Rydberg-London Potential for Diatomic Molecules and Unbonded Atom Pairs
Kevin Cahill, V. Adrian Parsegian
Abstract
We propose and test a pair potential that is accurate at all relevant distances and simple enough for use in large-scale computer simulations. A combination of the Rydberg potential from spectroscopy and the London inverse-sixth-power energy, the proposed form fits spectroscopically determined potentials better than the Morse, Varnshi, and Hulburt-Hirschfelder potentials and much better than the Lennard-Jones and harmonic potentials. At long distances, it goes smoothly to the correct London force appropriate for gases and preserves van der Waals's "continuity of the gas and liquid states," which is routinely violated by coefficients assigned to the Lennard-Jones 6-12 form.
Create a lesson
Related papers
Predicting protein structures at any folding stage from sequence
Lisheng Zhang, Qingsong Li, Zinan Xie et al.
Automatic Generation of Novel Highly-Functional Molecular Sequences
Vincent R. Ragusa, Chrisoph Adami
D2ML: Models for Direct-to-Biology Small Molecule Screening
AkshatKumar Nigam, Neri Amara, Hillary Dequina et al.
Contribution of chromosome-naïve transposon-seeded network of DNA templates to intracellular pools of protein dimers of liquid-liquid phase-separated condensate-forming proteins
Gennadi Glinsky
AI-driven structural informatics reveals diverse glycosylation machinery across double-stranded DNA viruses
Lan Na
A unified coarse-grained neural network potential for the dynamics of biomolecular complexes
Antonio Mirarchi, Stephen E. Farr, Adrià Peréz et al.