Zahra Alishahi, Mohammad Ali Zolfigol, Saeid Azizian, Morteza Torabi and Yanlong Gu
{"title":"Cu(OAc)2修饰的二茂铁基共价有机骨架-碳纳米管杂化物作为制备四氮唑的稳健催化剂。","authors":"Zahra Alishahi, Mohammad Ali Zolfigol, Saeid Azizian, Morteza Torabi and Yanlong Gu","doi":"10.1039/D5NA00566C","DOIUrl":null,"url":null,"abstract":"<p >The emergence of covalent organic framework-carbon nanotube hybrid composites (COF-CNT) has opened up a promising approach for the development of heterogeneous catalysis. In this research, a new ferrocene-based COF was wrapped onto the surface of a carbon nanotube and modified with Cu(OAc)<small><sub>2</sub></small> (denoted as FCOF-CNT-Cu(OAc)<small><sub>2</sub></small>) for boosting the catalytic performance for the preparation of tetrazoles. Ferrocene segments played a decisive role in assisting Cu(OAc)<small><sub>2</sub></small> as catalytically active sites for the preparation of 5-substituted 1<em>H</em>-tetrazoles and acrylonitrile-linked tetrazoles. FCOF-CNT-Cu(OAc)<small><sub>2</sub></small> had a high specific surface area of 117 m<small><sup>2</sup></small> g<small><sup>−1</sup></small>, which accelerated the catalytic process. Field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) analyses revealed that the catalyst was ordered with a tubular morphology and spherical COF grown on the outer surface of the CNT. This work presents FCOF-CNT-Cu(OAc)<small><sub>2</sub></small> as a superior catalyst toward the preparation of 5-substituted 1<em>H</em>-tetrazoles and acrylonitrile-linked tetrazole derivatives. Consequently, tetrazole derivatives were synthesized in short reaction times under green and mild reaction conditions.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":" 19","pages":" 6084-6097"},"PeriodicalIF":4.6000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12366523/pdf/","citationCount":"0","resultStr":"{\"title\":\"Ferrocene-based covalent organic framework-carbon nanotube hybrid modified with Cu(OAc)2 as a robust catalyst for the preparation of tetrazoles\",\"authors\":\"Zahra Alishahi, Mohammad Ali Zolfigol, Saeid Azizian, Morteza Torabi and Yanlong Gu\",\"doi\":\"10.1039/D5NA00566C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The emergence of covalent organic framework-carbon nanotube hybrid composites (COF-CNT) has opened up a promising approach for the development of heterogeneous catalysis. In this research, a new ferrocene-based COF was wrapped onto the surface of a carbon nanotube and modified with Cu(OAc)<small><sub>2</sub></small> (denoted as FCOF-CNT-Cu(OAc)<small><sub>2</sub></small>) for boosting the catalytic performance for the preparation of tetrazoles. Ferrocene segments played a decisive role in assisting Cu(OAc)<small><sub>2</sub></small> as catalytically active sites for the preparation of 5-substituted 1<em>H</em>-tetrazoles and acrylonitrile-linked tetrazoles. FCOF-CNT-Cu(OAc)<small><sub>2</sub></small> had a high specific surface area of 117 m<small><sup>2</sup></small> g<small><sup>−1</sup></small>, which accelerated the catalytic process. Field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) analyses revealed that the catalyst was ordered with a tubular morphology and spherical COF grown on the outer surface of the CNT. This work presents FCOF-CNT-Cu(OAc)<small><sub>2</sub></small> as a superior catalyst toward the preparation of 5-substituted 1<em>H</em>-tetrazoles and acrylonitrile-linked tetrazole derivatives. Consequently, tetrazole derivatives were synthesized in short reaction times under green and mild reaction conditions.</p>\",\"PeriodicalId\":18806,\"journal\":{\"name\":\"Nanoscale Advances\",\"volume\":\" 19\",\"pages\":\" 6084-6097\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12366523/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanoscale Advances\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/na/d5na00566c\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanoscale Advances","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/na/d5na00566c","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Ferrocene-based covalent organic framework-carbon nanotube hybrid modified with Cu(OAc)2 as a robust catalyst for the preparation of tetrazoles
The emergence of covalent organic framework-carbon nanotube hybrid composites (COF-CNT) has opened up a promising approach for the development of heterogeneous catalysis. In this research, a new ferrocene-based COF was wrapped onto the surface of a carbon nanotube and modified with Cu(OAc)2 (denoted as FCOF-CNT-Cu(OAc)2) for boosting the catalytic performance for the preparation of tetrazoles. Ferrocene segments played a decisive role in assisting Cu(OAc)2 as catalytically active sites for the preparation of 5-substituted 1H-tetrazoles and acrylonitrile-linked tetrazoles. FCOF-CNT-Cu(OAc)2 had a high specific surface area of 117 m2 g−1, which accelerated the catalytic process. Field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) analyses revealed that the catalyst was ordered with a tubular morphology and spherical COF grown on the outer surface of the CNT. This work presents FCOF-CNT-Cu(OAc)2 as a superior catalyst toward the preparation of 5-substituted 1H-tetrazoles and acrylonitrile-linked tetrazole derivatives. Consequently, tetrazole derivatives were synthesized in short reaction times under green and mild reaction conditions.