Abstract
Pd halide and hydride complexes of a new PNP pincer ligand with a central diarylamido moiety can be prepared via N-H cleavage in a neutral amine/diphosphine PNP ligand. The solid-state structure of (PNP)PdCl shows a meridional PNP ligand about an approximately square-planar Pd center. (PNP)PdH hydrodehalogenates alkyl and certain aryl halides, while (PNP)PdX (X=Cl, I, H, OAc) complexes catalyze Heck coupling of ethyl acrylate with aryl halides.
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CITATION STYLE
Fan, L., Foxman, B. M., & Ozerov, O. V. (2004). N-H cleavage as a route to palladium complexes of a new PNP pincer ligand. Organometallics, 23(3), 326–328. https://doi.org/10.1021/om034151x
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