8 research outputs found
Nonlinear Optical Chromophores with Aggregation Induced Emission Enhancement Based on 2-N,N-Dibutylamino-4-Phenyl Thiazole with FMR Characteristics
Dyeing of Polyester and Nylon with Semi-synthetic Azo Dye by Chemical Modification of Natural Source Areca Nut
Synthesis of heterocyclic monoazo dyes derived from 1H-benzo[g]pyrazolo[3,4-b]quinoline-3-ylamine: their antimicrobial activity and their dyeing performance on various fibers
A study on optimum transition state and tautomeric structures of a bis-heterocyclic monoazo dye
WOS:000351564600001In this study, possible tautomeric forms and ground state conformers of a bis-heterocyclic monoazo dye, 4-[ethyl 4'-methyl-5'-(phenylcarbamoyl) thiophene-3'-carboxylate-2'-ylazo]-3-methyl-1H-pyrazolin-5-one, have been calculated using density functional theory methods with 6-31G (d) basis set. H-1 and C-13 chemical shifts of tautomeric forms have been calculated. Calculated vibrational frequencies and chemical shifts have been compared with corresponding experimental data. Using time-dependent Hartree-Fock method, electronic absorption spectrum of title compound has been calculated and compared with experimental maximum wavelength data. Quantum Synchronous Transit2 approaches have been used for finding the optimum transition state and tautomeric forms of studied molecule. Calculations have shown that the most probable preferential form of this molecule in ground state is hydrazo-keto form. The calculations of frontier molecular orbitals and first order hyperpolarizability have also confirmed this stability.Karamanoglu Mehmetbey University-Scientific Research Projects Coordinating OfficeKaramanoglu Mehmetbey University [07-M-13]This work is supported by Karamanoglu Mehmetbey University-Scientific Research Projects Coordinating Office (Grant No. 07-M-13)