TY - JOUR
T1 - Spectroscopic constants of Pb and Eka-lead compounds
T2 - Comparison of different approaches
AU - Liu, Wenjian
AU - van Wüllen, Christoph
AU - Han, Young Kyu
AU - Choi, Yoon Jeong
AU - Lee, Yoon Sup
N1 - Publisher Copyright:
© 2001 by Academic Press.
PY - 2001
Y1 - 2001
N2 - Three independent relativistic approaches, four-component density functional theory (4c-DFT), two-component DFT-ZORA(MP) (Zeroth order regular approximation with model potentials) and two-component ECP-CCSD(T) (Effective core potentials, coupled-cluster theory with singles, doubles and perturbative triples), have been employed by three independent groups to calculate the bond lengths, binding energies and vibrational frequencies for the eka-lead (E114) compounds E114X (X = H, F, Cl, Br, I, O, O2) and the E114 dimer. For calibration, we also report results for homologous lead compounds. The dipole moments and dipole moment derivatives for the diatomic molecules are presented as well. The bonds in E114 compounds are considerably weaker than those of lead due to much larger relativistic (spin-orbit) effects It is predicted that E11402 is thermodynamically unstable with respect to the decomposition into E114 + O2, in contrast to PbO2 → Pb + O2. Both 2PbO2 → 2PbO + O2 and 2E114O2 → 2E114O + O2 are thermodynamically unstable. The agreement between the two-component (ZORA) and the four-component (BDF) density functional results is quite good even for the E114 compounds. However, this requires a careful construction of the Gaussian basis sets used in the ZORA calculations.
AB - Three independent relativistic approaches, four-component density functional theory (4c-DFT), two-component DFT-ZORA(MP) (Zeroth order regular approximation with model potentials) and two-component ECP-CCSD(T) (Effective core potentials, coupled-cluster theory with singles, doubles and perturbative triples), have been employed by three independent groups to calculate the bond lengths, binding energies and vibrational frequencies for the eka-lead (E114) compounds E114X (X = H, F, Cl, Br, I, O, O2) and the E114 dimer. For calibration, we also report results for homologous lead compounds. The dipole moments and dipole moment derivatives for the diatomic molecules are presented as well. The bonds in E114 compounds are considerably weaker than those of lead due to much larger relativistic (spin-orbit) effects It is predicted that E11402 is thermodynamically unstable with respect to the decomposition into E114 + O2, in contrast to PbO2 → Pb + O2. Both 2PbO2 → 2PbO + O2 and 2E114O2 → 2E114O + O2 are thermodynamically unstable. The agreement between the two-component (ZORA) and the four-component (BDF) density functional results is quite good even for the E114 compounds. However, this requires a careful construction of the Gaussian basis sets used in the ZORA calculations.
UR - http://www.scopus.com/inward/record.url?scp=0000679026&partnerID=8YFLogxK
U2 - 10.1016/s0065-3276(05)39019-8
DO - 10.1016/s0065-3276(05)39019-8
M3 - Review article
AN - SCOPUS:0000679026
SN - 0065-3276
VL - 39
SP - 325
EP - 355
JO - Advances in Quantum Chemistry
JF - Advances in Quantum Chemistry
IS - 1
ER -