Abstract
Brominated and chloromethylated styrene–divinylbenzene resins were used for the synthesis of polymer-bound dithio-β-diketones, obtained by anchoring the chelate ligand through the central position. The heterogenized dithio-β-diketone ligand was subsequently reacted either as sodium salt with a Ni(II) phosphino derivative or directly with a Ni(0) complex in the presence of a free phosphine and activated in situ with an aluminum co-catalyst for the selective dimerization of propylene to 2,3-dimethylbutenes. The hetetogenized catalysts so obtained showed, particulary when prepared starting from chloromethylated styrene/divinylbenzene resins, very high activity and selectivity towards 2,3-dimethylbutenes. Moreover, the above catalysts, at least under the adopted reaction conditions, did not display any appreciable metal leaching during the catalytic cycle, thus working as really heterogeneous systems. Copyright © 1999 John Wiley & Sons, Ltd.
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