Sökning: "fosfiner"
Visar resultat 1 - 5 av 7 avhandlingar innehållade ordet fosfiner.
1. Synthesis and Organocatalytic Evaluation of P-Chirogenic Phosphines
Sammanfattning : .... LÄS MER
2. Polymer Bound Water-Soluble Metal Phosphine Complexes-Preparation, Characterisation and Catalytic Application
Sammanfattning : Four new water-soluble phosphines have been prepared by utilising water-soluble polymers as charge carrying units. Coupling of methyl-4-(diphenylphosphino)-benzyl-amine or 4-diphenylphosphino benzaldehyde to poly-acrylic acid and poly-ethylene imine, respectively, afford the ligands PAA-PNH and PEI-PNH. LÄS MER
3. Cluster-Based Catalysts for Asymmetric Synthesis
Sammanfattning : In this work, the synthesis and characterisation of new low-valence transition metal carbonyl clusters, and an investigation into their viability to act as catalysts/catalyst precursors in asymmetric synthesis, are described. Carbonyl clusters based on ruthenium and osmium have been tested as (pre)catalysts for asymmetric hydrogenation of alpha-unsaturated carboxylic acids, and cobalt carbonyl clusters have been used as (pre)catalysts in (asymmetric) Pauson-Khand synthesis. LÄS MER
4. A Catalytic and Mechanistic Investigation of Palladium-Phosphine Catalysed Aqueous Hydroxycarbonylation. Steric and Electronic Properties of the Ligands
Sammanfattning : The steric and electronic properties of eight water-soluble phosphines (1-8) were investigated by different methods. Phosphines 1-6 were tested as ligands in palladium catalysed hydroxycarbonylation of styrene. LÄS MER
5. Phosphine ligands with triamine functionality - preparation and application in catalysis
Sammanfattning : Incorporation of the triamine, bis(2-diethylaminoethyl) amine as a side chain substituent on triphenylphosphine, (2S,4S)-4-diphenylphosphino-2-diphenylphosphino-methylpyrrolidine (PPM) or (R,R)-3,4-bis(diphenylphosphin)pyrrolidine (Pyrphos) gives the three new amphiphilic ligands N3P, N3PPM and N3-Pyrphos respectively. Because of the triamine functionality the distribution of the ligands and their complexes between water and an organic solvent is controlled by the pH of the aqueous phase. LÄS MER