Partition Function and Configurational Entropy in Non-Equilibrium States: A New Theoretical Model.

A new model of non-equilibrium thermodynamic states has been investigated on the basis of the fact that all thermodynamic variables can be derived from partition functions. We have thus attempted to define partition functions for non-equilibrium conditions by introducing the concept of pseudo-temperature distributions. These pseudo-temperatures are configurational in origin and distinct from kinetic (phonon) temperatures because they refer to the particular fragments of the system with specific energies.

Experimental and quantum-chemical studies on the thermochemical stabilities of mercury carbodiimide and mercury cyanamide.

Calorimetric dissolution measurements of the solid compounds mercury carbodiimide HgNCN(I) and mercury cyanamide HgNCN(II) in aqueous HCl that targeted at their thermochemical stabilities show the cyanamide species HgNCN(II) to be the more stable phase in terms of both enthalpy and Gibbs energy with an enthalpy difference of 2-3 kJ mol-1. While the stability ranking of HgNCN(I) and HgNCN(II) thus perfectly matches Pearson's HSAB concept, quantum-chemical stability predictions using common parametrizations of density functional theory appear to be fundamentally flawed. An analysis of the error is attempted on the basis of correlated wave functions for related molecules.