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Elastic constant calculations for molecular organic crystals

Record type: Article

Elastic constants of a set of molecular organic crystals have been calculated within the crystal modeling program DMAREL, which was developed to allow the use of highly accurate, anisotropic atom?atom potentials. A set of six molecular crystals (durene, m-dinitrobenzene, the ? form of resorcinol, pentaerythritol, urea, and hexamethylenetetramine) has been chosen to sample a range of intermolecular interactions and crystal symmetries. The sensitivity of such calculations to variations in empirical repulsion?dispersion parameters and the electrostatic model is determined and discussed relative to the other errors in the theoretical model and typical experimental uncertainties. We find that model potentials whose functional form has been simplified often reproduce crystal structures and lattice energies adequately but perform poorly when used to calculate elastic constants. This is because more theoretically justified potentials are required to satisfactorily model the curvature at the equilibrium geometries. The rigid-molecule approximation can result in exaggerated elastic constants, and the neglect of thermal effects also leads to significant overestimation of the stiffness constants

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Citation

Day, Graeme M., Price, Sarah L. and Leslie, Maurice (2001) Elastic constant calculations for molecular organic crystals Crystal Growth & Design, 1, (1), pp. 13-27. (doi:10.1021/cg0055070).

More information

Published date: 2001
Organisations: Organic Chemistry: Synthesis, Catalysis and Flow, Computational Systems Chemistry

Identifiers

Local EPrints ID: 343465
URI: http://eprints.soton.ac.uk/id/eprint/343465
ISSN: 1528-7483
PURE UUID: d03f8c09-4972-4828-9d51-c74a77259184
ORCID for Graeme M. Day: ORCID iD orcid.org/0000-0001-8396-2771

Catalogue record

Date deposited: 19 Oct 2012 14:05
Last modified: 18 Jul 2017 05:22

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Contributors

Author: Graeme M. Day ORCID iD
Author: Sarah L. Price
Author: Maurice Leslie

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