Mild P–P Bond Cleavage in the Methyldiphosphenyl Complex [Mo2Cp2(μ-PCy2)(μ-κ2:κ2-P2Me)(CO)2] To Give Novel Phosphide-Bridged Trinuclear Derivatives
Author:
Affiliation:
1. Departamento de Química Orgánica e Inorgánica/IUQOEM, Universidad de Oviedo, E-33071 Oviedo, Spain
2. Instituto Nacional del Carbón, Spanish Research Council for Scientific Research (CSIC), Francisco Pintado Fe 26, E-33011 Oviedo, Spain
Funder
Consejo Superior de Investigaciones Científicas
Ministerio de Economía y Competitividad
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ic501857f
Reference81 articles.
1. Mild P4 Activation To Give an Anionic Diphosphorus Complex with a Dual Binding Ability at a Single P Site
2. Reactivity of the Anionic Diphosphorus Complex [Mo2Cp2(μ-PCy2)(CO)2(μ-κ2:κ2-P2)]− Toward ER3X Electrophiles (E = C to Pb): Insights into the Multisite Donor Ability and Dynamics of the P2 Ligand
3. The chemistry of diphosphenes and their heavy congeners: synthesis, structure, and reactivity
4. Übergangsmetall‐substituierte Diphosphene, XIII. Zur Kenntnis von Rheniumdiphosphenylkomplexen (η 5 ‐C 5 Me 5 )(CO)(NO)RePPC 6 H 2 (tBu) 3 ‐(2,4,6) und (η 5 ‐C 5 Me 5 )(CO)(NO)Re[Cr(CO) 5 ]PPC 6 H 2 (tBu) 3 ‐(2,4,6)
5. übergangsmetall‐substituierte Diphosphene, V über (η 5 ‐C 5 Me 5 ) (CO)(NO)Mn – PP – C 6 H 2 ( t ‐Bu) 3 ‐(2,4,6), den ersten Mangandiphosphenylkomplex
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