Torsional anharmonicity in the conformational thermodynamics of flexible molecules

Abstract

We present an algorithm for calculating the conformational thermodynamics of large, flexible molecules that combines ab initio electronic structure theory calculations with a torsional path integral Monte Carlo (TPIMC) simulation. The new algorithm overcomes the previous limitations of the TPIMC method by including the thermodynamic contributions of non-torsional vibrational modes and by affordably incorporating the ab initio calculation of conformer electronic energies, and it improves the conventional ab initio treatment of conformational thermodynamics by accounting for the anharmonicity of the torsional modes. Using previously published ab initio results and new TPIMC calculations, we apply the algorithm to the conformers of the adrenaline molecule.

Acknowledgements

TFM and DCC acknowledge fellowships from the National Science Foundation and the Leverhulme Trust, respectively. Both authors would like to thank Professor John Simons for his many insights and encouragements.