Chalcogenoviologen Enhanced Host–Guest Recognition
Year: 2024
Type: article
Abstract: Open AccessCCS ChemistryRESEARCH ARTICLES25 Aug 2024Chalcogenoviologen Enhanced Host-Guest Recognition Yuanning Feng, Xingang Zhao, Daniel A. Appleton, Han Han, Ryan M. Young, Wenqi Liu, Christopher K. Lee, Weixingyue Li, Bai-Tong Liu, Yong Wu, Chun Tang, Aspen X.-Y. Chen, Charlotte L. Stern, Dong Jun Kim, Michael R. Wasielewski, Yunyan Qiu and J. Fraser Stoddart Yuanning Feng , Xingang Zhao , Daniel A. Appleton , Han Han , Ryan M. Young , Wenqi Liu , Christopher K. Lee , Weixingyue Li , Bai-Tong Liu , Yong Wu , Chun Tang , Aspen X.-Y. Chen , Charlotte L. Stern , Dong Jun Kim , Michael R. Wasielewski , Yunyan Qiu and J. Fraser Stoddart Cite this: CCS Chemistry. 2024;0:1–35https://doi.org/10.31635/ccschem.024.202404812 SectionsSupplemental MaterialAboutPDF ToolsAdd to favoritesDownload CitationsTrack Citations ShareFacebookTwitterLinked InEmail In the field of supramolecular chemistry, cyclophanes with novel properties are highly sought after since they can be tailored to fulfill specific tasks. In this article, we incorporate chalcogenoviologen-based units into tetracationic cyclophanes, resulting in enhanced host-guest recognition. The cyclophanes can be tuned through the addition of chalcogen bridging atoms-S, Se, and Te-which enhance their rigidity, regulate bond rotation and introduce additional steric bulk. Three cyclophanes containing chalcogen bridging atoms were synthesized and characterized in both the solution and solid states. The energy barriers for their interconversion between syn- and anti- conformations in solution were found to be correlated with chalcogen atom size. The photophysical properties of the cyclophanes are strongly dependent on the chalcogen atomic number, with intersystem crossing rates increasing from S to Se to Te. UV-Vis-NIR Spectroscopic and fluorometric titrations revealed that the chalcogenoviologen-based cyclophanes exhibit significantly stronger binding with electron-rich guests compared to the well-known, unsubstituted cyclobis(paraquat-p-phenylene). This enhancement in binding can be attributed to restricted rotation within the chalcogenoviologen units. This research provides insight into the rational design and tailored synthesis of cationic cyclophanes. Download figure Download PowerPoint Previous articleNext article FiguresReferencesRelatedDetails Issue AssignmentNot Yet AssignedSupporting Information Copyright & Permissions© 2024 Chinese Chemical Society Downloaded 0 times PDF downloadLoading ...
Source: CCS Chemistry
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: diamond
OpenAlex ID: W4401894201