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Reactions of bis(trifluoroacetylacetonato)palladium(II), [Pd(tfac)2], with tertiary phosphines followed by pyridine or its derivatives afforded a series of the [Pd(tfac(2–)-C,O)LL′]-type complexes which contain a C,O-chelating trifluoroacetylacetonate dianion and a couple of tertiary phosphine and/or heterocyclic nitrogen base ligands (L and L′). Their structures in solution were studied by 1H, 13C, 19F, and 31P NMR spectroscopy and the molecular structure in a crystal of [Pd(tfac(2–)-C,O)(PPh3)(2,6-Me2-py)]·C6H6 containing triphenylphosphine and 2,6-dimethylpyridine as L and L′ was determined by means of X-ray diffraction.
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Okeya et al. (1982) studied this question.
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