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Metallation of Ligands with Biological Activity: Synthesis and X‐ray Characterization of the New Sulfathiazolato Complexes of Gold(I) and Silver(I): [(sulfathiazolato)AuPPh<sub>3</sub>] and [Ag(sulfathiazolato)]<sub>2</sub> (sulfathiazole = N<sup>1</sup>‐2‐thiazolyl‐sulfanilamide)
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Citations
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References
2007
Year
Supramolecular AssemblyEngineeringSilver AtomsChemistryCompound 2Inorganic CompoundBiological Inorganic ChemistryHybrid MaterialsBiological ActivityInorganic ChemistryMaterials ScienceMetallic SilverBiochemistrySupramolecular ChemistryCrystallographyCrystal Structure DesignInorganic SynthesisNatural SciencesCoordination ComplexX‐ray CharacterizationMolecular ComplexNew Sulfathiazolato Complexes
Abstract Sulfathiazole reacts with [Ph 3 PAu(CH 3 COO)] in benzene and with Ag(CH 3 COO) in methanol giving [(sulfathiazolato)AuPPh 3 ] ( 1 ) and {[Ag(sulfathiazolato)] 2 } n ( 2 ). While the lattice of 1 contains single molecules with linear N–Au–P bonds, compound 2 performs a polymeric, one‐dimensional assembling of [Ag(sulfathiazolato)] 2 dimers linked through intermolecular Ag···O=S=O interactions along the crystallographic axis b . The silver atoms achieve a tetrahedral configuration through Ag–Ag contacts which measure 2.8427(4) Å, considerably shorter than the normal bonding distance of metallic silver.
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