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The synthesis and catalytic activity of long-chain NHC-stabilized RuNPs are presented. Full characterization of these novel nanostructures including surface state studies show that the ligand influences the number and the location of Ru active sites which impacts the NP catalytic activity, especially in hydrogenation reactions. The high stability and versatility of these nanosystems make them successful catalysts for both oxidation and hydrogenation reactions that can even be performed successively in a one pot-fashion. [ABSTRACT FROM AUTHOR]

Review: 74 refs. [ABSTRACT FROM AUTHOR]

Highlights: [•] Catalysts based on carbon-supported Pd nanoparticles (NPs) were prepared. [•] Catalysts activity was investigated in the hydrogenation of anthracene. [•] High conversions and selectivities towards the hydrogenated products were achieved. [•] No cracking or ring-opening products were obtained. [•] Reaction pathway for anthracene hydrogenation is proposed. [Copyright &y& Elsevier]

Abstract: Rhodium composite nanomaterials were synthesized by an innovating process called dry impregnation in a fluidized bed. It consists in spraying an aqueous colloidal suspension of rhodium on silica porous particles. The use of this precursor solution containing preformed nanoparticles avoids calcination/activation step. Different composite nanomaterials were prepared displaying various metal loadings. The operating conditions were tuned to modify τ s, the solvent vapour saturation rate value, in order to influence the deposit location: either uniform on the whole silica particles or at the particles surface like a coating. τ s is defined as the ratio between solvent content in the bed atmosphere and the maximum solvent content. The obtained samples were investigated in catalytic hydrogenation of aromatic compounds under very mild conditions. Their catalytic performances were compared to those of the original colloidal suspension in one hand and of a similar catalyst prepared through wet impregnation in another hand. Interesting activity and selectivity were observed. This illustrates the interest of the dry impregnation method: this way allows an easy control of the metal loading as well as of the metal loading location in the support particles. Moreover, the support particle size and morphology are preserved. [Copyright &y& Elsevier]

The synthesis of catalytic or not composite materials by dry impregnation in fluidized bed is described. This process can be carried out under mild conditions from solutions of organometallic precursors or colloidal solutions of preformed nanoparticles giving rise to reproducible metallic nanoparticles containing composite materials with a high reproducibility. The adequate choice of the reaction conditions makes possible to deposit uniformly the metal precursor within the porous matrix or on the support surface. When the ratio between the drying time and the capillary penetration time ( tsec/ tcap) is higher than 10, the impregnation under soft drying conditions leads to a homogeneous deposit inside the pores of the particles of support. The efficiency of the metal deposition is close to 100%, and the size of the formed metal nanoparticles is controlled by the pores diameter. Finally, some of the presented composite materials have been tested as catalysts: iron-based materials were used in carbon-nanotubes synthesis, while Pd and Rh composite materials have been investigated in hydrogenation reactions. [ABSTRACT FROM AUTHOR]

Abstract: The organometallic synthesis of ruthenium nanoparticles stabilized by water-soluble alkyl sulfonated diphosphines as ligands is described for the first time. After isolation, the so-obtained nanoparticles could be easily dispersed into water giving rise to stable aqueous colloidal solutions without precipitation over the course of several months. The catalytic behaviour of these aqueous colloidal solutions has been investigated in the hydrogenation of unsaturated substrates (tetradecene, styrene and acetophenone) in biphasic liquid–liquid conditions, showing interesting results in terms of reactivity. Interestingly, small structural differences in the backbone of the diphosphine ligands influence the catalytic activity of these nanocatalysts. In addition, preliminary tests of recycling showed promising results with neither loss of activity or significant precipitation. [Copyright &y& Elsevier]