Por favor, use este identificador para citar o enlazar a este item:
http://hdl.handle.net/10261/52333
COMPARTIR / EXPORTAR:
SHARE CORE BASE | |
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
Título: | Behavior of Neutral Phosphido Derivatives of Platinum and Palladium toward Silver Centers |
Autor: | Forniés, Juan CSIC; Fortuño, Consuelo CSIC ORCID; Ibáñez, Susana CSIC ORCID; Martín, Antonio CSIC ORCID | Fecha de publicación: | 2011 | Editor: | American Chemical Society | Citación: | Inorganic Chemistry 50(21): 10798-10809 (2011) | Resumen: | The reaction of the neutral binuclear complexes [(RF) 2Pt(μ-PPh2)2M(phen)] (phen = 1,10-phenanthroline, RF = C6F5; M = Pt, 1; M = Pd, 2) with AgClO4 or [Ag(OClO3)(PPh3)] affords the trinuclear complexes [AgPt2(μ-PPh2) 2(RF)2(phen)(OClO3)] (7a) or [AgPtM(μ-PPh2)2(RF)2(phen) (PPh3)][ClO4] (M = Pt, 8; M = Pd, 9), which display an >open-book> type structure and two (7a) or one (8, 9) Pt-Ag bonds. The neutral diphosphine complexes [(RF)2Pt(μ-PPh 2)2M(P-P)] (P-P = 1,2-bis(diphenylphosphino)methane, dppm, M = Pt, 3; M = Pd, 4; P-P = 1,2-bis(diphenylphosphino)ethane, dppe, M = Pt, 5; M = Pd, 6) react with AgClO4 or [Ag(OClO3)(PPh 3)], and the nature of the resulting complexes is dependent on both M and the diphosphine. The dppm Pt-Pt complex 3 reacts with [Ag(OClO 3)(PPh3)], affording a silver adduct 10 in which the Ag atom interacts with the Pt atoms, while the dppm Pt-Pd complex 4 reacts with [Ag(OClO3)(PPh3)], forming a 1:1 mixture of [AgPdPt(μ-PPh2)2(RF)2(OClO 3)(dppm)] (11), in which the silver atom is connected to the Pt-Pd moiety through Pd-(μ-PPh2)-Ag and Ag-P(k1-dppm) interactions, and [AgPdPt(μ-PPh2)2(RF) 2(OClO3)(PPh3)2][ClO4] (12). The reaction of complex 4 with AgClO4 gives the trinuclear derivative 11 as the only product. Complex 11 shows a dynamic process in solution in which the silver atom interacts alternatively with both Pd-μPPh2 bonds. When P-P is dppe, both complexes 5 and 6 react with AgClO4 or [Ag(OClO3)(PPh3)], forming the saturated complexes [(PPh2C6F5)(R F)Pt(μ-PPh2)(μ-OH)M(dppe)][ClO4] (M = Pt, 13; Pd, 14), which are the result of an oxidation followed by a PPh 2/C6F5 reductive coupling. Finally, the oxidation of trinuclear derivatives [(RF)2Pt II(μ-PPh2)2PtII(μ-PPh 2)2PtIIL2] (L2 = phen, 15; L = PPh3, 16) by AgClO4 results in the formation of the unsaturated 46 VEC complexes [(RF)2Pt III(μ-PPh2)2PtIII(μ-PPh 2)2PtIIL2][ClO4] 2 (17 and 18, respectively) which display Pt(III)-Pt(III) bonds. © 2011 American Chemical Society. | URI: | http://hdl.handle.net/10261/52333 | DOI: | 10.1021/ic201354s | Identificadores: | doi: 10.1021/ic201354s issn: 0020-1669 e-issn: 1520-510X |
Aparece en las colecciones: | (ICMA) Artículos |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
---|---|---|---|---|
accesoRestringido.pdf | 15,38 kB | Adobe PDF | Visualizar/Abrir |
CORE Recommender
SCOPUSTM
Citations
23
checked on 22-abr-2024
WEB OF SCIENCETM
Citations
22
checked on 16-feb-2024
Page view(s)
317
checked on 23-abr-2024
Download(s)
116
checked on 23-abr-2024
Google ScholarTM
Check
Altmetric
Altmetric
NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.