Synthesis, Crystal And Molecular Structure, And Characterization Of 2-((2-Aminopyridin-3-Yl)Methylene)-N-Ethylhydrazinecarbothioamide Using Spectroscopic (H-1 And C-13 Nmr, Ft-Ir, Ft-Raman, Uv-Vis) And Dft Methods And Evaluation Of Its Anticancer Activity

2-((2-aminopyridin-3-yl)methylene)-N-ethylhydrazinecarbothioamide was synthesized. It was characterized by making elemental analysis, assisted by experimental H-1 NMR, C-13 NMR, FT-Raman (400050 cm(-1)), FT-IR (4000-400 cm(-1)), and UV-Vis (200-400 nm) spectra and evaluating its anticancer activity, for human carcinoma cell lines HeLa (cervical), IMR-32 (neuroblastoma) and A549 (lung). Crystal and molecular structure of the molecule was determined by means of X-ray diffractometry, which showed that it belongs to triclinic crystal system, with space group P-1, having two molecules per unit cell (Z = 2). The parameters of the unit cell are a = 6.0960 (6) angstrom, b = 7.4119 (8) angstrom, c = 11.9959 (13) angstrom, alpha = 82.1695 (4)degrees, beta = 81.6407 (4)degrees, gamma = 88.3283 (4)degrees at 100 K. Quantum chemical computations were made using density functional theory (DFT), B3LYP functional and 6-311++G (d, p) basis set in order to determine optimized structure parameters, general valence force field, harmonic vibrational frequencies, potential energy distribution, infrared and Raman intensities, NLO properties, frontier molecular orbital parameters and NBO characteristics. Its time-dependent variant (TD-DFT) was used to calculate the oscillator strengths and absorption maxima (lambda(max)) in DMSO-d(6) as a solvent, of various electronic transitions. There was a good agreement between the theoretical and experimental parameters such as molecular structure parameters, IR, Raman and UV-Vis spectra. The rms error between measured and estimated vibrational frequencies was 6.9 cm(-1). The calculations showed that the molecule under investigation was good for NLO applications, which was supported by NBO analysis. (C) 2019 Elsevier B.V. All rights reserved.