Palladium(ii) complexes with an NNN type pincer ligand (pipNNN = 2,6-bis(piperdyl-methyl)pyridine) are synthesized and characterized. Electronic and H NMR spectra point to decreasing filled/filled repulsions between the dπ(Pd) orbitals and the halide lone pair orbitals along the Cl < Br < I series. For all complexes, the most downfield α-piperidyl resonance of the pipNNN ligand is sensitive to changes in the coordinated halide while the -pyridyl and benzylic resonances are sensitive to changes in the counter anion. This sensitivity is utilized to study halide association and exchange at the fourth coordination site. Conductivity and H NMR spectroscopy confirm the interaction between the exogenous anion (Cl, Br, BF ) and Pd(pipNNN)X (X = Cl, Br).
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| http://dx.doi.org/10.1039/c9ra05423e | DOI Listing |
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