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Chlorine pentafluoride is an interhalogen compound with formula ClF 5. This colourless gas is a strong oxidant that was once a candidate oxidizer for rockets. The molecule adopts a square pyramidal structure with C 4v symmetry, [1] as confirmed by its high-resolution 19 F NMR spectrum. [2] It was first synthesized in 1963. [3]
Fluorine forms a great variety of chemical compounds, within which it always adopts an oxidation state of −1. With other atoms, fluorine forms either polar covalent bonds or ionic bonds. Most frequently, covalent bonds involving fluorine atoms are single bonds, although at least two examples of a higher order bond exist. [2]
[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.
Chlorine monofluoride: Chlorine trifluoride: Chlorine pentafluoride: Molar mass: 54.45 g/mol 92.45 g/mol 130.45 g/mol CAS number: Melting point: −155.6 °C −76.3 °C −103 °C Boiling point: −100 °C 11.8 °C −13.1 °C Standard enthalpy of formation Δ f H° gas: −50.29 kJ/mol −158.87 kJ/mol −238.49 kJ/mol
Structure of xenon oxytetrafluoride, an example of a molecule with the square pyramidal coordination geometry. Square pyramidal geometry describes the shape of certain chemical compounds with the formula ML 5 where L is a ligand. If the ligand atoms were connected, the resulting shape would be that of a pyramid with a square base.
Phosphorus pentafluoride. There are 2 possible structures with an axial ionic bond, plus 3 possible structures with an equatorial ionic bond. For a hexacoordinate molecule such as sulfur hexafluoride, each of the six bonds is the same length. The rationalization described above can be applied to generate 15 resonance structures each with four ...
Phosphorus pentafluoride is a relatively inert gas, notable as a mild Lewis acid and a fluoride ion acceptor. It is a fluxional molecule in which the axial (ax) and equatorial (eq) fluorine atoms interchange positions by the Berry pseudorotation mechanism .
The carbon–fluorine bond is a polar covalent bond between carbon and fluorine that is a component of all organofluorine compounds. It is one of the strongest single bonds in chemistry (after the B–F single bond, Si–F single bond, and H–F single bond), and relatively short, due to its partial ionic character.