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Synthesis and characterization of mononuclear and dinuclear zinc-arylazoimidazole complexes. single-crystal x-ray structure of [Zn(HaaiEt)<sub>4</sub>](ClO<sub>4</sub>)<sub>2</sub> and [Zn(HaaiMe) (<b>μ</b>-1,1-N<sub>3</sub>)(N<sub>3</sub>)]<sub>2</sub> [HaaiEt = 1-ethyl-2-(phenylazo)imidazole; HaaiMe = 1-methyl-2-(phenylazo)imidazole]
25
Citations
13
References
2004
Year
Inorganic ChemistrySingle-crystal X-ray StructureEngineeringBiochemistryNatural SciencesCoordination ComplexMolecular ComplexChemistryDimeric Azido-complexesExcess Sodium AzideCrystallographyInorganic SynthesisBiomolecular EngineeringDinuclear Zinc-arylazoimidazole ComplexesInorganic Compound
Zn(ClO4)2·6H2O reacts with 1-alkyl-2-(arylazo)imidazoles [RaaiR′, where R = H (a), Me (b); R′ = Me (1), Et (2)] affording orange–yellow [Zn(RaaiR′)4](ClO4)2 (3,4) complexes. When excess sodium azide is added to the reaction, orange–red, dimeric azido-complexes of the type [Zn(RaaiR′)(N3)(μ-1,1-N3)]2 (5,6) are obtained. Both types of complex were characterized. Structures were confirmed by single-crystal X-ray diffraction studies of [Zn(HaaiEt)4](ClO4)2 (3b) and [Zn(HaaiMe)(N3)(μ-1,1-N3)]2 (5a).
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