The experimental charge-density approach in the evaluation of intermolecular interactions. Application of a new module of the XD programming package to several solids including a pentapeptide

A new module interfaced to the XD programming package has been used in the evaluation of intermolecular interactions and lattice energies of the cryst als of p-nitroaniline, L-asparagine monohydrate and the pentapeptide Boc-Gl n-D-Iva-Hyp-Ala-Phol (Boc = butoxycarbonyl, Iva = isovaline = ethylalanine, Phol = phenylalaninol). The electrostatic interactions are evaluated with the atom-centered distributed multipoles from KRMM (kappa'-restricted multi pole model) refinements, using the Buckingham expression for non-overlappin g charge densities. Results for p-nitroaniline are compared with Hartree-Fo ck (HF), density functional (DFT) and Moller-Plesset (MP2) supermolecular c alculations and with HF and DFT periodic calculations. The HF and DFT metho ds fail to predict the stability of the p-nitroaniline crystal but the resu lts of the experimental charge-density approach (ECDA) are in good agreemen t with both MP2 interaction energies and the experimental lattice energy. E CDA results for l-asparagine monohydrate compare well with those from DFT s upermolecular and periodic HF calculations. The disorder of the terminal gr oup in the pentapeptide, which persists at the experimental temperature of 20 K, corresponds to an energy difference of only 0.35 kJ mol(-1), which is too small to be reproduced with current methods.