English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/112909
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Exportar a otros formatos:

Title

Deprotonation of C-Alkyl groups of cationic triruthenium clusters containing cyclometalated C-Alkylpyrazinium ligands: Experimental and computational studies

AuthorsCabeza, Javier A.; Fernández-Colinas, José M.; García-Álvarez, Pablo; Pérez-Carreño, E. ; Pruneda, Vanessa; Maelen, Juan F. van der
Issue Date2013
PublisherWiley-VCH
CitationChemistry - A European Journal 19(28): 9251-9260 (2013)
AbstractThe C-alkyl groups of cationic triruthenium cluster complexes of the type [Ru3(μ-H)(μ-κ2N1,C2 -L)(CO)10]+ (HL represents a generic C-alkyl-N- methylpyrazium species) have been deprotonated to give kinetic products that contain unprecedented C-alkylidene derivatives and maintain the original edge-bridged decacarbonyl structure. When the starting complexes contain various C-alkyl groups, the selectivity of these deprotonation reactions is related to the atomic charges of the alkyl H atoms, as suggested by DFT/natural-bond orbital (NBO) calculations. Three additional electronic properties of the C-alkyl C-H bonds have also been found to correlate with the experimental regioselectivity because, in all cases, the deprotonated C-H bond has the smallest electron density at the bond critical point, the greatest Laplacian of the electron density at the bond critical point, and the greatest total energy density ratio at the bond critical point (computed by using the quantum theory of atoms in molecules, QTAIM). The kinetic decacarbonyl products evolve, under appropriate reaction conditions that depend upon the position of the C-alkylidene group in the heterocyclic ring, toward face-capped nonacarbonyl derivatives (thermodynamic products). The position of the C-alkylidene group in the heterocyclic ring determines the distribution of single and double bonds within the ligand ring, which strongly affects the stability of the neutral decacarbonyl complexes and the way these ligands coordinate to the metal atoms in the nonacarbonyl products. The mechanisms of these decacarbonylation processes have been investigated by DFT methods, which have rationalized the structures observed for the final products and have shed light on the different kinetic and thermodynamic stabilities of the reaction intermediates, thus explaining the reaction conditions experimentally required by each transformation. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publisher version (URL)http://dx.doi.org/10.1002/chem.201204250
URIhttp://hdl.handle.net/10261/112909
DOI10.1002/chem.201204250
Identifiersdoi: 10.1002/chem.201204250
issn: 0947-6539
e-issn: 1521-3765
Appears in Collections:(CINN) Artículos
Files in This Item:
File Description SizeFormat 
Manuscript-cej R2.pdf5,45 MBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 

Related articles:


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.