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The reaction of phosphorus pentoxide and PCl 5 produces POCl 3 : [18] [page needed] 6 PCl 5 + P 4 O 10 → 10 POCl 3. PCl 5 chlorinates nitrogen dioxide to form unstable nitryl chloride: PCl 5 + 2 NO 2 → PCl 3 + 2 NO 2 Cl 2 NO 2 Cl → 2 NO 2 + Cl 2. PCl 5 is a precursor for lithium hexafluorophosphate, LiPF 6.
Structure of iodine heptafluoride, an example of a molecule with the pentagonal-bipyramidal coordination geometry. In chemistry, a pentagonal bipyramid is a molecular geometry with one atom at the centre with seven ligands at the corners of a pentagonal bipyramid. A perfect pentagonal bipyramid belongs to the molecular point group D 5h.
This is unlike phosphorus pentachloride which exists as neutral PCl 5 molecules in the gas and liquid states but adopts the ionic form [PCl 4] + [PCl 6] − (tetrachlorophosphonium hexachlorophosphate(V)) in the solid state. The average bond lengths in the crystal structure of POCl 3 are 1.98 Å for P–Cl and 1.46 Å for P=O. [5]
Phosphorus pentachloride, phosphorus pentabromide, and phosphorus heptabromide are ionic in the solid and liquid states; PCl 5 is formulated as PCl 4 + PCl 6 –, but in contrast, PBr 5 is formulated as PBr 4 + Br −, and PBr 7 is formulated as PBr 4 + Br 3 −. They are widely used as chlorinating and brominating agents in organic chemistry.
The reaction field method is used in molecular simulations to simulate the effect of long-range dipole-dipole interactions for simulations with periodic boundary conditions. Around each molecule there is a 'cavity' or sphere within which the Coulomb interactions are treated explicitly.
Phosphorus pentafluoride is a Lewis acid.This property is relevant to its ready hydrolysis. A well studied adduct is PF 5 with pyridine.With primary and secondary amines, the adducts convert readily to dimeric amido-bridged derivatives with the formula [PF 4 (NR 2)] 2.
In organic chemistry, a dipolar compound or simply dipole is an electrically neutral molecule carrying a positive and a negative charge in at least one canonical description. In most dipolar compounds the charges are delocalized . [ 1 ]
The polarizability of an atom or molecule is defined as the ratio of its induced dipole moment to the local electric field; in a crystalline solid, one considers the dipole moment per unit cell. [1] Note that the local electric field seen by a molecule is generally different from the macroscopic electric field that would be measured externally.