Publication | Open Access
Novel biologically active polyurea derivatives and its TiO<sub>2</sub>-doped nanocomposites
18
Citations
57
References
2020
Year
A new series of polyurea derivatives and its nanocomposites were synthesised by the solution polycondensation method through the interaction between 4(2-aminothiazol-4-ylbenzylidene)-4-(tert-butyl) cyclohexanone and diisocyanate compound in pyridine. The PU<sub>1-3</sub> structure was confirmed using Fourier transform-infrared (FTIR) spectroscopy and characterised by solubility, viscometry, gel permeation chromatography (GPC), and X-ray diffraction (XRD) analysis. In addition, PU<sub>1-3</sub> was evaluated by TGA. Polyurea-TiO<sub>2</sub>nanocomposites were synthesised using the same technique as that of PU<sub>1-3</sub> by adding TiO<sub>2</sub> as a nanofiller. The thermal properties of PU<sub>2</sub>TiO<sub>2</sub>a-d were evaluated by TGA. Moreover, the morphological properties of a selected sample were examined by SEM and TEM. In addition, PU<sub>1-3</sub> and PU<sub>2</sub>TiO<sub>2</sub>a-d were examined for antimicrobial activity against certain bacteria and fungi. The PU<sub>1-3</sub> showed antibacterial activity against some of the tested bacteria and fungi, as did PU<sub>2</sub>TiO<sub>2</sub>a-d, which increased with the increase in TiO<sub>2</sub> content. Furthermore, molecular docking studies were displayed against all PU<sub>1-3</sub> derivatives against two types of proteins. The results show that the increase in the strength of π-H interactions and H-donors contributed to improved binding of PU2 compared to PU1 andPU<sub>3.</sub> The docking of 1KZN against the tested polymers suggests an increase in the docking score of PU<sub>2,</sub> then PU<sub>1</sub>, and PU<sub>3</sub>, which is in agreement with the antibacterial study.
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