English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/65339
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
Exportar a otros formatos:

Trapping of a 12-valence-electron osmium intermediate

AuthorsBuil, María L. ; Esteruelas, Miguel A. ; Garcés, Karin ; García-Raboso, Jorge ; Oliván, Montserrat
Issue Date2009
PublisherAmerican Chemical Society
CitationOrganometallics 28(15): 4606-4609 (2009)
AbstractThe hydride-dikydrogen complex [OsH(η2-H2) {κ3N,C,C-CH2=CH-o-C5H4N} (PiPr3)2] BF4 (1) is a >functional equivalent> of the 12-valence-electron monohydride cation >[OsH(PiPr3)2]+>, which is trapped by aromatic solvents, such as toluene, benzene, and fluorobenzene to form the arene derivatives [OsH(η6-C6H5R) (PiPr3)2] BF4 (R = CH3 (2), H (3), F (4)). This >functionalequivalent> can be also generated by protonation of the hexahydride OsH6-(PiPr 3)2 (5) with 1 equiv of HBF4 and subsequent release of three hydrogen molecules. The monohydride is also trapped by S. The protonation of the latter with 0.5 equiv of HBF4 yields the heptahydride dimer [{OsH2(PiPr3) 2}2(μ-H)3] BF4 (6), which does not undergo exchange of bridging and terminal hydrides. © 2009 American Chemical Society.
Identifiersdoi: 10.1021/om9002544
issn: 0276-7333
e-issn: 1520-6041
Appears in Collections:(ICMA) Artículos
Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 kBAdobe PDFThumbnail
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.