EPR Study of Electronic Structure of [CoF6]3−and B18N18 Nano Ring Field Effects on Octahedral Complex
Tóm tắt
Density functional theory calculations (DFT), as well as hybrid methods (B3LYP) for B18N18-[CoF6]3− complex have been carried out to study the non-bonded interaction. The geometry of the B18N18 has been optimized at B3LYP method with EPR-II basis set and geometry of the [CoF6]3− have been optimized at B3LYP method with Def2-TZVP basis set and Stuttgart RSC 1997 Effective Core Potential. The electromagnetic interactions of the [CoF6]3− molecule embedded in the B18N18 Nano ring have been investigated at B3LYP and total atomic charges, spin densities, dipole moment and isotropic Fermi coupling constants parameters in different loops and bonds of the B18N18-[CoF6]3− system have been calculated. Also NBO analysis such as electronic delocalization between donor and acceptor bonds has been studied by DFT method. Then we have been investigated the lowest unoccupied molecular orbital (LUMO) and the highest occupied molecular orbital (HOMO) for the lowest energy have been derived to estimate the structural stability of the B18N18-[CoF6]3− system, and the coefficients of s, p and d orbitals of Co-F bonds involved in B18N18-[CoF6]3−.Thus, hybridization of Co and F atoms can be distinguished based on these NBO data. The Gaussian quantum chemistry package is used for all calculations.
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