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Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As)

The reaction of [Cp(2)Mo(2)(CO)(4)(μ,η(2:2)‐E(2))] (A: E=P, B: E=As, Cp=C(5)H(5)) with the WCA‐containing Cu(I) salts ([Cu(CH(3)CN)(4)][Al{OC(CF(3))(3)}(4)] (CuTEF, C), [Cu(CH(3)CN)(4)][BF(4)] (D) and [Cu(CH(3)CN)(3.5)][FAl{OC(6)F(10)(C(6)F(5))}(3)] (CuFAl, E)) affords seven unprecedented coordinati...

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Detalles Bibliográficos
Autores principales: Schiller, Jana, Schreiner, Andrea, Seidl, Michael, Balázs, Gábor, Scheer, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756472/
https://www.ncbi.nlm.nih.gov/pubmed/32614109
http://dx.doi.org/10.1002/chem.202003133
Descripción
Sumario:The reaction of [Cp(2)Mo(2)(CO)(4)(μ,η(2:2)‐E(2))] (A: E=P, B: E=As, Cp=C(5)H(5)) with the WCA‐containing Cu(I) salts ([Cu(CH(3)CN)(4)][Al{OC(CF(3))(3)}(4)] (CuTEF, C), [Cu(CH(3)CN)(4)][BF(4)] (D) and [Cu(CH(3)CN)(3.5)][FAl{OC(6)F(10)(C(6)F(5))}(3)] (CuFAl, E)) affords seven unprecedented coordination compounds. Depending on the E(2) ligand complex, the counter anion of the copper salt and the stoichiometry, four dinuclear copper dimers and three trinuclear copper compounds are accessible. The latter complexes reveal first linear Cu(3) arrays linked by E(2) units (E=P, As) coordinated in an η(2:1:1) coordination mode. All compounds were characterized by X‐ray crystallography, NMR and IR spectroscopy, mass spectrometry and elemental analysis. To define the nature of the Cu⋅⋅⋅Cu⋅⋅⋅Cu interactions, DFT calculations were performed.