High level of ab initio and density functional theory computational study of structural and energetic properties of tetrafluorhydrazine rotamers

Abstract

The HF, MP2, MP3, MP4, and QCISD ab initio methods were compared with local, hybrid, and gradient-corrected density functional theory (DFT) methods for computing structures and energies of N2F4 rotamers. In all DFT calculations 6-311+G(2d) basis set was used. The generated structures energies of trans- and gauche-N 2F 4 rotamers, and their dissociation energies to nitrogen difluoride were compared with experimental data. Suitable hybrid and gradient-corrected DFT methods for determining structures and energies for these and similar molecular systems were discussed.