A series of novel neutral and cationic methylpalladium complexes bearing N -alkyl-2,2′-dipyridylaldiminato ligands were prepared and characterized. In the presence of ethylene, the cationic complexes were active as dimerization catalysts, producing a mixture of 1- and 2-butenes. A Pd–ethyl π-ethylene species was identified as the catalyst resting state by low-temperature spectroscopic and DFT studies, which provided insights into the effect of both steric and electronic factors on the observed reactivity.
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Swarts et al. (2014) studied this question.
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