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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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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
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author Schiller, Jana
Schreiner, Andrea
Seidl, Michael
Balázs, Gábor
Scheer, Manfred
author_facet Schiller, Jana
Schreiner, Andrea
Seidl, Michael
Balázs, Gábor
Scheer, Manfred
author_sort Schiller, Jana
collection PubMed
description 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.
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spelling pubmed-77564722020-12-28 Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As) Schiller, Jana Schreiner, Andrea Seidl, Michael Balázs, Gábor Scheer, Manfred Chemistry Communications 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. John Wiley and Sons Inc. 2020-10-08 2020-11-17 /pmc/articles/PMC7756472/ /pubmed/32614109 http://dx.doi.org/10.1002/chem.202003133 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Schiller, Jana
Schreiner, Andrea
Seidl, Michael
Balázs, Gábor
Scheer, Manfred
Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As)
title Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As)
title_full Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As)
title_fullStr Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As)
title_full_unstemmed Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As)
title_short Linking of Cu(I) Units by Tetrahedral Mo(2)E(2) Complexes (E=P, As)
title_sort linking of cu(i) units by tetrahedral mo(2)e(2) complexes (e=p, as)
topic Communications
url 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
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