Rémi Beucher, Emmanuel Lacôte, Jérôme Canivet and David Farrusseng
{"title":"Molecular copper complexes embedded within porous polymer macroligands for the heterogeneously catalyzed aerobic oxidative formation of N–N bonds†","authors":"Rémi Beucher, Emmanuel Lacôte, Jérôme Canivet and David Farrusseng","doi":"10.1039/D4NJ03498H","DOIUrl":null,"url":null,"abstract":"<p >Here we report the synthesis of series of bipyridine-based porous polymers as macroligands for molecular copper complexes. The resulting Cu@N-POP solids efficiently catalyze the dehydrogenative N–N coupling of di-<em>p</em>-tolylamine into the corresponding hydrazine using oxygen as the oxidant. The heterogenization of the Cu-based catalyst within porous macroligands improved the catalytic activity with regard to previously reported Cu-based molecular homogeneous systems. Increasing the availability of the bipyridine sites to Cu coordination led to enhanced catalytic performances.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 45","pages":" 19167-19174"},"PeriodicalIF":2.7000,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03498h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Here we report the synthesis of series of bipyridine-based porous polymers as macroligands for molecular copper complexes. The resulting Cu@N-POP solids efficiently catalyze the dehydrogenative N–N coupling of di-p-tolylamine into the corresponding hydrazine using oxygen as the oxidant. The heterogenization of the Cu-based catalyst within porous macroligands improved the catalytic activity with regard to previously reported Cu-based molecular homogeneous systems. Increasing the availability of the bipyridine sites to Cu coordination led to enhanced catalytic performances.