Zeolite- and MgO-supported rhodium complexes and rhodium clusters: Tuning catalytic properties to control carbon–carbon vs. carbon–hydrogen bond formation reactions of ethene in the presence of H2

Abstract

Essentially molecular rhodium catalysts were made from Rh(C2H4)2(acetylacetonate) on zeolite HY and on MgO and characterized by infrared and X-ray absorption spectroscopies. The supported rhodium species anchored to the zeolite, initially in the form of Rh(C2H4)2, selectively catalyzed ethene dimerization, typically at 298K and 1bar, but when the catalyst was poisoned by CO, or the support was changed to MgO or zeolite NaY, or the rhodium was converted into small clusters, the ethene underwent predominantly hydrogenation. The preciseness of the synthesis of the supported rhodium species facilitated determination of structure-catalyst performance relationships that led to a schematic representation of how the dimerization proceeds by a mechanism involving both the rhodium complexes and zeolite surface OH groups. The reaction is facilitated by H2 and proceeds as one ethene molecule is activated by an isolated rhodium complex and another by a weakly acidic Si–OH–Al group.