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- W3041786019 abstract "In solution-state and solid-state MAS (Magic Angle Spinning) NMR (Nuclear Magnetic Resonance) spectroscopy, a comprehensive product operator formalism applicable to general two-spin 1/2 systems, including strongly-coupled systems, is proposed. The formalism employs standard product operators, based on the orthogonal coordinate system, easily evaluating the effects of RF (Radio Frequency) pulse sequences. Solid-state anisotropic interactions modulated by MAS are treated in the perturbation theory, yielding striking solid-state effects, whereas the absence of those interactions leads to solution-state cases with strong couplings. Solid-state MAS INADEQUATE spectra are found to give rise to auto-correlation signals even for the spin pairs possessing an identical isotropic chemical shift. In solution-state and solid-state MAS NMR spectroscopy, a comprehensive product operator formalism applicable to two-spin systems, involving strong couplings, is proposed. MAS INADEQUATE yields auto-correlation signals for the spin pairs possessing an identical isotropic chemical shift: The above S(τ) determining their intensities, calculated with various chemical-shift differences δ (Hz), demonstrates that S(τ) does not vanish even for δ = 0." @default.
- W3041786019 created "2020-07-16" @default.
- W3041786019 creator A5091154932 @default.
- W3041786019 date "2020-12-15" @default.
- W3041786019 modified "2023-09-27" @default.
- W3041786019 title "A Theoretical Study on a Novel Cartesian Product Operator Formalism Applicable to Strongly-Coupled Two-Spin 1/2 Systems in Solution-State and Solid-State MAS NMR Spectroscopy" @default.
- W3041786019 doi "https://doi.org/10.1246/bcsj.20200072" @default.
- W3041786019 hasPublicationYear "2020" @default.
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