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  2. CPK coloring - Wikipedia

    en.wikipedia.org/wiki/CPK_coloring

    Several of the CPK colors refer mnemonically to colors of the pure elements or notable compound. For example, hydrogen is a colorless gas, carbon as charcoal, graphite or coke is black, sulfur powder is yellow, chlorine is a greenish gas, bromine is a dark red liquid, iodine in ether is violet, amorphous phosphorus is red, rust is dark orange-red, etc.

  3. Thiophosphoryl fluoride - Wikipedia

    en.wikipedia.org/wiki/Thiophosphoryl_fluoride

    3D model [3]: Interactive ... acids suggest that the phosphorus atom is at least as electrophilic as in phosphoryl fluoride. [10] Autodecomposition from heat gives ...

  4. Molecular graphics - Wikipedia

    en.wikipedia.org/wiki/Molecular_graphics

    These early models also established the CPK coloring scheme that is still used today to differentiate the different types of atoms in molecular models (e.g. carbon = black, oxygen = red, nitrogen = blue, etc). This early model was improved upon in 1966 by W.L. Koltun and are now known as Corey-Pauling-Koltun (CPK) models. [5]

  5. Electron configurations of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Electron_configurations_of...

    For each atom the subshells are given first in concise form, then with all subshells written out, followed by the number of electrons per shell. For phosphorus (element 15) as an example, the concise form is [Ne] 3s 2 3p 3 .

  6. Methylenetriphenylphosphorane - Wikipedia

    en.wikipedia.org/wiki/Methylenetriphenylphosphorane

    Crystallographic characterization of the colourless ylide reveals that the phosphorus atom is approximately tetrahedral. The PCH 2 centre is planar and the P=CH 2 distance is 1.661 Å, which is much shorter than the P-Ph distances (1.823 Å). [5] The compound is usually described as a combination of two resonance structures: Ph 3 P + CH 2 − ...

  7. Phosphorine - Wikipedia

    en.wikipedia.org/wiki/Phosphorine

    Phosphorine (IUPAC name: phosphinine) is a heavier element analog of pyridine, containing a phosphorus atom instead of an aza-moiety. It is also called phosphabenzene and belongs to the phosphaalkene class. It is a colorless liquid that is mainly of interest in research.

  8. Allotropes of phosphorus - Wikipedia

    en.wikipedia.org/wiki/Allotropes_of_phosphorus

    Black phosphorus has an orthorhombic pleated honeycomb structure and is the least reactive allotrope, a result of its lattice of interlinked six-membered rings where each atom is bonded to three other atoms. [21] [22] In this structure, each phosphorus atom has five outer shell electrons. [23]

  9. Phosphoryl chloride difluoride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride_difluoride

    Along the b-axis there is a zigzag of O atoms close to a P atom in the other position. [2] The density of the solid is as calculated from crystal data is 2.177 g/cm 3. [2] In the 31 P-NMR spectrum (in H 3 PO 4), the phosphorus atom of POClF 2 is a triplet at 15 ppm. [4]