Synthesis, structural characterization and comparison of experimental and theoretical results by DFT level of molecular structure of 4-(4-methoxyphenethyl)-3,5-dimethyl-4H-1,2,4-triazole

• Published in: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Vol. 108; pp. 329 - 337
• Main Authors: Düğdü, Esra, Ünver, Yasemin, Ünlüer, Dilek, Tanak, Hasan, Sancak, Kemal, Köysal, Yavuz, Işık, Şamil
• Format: Journal Article
• Language: English
• Published: England Elsevier B.V 01-05-2013
• Subjects: 1,2,4-Triazole; Crystallography, X-Ray; Density functional theory; FT-IR spectroscopy; Hydrogen Bonding; Magnetic Resonance Spectroscopy; Mass Spectrometry; MEP; Models, Molecular; Molecular Conformation; NLO; Nonlinear Dynamics; Quantum Theory; Spectroscopy, Fourier Transform Infrared; Static Electricity; Thermodynamics; Triazoles - chemical synthesis; Triazoles - chemistry; Vibration; 1,2,4-Triazole; NLO; Density functional theory; MEP; FT-IR spectroscopy
• ISSN: 1386-1425; 1873-3557
• DOI: 10.1016/j.saa.2012.09.060

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► 4-(4-methoxyphenethyl)-3,5-dimethyl-4H-1,2,4-triazole was synthesized. ► The compound has been synthesized and characterized based on elemental analysis, 1H- and 13C-NMR spectra, mass spectra and IR. ► In addition, the compound has been characterized by combination of X-ray crystallography and theoretical methods using the density functional theory (DFT/B3LYP) method with 6-31G(d) basis set, and compared with the experimental findings. ► Theoretical and experimental findings are supported each other and the structure of the compound is put forth clearly.
4-(4-Methoxyphenethyl)-3,5-dimethyl-4H-1,2,4-triazole (3) was synthesized from the reaction of ethyl N′-acetylacetohydrazonate (1) with 2-(4-methoxyphenyl)ethanamine (2). The structure of the title compound 3 has been inferred through IR, 1H/13C NMR, mass spectrometry, elemental analyses and combination of X-ray crystallography and theoretical methods. In addition to the molecular geometry from X-ray determination, the molecular geometry and vibrational frequencies of the title compound 3 in the ground state, were calculated using the density functional method (B3LYP) with the 6-31G(d) basis set. The calculated results show that the optimized geometry can well reproduce the crystal structure and the theoretical vibrational frequencies show good agreement with experimental values. The nonlinear optical properties are also addressed theoretically. The predicted nonlinear optical properties of 3 are greater than ones of urea. In addition, DFT calculations of molecular electrostatic potentials and frontier molecular orbitals of the title compound were carried out at the B3LYP/6-31G(d) level of theory.