RuMCM-41 catalysts were prepared by deposition of several complexes from th
eir solvents: of Ru acetylacetonate from its ether solution, of cis-dichlor
obis(2,2 ' -bipyridine) Ru in chloroform, of di-mu chlorobis((p-cymene)chlo
ro Ru(II)) in chloroform and of dichloro(l,5-cyclooctadiene) Ru(II) dissolv
ed in pyridine. The catalysts were characterized as prepared and after seve
ral reactions cycles by: adsorption-desorption isotherms of N-2 at 77 K, XR
D, FTIR, and XPS. The above catalysts were used in the liquid phase hydroge
nation of a F prostaglandin intermediate. A strong leaching of Ru was obser
ved, but after four cycles the catalysts remained unchanged in activity and
diastereoselectivity. The stereoselectivity was found to be influenced by
the nature of the precursor complex. In the presence of the catalyst prepar
ed from di-mu chlorobis((p-cymene)chloro Ru(II)) the natural-like product w
as obtained. (C) 2001 Elsevier Science B.V. All rights reserved.