Coordination Chemistry of Violurate Complexes

Summary

Violurate complexes arise from the deprotonation of violuric acid, a pyrimidine tetrone oxime, which functions as a versatile chelating ligand. The conjugate violurate anion exhibits multiple donor sites, including carbonyl and oxime oxygen atoms, enabling mono-, bi- and polynuclear assemblies with a broad range of transition metals. Coordination modes span monodentate to tridentate binding, often giving rise to square-planar, tetrahedral or distorted octahedral geometries. The inherent planarity of the ligand backbone facilitates π-stacking and hydrogen-bonded networks that stabilise solid-state structures and promote extended frameworks. Recent efforts have explored how subtle variations in pH, solvent and counter-ions tune the coordination environment, modulating redox properties, magnetic interactions and photophysical responses. Applications under investigation include catalytic oxidation, redox-switchable materials and luminescent sensors, reflecting the global interest in designing multifunctional metal–organic architectures derived from simple oxime templates.

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Coordination Chemistry of Violurate Complexes publication trend

The graph below shows the total number of articles in coordination chemistry of violurate complexes across all publications each year (not limited to Nature Index journals).

Technical terms

Violuric acid: Organic pyrimidine tetrone oxime that, upon deprotonation, acts as a multidentate ligand.

Ligand: An atom or molecule that donates one or more electron pairs to a central metal ion to form a coordination complex.

Coordination geometry: The spatial arrangement of ligands around a central metal ion.

Bidentate ligand: A ligand that binds to a metal centre through two donor atoms.

Octahedral geometry: A coordination geometry in which six ligands occupy the vertices of an octahedron around the central metal.

References

  1. Violuric acid monohydrate: a definitive redetermination at 150 K. Acta Crystallographica Section E: Crystallographic Communications (2005).
  2. Hydrogen-bonding and carbon­yl–carbonyl inter­actions in violuric acid methanol solvate. Acta Crystallographica Section C: Structural Chemistry (2005).

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