenes.

Graphic abstract

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