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Halogen-Halogen Nonbonded Interactions.

ABSTRACT: Halogen-halogen nonbonded interactions were studied for methyl halides and phenyl halides using both B3LYP and MP2 along with 6-311+G* and aug-cc-pVTZ. With the methyl halides, the linear approach was found to lead to little stabilization, whereas the "90°" approach gave 1-2 kcal/mol. This modest stabilization was due to long-range electron correlation effects. The lowest-energy arrangement had the molecules side-by-side, with the major stabilization being derived from halogen-hydrogen interactions. The results for methyl bromide were quite similar. Chlorobenzene dimer with the 90° orientation gave a small stabilization energy, but the best arrangement had the two benzene rings oriented over each other. The meta orientation of the chlorines had a lower energy than ortho or para. The dimerization energy was larger than that for two benzene rings sitting directly above each other, suggesting that whereas Cl···Cl interaction is not very important, the effect of the halogen on the electron distribution does have an effect. This suggests that much of the crystallographic results for these compounds may not be due to halogen-halogen interactions but rather the interaction between the substituted benzene rings along with crystal forces.

SUBMITTER: Wiberg KB

PROVIDER: S-EPMC8210438 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:There is a small, but growing, body of literature describing the use of osmotic coefficient measurements to validate and reparametrize simulation force fields. Here we have investigated the ability of five very commonly used force field and water model combinations to reproduce the osmotic coefficients of seven neutral amino acids and five small molecules. The force fields tested include AMBER ff99SB-ILDN, CHARMM36, GROMOS54a7, and OPLS-AA, with the first of these tested in conjunction with the TIP3P and TIP4P-Ew water models. In general, for both the amino acids and the small molecules, the tested force fields produce computed osmotic coefficients that are lower than experiment; this is indicative of excessively favorable solute-solute interactions. The sole exception to this general trend is provided by GROMOS54a7 when applied to amino acids: in this case, the computed osmotic coefficients are consistently too high. Importantly, we show that all of the force fields tested can be made to accurately reproduce the experimental osmotic coefficients of the amino acids when minor modifications-some previously reported by others and some that are new to this study-are made to the van der Waals interactions of the charged terminal groups. Special care is required, however, when simulating Proline with a number of the force fields, and a hydroxyl-group specific modification is required in order to correct Serine and Threonine when simulated with AMBER ff99SB-ILDN. Interestingly, an alternative parametrization of the van der Waals interactions in the latter force field, proposed by the Nerenberg and Head-Gordon groups, is shown to immediately produce osmotic coefficients that are in excellent agreement with experiment. Overall, this study reinforces the idea that osmotic coefficient measurements can be used to identify general shortcomings in commonly used force fields' descriptions of solute-solute interactions and further demonstrates that modifications to van der Waals parameters provide a simple route to optimizing agreement with experiment.

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Halogen-Halogen Nonbonded Interactions.

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