Şener İ., Şener N., Gür M.Sener, I, Sener, N, Gur, M2023-05-092023-05-092018-12-152018.01.010022-2860https://hdl.handle.net/20.500.12597/12975A series of carbocyclic amines was reacted with 3-aminocrotonitrile to give the 2-arylhydrazone-3-ketiminobutyronitriles 1(a–m). Separately, 2-aminobenzothiazole was treated with hydrazine monohydrate to afford 2-hydrazinobenzothiazole. Then, compounds 1(a–m) were reacted with 2-hydrazinobenzimidazole under reflux in ethanol to give the 1-(1,3-benzothiazol-2-yl)-3-methyl-4-arylazo-5-aminopyrazole compounds 2(a–m). The structures of the synthesized compounds were investigated using FT-IR and 1H NMR spectroscopic methods and elemental analysis. Furthermore, the absorption profiles of the dyes in different solvents and in acidic and basic media were investigated.falseBenzothiazole | Diazo-coupling reaction | Mono-azo dye | SolvatochromismArticle10.1016/j.molstruc.2018.04.05210.1016/j.molstruc.2018.04.0522-s2.0-85054573372WOS:000449132500004121711741872-8014