Study of the catalytic activity of metal complexes on solid supports. 5. Immobilized rhodium complexes in hydrogen transfer from 2-propanol to ketones and olefins

1.	Rhodium complexes [RhCl(COD)]2, RhCl(PPh3)3, and RhCl3 immobilized on silica gel modified by aminophosphine groups catalyze the transfer of hydrogen from 2-propanol to cyclohexanone, styrene, and 2-cyclohexenone and the isomerization of allylbenzene in an argon atmosphere.
2.	The reduction of cyclohexanone to cyclohexanol is promoted by alkali. The reaction rate is proportional to the amount of catalyst, 2-propanol concentration, and cyclohexanone. The reaction rate decreases at high ketone concentrations.
3.	Styrene is reduced to ethylbenzene extremely slowly. Under these conditions, allylbenzene is not reduced, but rather undergoes isomerization with the predominant formation of trans-propenylbenzene.
4.	The reduction of 2-cyclohexenone to cyclohexanol occurs by the initial reduction of the C=C bond and the subsequent reduction of the C=O group.

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1223–1228, June, 1988.