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Crystal structure of catena -poly[[methanoldioxidouranium(VI)]-μ-2-[5-(2-oxidophen-yl)-1 H -1,2,4-triazol-3-yl]acetato-κ 2 O : O '].

Oleksandr V VashchenkoDmytro M KhomenkoRoman O DoroshchukAlexandru-Constantin StoicaOlga Yu VassilyevaRostislav D Lampeka
Published in: Acta crystallographica. Section E, Crystallographic communications (2024)
In the title complex, [U(C 10 H 7 N 3 O 3 )O 2 (CH 3 OH)] n , the U VI cation has a typical penta-gonal-bipyramidal environment with the equatorial plane defined by one N and two O atoms of one doubly deprotonated 2-[5-(2-hy-droxy-phen-yl)-1 H -1,2,4-triazol-3-yl]acetic acid ligand, a carboxyl-ate O atom of the symmetry-related ligand and the O atom of the methanol mol-ecule [U-N/O eq 2.256 (4)-2.504 (5) Å]. The axial positions are occupied by two oxide O atoms. The equatorial atoms are almost coplanar, with the largest deviation from the mean plane being 0.121 Å for one of the O atoms. The benzene and triazole rings of the tetra-dentate chelating-bridging ligand are twisted by approximately 21.6 (2)° with respect to each other. The carboxyl-ate group of the ligand bridges two uranyl cations, forming a neutral zigzag chain reinforced by a strong O-H⋯O hydrogen bond. In the crystal, adjacent chains are linked into two-dimensional sheets parallel to the ac plane by C/N-H⋯N/O hydrogen bonding and π-π inter-actions. Further weak C-H⋯O contacts consolidate the three-dimensional supra-molecular architecture. In the solid state, the compound shows a broad medium intensity LMCT transition centred around 463 nm, which is responsible for its red colour.
Keyphrases
  • solid state
  • ionic liquid
  • molecular dynamics
  • photodynamic therapy
  • high intensity
  • single molecule
  • room temperature
  • drug induced