Affiliations: [a] Faculty of Pharmacy, University of Sarajevo, Sarajevo, Bosnia and Herzegovina | [b] Cumhuriyet University, Faculty of Science, Department of Chemistry, Sivas, Turkey | [c] NMR Centre, Ru\djer Bošković Institute, Zagreb, Croatia
Correspondence:
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Corresponding author: Ervina Bečić, Faculty of Pharmacy, University of Sarajevo, Zmaja od Bosne 8, 71000 Sarajevo, Bosnia and Herzegovina. E-mail: ervina.becic@ffsa.unsa.ba. ORCID ID: 0000-0001-6371-9504.
Abstract: BACKGROUND: Computational research plays an important role in predicting the chemical and physical properties of biologically active compounds important in future structural modifications to improve or modify biological activity. OBJECTIVE: This research focuses on quantum chemical and spectroscopic investigations properties of synthesized 4-hydroxycoumarin derivatives. METHODS: Quantum chemical calculations were obtained using B3LYP, HF, and M06-2x level methods with the 6-31++G (d,p) basis set. Afterward, IR, 1H, 13C, UV-Visible experimentally parameters were compared with the results obtained using the B3LYP/6-31+G*(d) basis set of the molecules to be able to characterize the structures. RESULTS: Based on the quantum chemical calculations compound with acetamido group on the phenyl ring is the most reactive, and compound with nitro substituent is the least reactive and the the strongest electrophile among tested compounds. With the exception of compounds with dimethylamino group, all other compounds have a pronounced tautomer between OH and C = O group. The calculated and experimental values are in agreement with each other. CONCLUSION: The molecular structure in the ground state of six 3-cinnamoyl 4-hydroxycoumarin derivatives was optimized using density functional theory. The observed and computed values were compared and it can be concluded that the theoretical results were in good linear agreement with the experimental data.
Keywords: Density functional theory (DFT), coumarin derivatives, quantum chemical calculations
