Crystal field effects on the topological properties of the electron density in molecular crystals: The case of urea

Abstract

The Quantum Theory of Atoms in Molecules, due to Bader, is applied to periodic systems. Results for molecular and crystalline urea are presented. Changes in both bondcritical points and atomic properties due to changes of chemical environment are described. A rationale for the different lengths of the in‐plane and out‐of‐plane hydrogen bonds and for the lengthening of the CO bond in bulk urea is provided in terms of the properties of the Laplacian of the oxygen atom electron density distribution. An evaluation of molecular and atomic volume changes indicates that the decrease of molecular volume upon change of phase from gas to solid originates primarily from a contraction of the atomic basins directly involved in hydrogen bonds. Other atoms show a small expansion. The considerable decrease of oxygen and hydrogen atomic volumes is related to the mutual penetration of their van der Waals envelopes following hydrogen bond formation. The results confirm that urea is more polar in the solid phase.