María Moreno-Latorre, María C. de la Torre*, Heinz Gornitzka, Catherine Hemmert and Miguel A. Sierra*,
{"title":"单核和双核 1-(2-吡啶基)-4-苯基-1,2,3-三唑基 Ir(III) 和 Rh(III) 配合物","authors":"María Moreno-Latorre, María C. de la Torre*, Heinz Gornitzka, Catherine Hemmert and Miguel A. Sierra*, ","doi":"10.1021/acs.organomet.4c00079","DOIUrl":null,"url":null,"abstract":"<p >The synthesis and characterization of a series of mono-, homo-, and heterobimetallic complexes involving iridium and rhodium centers have been achieved through the reaction of the proligand, 1-pyridyl-4-phenyl-1,2,3-triazole, and [M(Cp)*Cl<sub>2</sub>]<sub>2</sub> (M = Ir, Rh). The ligand undergoes coordination of the <i>N,N</i> fragment and subsequent <i>N</i>-directed C–H activation at the 1,2,3-triazole and phenyl or pyridyl moieties. Alternatively, direct <i>N</i>-directed C–H activation can be achieved. The structures of the prepared complexes were determined using spectroscopic techniques and confirmed by X-ray crystallography. The electrochemical properties of the complexes show a differentiate redox behavior between Ir–Ir centers and a clear influence of the second metal in heterobimetallic complexes. This flexible approach could have potential applications in catalysis and other areas of chemistry.</p>","PeriodicalId":56,"journal":{"name":"Organometallics","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.organomet.4c00079","citationCount":"0","resultStr":"{\"title\":\"Mono- and Dinuclear 1-(2-Pyridyl)-4-phenyl-1,2,3-triazole-Based Ir(III) and Rh(III) Complexes\",\"authors\":\"María Moreno-Latorre, María C. de la Torre*, Heinz Gornitzka, Catherine Hemmert and Miguel A. Sierra*, \",\"doi\":\"10.1021/acs.organomet.4c00079\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The synthesis and characterization of a series of mono-, homo-, and heterobimetallic complexes involving iridium and rhodium centers have been achieved through the reaction of the proligand, 1-pyridyl-4-phenyl-1,2,3-triazole, and [M(Cp)*Cl<sub>2</sub>]<sub>2</sub> (M = Ir, Rh). The ligand undergoes coordination of the <i>N,N</i> fragment and subsequent <i>N</i>-directed C–H activation at the 1,2,3-triazole and phenyl or pyridyl moieties. Alternatively, direct <i>N</i>-directed C–H activation can be achieved. The structures of the prepared complexes were determined using spectroscopic techniques and confirmed by X-ray crystallography. The electrochemical properties of the complexes show a differentiate redox behavior between Ir–Ir centers and a clear influence of the second metal in heterobimetallic complexes. This flexible approach could have potential applications in catalysis and other areas of chemistry.</p>\",\"PeriodicalId\":56,\"journal\":{\"name\":\"Organometallics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-05-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acs.organomet.4c00079\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organometallics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.organomet.4c00079\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organometallics","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.organomet.4c00079","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Mono- and Dinuclear 1-(2-Pyridyl)-4-phenyl-1,2,3-triazole-Based Ir(III) and Rh(III) Complexes
The synthesis and characterization of a series of mono-, homo-, and heterobimetallic complexes involving iridium and rhodium centers have been achieved through the reaction of the proligand, 1-pyridyl-4-phenyl-1,2,3-triazole, and [M(Cp)*Cl2]2 (M = Ir, Rh). The ligand undergoes coordination of the N,N fragment and subsequent N-directed C–H activation at the 1,2,3-triazole and phenyl or pyridyl moieties. Alternatively, direct N-directed C–H activation can be achieved. The structures of the prepared complexes were determined using spectroscopic techniques and confirmed by X-ray crystallography. The electrochemical properties of the complexes show a differentiate redox behavior between Ir–Ir centers and a clear influence of the second metal in heterobimetallic complexes. This flexible approach could have potential applications in catalysis and other areas of chemistry.
期刊介绍:
Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.