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 dimeri

SUBMITTER: Wiberg KB 

PROVIDER: S-EPMC8210438 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature