Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/19100
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Título : Formation of PPh2C6F5 through phosphido platinum and/or palladium(III) intermediates
Autor : Ara, Irene, Chaouche, Naima, Forniés, Juan, Fortuño, Consuelo, Kribii, Abdelaziz, Tsipis, Athanassios C.
Fecha de publicación : 1-Feb-2006
Editor: American Chemical Society
Resumen: The two-electron oxidation reactions of the neutral [(C6F5)2M(μ-PR2)2M‘(NCCH3)2] (M = M‘ = Pt or Pd, M = Pt, M‘ = Pd) complexes using I2 as oxidant have been investigated by experimental (R = Ph) and electronic structure calculation methods (R = H). It was found that a reductive coupling of PR2 and C6F5 takes place along the reaction pathway for all oxidized complexes. The most salient structural features of the [(C6F5)2Pt(μ-PR2)2Pd(C6F5)2]2-, [(C6F5)2Pd(μ-PR2)2Pd(acac)]-, and [(C6F5)2Pt(μ-PR2)2PtI2] complexes (experimental R = Ph) are reproduced very well by the B3LYP/lanl2dz calculations (R = H).
Descripción : 8 pages, 5 figures, 3 tables.
Versión del editor: http://dx.doi.org/10.1021/om0508029
URI : http://hdl.handle.net/10261/19100
ISSN: 0276-7333
DOI: 10.1021/om0508029
Citación : Organometallics 25(5): 1084-1091 (2006)
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