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Integral contour for deriving Kramers–Kronig relations. The proof begins with an application of Cauchy's residue theorem for complex integration. Given any analytic function in the closed upper half-plane, the function ′ (′) / (′), where is real, is analytic in the (open) upper half-plane.
The binding constant, or affinity constant/association constant, is a special case of the equilibrium constant K, [1] and is the inverse of the dissociation constant. [2] It is associated with the binding and unbinding reaction of receptor (R) and ligand (L) molecules, which is formalized as: R + L ⇌ RL
= , where k B is the Boltzmann constant, and Ω denotes the volume of macrostate in the phase space or otherwise called thermodynamic probability. d S = δ Q T {\displaystyle dS={\frac {\delta Q}{T}}} , for reversible processes only
The Boltzmann constant (k B or k) is the proportionality factor that relates the average relative thermal energy of particles in a gas with the thermodynamic temperature of the gas. [2] It occurs in the definitions of the kelvin (K) and the gas constant , in Planck's law of black-body radiation and Boltzmann's entropy formula , and is used in ...
kT (also written as k B T) is the product of the Boltzmann constant, k (or k B), and the temperature, T.This product is used in physics as a scale factor for energy values in molecular-scale systems (sometimes it is used as a unit of energy), as the rates and frequencies of many processes and phenomena depend not on their energy alone, but on the ratio of that energy and kT, that is, on E ...
where log denotes a logarithm to base 10 or common logarithm, and K diss is a stepwise acid dissociation constant. For bases, the base association constant, pK b is used. For any given acid or base the two constants are related by pK a + pK b = pK w, so pK a can always be used in calculations.
K b, the ebullioscopic constant, which is dependent on the properties of the solvent. It can be calculated as K b = RT b 2 M/ΔH v, where R is the gas constant, and T b is the boiling temperature of the pure solvent [in K], M is the molar mass of the solvent, and ΔH v is the heat of vaporization per mole of the solvent.
This would thus allow the calculation of K −1. By plotting a graph of ε HG versus K −1, the result would be a linear relationship. When the procedure is repeated for a series of concentrations and plotted on the same graph, the lines intersect at a point giving the optimum value of ε HG and K −1.