Hexaaquazinc(II) dinitrate bis[5-(pyridinium-3-yl)tetrazol-1-ide]
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Archivos
Fecha
2018
Profesor/a Guía
Facultad/escuela
Idioma
en
Título de la revista
ISSN de la revista
Título del volumen
Editor
International Union of Crystallography
Nombre de Curso
Licencia CC
Licencia CC
Resumen
Hexaaquazinc(II) dinitrate 5-(pyridinium-3-yl)tetrazol-1-ide, [Zn(H2 O)6](NO 3)2 ·2C6H5 N 5, crystallizes in the space group P. The asymmetric unit contains one zwitterionic 5-(pyridinium-3-yl)tetrazol-1-ide molecule, one NO3-anion and one half of a [Zn(H2 O)6]2+ cation (symmetry). The pyridinium and tetrazolide rings in the zwitterion are nearly coplanar, with a dihedral angle of 5.4 (2)°. Several O-H..N and N-H..O hydrogen-bonding interactions exist between the [Zn(H2 O)6]2+ cation and the N atoms of the tetrazolide ring, and between the nitrate anions and the N-H groups of the pyridinium ring, respectively, giving rise to a three-dimensional network. The 5-(pyridinium-3-yl)tetrazol-1-ide molecules show parallel-displaced π-π stacking interactions; the centroid-centroid distance between adjacent tetrazolide rings is 3.6298 (6) Å and that between the pyridinium and tetrazolide rings is 3.6120 (5) Å. © 2018 Chi-Duran et al.
Notas
Indexación Scopus
Palabras clave
1H-Tetrazole, Coordination Polymer, Metal-Organic Frameworks, Crystal stryucture, Hexaaquazinc(II) complex, Hydrogen-bonding, Pyridin-3-yltetrazole, π-π stacking
Citación
Acta Crystallographica Section E: Crystallographic Communications Volume 74, Pages 1231 - 1234 2018
DOI
10.1107/S205698901801112X