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Formation of PPh2C6F5 through phosphido platinum and/or palladium(III) intermediates

AuthorsAra, Irene ; Chaouche, Naima; Forniés, Juan ; Fortuño, Consuelo ; Kribii, Abdelaziz; Tsipis, Athanassios C.
Issue Date1-Feb-2006
PublisherAmerican Chemical Society
CitationOrganometallics 25(5): 1084-1091 (2006)
AbstractThe 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).
Description8 pages, 5 figures, 3 tables.
Publisher version (URL)http://dx.doi.org/10.1021/om0508029
Appears in Collections:(ICMA) Artículos
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