Home > Research > Publications & Outputs > Multinuclear solid-state NMR investigation of H...

Electronic data

  • Submission confirmation Revision2 - Inorg Chem

    Rights statement: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © 2016 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.6b00345

    Accepted author manuscript, 2.73 MB, PDF document

    Available under license: CC BY-NC: Creative Commons Attribution-NonCommercial 4.0 International License

Links

Text available via DOI:

View graph of relations

Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published

Standard

Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds. / Deblonde, Gauthier J.-P.; Coelho-Diogo, Cristina; Chagnes, Alexandre et al.
In: Inorganic Chemistry, Vol. 55, No. 12, 20.06.2016, p. 5946-5956.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Deblonde, GJ-P, Coelho-Diogo, C, Chagnes, A, Cote, G, Smith, ME, Hanna, JV, Iuga, D & Bonhomme, C 2016, 'Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds', Inorganic Chemistry, vol. 55, no. 12, pp. 5946-5956. https://doi.org/10.1021/acs.inorgchem.6b00345

APA

Deblonde, G. J.-P., Coelho-Diogo, C., Chagnes, A., Cote, G., Smith, M. E., Hanna, J. V., Iuga, D., & Bonhomme, C. (2016). Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds. Inorganic Chemistry, 55(12), 5946-5956. https://doi.org/10.1021/acs.inorgchem.6b00345

Vancouver

Deblonde GJP, Coelho-Diogo C, Chagnes A, Cote G, Smith ME, Hanna JV et al. Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds. Inorganic Chemistry. 2016 Jun 20;55(12):5946-5956. Epub 2016 Jun 1. doi: 10.1021/acs.inorgchem.6b00345

Author

Deblonde, Gauthier J.-P. ; Coelho-Diogo, Cristina ; Chagnes, Alexandre et al. / Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds. In: Inorganic Chemistry. 2016 ; Vol. 55, No. 12. pp. 5946-5956.

Bibtex

@article{fca3011f03d340a9b47c3870e02b04f0,
title = "Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds",
abstract = "This work determines the potential of solid-state NMR techniques to probe proton, alkali, and niobium environments in Lindqvist salts. Na7HNb6O19·15H2O (1), K8Nb6O19·16H2O (2), and Na8Ta6O19·24.5H2O (3) have been studied by solid-state static and magic angle spinning (MAS) NMR at high and ultrahigh magnetic field (16.4 and 19.9 T). 1H MAS NMR was found to be a convenient and straightforward tool to discriminate between protonated and nonprotonated clusters AxH8–xM6O19·nH2O (A = alkali ion; M = Nb, Ta). 93Nb MAS NMR studies at different fields and MAS rotation frequencies have been performed on 1. For the first time, the contributions of NbO5Oμ2H sites were clearly distinguished from those assigned to NbO6 sites in the hexaniobate cluster. The strong broadening of the resonances obtained under MAS was interpreted by combining chemical shift anisotropy (CSA) with quadrupolar effects and by using extensive fitting of the line shapes. In order to obtain the highest accuracy for all NMR parameters (CSA and quadrupolar), 93Nb WURST QCPMG spectra in the static mode were recorded at 16.4 T for sample 1. The 93Nb NMR spectra were interpreted in connection with the XRD data available in the literature (i.e., fractional occupancies of the NbO5Oμ2H sites). 1D 23Na MAS and 2D 23Na 3QMAS NMR studies of 1 revealed several distinct sodium sites. The multiplicity of the sites was again compared to structural details previously obtained by single-crystal X-ray diffraction (XRD) studies. The 23Na MAS NMR study of 3 confirmed the presence of a much larger distribution of sodium sites in accordance with the 10 sodium sites predicted by XRD. Finally, the effect of Nb/Ta substitutions in 1 was also probed by multinuclear MAS NMR (1H, 23Na, and 93Nb).",
author = "Deblonde, {Gauthier J.-P.} and Cristina Coelho-Diogo and Alexandre Chagnes and G{\'e}rard Cote and Smith, {Mark Edmund} and Hanna, {John V.} and Dinu Iuga and Christian Bonhomme",
note = "This document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright {\textcopyright} 2016 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.6b00345",
year = "2016",
month = jun,
day = "20",
doi = "10.1021/acs.inorgchem.6b00345",
language = "English",
volume = "55",
pages = "5946--5956",
journal = "Inorganic Chemistry",
issn = "0020-1669",
publisher = "American Chemical Society",
number = "12",

}

RIS

TY - JOUR

T1 - Multinuclear solid-state NMR investigation of Hexaniobate and Hexatantalate compounds

AU - Deblonde, Gauthier J.-P.

