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where μ is the electric dipole moment of the effectively polarized water molecule (2.35 D for the SPC/E model), μ 0 is the dipole moment of an isolated water molecule (1.85 D from experiment), and α i is an isotropic polarizability constant, with a value of 1.608 × 10 −40 F·m 2. Since the charges in the model are constant, this ...
Polarizability increases down on columns of the periodic table. [9] Likewise, larger molecules are generally more polarizable than smaller ones. Water is a very polar molecule, but alkanes and other hydrophobic molecules are more polarizable. Water with its permanent dipole is less likely to change shape due to an external electric field.
Dispersion of gravity waves on a fluid surface. Phase and group velocity divided by shallow-water phase velocity √ gh as a function of relative depth h / λ. Blue lines (A): phase velocity; Red lines (B): group velocity; Black dashed line (C): phase and group velocity √ gh valid in shallow water.
Spatial dispersion means that light travelling in different directions (different wavevectors) sees a slightly different permittivity tensor. Natural optical rotation requires a special material, but it also relies on the fact that the wavevector of light is nonzero, and a nonzero wavevector bypasses the symmetry restrictions on the local (zero ...
The waves propagate over an elliptic-shaped underwater shoal on a plane beach. This example combines several effects of waves and shallow water, including refraction, diffraction, shoaling and weak non-linearity. In fluid dynamics, the Boussinesq approximation for water waves is an approximation valid for weakly non-linear and fairly long waves.
London dispersion forces are also known as 'dispersion forces', 'London forces', or 'instantaneous dipole–induced dipole forces'. The strength of London dispersion forces is proportional to the polarizability of the molecule, which in turn depends on the total number of electrons and the area over which they are spread.
An Ion of charge and a nonpolar molecule of polarizability . The Lifshitz theory can be expressed as an effective Hamaker constant in the van der Waals theory. Consider, for example, the interaction between an ion of charge Q {\textstyle Q} , and a nonpolar molecule with polarizability α 2 {\textstyle \alpha _{2}} at distance r {\textstyle r} .
For example, the Kamlet-Taft parameters are dipolarity/polarizability (π*), hydrogen-bonding acidity (α) and hydrogen-bonding basicity (β). These can be calculated from the wavelength shifts of 3–6 different solvatochromic dyes in the solvent, usually including Reichardt's dye , nitroaniline and diethylnitroaniline .