Synthesis, characterization, electrochemistry and optical properties of new 1,3,5-trisubstituted ferrocenyl pyrazolines and pyrazoles containing sulfonamide moiety

This article describes the synthesis and characterization of a series of new 3-ferrocenyl-1-(4-sulphamylphenyl)-5-aryl-4,5-dihydro-1H-pyrazolines and the corresponding pyrazole derivatives derived from ferrocenyl chalcones and 4-hydrazino benzenesulfonamide hydrochloride. The compounds were characterized by spectroscopic means and the structure of the new ferrocenyl pyrazoline (3a) was determined by means of X-ray crystallography. The optical properties of these compounds were studied by means of UV/visible absorption spectroscopy and fluorescence spectroscopy (both steady state and time-resolved) in dichloromethane solvent. Electrochemical study revealed that all the compounds exhibited reversible oxidation behavior at 521–543 mV corresponding to ferrocene pyrazolines (3a–l) and 621–645 mV corresponding to ferrocene pyrazoles (4a–j) respectively, as confirmed by the ipc/ipa = 0.92–1.00.

A series of new ferrocenyl 1,3,5-trisubstituted pyrazoline and pyrazole derivatives having sulfonamide moiety have been prepared and characterized by spectral and single crystal X-ray techniques. Cyclic voltammetric and optical properties like absorption, fluorescence emission, decay (lifetime) are also studied.Figure optionsDownload as PowerPoint slideHighlights
► New hybrid compounds containing sulfonamide group on ferrocenyl pyrazoline and pyrazole ring are reported.
► The crystal structure of the ferrocenyl pyrazoline is reported.
► The fluorescence spectra, the quantum yields and lifetime measurement are reported.
► Intermolecular 8-member hydrogen bond ring between two different ferrocenyl pyrazoline moieties.