AU - Coelho-Diogo, Cristina

AU - Chagnes, Alexandre

AU - Cote, Gérard

AU - Smith, Mark Edmund

AU - Hanna, John V.

AU - Iuga, Dinu

AU - Bonhomme, Christian

N1 - This document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © 2016 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/acs.inorgchem.6b00345

PY - 2016/6/20

Y1 - 2016/6/20

N2 - This work determines the potential of solid-state NMR techniques to probe proton, alkali, and niobium environments in Lindqvist salts. Na7HNb6O19·15H2O (1), K8Nb6O19·16H2O (2), and Na8Ta6O19·24.5H2O (3) have been studied by solid-state static and magic angle spinning (MAS) NMR at high and ultrahigh magnetic field (16.4 and 19.9 T). 1H MAS NMR was found to be a convenient and straightforward tool to discriminate between protonated and nonprotonated clusters AxH8–xM6O19·nH2O (A = alkali ion; M = Nb, Ta). 93Nb MAS NMR studies at different fields and MAS rotation frequencies have been performed on 1. For the first time, the contributions of NbO5Oμ2H sites were clearly distinguished from those assigned to NbO6 sites in the hexaniobate cluster. The strong broadening of the resonances obtained under MAS was interpreted by combining chemical shift anisotropy (CSA) with quadrupolar effects and by using extensive fitting of the line shapes. In order to obtain the highest accuracy for all NMR parameters (CSA and quadrupolar), 93Nb WURST QCPMG spectra in the static mode were recorded at 16.4 T for sample 1. The 93Nb NMR spectra were interpreted in connection with the XRD data available in the literature (i.e., fractional occupancies of the NbO5Oμ2H sites). 1D 23Na MAS and 2D 23Na 3QMAS NMR studies of 1 revealed several distinct sodium sites. The multiplicity of the sites was again compared to structural details previously obtained by single-crystal X-ray diffraction (XRD) studies. The 23Na MAS NMR study of 3 confirmed the presence of a much larger distribution of sodium sites in accordance with the 10 sodium sites predicted by XRD. Finally, the effect of Nb/Ta substitutions in 1 was also probed by multinuclear MAS NMR (1H, 23Na, and 93Nb).

AB - This work determines the potential of solid-state NMR techniques to probe proton, alkali, and niobium environments in Lindqvist salts. Na7HNb6O19·15H2O (1), K8Nb6O19·16H2O (2), and Na8Ta6O19·24.5H2O (3) have been studied by solid-state static and magic angle spinning (MAS) NMR at high and ultrahigh magnetic field (16.4 and 19.9 T). 1H MAS NMR was found to be a convenient and straightforward tool to discriminate between protonated and nonprotonated clusters AxH8–xM6O19·nH2O (A = alkali ion; M = Nb, Ta). 93Nb MAS NMR studies at different fields and MAS rotation frequencies have been performed on 1. For the first time, the contributions of NbO5Oμ2H sites were clearly distinguished from those assigned to NbO6 sites in the hexaniobate cluster. The strong broadening of the resonances obtained under MAS was interpreted by combining chemical shift anisotropy (CSA) with quadrupolar effects and by using extensive fitting of the line shapes. In order to obtain the highest accuracy for all NMR parameters (CSA and quadrupolar), 93Nb WURST QCPMG spectra in the static mode were recorded at 16.4 T for sample 1. The 93Nb NMR spectra were interpreted in connection with the XRD data available in the literature (i.e., fractional occupancies of the NbO5Oμ2H sites). 1D 23Na MAS and 2D 23Na 3QMAS NMR studies of 1 revealed several distinct sodium sites. The multiplicity of the sites was again compared to structural details previously obtained by single-crystal X-ray diffraction (XRD) studies. The 23Na MAS NMR study of 3 confirmed the presence of a much larger distribution of sodium sites in accordance with the 10 sodium sites predicted by XRD. Finally, the effect of Nb/Ta substitutions in 1 was also probed by multinuclear MAS NMR (1H, 23Na, and 93Nb).

U2 - 10.1021/acs.inorgchem.6b00345

DO - 10.1021/acs.inorgchem.6b00345

M3 - Journal article

VL - 55

SP - 5946

EP - 5956

JO - Inorganic Chemistry

JF - Inorganic Chemistry

SN - 0020-1669

IS - 12

ER -