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  • 1.
    Aleksis, Rihards
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Carvalho, José P.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Jaworski, Aleksander
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Pell, Andrew J.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
    Artefact-free broadband 2D NMR for separation of quadrupolar and paramagnetic shift interactions2019Inngår i: Solid State Nuclear Magnetic Resonance, ISSN 0926-2040, E-ISSN 1527-3326, Vol. 101, s. 51-62Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Two new two-dimensional, broadband, solid-state NMR experiments for separating and correlating the quadrupolar and shift interactions of spin I = 1 nuclei in paramagnetic systems are proposed. The new pulse sequences incorporate the short, high-power adiabatic pulses (SHAPs) into the shifting d-echo experiment of Walder et al. [J. Chem. Phys., 142, 014201 (2015)], in two different ways, giving double and quadruple adiabatic shifting d-echo sequences. These new experiments have the advantage over previous methods of both suppressing spectral artefacts due to pulse imperfections, and exhibiting a broader excitation bandwidth. Both experiments are analysed with theoretical calculations and simulations, and are applied experimentally to the H-2 NMR of deuterated CuCl2 center dot 2H(2)O, and two deuterated samples of the ion conductor oxyhydride BaTiO3-xHy prepared using two different methods. For the CuCl2 center dot 2H(2)O sample, both new methods obtain very high-quality spectra from which the parameters describing the shift and quadrupolar interaction tensors, and their relative orientation, were extracted. The two BaTiO3-xHy samples exhibited different local hydride environments with different tensor parameters. The H-2 spectra of these oxyhydrides exhibit inhomogeneous broadening of the H-2 shifts, and so whilst the quadrupolar interaction parameters were easily extracted, the measurement of the shift parameters was more complex. However, effective shift parameters were extracted, which combine the effects of both the paramagnetic shift tensor and the inhomogeneous broadening.

  • 2.
    Eden, Mattias
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi.
    Homonuclear dipolar recoupling of half-integer spin quadrupolar nuclei: techniques and applications2009Inngår i: Solid State Nuclear Magnetic Resonance, ISSN 0926-2040, E-ISSN 1527-3326, Vol. 36, nr 1, s. 1-10Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We review recent advances in solid state NMR methodology for recovering homonuclear dipolar interactions among half-integer quadrupolar spins undergoing sample rotation. Existing dipolar recoupling techniques are contrasted, based on (i) the form of their associated dipolar Hamiltonian, (ii) the different experimental conditions necessitating their realization and (iii) their roles as components in multi-dimensional NMR correlation spectroscopy. Various types of structural information accessible from such solid state NMR experimentation is reviewed. Promises and limitations of methodologies targeting homonuclear dipolar couplings between half-integer spins under high-resolution conditions are discussed, with particular focus on the demands set for structural investigations of crystalline as well as structurally disordered (amorphous) inorganic network materials

  • 3.
    Hedin, Niklas
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi.
    Ng, JBS
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi.
    Stilbs, P
    Spectral Deconvolution of NMR Cross Polarization Data Sets2009Inngår i: Solid State Nuclear Magnetic Resonance, ISSN 0926-2040, E-ISSN 1527-3326, Vol. 35, s. 208-213Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The COmponent-REsolved (CORE) strategy has been employed, for the first time to solid state NMR spectroscopy. CORE was used to extract two time-dependent spectral components in 24 Si-29(H-1) NMR spectra, recorded on a meso-structured silica material under conditions of cross polarization evolution. No prior assumptions were made about the component bandshapes, which were both found to be skewed to higher chemical shifts. For the silica fragments close to protons this skewness could be rationalized by a distribution of the degree of condensation in the silica network; however, for the other component the non-Gaussian shape was unexpected. We expect that the same strategy could be applied to a range of experiments in solid-state NMR spectroscopy, where spectral distributions or kinetic parameters need to be accurately extracted

  • 4.
    Leonova, Ekaterina
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi.
    Grins, Jekabs
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi.
    Shariatgorji, Mohammadreza
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för analytisk kemi.
    Ilag, Leopold L.
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för analytisk kemi.
    Eden, Mattias
    Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi.
    Solid-state NMR investigations of Si-29 and N-15 enriched silicon nitride2009Inngår i: Solid State Nuclear Magnetic Resonance, ISSN 0926-2040, E-ISSN 1527-3326, Vol. 36, nr 1, s. 11-18Artikkel i tidsskrift (Fagfellevurdert)
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