NMR parameters in column 13 metal fluoride compounds (AlF3, GaF3, InF3 and TlF) from first principle calculations - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Solid State Nuclear Magnetic Resonance Année : 2014

NMR parameters in column 13 metal fluoride compounds (AlF3, GaF3, InF3 and TlF) from first principle calculations

Résumé

The relationship between the experimental 19F isotropic chemical shift and the 19F isotropic shielding calculated using the gauge including projector augmented-wave (GIPAW) method with PBE functional is investigated in the case of GaF3, InF3, TlF and several AlF3 polymorphs. It is shown that the linear correlation between experimental and DFT-PBE calculated values previously established on alkali, alkaline earth and rare earth of column 3 basic fluorides (Sadoc et al., Phys. Chem. Chem. Phys. 13 (2011) 18539–18550) remains valid in the case of column 13 metal fluorides, indicating that it allows predicting 19F solid state NMR spectra of a broad range of crystalline fluorides with a relatively good accuracy. For the isostructural α-AlF3, GaF3 and InF3 phases, PBE-DFT geometry optimization leads to noticeably overbended M–F–M bond angles and underestimated 27Al, 71Ga and 115In calculated quadrupolar coupling constants. For the studied compounds, whose structures are built of corner shared MF6 octahedra, it is shown that the electric field gradient (EFG) tensor at the cationic sites is not related to distortions of the octahedral units, in contrast to what previously observed for isolated AlF6 octahedra in fluoroaluminates.

Domaines

Matériaux
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Dates et versions

hal-01085225 , version 1 (20-11-2014)

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Citer

Aymeric Sadoc, Mamata Biswal, Monique Body, Christophe Legein, Florent Boucher, et al.. NMR parameters in column 13 metal fluoride compounds (AlF3, GaF3, InF3 and TlF) from first principle calculations. Solid State Nuclear Magnetic Resonance, 2014, 59-60, pp.1-7. ⟨10.1016/j.ssnmr.2014.01.001⟩. ⟨hal-01085225⟩
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