Conformational stability, the spectroscopic (FT-IR and UV), first order hyperpolarizability, NBO analysis, HOMO and LUMO analysis of 6,8-diphenylimidazo[1,2-α]pyrazine molecule by ab initio HF and density functional methods

• Published in: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Vol. 81; no. 1; pp. 339 - 352
• Main Authors: Sıdır, İsa, Sıdır, Yadigar Gülseven, Kayagil, İsmail
• Format: Journal Article
• Language: English
• Published: England Elsevier B.V 15-10-2011
• Subjects: 6,8-Diphenylimidazo[1,2-α]pyrazine; Drug Stability; First order hyperpolarizability; Fluorescence Polarization; FT-IR; Hydrogen Bonding; Imidazoles - chemistry; Imidazoles - pharmacokinetics; Intramolecular charge transfer; Models, Biological; Models, Molecular; Molecular Conformation; Molecular Dynamics Simulation; NBO analysis; Optical Rotation; Pyrazines - chemistry; Pyrazines - pharmacokinetics; Quantum Theory; Spectrophotometry, Ultraviolet - methods; Spectroscopy, Fourier Transform Infrared - methods; Static Electricity; Stereoisomerism; TD-DFT; UV–vis; UV–vis; First order hyperpolarizability; FT-IR; 6,8-Diphenylimidazo[1,2-α]pyrazine; Intramolecular charge transfer; NBO analysis; TD-DFT
• ISSN: 1386-1425; 1873-3557
• DOI: 10.1016/j.saa.2011.06.021

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• Conformation, molecular structure, FT-IR and UV spectra along with first order hyperpolarizability and NBO analysis of 6,8-diphenylimidazo[1,2-α]pyrazine were reported. • Comparison to the experimental results, the calculated vibrational frequencies obtained by DFT method are better than those of HF method.
The conformational analysis of 6,8-diphenylimidazo[1,2-α]pyrazine molecule (abbreviated as 68DIP) was performed by using B3LYP/6-31G(d) level of theory to find the most stable form. Two staggered stable conformers were observed on the torsional potential energy surface. The equilibrium geometry, bonding features and vibrational frequencies of 68DIP have been investigated by using the DFT (B3LYP) and HF methods for the lowest energy conformer. The first order hyperpolarizability (
β
total) of this molecular system and related properties (
β,
μ, 〈
α〉 and Δ
α) are calculated using HF/6-311++G(d,p) and B3LYP/6-311++G(d,p) methods based on the finite-field approach. Stability of the molecule arising from hyperconjugative interactions, charge delocalization and C–H⋯N intramolecular hydrogen-bond-like weak interaction has been analyzed using natural bond orbital (NBO) analysis by using B3LYP/6-311++G(d,p) method. The results show that electron density (ED) in the σ* and π* antibonding orbitals and second order delocalization energies
E
(2) confirm the occurrence of intramolecular charge transfer (ICT) within the molecule. UV–vis spectrum of the compound was recorded and electronic properties, such as HOMO, LUMO energies, excitation energies and wavelength were performed by TD-DFT/B3LYP, CIS and TD-HF methods by using 6-311++G(d,p) basis set. Finally, the calculation results were applied to simulated infrared spectra of the title compound which show good agreement with observed spectra.