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https://open.uns.ac.rs/handle/123456789/20011
Nаziv: | Theoretical Studies on the Structure and Various Physico-Chemical and Biological Properties of a Terphenyl Derivative with Immense Anti-Protozoan Activity | Аutоri: | Mary Y. Sheena Mary Y. Shyma Thomas Renjith Narayana B. Samshuddin S. Sarojini Baladka K. Armaković Stevan Armaković Sanja Pillai Girinath G. |
Dаtum izdаvаnjа: | 2019 | Čаsоpis: | Polycyclic Aromatic Compounds | Sažetak: | © 2019, © 2019 Taylor & Francis Group, LLC. Theoretical calculations at the B3LYP/CC-pVDZ level were used to find the IR, Raman, VCD, and various molecular properties of a terphenyl derivative. Experimental and theoretical spectra agree within their respective limits. Partial density of states shows which parts of the molecules have the most important contribution to the FMO. Fluorine, sulfur, oxygen, and nitrogen atoms have practically insignificant contribution to the HOMO. Time dependent DFT calculations were used to study excitations, while natural transition orbitals were used to study the charge transfer in the strongest excitation. The experimentally observed FTIR modes are compared with calculated wavenumbers. Natural bond orbital analysis gives the idea about stability of molecules. MD simulations are used for calculating solubility parameters. Autoxidation and bond dissociation studies indicate stability of the compound. The docked ligands form secure complexes with the receptor methionyl-tRNA synthetase which indicates new anti-protozoan drugs. | URI: | https://open.uns.ac.rs/handle/123456789/20011 | ISSN: | 1040-6638 | DOI: | 10.1080/10406638.2019.1624974 |
Nаlаzi sе u kоlеkciјаmа: | PMF Publikacije/Publications |
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