Abstract
A series of novel 1-ferrocenyl-2-(3-phenyl-1 H-1,2,4-triazol-5-ylthio)ethanone derivatives was synthesized by the reaction of 3-substituted-1 H-1,2,4-triazole-5-thiol and chloroacetyl ferrocene in the presence of sodium hydride and potassium iodide at reflux. The structures of the new compounds were determined by IR and 1H NMR spectroscopy and HRMS. The structure of compound 5c was established by X-ray crystallography. UV–vis absorption and fluorescence spectra were recorded in ethanol and dichloromethane. The results showed that compounds 5a–g display similar absorptions ranging from 300 to 500 nm and maximal emission bands are about 566 nm. The intensity of fluorescence and maximal emission bands are dependent on the groups bonded to triazole rings.
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More From: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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