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  2. Triphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine

    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 ...

  3. Triphenylphosphine oxide - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine_oxide

    Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C 6 H 5) 3, also written as Ph 3 PO or PPh 3 O (Ph = C 6 H 5). It is one of the more common phosphine oxides .

  4. Phosphine oxides - Wikipedia

    en.wikipedia.org/wiki/Phosphine_oxides

    The nature of the P–O bond was once hotly debated. Some discussions invoked a role for phosphorus-centered d-orbitals in bonding, but this analysis is not supported by computational analyses. In terms of simple Lewis structure, the bond is more accurately represented as a dative bond, as is currently used to depict an amine oxide. [3] [4]

  5. Transition metal complexes of phosphine oxides - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Principal resonance structures for phosphine oxides. The structure of the phosphine oxide is not strongly perturbed by coordination. The geometry at phosphorus remains tetrahedral. The P-O distance elongates by ca. 2%. In triphenylphosphine oxide, the P-O distance is 1.48 Å. [3] In NiCl 2 [OP(C 6 H 5) 3] 2, the distance is 1.51 Å (see figure).

  6. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    The methylation of triphenylphosphine is the first step in the preparation of the Wittig reagent. Illustrative phosphorus(V) compounds: the phosphonium ion P(CH 2 OH) 4 +, two resonance structures for the Wittig reagent Ph 3 PCH 2, and pentaphenylphosphorane, a rare pentaorganophophorus compound. The parent phosphorane (σ 5 λ 5) is PH 5 ...

  7. Metal-phosphine complex - Wikipedia

    en.wikipedia.org/wiki/Metal-phosphine_complex

    One of the first applications of phosphine ligands in catalysis was the use of triphenylphosphine in "Reppe" chemistry (1948), which included reactions of alkynes, carbon monoxide, and alcohols. [16] In his studies, Reppe discovered that this reaction more efficiently produced acrylic esters using NiBr 2 ( PPh 3 ) 2 as a catalyst instead of ...

  8. List of chemical elements - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical_elements

    A chemical element, often simply called an element, is a type of atom which has a specific number of protons in its atomic nucleus (i.e., a specific atomic number, or Z). [ 1 ] The definitive visualisation of all 118 elements is the periodic table of the elements , whose history along the principles of the periodic law was one of the founding ...

  9. Tris(4-methoxyphenyl)phosphine - Wikipedia

    en.wikipedia.org/wiki/Tris(4-methoxyphenyl)phosphine

    Chemical formula. P(C 6 H 4 OCH 3) 3 Appearance white solid Melting point: 131 °C (268 °F; 404 K) ... Triphenylphosphine; 2-(Diphenylphosphino)anisole; References