Tian-Cai Yue, Xin-Fang Wang, Jian-Bo Huang, Lu-Lu Wang, Duo-Zhi Wang
{"title":"Assembly of functional Co(II)−organic frameworks through a mixed ligand strategy: structure, photocatalytic oxidation of sulfides and CO2 conversion","authors":"Tian-Cai Yue, Xin-Fang Wang, Jian-Bo Huang, Lu-Lu Wang, Duo-Zhi Wang","doi":"10.1016/j.jcat.2026.116700","DOIUrl":null,"url":null,"abstract":"<div><div>Four new Co(II)-based metal–organic frameworks (MOFs) were successfully synthesized by a mixed ligand strategy. The controllable transformation of the bridging groups in the secondary structural units was achieved by modulating the anions in MOFs <strong>1</strong>–<strong>4</strong>. The catalytic performance study indicated that MOF <strong>1</strong> exhibited excellent photocatalytic activity for the oxidation of sulfides to sulfoxides under the air atmosphere and •O<sub>2</sub><sup>−</sup> and <sup>1</sup>O<sub>2</sub> were the main active species in the photocatalytic reaction process. Furthermore, MOF <strong>1</strong> also could efficiently catalyze the carboxylative cyclization of propargylic amines with CO<sub>2</sub> and the possible catalytic mechanism was explored in detail. Importantly, MOF <strong>1</strong> can exhibit remarkable catalytic activity after five cycles in both reactions. Therefore, MOF <strong>1</strong> can be used as an efficient and stable heterogeneous catalyst for the oxidation of sulfides and the carboxylative cyclization of propargylic amines with CO<sub>2</sub>.</div></div>","PeriodicalId":346,"journal":{"name":"Journal of Catalysis","volume":"455 ","pages":"Article 116700"},"PeriodicalIF":6.5000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021951726000345","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/13 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Four new Co(II)-based metal–organic frameworks (MOFs) were successfully synthesized by a mixed ligand strategy. The controllable transformation of the bridging groups in the secondary structural units was achieved by modulating the anions in MOFs 1–4. The catalytic performance study indicated that MOF 1 exhibited excellent photocatalytic activity for the oxidation of sulfides to sulfoxides under the air atmosphere and •O2− and 1O2 were the main active species in the photocatalytic reaction process. Furthermore, MOF 1 also could efficiently catalyze the carboxylative cyclization of propargylic amines with CO2 and the possible catalytic mechanism was explored in detail. Importantly, MOF 1 can exhibit remarkable catalytic activity after five cycles in both reactions. Therefore, MOF 1 can be used as an efficient and stable heterogeneous catalyst for the oxidation of sulfides and the carboxylative cyclization of propargylic amines with CO2.
期刊介绍:
The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes.
The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods.
The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.