A quantum Monte Carlo and density functional theory study of the electronic structure of peroxynitrite anion

Abstract

Single point calculations of the ground state electronic structure of peroxynitrite anion have been performed at the optimized cis geometry using the restricted Hartree–Fock (RHF), Møller Plesset second order perturbation theory (MP2), generalized gradient approximation density functional theory (GGA DFT) in the B3LYP form and two quantum Monte Carlo (QMC) methods, variational Monte Carlo (VMC) and diffusion Monte Carlo (DMC). These calculations reveal differences in atomization energies estimated by B3LYP (287.03 kcal/mol), MP2 (290.84 kcal/mol), and DMC, 307.4(1.9) kcal/mol, as compared to experiment, 313(1) kcal/mol. The error associated with MP2 and B3LYP methods is attributed largely to differential recovery of correlation energies for neutral nitrogen and oxygen atoms relative to the oxygen and peroxynitrite anions. In addition, basis set studies were carried out to determine potential sources of error in MP2 and B3LYP valence energy values. Our studies indicate that MP2 and B3LYP valence energies are strongly dependent on the presence of diffuse functions for the negative ions O− and ONOO−.