| Literature DB >> 29389130 |
Manoj K Kesharwani1, Debashree Manna1, Nitai Sylvetsky1, Jan M L Martin1.
Abstract
We have re-evaluated the X40×10 benchmark for halogen bonding using conventional and explicitly correlated coupled cluster methods. For the aromatic dimers at small separation, improved CCSD(T)-MP2 "high-level corrections" (HLCs) cause substantial reductions in the dissociation energy. For the bromine and iodine species, (n-1)d subvalence correlation increases dissociation energies and turns out to be more important for noncovalent interactions than is generally realized; (n-1)sp subvalence correlation is much less important. The (n-1)d subvalence term is dominated by core-valence correlation; with the smaller cc-pVDZ-F12-PP and cc-pVTZ-F12-PP basis sets, basis set convergence for the core-core contribution becomes sufficiently erratic that it may compromise results overall. The two factors conspire to generate discrepancies of up to 0.9 kcal/mol (0.16 kcal/mol RMS) between the original X40×10 data and the present revision.Entities:
Year: 2018 PMID: 29389130 DOI: 10.1021/acs.jpca.7b10958
Source DB: PubMed Journal: J Phys Chem A ISSN: 1089-5639 Impact factor: 2.781