Artigo Revisado por pares

Contrasting Reactivity of Fluoropyridines at Palladium and Platinum: C−F Oxidative Addition at Palladium, P−C and C−F Activation at Platinum

2004; American Chemical Society; Volume: 23; Issue: 26 Linguagem: Inglês

10.1021/om049448p

ISSN

1520-6041

Autores

Naseralla A. Jasim, Robin N. Perutz, Adrian C. Whitwood, Thomas Braun, J. Izundu, Beate Neumann, S. Rothfeld, Hans‐Georg Stammler,

Tópico(s)

Organometallic Complex Synthesis and Catalysis

Resumo

The divergent behavior of palladium(0) and platinum(0) is revealed in the reactivity of [M(PR3)2] (M = Pd or Pt; R = Cy or iPr) toward pentafluoropyridine and 2,3,5,6-tetrafluoropyridine. The palladium complexes react with pentafluoropyridine at 100 °C to yield the fluoride complexes trans-[Pd(F)(4-C5NF4)(PR3)2]. They do not react with 2,3,5,6-tetrafluoropyridine. The reaction of platinum(0) complexes [Pt(PR3)2] with pentafluoropyridine in THF at ambient temperature yields trans-[Pt(R)(4-C5NF4)(PR3)(PFR2)] complexes, whereas the reaction of [Pt(PCy3)2] with 2,3,5,6-tetrafluoropyridine results in C−H activation to form cis-[Pt(H)(4-C5NF4)(PCy3)2]; this complex may be converted to the trans isomer by photolysis. The cis-hydride also forms during the reaction of [Pt(PCy3)2] with C5NF5 in hexane. These reactions also contrast with earlier studies of the reactivity of the same substrates toward {Ni(PEt3)2}, which yield [Ni(F)(2-C5NF5)(PEt3)2] with pentafluoropyridine and [Ni(F)(2-C5NF4H)(PEt3)2] with tetrafluoropyridine. Thus palladium has different regioselectivity from nickel and is the least reactive. Platinum is capable of both C−F and C−H activation and is alone in the triad in undergoing rearrangement to the alkyl complex with the fluorophosphine ligand. Mechanisms for the rearrangement are proposed. The platinum dihydride complex trans-[Pt(H)2(PR3)2] reacts with pentafluoropyridine at room temperature, yielding a 1:1:1 mixture of trans-[PtH(FHF)(PR3)2], trans-[Pt(H)(4-C5NF4)(PR3)2], and trans-[Pt(R)(4-C5NF4)(PR3)(PFR2)]. Crystal structures are reported for trans-[Pd(F)(4-C5NF4)(PCy3)2]·H2O·C6H6, trans-[Pd(F)(4-C5NF4)(PiPr3)2], trans-[Pt(C6H11)(4-C5NF4)(PCy3)(PFCy2)]· CH2Cl2, and cis-[Pt(H)(4-C5NF4)(PCy3)2].

Referência(s)
Altmetric
PlumX