The effect of Zr modification on the catalytic activity of Co/SiO 2 was investigated for nonoxidative propane dehydrogenation. Isolated Zr on SiO 2 surface sites were prepared by organometallic synthesis using Zr(O t Bu) 4 as a precursor. The resulting Zr/SiO 2 support was functionalized with Co 2+ ions via strong electrostatic adsorption. Spectroscopic (diffuse reflectance infrared Fourier transform spectroscopy, UV–vis, electron paramagnetic resonance) and microscopic characterization (transmission electron microscopy, scanning transition electron microscopy) results are consistent with single-site cobalt that preferentially associates with the mono-dispersed Zr at a variety of loadings and Co/Zr ratios. The oxidation state of Co in the as-prepared Co/SiO 2 and Co–Zr/SiO 2 was both +2 with tetrahedral and octahedral geometries, respectively. In situ X-ray absorption near edge structure and extended X-ray absorption fine structure results confirmed that the oxidation state of Co remained as +2 under reaction condition for both Co/SiO 2 and Co–Zr/SiO 2 samples and both catalysts have tetrahedral Co 2+ as the active catalyst. Despite similar Co coordination environments, the catalytic activity and selectivity was significantly improved by the Zr modification of the silica support versus Co/SiO 2 . This was attributed to the change in oxygen donor ability and Co–O bond strength of the ≡SiO–Zr–O sites of Co–Zr/SiO 2 compared with the ≡SiO– ligands in Co/SiO 2 . These results show that tuning of the support SiO 2 oxygen donation ability by use of an anchoring site (e.g., ≡SiO–Zr–O – ) can be used to alter both rate and selectivity of propane dehydrogenation with single-site heterogeneous catalysts. These results also show some preference for Co 2+ active sites to associate with ≡SiO–Zr–O – sites over ≡SiO–.

A novel Rh 2 (OAc) 4 -catalyzed three-component reaction of diazoacetates, anilines, and activated ketones via ammonium ylide trapping processes is reported. The reaction of isatins afforded a-amino-b-hydroxy esters bearing the 3-substituted 3-hydroxyindolin-2-one moiety with vicinal quaternary carbon centers in one step with high chemo-and diastereoselectivity. Extension of the reaction to acyclic a-keto esters afforded 2-hydroxy-2-alkyl-3-aryl-3-(phenylamino) succinates in moderate yield and diastereoselectivity.

Aminocarboxylic acids (hydrazinocarboxylic acids) and esters Q 0440Trapping of an Ammonium Ylide with Activated Ketones: Synthesis of β-Hydroxy-α-amino Esters with Adjacent Quaternary Stereocenters. -The Rh-catalyzed reaction of carbonyl compounds with ammonium ylides, generated in situ from diazoesters and anilines, yields β-hydroxy-α-amino esters with moderate diastereoselectivity. -(GUO, X.; YUE, Y.; HU, G.; ZHOU, J.; ZHAO, Y.; YANG, L.; HU