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Hans Jørgen Jakobsen

Direct observation of 17O-185/187Re 1J-coupling in perrhenates by solid-state 17O VT MAS NMR: Temperature and self-decoupling effects

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  • Hans Jørgen Jakobsen
  • Henrik K. Bildsøe, Danmark
  • M. Brorson, Haldor Topsøe A/S, Danmark
  • Z. Gan, National High Magnetic Field Laboratory, USA
  • I. Hung, National High Magnetic Field Laboratory, USA
O MAS NMR spectra recorded at 14.1 T and room temperature (RT) for O-enriched samples of the two perrhenates, KReO and NHReO, exhibit very similar overall appearances of the manifold of spinning sidebands (ssbs) for the satellite transitions (STs) and the central transition (CT). These overall appearances of the spectra are easily simulated in terms of the usual quadrupole coupling and chemical shift interaction parameters. However, a detailed inspection of the line shapes for the individual ssbs of the STs and, in particular, for the CT in the spectrum of KReO reveals line-shape features, which to our knowledge have not before been observed experimentally in 1D MAS NMR spectra for any quadrupolar nucleus, nor emerged from simulations for any combination of second-order quadrupolar interaction and chemical shift anisotropy. In contrast, such line-shape features are not observed for the corresponding ssbs (STs and CT) in the 14.1 T RT O MAS NMR spectrum of NHReO. Considering the additional interaction of a combination of residual heteronuclear O-Re dipolar and scalar J coupling between this spin pair of two quadrupolar nuclei, spectral simulations for KReO show that these interactions are able to account for the observed line shapes, although the expected J( O-Re) six-line spin-spin splittings are not resolved. Low-temperature, high-field (21.1 T) O VT MAS NMR spectra of both KReO and NHReO show that full resolution into six-line multiplets for the centerbands are achieved at -90 °C and -138 °C, respectively. This allows determination of J(O-Re) = -268 Hz and -278 Hz for KReO and NHReO, respectively, i.e., an isotropic J coupling and its sign between two quadrupolar nuclei, observed for the first time directly from solid-state one-pulse 1D MAS NMR spectra, without resort to additional 1D or 2D experiments. Determination of T(Re) spin-lattice relaxation times, observed indirectly through a 2D O EXSY experiment for NH ReO at several low temperatures, show that the dynamics observed for the ReO4- anion in the O VT MAS NMR spectra at low temperatures are caused by self-decoupling of J(O- Re). The J(O-Re) values determined here for ReO4- from solid-state O MAS NMR, along with literature J(O-M) values for oxoanions (M being a quadrupolar nucleus) obtained from liquid-state NMR, have allowed correlations to be established between the reduced coupling constant K( O-M) = 2π J(O-M)/(γ γ ℏ) and the atomic number of M.
OriginalsprogEngelsk
TidsskriftJournal of Magnetic Resonance
Vol/bind230
Sider (fra-til)98-110
Antal sider13
ISSN1090-7807
DOI
StatusUdgivet - 2013

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