Pei Chen, Mingxuan Liu, Ruofan Li, Xi Su, Guolong Xing, Xiao-Rui Ren, Dong Wang, Jian Zhang, Long Chen
{"title":"Multidentate Macrocyclic Salphen-Based 2D Conjugated Metal-Organic Framework.","authors":"Pei Chen, Mingxuan Liu, Ruofan Li, Xi Su, Guolong Xing, Xiao-Rui Ren, Dong Wang, Jian Zhang, Long Chen","doi":"10.1002/anie.202511048","DOIUrl":null,"url":null,"abstract":"<p><p>Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) represent an emerging class of crystalline porous materials with promising electrochemical applications. The design of novel organic ligands for constructing 2D c-MOFs remains a crucial research frontier. While the incorporation of macrocycle blocks into 2D c-MOFs can introduce intrinsic cavities with advantageous properties, most existing reports are limited to coordinating with only one equivalent metal ion per macrocyclic cavity. In this work, we developed a triangular-shaped Salphen macrocycle-based 2D c-MOF (SM-MOF-Cu) featuring multidentate internal coordination sites. SM-MOF-Cu exhibits high crystallinity, permanent porosity, and abundant accessible metal sites. Remarkably, this material demonstrates exceptional performance in the electrocatalytic hydrogenation of acetylene to ethylene (E-HAE), achieving a Faradaic efficiency of 96.6% for ethylene production at -0.85 V versus the reversible hydrogen electrode (RHE) under continuous pure acetylene feed. This study not only broadens the family of macrocycle-based 2D c-MOFs but also provides new insights into their potential for advanced electrocatalysis.</p>","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202511048"},"PeriodicalIF":16.9000,"publicationDate":"2025-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie (International ed. in English)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/anie.202511048","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) represent an emerging class of crystalline porous materials with promising electrochemical applications. The design of novel organic ligands for constructing 2D c-MOFs remains a crucial research frontier. While the incorporation of macrocycle blocks into 2D c-MOFs can introduce intrinsic cavities with advantageous properties, most existing reports are limited to coordinating with only one equivalent metal ion per macrocyclic cavity. In this work, we developed a triangular-shaped Salphen macrocycle-based 2D c-MOF (SM-MOF-Cu) featuring multidentate internal coordination sites. SM-MOF-Cu exhibits high crystallinity, permanent porosity, and abundant accessible metal sites. Remarkably, this material demonstrates exceptional performance in the electrocatalytic hydrogenation of acetylene to ethylene (E-HAE), achieving a Faradaic efficiency of 96.6% for ethylene production at -0.85 V versus the reversible hydrogen electrode (RHE) under continuous pure acetylene feed. This study not only broadens the family of macrocycle-based 2D c-MOFs but also provides new insights into their potential for advanced electrocatalysis.