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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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Espeau, Philippe
Unité de Technologies Chimiques et Biologiques pour la Santé
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Publications (5/5 displayed)
- 2017Determination of the glass transition temperature of difficult samples by Flash DSC
- 2016Crystal structure determination and thermal behavior upon melting of p-synephrinecitations
- 2013Crystallographic and Pressure-Temperature State Diagram Approach for the Phase Behavior and Polymorphism Study of Glutaric Acidcitations
- 2011Physicochemical Stability of Solid Dispersions of Enantiomeric or Racemic Ibuprofen in Stearic Acidcitations
- 2011Solid-State Characterization of Enantiomeric and Racemic Hydrated and Anhydrous Zinc-Pidolate Complexescitations
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article
Solid-State Characterization of Enantiomeric and Racemic Hydrated and Anhydrous Zinc-Pidolate Complexes
Abstract
Zn(II) L- and DL-pidolates diaqua complexes dehydrate at around 407 K, leading to amorphous anhydrous complexes. Only amorphous anhydrous Zn(II) L-pidolate was found to crystallize on heating into a crystalline anhydrous phase whose crystal structure was solved from a high-resolution X-ray powder diffraction pattern. Orthorhombic anhydrous Zn(II) L-pidolate exhibits a structure in which (4 + 2)-coordinated Zn atoms (with four usual and two additional Zn-O distances of 2.53 and 2.69 Å) and L-pidolate ligands alternate so as to form a three-dimensional polymerized network. Room-temperature rehydration processes under saturating water vapor for amorphous and crystalline anhydrous complexes were found to be different from each other, although they all led back to crystalline diaqua complexes whose relative stabilities were inferred from measurements of their solubilities in water.