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Chemically induced symmetry breaking in the crystal structure of guanidinium uranyl sulfate

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Gurzhiy V. V. et al. Chemically induced symmetry breaking in the crystal structure of guanidinium uranyl sulfate // Mendeleev Communications. 2019. Vol. 29. No. 4. pp. 408-410.
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Gurzhiy V. V., Tyumentseva O. S., Belova O. V., Krivovichev S. V. Chemically induced symmetry breaking in the crystal structure of guanidinium uranyl sulfate // Mendeleev Communications. 2019. Vol. 29. No. 4. pp. 408-410.
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TY - JOUR
DO - 10.1016/j.mencom.2019.07.017
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.07.017
TI - Chemically induced symmetry breaking in the crystal structure of guanidinium uranyl sulfate
T2 - Mendeleev Communications
AU - Gurzhiy, Vladislav V
AU - Tyumentseva, Olga Sergeevna
AU - Belova, Olga V
AU - Krivovichev, Sergei Vladimirovich
PY - 2019
DA - 2019/07/01
PB - Mendeleev Communications
SP - 408-410
IS - 4
VL - 29
ER -
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@article{2019_Gurzhiy,
author = {Vladislav V Gurzhiy and Olga Sergeevna Tyumentseva and Olga V Belova and Sergei Vladimirovich Krivovichev},
title = {Chemically induced symmetry breaking in the crystal structure of guanidinium uranyl sulfate},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.07.017},
number = {4},
pages = {408--410},
doi = {10.1016/j.mencom.2019.07.017}
}
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Gurzhiy, Vladislav V., et al. “Chemically induced symmetry breaking in the crystal structure of guanidinium uranyl sulfate.” Mendeleev Communications, vol. 29, no. 4, Jul. 2019, pp. 408-410. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.07.017.

Abstract

The novel uranyl sulfate templated by protonated guanidinium molecules was obtained from aqueous solution under ambient conditions. Its crystal structure was determined by the single crystal X-ray diffraction analysis and evaluated using a topological approach and information-based complexity calculations. The Se-for-S substitution resulted in a symmetry breaking (from orthorhombic in sulfate to monoclinic in selenate) due to the rearrangement of oxygen atoms, so the resulting symmetry is a consequence of interplay between the template-substructure interactions and size of the tetrahedral cation.

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