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  2. Phosphine - Wikipedia

    en.wikipedia.org/wiki/Phosphine

    Phosphine (IUPAC name: phosphane) is a colorless, flammable, highly toxic compound with the chemical formula P H 3, classed as a pnictogen hydride. Pure phosphine is odorless, but technical grade samples have a highly unpleasant odor like rotting fish, due to the presence of substituted phosphine and diphosphane ( P 2 H 4 ).

  3. Phosgene - Wikipedia

    en.wikipedia.org/wiki/Phosgene

    Phosgene is an organic chemical compound with the formula COCl 2. It is a toxic, colorless gas; in low concentrations, its musty odor resembles that of freshly cut ...

  4. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    Compounds related to phosphine oxides include phosphine imides (R 3 PNR') and related chalcogenides (R 3 PE, where E = S, Se, Te). These compounds are some of the most thermally stable organophosphorus compounds. In general, they are less basic than the corresponding phosphine oxides, which can adduce to thiophosphoryl halides: [7]: 73

  5. Tributylphosphine - Wikipedia

    en.wikipedia.org/wiki/Tributylphosphine

    Tributylphosphine is the organophosphorus compound with the chemical formula P(CH 2 CH 2 CH 2 CH 3) 3, often abbreviated as PBu 3.It is a tertiary phosphine.It is an oily liquid at room temperature, with a nauseating odor.

  6. Organophosphine - Wikipedia

    en.wikipedia.org/wiki/Organophosphine

    The reaction with oxygen is spin-forbidden but still proceeds at sufficient rate that samples of tertiary phosphines are characteristically contaminated with phosphine oxides. Qualitatively, the rates of oxidation are higher for trialkyl vs triarylphosphines. Faster still are oxidations using hydrogen peroxide. Primary and secondary phosphines ...

  7. Metal-phosphine complex - Wikipedia

    en.wikipedia.org/wiki/Metal-phosphine_complex

    The first reported phosphine complexes were cis- and trans-PtCl 2 (PEt 3) 2 reported by Cahours and Gal in 1870. [5] Often the phosphine serves both as a ligand and as a reductant. This property is illustrated by the synthesis of many platinum-metal complexes of triphenylphosphine: [6] RhCl 3 (H 2 O) 3 + 4 PPh 3 → RhCl(PPh 3) 3 + OPPh 3 + 2 ...

  8. Phosphazene - Wikipedia

    en.wikipedia.org/wiki/Phosphazene

    One class of phosphazenes have the formula R−N=P(−NR 2) 3. These phosphazenes are also known as iminophosphoranes and phosphine imides. They are superbases. [1]

  9. Category:Phosphines - Wikipedia

    en.wikipedia.org/wiki/Category:Phosphines

    Phosphines or phosphanes are phosphorus compounds derived from phosphine and have the general structure R 3 P. For the nitrogen analogues, please see Category:Inorganic amines . Wikimedia Commons has media related to Phosphines .