A theoretical study of the <sup>77</sup>Se NMR and vibrational spectroscopic properties of Se<i><sub>n</sub></i>S<sub>8</sub><i><sub>n</sub></i> ring molecules
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Abstract
The structures and spectroscopic properties of Se n S 8 n ring molecules have been studied by the use of ab initio molecular orbital techniques and density functional techniques involving Stuttgart relativistic large core effective core potential approximation with double zeta basis sets for valence orbitals augmented by two polarization functions for both sulfur and selenium. Full geometry optimizations have been carried out for all 30 isomers at the Hartree-Fock level of theory. The optimized geometries and the calculated fundamental vibrations and Raman intensities of the Se n S 8 n molecules agree closely with experimental information where available. The nuclear magnetic shielding tensor calculations have been carried out by the Gauge-independent atomic orbital method at the DFT level using Becke's three-parameter hybrid functional with Perdew/Wang 91 correlation. The isotropic shielding tensors correlate well with the observed chemical shift data. The calculated chemical shifts provide a definite assignment of the observed 77 Se NMR spectroscopic data and can be used in the prediction of the chemical shifts of unknown Se n S 8 n ring molecules.Key words: selenium sulfides, ab initio, DFT, effective core potentials, geometry optimization, energetics, fundamental vibrations, 77 Se chemical shifts.
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| Category | Codex | Gemma |
|---|---|---|
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| Open science | 0.001 | 0.000 |
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| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
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