Jialin Liu, Yan Huang, Qixia Bai, Qiaoan Yang, Xinyi Wu, Limin Zhang, Tun Wu, Pingshan Wang, Jianqiao Wang and Zhe Zhang
{"title":"Self-assembly and dynamic exchange of cuboctahedral metal–organic cages†","authors":"Jialin Liu, Yan Huang, Qixia Bai, Qiaoan Yang, Xinyi Wu, Limin Zhang, Tun Wu, Pingshan Wang, Jianqiao Wang and Zhe Zhang","doi":"10.1039/D4DT01169D","DOIUrl":null,"url":null,"abstract":"<p >Due to their unique physical and chemical properties, metal–organic cage structures have great potential for applications in various fields. However, current studies have mainly focused on highly symmetric structures assembled from single metal ions and organic ligands, limiting their diversity and complexity, and there are still relatively few studies on the dynamic formation process of metal–organic cages. Herein, we constructed a series of metal–organic cages with different sizes assembled from the highly-stable coordination of 2,2′:6′,2′′-terpyridine-based tetratopic ligands and various metals ions such as Zn, Cu, Co and Fe. Furthermore, the intermolecular exchange process between the metal–organic cages was explored through the dynamic exchange of ligands, and the formation of a series of hybrid supramolecular nanocages together with their final tendency to form a predominant structure of <strong>M<small><sub>24</sub></small>L1<small><sub>4</sub></small>L2<small><sub>8</sub></small></strong> was observed. In addition, the binding of metal–organic cages with 5,10,15,20-tetrakis(3,4,5-trimethoxyphenyl) porphyrin-Zn was also investigated. This study not only expands the complexity and diversity of metal–organic cages, but also provides a new perspective for studying the dynamic behaviour of metal–organic cages.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 35","pages":" 14701-14709"},"PeriodicalIF":3.5000,"publicationDate":"2024-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/dt/d4dt01169d","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Due to their unique physical and chemical properties, metal–organic cage structures have great potential for applications in various fields. However, current studies have mainly focused on highly symmetric structures assembled from single metal ions and organic ligands, limiting their diversity and complexity, and there are still relatively few studies on the dynamic formation process of metal–organic cages. Herein, we constructed a series of metal–organic cages with different sizes assembled from the highly-stable coordination of 2,2′:6′,2′′-terpyridine-based tetratopic ligands and various metals ions such as Zn, Cu, Co and Fe. Furthermore, the intermolecular exchange process between the metal–organic cages was explored through the dynamic exchange of ligands, and the formation of a series of hybrid supramolecular nanocages together with their final tendency to form a predominant structure of M24L14L28 was observed. In addition, the binding of metal–organic cages with 5,10,15,20-tetrakis(3,4,5-trimethoxyphenyl) porphyrin-Zn was also investigated. This study not only expands the complexity and diversity of metal–organic cages, but also provides a new perspective for studying the dynamic behaviour of metal–organic cages.
期刊介绍:
Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.