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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Walton, Richard
University of Warwick
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (5/5 displayed)
- 2024Site-directed cation ordering in chabazite-type Al x Ga 1–x PO 4 -34 frameworks revealed by NMR crystallographycitations
- 2024Site-directed cation ordering in chabazite-type AlxGa1–xPO4-34 frameworks revealed by NMR crystallographycitations
- 2021Hydrothermal Synthesis of Iridium-Substituted NaTaO3 Perovskitescitations
- 2017A gel aging effect in the synthesis of open-framework gallium phosphatescitations
- 2013Adsorption of N/S heterocycles in the flexible metal–organic framework MIL-53(FeIII) studied by in situ energy dispersive X-ray diffractioncitations
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article
Site-directed cation ordering in chabazite-type AlxGa1–xPO4-34 frameworks revealed by NMR crystallography
Abstract
We report the first synthesis of the mixed-metal chabazite-type Al<sub>x</sub>Ga<sub>1–x</sub>PO<sub>4</sub>-34(mim) solid solution, containing 1- methylimidazolium, mim, as structure directing agent (SDA), from the parent mixed-metal oxide solid solution, γ-(Al<sub>x</sub>Ga<sub>1– x</sub>)<sub>2</sub>O<sub>3</sub>. This hitherto unreported family of materials exhibits complex disorder, arising from the possible distributions of cations over available sites, the orientation of the SDA and the presence of variable amounts of water, which provides a prototype for understanding structural subtleties in nanoporous materials. In the as-made forms of the phosphate frameworks, there are three crystallographically distinct metal sites: two tetrahedral MO<sub>4</sub> and one octahedral MO<sub>4</sub>F2 (M = Al, Ga). A combination of solid-state NMR spectroscopy and periodic DFT calculations reveal that the octahedral site is preferentially occupied by Al and the tetrahedral sites by Ga, leading to a non-random distribution of cations within the framework. Upon calcination to the Al<sub>x</sub>Ga<sub>1–x</sub>PO<sub>4</sub>-34 framework, all metal sites are tetrahedral and crystallographically equivalent in the average R3 symmetry. The cation distribution was explored by <sup>31</sup>P solid-state NMR spectroscopy, and it is shown that the non-random distribution demonstrated to exist in the as-made materials would be expected to give remarkably similar patterns of peak intensities to a random distribution owing to the change in average symmetry in the calcined materials.