High 1,4-NADH selectivity (90% at full conversion) has been achieved in H 2 -driven NAD + reduction using a PtSn/SiO bimetallic catalyst, offering strategy for the development of heterogeneous catalysts NADH regeneration.

Background Catalysts improve the rate or selectivity of chemical reactions without being consumed in the chemical reaction. “Supported heterogeneous catalysts” consist of catalytic active sites carried on the surfaces of porous solids, known as “supports”. Such catalytic materials are especially important for chemical manufacturing because they minimize the loss of valuable catalytic materials ...

A bimetallic heme-DNA cofactor, containing an iron and a copper center, was synthesized for the design of novel hybrid catalysts for stereoselective synthesis. The cofactor was used for the reconstitution of apo-myoglobin. Both the cofactor alone and its myoglobin adduct were used to catalyze a model Diels Alder reaction. Stereoselectivity of this conversion was analyzed by chiral HPLC. Reactio...

Bimetallic AuPd supported on different carbonaceous materials and TiO2 was tested in the liquid phase oxidation of commercial grade and raw glycerol. The latter was directly obtained from the base-catalyzed transesterification of edible rapeseed oil using KOH. The best catalytic results were obtained using activated carbon and nitrogen-functionalized carbon nanofibers as supports. In fact, the ...

Ruthenium-based bimetallic electrocatalysts with non-noble metals such as Ti, Cr, Fe, Co and Pb were synthesized on a porous carbon support sing a chelation process. Rotating ring disk electrode measurements indicated that RuFeNx/C showed the catalytic activity and selectivity toward he four-electron reduction of oxygen to water comparable to those of the conventional Pt/C catalysts. The perfor...

Dinickel bisphenoxyiminato complexes based on highly substituted p- and m-terphenyl backbones were synthesized, and the corresponding atropisomers were isolated. In the presence of a phosphine scavenger, Ni(COD)2, the phosphine-ligated syn-dinickel complexes copolymerized α-olefins and ethylene in the presence of amines to afford 0.2-1.3% α-olefin incorporation and copolymerized amino olefins a...

The structure evolution behaviors of NiAu nanospindles in oxidizing/vacuum conditions were studied by in situ scanning transmission electron microscopy. The spindle structure transforms into Ni@Au@NiO multi-shell structure in the oxidizing atmosphere following an oxidation-driving multilayer reconstruction mechanism. In the vacuum condition, the NiAu nanospindles evolve along four distinct stag...

5 1 Conceptual approach 8 1.1 Scope of this thesis 8 1.2 Electronic and geometric effects in bimetallic catalysts 10 1.3 Mixed Oxides 11 1.4 (Strong) metal-support interaction 12 1.5 The role of the Pd-hydride phases 14 1.6 Oxide-supported Pd bimetallics in methanol steam reforming 14 1.7 Model Systems 21 2 Appendix: Experimental approach and methods 25 2.1 Electron Microscopy and related techn...

The μ-amino-borane complexes [Rh2 (L(R) )2 (μ-H)(μ-H2 B=NHR')][BAr(F) 4 ] (L(R) =R2 P(CH2 )3 PR2 ; R=Ph, (i) Pr; R'=H, Me) form by addition of H3 B⋅NMeR'H2 to [Rh(L(R) )(η(6) -C6 H5 F)][BAr(F) 4 ]. DFT calculations demonstrate that the amino-borane interacts with the Rh centers through strong Rh-H and Rh-B interactions. Mechanistic investigations show that these dimers can form by a boronium-me...

Bimetallic Mo-Fe and Mo-Co sulfide clusters were anchored on AI,O, and used for CO hydrogenation. In addition to methane, significant amounts of dimethyl ether were produced. The reaction orders obtained from power rate laws for methanation indicated that the surfaces of the catalytic ensembles were not completely saturated by CO, in contrast to the observations for most conventional CO hydroge...