{"title":"Inclusion of organic molecule guests by sulfinyl bridged bis-salicylic acid-type open-chain host with flexible change of crystal structure","authors":"Naoya Morohashi, Takanori Shimazaki, Yuki Akahira, Tetsutaro Hattori","doi":"10.1007/s10847-022-01166-x","DOIUrl":null,"url":null,"abstract":"<div><p>To develop an open-chain host that can accommodate organic molecule guests via the formation of a recognition space, such as a pseudo-cyclic structure in the solid state, we designed and synthesized host molecules <b>4</b> and <b>5</b> comprising sulfur- and sulfinyl-bridged salicylic acids. X-ray structural analysis revealed that compound <b>5</b> affords the desired pseudo-cyclic structure in the solid state by the association of two of its molecules via <i>syn</i>-oriented salicylic acid units, presumably owing to the dipole repulsion against its sulfinyl group. Host <b>5</b> successfully formed inclusion crystals with specific organic molecules such as chloroform and 1,1,2,2-tetrachloroethane. We observed conformational and packing structure flexibility of host <b>5</b> based on the structure of guest molecules. <b>5</b>·CHCl<sub>3</sub> and <b>5</b>·[CHCl<sub>2</sub>CHCl<sub>2</sub>]<sub>3</sub> formed columnar and sheet structures, respectively, because of the differences in their host–guest interactions and the size of guest molecules.</p></div>","PeriodicalId":54324,"journal":{"name":"Journal of Inclusion Phenomena and Macrocyclic Chemistry","volume":"102 11-12","pages":"861 - 869"},"PeriodicalIF":1.7000,"publicationDate":"2022-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","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/s10847-022-01166-x","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
Abstract
To develop an open-chain host that can accommodate organic molecule guests via the formation of a recognition space, such as a pseudo-cyclic structure in the solid state, we designed and synthesized host molecules 4 and 5 comprising sulfur- and sulfinyl-bridged salicylic acids. X-ray structural analysis revealed that compound 5 affords the desired pseudo-cyclic structure in the solid state by the association of two of its molecules via syn-oriented salicylic acid units, presumably owing to the dipole repulsion against its sulfinyl group. Host 5 successfully formed inclusion crystals with specific organic molecules such as chloroform and 1,1,2,2-tetrachloroethane. We observed conformational and packing structure flexibility of host 5 based on the structure of guest molecules. 5·CHCl3 and 5·[CHCl2CHCl2]3 formed columnar and sheet structures, respectively, because of the differences in their host–guest interactions and the size of guest molecules.
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.