Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2066
Title: Synthesis and Evaluation of Coupler 4-Aryl-2-Aminothiophene-3- Carbonitrile and its Derivatives as Potential Coupling Component in Dye Synthesis
Authors: ISHEGBE, Joyce
Keywords: Heterocyclic compounds; ;
synthesis; absorption spectroscopy
NMR;
Gewald reaction
Issue Date: 2020
Publisher: Ariviyal publishing
Citation: Synthesis and Evaluation of Coupler 4-Aryl-2-Aminothiophene-3- Carbonitrile and its Derivatives as Potential Coupling Component in Dye Synthesis J. E. Ishegbe,* K. A. Bello, P. O. Nkeonye and A. A. Kogo
Abstract: Thiophene nucleus has been established as the potential entity in the large growing chemical world of heterocyclic compounds possessing promising coupling characteristics. A series of coupler 4-aryl-2-aminothiophene-3- carbonitrile derivatives were synthesized. The synthetic method involves the reaction of ketones, aldehydes or 1,3- dicarbonyl species with activated nitriles and elemental sulphur in the presence of an amine base. Characterization of these coupling components was carried out by UV-Visible spectroscopy, Fourier-transform infrared spectroscopy (FTIR), gas chromatography–mass spectrometry (GC-MS) and nuclear magnetic resonance spectroscopy (NMR) analysis. The synthesized compounds were purified, characterized and evaluated for spectroscopic properties. They were found to possess good coupling properties as well as high degree of brightness and a colour deepening effect compared to other heterocyclic couplers.
URI: http://localhost:8080/xmlui/handle/123456789/2066
Appears in Collections:Research Articles

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