In this paper, the trans influence of boryl ligands, together with that of other ligands commonly believed to have a strong trans influence, has been investigated theoretically via density functional theory (DFT) calculations on a series of square-planar platinum(II) complexes of the form trans-[PtL(Cl) (PMe3)(2)].
B3LYP density functional theory calculations have been carried out to examine the structural and energetic aspects of β-hydrogen elimination in several metallacyclic complexes of ruthenium and platinum. Factors affecting barriers of the elimination reactions have been examined. It was found that favorable structural arrangements, in which the transferring β-hydrogen is in close proximity to the metal center, for β-hydrogen elimination exist in certain ring conformations of metallacyclic complexes.
The η2-dihydrogen complex [TpRu(L2)(H2)]+ (L2 = dppm, dppp, or (PPh3)2) prepared in situ by protonation of the hydride precursor reacts with O2 to yield the paramagnetic RuIII-superoxo complex [TpRuIII(L2)(O2)]+, in which antiferromagnetic coupling between the RuIII ion (d5, S = 1/2) and the coordinated superoxide radical (S = 1/2) does not seem to be present.
Plausible mechanisms for reactions of the ionized O-3 with N-2 are studied by DFT and electron correlation methods. Calculations show that formation of the primary products O-2(+) + N2O and N2O+ + O-2 arises from an intermediate [O-2...ON2](+) in the ground state and its charge-transfer excited state, respectively. New routes to NO2 + NO+ through an intermediate [ON2...O-2](+) and to [ON...NO](+) + O-2 via the reactions of O-3(+) with N2O are proposed.
Density functional calculations for copper clusters Cu and their monocarbonyls CunCO (n less than or equal to 13) have been performed using the relativistic ECP plus DZ basis set augmented by an f polarization function for copper atom. Equilibrium geometries, harmonic frequencies, and static mean polarizabilities of Cu-n and CunCO are determined. The feature of CO adsorption on the copper cluster and the effect of CO adsorption on stability and polarizability of the cluster are investigated.
Density functional theory with the B3LYP functional is used to calculate the equilibrium geometries and harmonic vibrational frequencies of nitryl halogenides XNO2 and XONO (X = F, Cl, Br, I). Stabilities and isomerizations of these isomers are investigated. Dissociation energies of the X-N bond in XNO2 are predicted at the B3LYP/6-311G* and QCISD(T)/ce-pvTZ levels. The electronic transition energies of the most stable XNO2 species have been estimated by time-dependent B3LYP calculations.
Welcome Yulei Hao to join our group!
Welcome Jingjing Wu to join our group!