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https://open.uns.ac.rs/handle/123456789/20420
Nаziv: | Exploring the detailed spectroscopic characteristics, chemical and biological activity of two cyanopyrazine-2-carboxamide derivatives using experimental and theoretical tools | Аutоri: | Beegum Shargina Mary Y. Sheena Mary Y. Shyma Thomas Renjith Armaković Stevan Armaković Sanja Zitko Jan Dolezal Martin Van Alsenoy C. |
Dаtum izdаvаnjа: | 2020 | Čаsоpis: | Spectrochimica Acta. Part A: Molecular and Biomolecular Spectroscopy | Sažetak: | © 2019 Elsevier B.V. This article represents the spectroscopic and computational studies of two new pyrazine compounds. In order to establish the structure and functional nature of the compounds, we have employed Fourier transformed infrared (FT-IR) and Raman spectra, nuclear magnetic resonance (NMR) spectra, and ultraviolet (UV) absorptions and have compared them with the simulated computational spectra and found that they are in the agreeable range. Simulated hyperpolarisability values are used to obtain the nonlinear optic (NLO) activity of the compound, to be used in organic electronic materials. The charge transfer and related properties was investigated by the simulation of electronic spectrum with time dependent density functional theory (TD-DFT). Natural transition orbitals (NTO) provides information about which region of the molecules are more involved in the electronic transitions and the charge transfer properties for the lowest energy excitation have been analyzed on the basis of electron density variation. Molecular dynamics simulations provide information about the behavior of the molecule in solutions. Frontier orbital analysis and study of various reactivity descriptors like ALIE and Fukui provided deep knowledge on the reactivity side. Molecular docking has been also performed to investigate the interaction between title molecules and exhibits inhibitory activity against Pseudomonas aeruginosa Enoyl-Acyl carrier protein reductase (Fabl). | URI: | https://open.uns.ac.rs/handle/123456789/20420 | ISSN: | 1386-1425 | DOI: | 10.1016/j.saa.2019.117414 |
Nаlаzi sе u kоlеkciјаmа: | PMF Publikacije/Publications |
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