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Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C 6 H 5) 3 and often abbreviated to P Ph 3 or Ph 3 P. It is versatile compound that is widely used as a reagent in organic synthesis and as a ligand for transition metal complexes, including ones that serve as catalysts in organometallic chemistry.
A metal-phosphine complex is a coordination complex containing one or more phosphine ligands. Almost always, the phosphine is an organophosphine of the type R 3 P (R = alkyl, aryl).
A spectrochemical series is a list of ligands ordered by ligand "strength", and a list of metal ions based on oxidation number, group and element.For a metal ion, the ligands modify the difference in energy Δ between the d orbitals, called the ligand-field splitting parameter in ligand field theory, or the crystal-field splitting parameter in crystal field theory.
A ligand exchange (also called ligand substitution) is a chemical reaction in which a ligand in a compound is replaced by another. Two general mechanisms are recognized: associative substitution or by dissociative substitution. A generalized example of ligand association. Associative substitution closely resembles the S N 2 mechanism in organic ...
Skeletal formula of a generic diphosphine ligand. R represents a side chain.The phosphine donors are connected by a backbone linker. Diphosphines, sometimes called bisphosphanes, are organophosphorus compounds most commonly used as bidentate phosphine ligands in inorganic and organometallic chemistry.
The four phosphorus atoms are at the corners of a tetrahedron surrounding the palladium(0) center. This structure is typical for four-coordinate 18 e − complexes. [2] The corresponding complexes Ni(PPh 3) 4 and Pt(PPh 3) 4 are also well known.
A typical example of this category viz. novel hexacoordinated orthometalated rhodium(III) thiolato complex trans-[Rh(C ∧ N ∧ S)Cl(PPh 3) 2] was synthesized from benzyl 2-(phenylazo)phenyl thioether and RhCl 3 ·3H 2 O in the presence of excess PPh 3 via in situ C(sp 2)−H and C(sp 3)−S bond scissions. This is the first example for a ...
The introduction of phosphine ligands led to improved reactivity and numerous asymmetric allylic alkylation strategies. Many of these strategies are driven by the advent of chiral ligands, which are often able to provide high enantioselectivity and high diastereoselectivity under mild conditions. This modification greatly expands the utility of ...