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Ru-MCM-41 catalysts for diastereoselective hydrogenation

✍ Scribed by M Florea; M Sevinci; V.I Pârvulescu; G Lemay; S Kaliaguine


Book ID
104430383
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
241 KB
Volume
44-45
Category
Article
ISSN
1387-1811

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✦ Synopsis


Ru-MCM-41 catalysts were prepared by deposition of several complexes from their solvents: of Ru acetylacetonate from its ether solution, of cis-dichlorobis(2,2 H -bipyridine) Ru in chloroform, of di-lchlorobis((p-cymene)chloro Ru(II)) in chloroform and of dichloro(1,5-cyclooctadiene) Ru(II) dissolved in pyridine. The catalysts were characterized as prepared and after several reactions cycles by: adsorption±desorption isotherms of N 2 at 77 K, XRD, FTIR, and XPS. The above catalysts were used in the liquid phase hydrogenation of a F prostaglandin intermediate. A strong leaching of Ru was observed, but after four cycles the catalysts remained unchanged in activity and diastereoselectivity. The stereoselectivity was found to be in¯uenced by the nature of the precursor complex. In the presence of the catalyst prepared from di-lchlorobis((p-cymene)chloro Ru(II)) the natural-like product was obtained.


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Stereocontrolled hydrogenation of prosta
✍ S Coman; V.I Pârvulescu; B Tesche; H Bönnemann; J.F Roux; S Kaliaguine; P.A Jaco 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 655 KB

Ru-MCM-41 catalysts were investigated in the diastereoselective hydrogenation of class F prostaglandin intermediates. Ž The catalysts were prepared by deposition of Ru from different precursors ruthenium acetylacetonate, ruthenium chloride or . ruthenium hexaamine chloride . These catalysts were ch