English   español  
Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/111758
Compartir / Impacto:
Estadísticas
Add this article to your Mendeley library MendeleyBASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Título

Hydridorhodathiaboranes: Synthesis, characterization, and reactivity

AutorÁlvarez, Álvaro; Calvo, Beatriz ; Macías, Ramón ; Lahoz, Fernando J. ; Oro, Luis A.
Fecha de publicación2014
EditorAmerican Chemical Society
CitaciónOrganometallics 33(12): 3137-3153 (2014)
ResumenThe reaction between pyridine and [8,8-(PPh3) 2-nido-8,7-RhSB9H10] (1) has given the opportunity to synthesize a new family of 11-vertex hydridorhodathiaboranes that feature boron-bound N-heterocyclic ligands. To explore the scope of this reaction, 1 has been treated with the methylpyridine isomers (picolines) 2-Me-NC5H4, 3-Me-NC5H4, and 4-Me-NC5H4, affording the picoline ligated clusters [8,8,8-(H)(PPh3)2-9-(L)-nido-8,7-RhSB9H 9], where L = 2-Me-NC5H4 (3), 3-Me-NC 5H4 (4), 4-Me-NC5H4 (5). Thermal treatment of these nido clusters leads to dehydrogenation and the formation of isonido/closo-[1,1-(PPh3)2-3-(L)-1,2-RhSB 9H8] (9-11). Compounds 3-5 react with ethylene to form [1,1-(η2-C2H4)(PPh3)-3-(L)-1,2- RhSB9H8] (13-15). Similarly, treatment of 3-5 with carbon monoxide produces [1,1-(CO)(PPh3)-3-(L)-1,2-RhSB9H 8] (17-19). These series of η2-C2H 4 and CO ligated 11-vertex isonido/closo-rhodathiaboranes result from the substitution of one PPh3 ligand by ethylene or CO together with H2 loss and a concomitant nido to closo/isonido cluster structural transformation. The reactivity of 3-5 with propene, 1-hexene, and cyclohexene under a hydrogen atmosphere is also reported and compared with the reactivity of the pyridine ligated analogue [8,8,8-(H)(PPh3)2-9- (NC5H5)-nido-8,7-RhSB9H9] (2). Low-temperature NMR studies have allowed the characterization of intermediates which undergo inter- and intramolecular exchange processes, depending on the nature of the N-heterocyclic ligand. The CO ligand enhances the nonrigidity of the cluster, opening mechanisms of H2 loss. © 2014 American Chemical Society.
Versión del editorhttp://dx.doi.org/10.1021/om500374g
URIhttp://hdl.handle.net/10261/111758
DOI10.1021/om500374g
Identificadoresdoi: 10.1021/om500374g
issn: 0276-7333
e-issn: 1520-6041
Aparece en las colecciones: (ISQCH) Artículos
Ficheros en este ítem:
Fichero Descripción Tamaño Formato  
Alvaro_Organometallics-2014.pdf2,18 MBAdobe PDFVista previa
Visualizar/Abrir
Mostrar el registro completo
 

Artículos relacionados:


NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.