enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. Phosphine oxide - Wikipedia

    en.wikipedia.org/wiki/Phosphine_oxide

    Phosphine oxide is the inorganic compound with the formula H 3 PO. Although stable as a dilute gas, liquid or solid samples are unstable. Unlike many other compounds of the type PO x H y, H 3 PO is rarely discussed and is not even mentioned in major sources on main group chemistry.

  4. Phosphorine - Wikipedia

    en.wikipedia.org/wiki/Phosphorine

    Halophosphorines do undergo noble-metal- or zirconocene-catalyzed substitution, and λ 5-phosphorines exhibit a much more traditional substitution chemistry. [6] Unlike arsabenzene, phosphorine rarely participates in Diels-Alder-type cycloadditions; when it does, the coupling partner must be an extremely electron-poor alkyne.

  5. Pnictogen - Wikipedia

    en.wikipedia.org/wiki/Pnictogen

    Going down the group, to phosphane (phosphine), arsane (arsine), stibane (stibine), and finally bismuthane (bismuthine), each pnictogen hydride becomes progressively less stable (more unstable), more toxic, and has a smaller hydrogen-hydrogen angle (from 107.8° in ammonia [6] to 90.48° in bismuthane). [7] (Also, technically, only ammonia and ...

  6. Organophosphine - Wikipedia

    en.wikipedia.org/wiki/Organophosphine

    The latter is a common feature of the chemistry of phosphorus. As a result, the lone pair of trimethylphosphine has predominantly s-character as is the case for phosphine, PH 3. [10] Tertiary phosphines are pyramidal. When the organic substituents all differ, the phosphine is chiral and

  7. Phosphorus - Wikipedia

    en.wikipedia.org/wiki/Phosphorus

    Phosphine (PH 3) and its organic derivatives (PR 3) are structural analogues of ammonia (NH 3), but the bond angles at phosphorus are closer to 90° for phosphine and its organic derivatives. Phosphine is an ill-smelling, toxic gas. Phosphorus has an oxidation number of −3 in phosphine. Phosphine is produced by hydrolysis of calcium phosphide ...

  8. Phosphonium - Wikipedia

    en.wikipedia.org/wiki/Phosphonium

    In chemistry, the term phosphonium (more obscurely: phosphinium) describes polyatomic cations with the chemical formula PR + 4 (where R is a hydrogen or an alkyl, aryl, or halide group). These cations have tetrahedral structures. The salts are generally colorless or take the color of the anions. [1]

  9. 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. It reacts slowly with atmospheric oxygen, and rapidly with other oxidizing agents, to give tributylphosphine oxide.