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Synthesis and Evaluation of Coupler 4-Aryl-2-Aminothiophene-3- Carbonitrile and its Derivatives as Potential Coupling Component in Dye Synthesis

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dc.contributor.author ISHEGBE, Joyce
dc.date.accessioned 2024-06-17T15:40:00Z
dc.date.available 2024-06-17T15:40:00Z
dc.date.issued 2020
dc.identifier.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 en_US
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/2066
dc.description.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. en_US
dc.description.sponsorship Self en_US
dc.language.iso en en_US
dc.publisher Ariviyal publishing en_US
dc.subject Heterocyclic compounds; ; en_US
dc.subject synthesis; absorption spectroscopy en_US
dc.subject NMR; en_US
dc.subject Gewald reaction en_US
dc.title Synthesis and Evaluation of Coupler 4-Aryl-2-Aminothiophene-3- Carbonitrile and its Derivatives as Potential Coupling Component in Dye Synthesis en_US
dc.type Article en_US


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