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  2. Allotropes of phosphorus - Wikipedia

    en.wikipedia.org/wiki/Allotropes_of_phosphorus

    The lattice structure of violet phosphorus has been obtained by single-crystal x-ray diffraction to be monoclinic with space group of P2/n (13) (a = 9.210, b = 9.128, c = 21.893 Å, β = 97.776°, CSD-1935087). The optical band gap of the violet phosphorus was measured by diffuse reflectance spectroscopy to be around 1.7 eV.

  3. Phosphazene - Wikipedia

    en.wikipedia.org/wiki/Phosphazene

    One example is hexachlorocyclotriphosphazene (−N=P(−Cl) 2 −) 3. Bis(triphenylphosphine)iminium chloride [Ph 3 P=N=PPh 3] + Cl − is also referred to as a phosphazene, where Ph = phenyl group. The present article focuses on those phosphazenes with the formula R−N=P(−NR 2) 3.

  4. White phosphorus - Wikipedia

    en.wikipedia.org/wiki/White_phosphorus

    White phosphorus, yellow phosphorus, or simply tetraphosphorus (P 4) is an allotrope of phosphorus.It is a translucent waxy solid that quickly yellows in light (due to its photochemical conversion into red phosphorus), [2] and impure white phosphorus is for this reason called yellow phosphorus.

  5. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  6. Phosphorus - Wikipedia

    en.wikipedia.org/wiki/Phosphorus

    Download as PDF; Printable version; ... It is more common, has cubic crystal structure and at 195.2 K (−78.0 °C), it transforms into β-form, which has hexagonal ...

  7. Tetrahedrane - Wikipedia

    en.wikipedia.org/wiki/Tetrahedrane

    Tetrahedrane is a hypothetical platonic hydrocarbon with chemical formula C 4 H 4 and a tetrahedral structure. The molecule would be subject to considerable angle strain and has not been synthesized as of 2023. However, a number of derivatives have been prepared.

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  9. Phosphonium iodide - Wikipedia

    en.wikipedia.org/wiki/Phosphonium_iodide

    Phosphonium iodide is a powerful substitution reagent in organic chemistry; for example, it can convert a pyrilium into a phosphinine via substitution. [3] In 1951, Glenn Halstead Brown found that PH 4 I reacts with acetyl chloride to produce an unknown phosphine derivative, possibly CH 3 C(=PH)PH 2 ·HI .