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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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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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Kočí, Jan | Prague |
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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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Boss, S. R.
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article
Hydride encapsulation by a molecular main-group-metal cluster: Single-crystal neutron diffraction structure of [{Ph(2-C5H4N}(6)HLi8](+)
Abstract
The new very-intense vertical-axis Laue diffractometer (VIVALDI) at the Institut Laue-Langevin has been used to probe the single-crystal structure of [(t-Bu2AlMe2)(2)Li](-)[{Ph(2-C5H4N)N}(6)HLi8](+), with data proving that the molecular main-group-metal cluster cation component incorporates interstitial hydride. Variations in nitrogen coordination mode and distortion of the metal core are in accord with octahedral hydride coordination (H-Li = 1.92(2), 2.04(2), 2.07(2) Angstrom), two metal centers being nonbonding with respect to hydride ((HLi)-Li-... = 2.86(2) Angstrom).