3.2.3. Hydroformylation 2467 3.2.4. Dimerization 2468 3.2.5. Oxidative Cleavage and Ozonolysis 2469 3.2.6. Metathesis 2470 4. Terpenes 2472 4.1. Pinene 2472 4.1.1. Isomerization: R-Pinene 2472 4.1.2. Epoxidation of R-Pinene 2475 4.1.3. Isomerization of R-Pinene Oxide 2477 4.1.4. Hydration of R-Pinene: R-Terpineol 2478 4.1.5. Dehydroisomerization 2479 4.2. Limonene 2480 4.2.1. Isomerization 2480 4.2.2. Epoxidation: Limonene Oxide 2480 4.2.3. Isomerization of Limonene Oxide 2481 4.2.4. Dehydroisomerization of Limonene and Terpenes To Produce Cymene 2481

Chemical Routes for the Transformation of Biomass into Chemicals

Size- and support-dependency in the catalysis of gold

ion from a primary OH group of glyc-erol. 223,231 A similar mechanism was proposed manyyears ago for alcohol oxidation on Pt/C, involving asecond step, the transfer of a hydride ion to the Ptsurface (Scheme 11). 8,87,237 We consider it more feasible that the rate-deter-mining step is the cleavage of the C-H bond at theR-carbon atom. A similar mechanism is now generallyaccepted for Au electrodes (Scheme 12). 238 Despite thestructural differences between Au nanoparticles andan extended Au electrode surface, there are alsosimilarities, such as the critical role of aqueousalkaline medium and the absence of deactivation dueto decomposition products (CO and C x H y frag-ments). 239,240 An important question is the nature of active siteson Au nanoparticles. Electrooxidation of ethanol onAu nanoparticles supported on glassy carbon re-quired the partial coverage of Au surface by oxides. 241 Another analogy might be the model proposed for COoxidation. 219,242,243 According to this suggestion, theactive site consists of an ensemble of metallic Auatoms and a cationic Au

Oxidation of Alcohols with Molecular Oxygen on Solid Catalysts

Selective Vapor-Phase Epoxidation of Propylene over Au/TiO2Catalysts in the Presence of Oxygen and Hydrogen

Despite occasional references in the older literature to the ability of gold to catalyze certain reactions, the metal has until recently had the reputation of being one of the least catalytically useful. The recent discovery that some supported gold catalysts can affect the oxidation of carbon monoxide at or below ambient temperature has, however, focused attention on the metal's ability in this respect. For oxidation of carbon monoxide at low temperature, catalysts comprising small (<5 nm) gold particles supported preferably on an oxide of the first transition series (e.g., TiO2, α-Fe2O3) are needed. Deposition–precipitation and coprecipitation are better methods than impregnation for this purpose and provide the desired intimacy of contact between metal and support. High activity may well originate at sites at the gold–support interface, with the support making a vital contribution. Stable activity can result by optimizing aging in solution during the preparation, and low calcination temperatures are ge...

Catalysis By Gold

Selective Oxidation of Cinnamyl Alcohol to Cinnamaldehyde with Air over Bi-Pt/Alumina Catalysts

Carbon-Monoxide Oxidation over Catalysts Prepared by in-Situ Activation of Amorphous Gold-Silver-Zirconium and Gold-Iron-Zirconium Alloys

Direct Oxidation of L-Sorbose to 2-Keto-L-gulonic Acid with Molecular Oxygen on Platinum- and Palladium-Based Catalysts

The distribution and chemical state of Si in a synthetic 2-line ferrihydrite with a Si/(Si + Fe) molar ratio of 0.11 was studied. Heat treatment under oxidizing conditions shows that Si-rich ferrihydrite is stable to 400°C. The transformation to hematite and the formation of a polymerized amorphous-silica phase occur at 850°C. At this temperature, the specific surface area decreases greatly and the average pore diameter increases, which is indicative of sintering. Heating under severe reducing conditions causes a segregation of Si from Fe and results in a mixture of elemental Fe and SiO2. Surface and structural data suggest that Si is located near the particle surface where it limits the rearrangement of Fe octahedra to form hematite.

P. Hug

Papers

Selective Oxidation of Cinnamyl Alcohol to Cinnamaldehyde with Air over Bi-Pt/Alumina Catalysts

Carbon-Monoxide Oxidation over Catalysts Prepared by in-Situ Activation of Amorphous Gold-Silver-Zirconium and Gold-Iron-Zirconium Alloys

Direct Oxidation of L-Sorbose to 2-Keto-L-gulonic Acid with Molecular Oxygen on Platinum- and Palladium-Based Catalysts

Inhibition of Sintering by Si During the Conversion of Si-Rich Ferrihydrite to Hematite

Thermal degradation of copper(1) thiolate clusters and the crystal structure of solvent-free (Ph4P)2 [Cu4(SPh)6]