Coupled cluster and DFT calculations of ~(14)N nuclear quadrupole coupling constants

摘要

The dependence of ~(14)N quadrupole coupling constants calculated using coupled cluster theory on the level of approximation is examined for a series of small molecules. For HCN, HNC, CH _3CN, and CH _3NC, we use the coupled cluster singles-and-doubles with a noniterative perturbative triples correction - CCSD(T) - approach, and we analyze the basis set dependence of the results. For aziridine, diazirine, and cyclopropyl cyanide, we use the CCSD(T) approach, but smaller basis sets, and for the largest studied molecules - quinuclidine and hexamine - we present CCSD results. The differences between computed and experimental values for the best basis sets used are ≈ 5% at the CCSD level and decrease noticeably at the CCSD(T) level. The - N≡C bonds are an exception - in this case the quadrupole coupling constants are very small, hence the differences between theory and experiment become larger (up to 9%). We also consider the performance of density functional theory, comparing the results for different density functionals with the coupled cluster values of the same constants. Most of the functionals provide results systematically improved with respect to the Hartree-Fock values, with ~(14)N coupling constants in - N≡C bonds being again an exception.