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Jacobson D, Stratt RM. The inherent dynamics of a molecular liquid: geodesic pathways through the potential energy landscape of a liquid of linear molecules. J Chem Phys. 2014;140(17):174503doi: 10.1063/1.4872363.
Jacobson, D., & Stratt, R. M. (2014). The inherent dynamics of a molecular liquid: geodesic pathways through the potential energy landscape of a liquid of linear molecules. The Journal of chemical physics, 140(17), 174503. https://doi.org/10.1063/1.4872363
Jacobson, Daniel, and Stratt, Richard M. "The inherent dynamics of a molecular liquid: geodesic pathways through the potential energy landscape of a liquid of linear molecules." The Journal of chemical physics vol. 140,17 (2014): 174503. doi: https://doi.org/10.1063/1.4872363
Jacobson D, Stratt RM. The inherent dynamics of a molecular liquid: geodesic pathways through the potential energy landscape of a liquid of linear molecules. J Chem Phys. 2014 May 07;140(17):174503. doi: 10.1063/1.4872363. PMID: 24811642.
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J Chem Phys. 2014 May 07;140(17):174503. doi: 10.1063/1.4872363.

The inherent dynamics of a molecular liquid: geodesic pathways through the potential energy landscape of a liquid of linear molecules.

The Journal of chemical physics

Daniel Jacobson, Richard M Stratt

Affiliations

  1. Department of Chemistry, Brown University, Providence, Rhode Island 02912, USA.

PMID: 24811642 DOI: 10.1063/1.4872363

Abstract

Because the geodesic pathways that a liquid follows through its potential energy landscape govern its slow, diffusive motion, we suggest that these pathways are logical candidates for the title of a liquid's "inherent dynamics." Like their namesake "inherent structures," these objects are simply features of the system's potential energy surface and thus provide views of the system's structural evolution unobstructed by thermal kinetic energy. This paper shows how these geodesic pathways can be computed for a liquid of linear molecules, allowing us to see precisely how such molecular liquids mix rotational and translational degrees of freedom into their dynamics. The ratio of translational to rotational components of the geodesic path lengths, for example, is significantly larger than would be expected on equipartition grounds, with a value that scales with the molecular aspect ratio. These and other features of the geodesics are consistent with a picture in which molecular reorientation adiabatically follows translation-molecules largely thread their way through narrow channels available in the potential energy landscape.

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