| Autor: |
Yadav, Bhoopendra, Yadav, Rohit Kumar, Srivastav, Gaurav, Yadav, R. A. |
| Předmět: |
|
| Zdroj: |
Polycyclic Aromatic Compounds; 2024, Vol. 44 Issue 3, p1609-1643, 35p |
| Abstrakt: |
Molecular structural, conformational and spectroscopic investigations on the isorhamnetin molecule have been carried out at the B3LYP/6-311++G(d,p) level. Experimental FTIR, Raman and UV–vis spectra have been recorded and analyzed in light of the computed quantities and potential energy distributions (PEDs). In addition, MEP, Iso-surface plot of ESP and HOMO-LUMO energies, the barrier heights for the internal rotations about different axes and different thermodynamic functions were computed. Moreover, the wavefunction properties like reduced density gradient and electron localization function were computed. To investigate the biological properties, the bioactivity scores were computed and the molecular docking was also performed. The planarity of the flavone skeleton was stabilized by intramolecular interactions of O16.H24, and O26...H22. The barrier heights for bound OH tops were three times than the free OH tops. The bond length of the C-C linkage was found to be the longest among all the C-C bonds. Out of 99 normal modes, only 66 normal modes were seen to be conformer dependent. The sites near the H and O-atoms of free OH groups are more effective for nucleophilic and electrophilic attacks. The HOMO-LUMO analysis suggests that the molecule is chemically soft. From the observed UV-Vis spectral analysis bathochromic shift was noticed. Thermodynamic functions varied non-linearly with temperature. The bioactivity scores and molecular docking suggest that the molecule is a bioactive molecule. The results of the present investigations made on the isorhamnetin molecule are reported for the first time. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
