Spectral analysis and DFT investigation of some benzopyran analogues and their self-assemblies with graphene

Al-Otaibi J. S., Mary Y. S., Mary Y. S., KAYA S., ERKAN S.

JOURNAL OF MOLECULAR LIQUIDS, cilt.317, 2020 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 317
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1016/j.molliq.2020.113924
  • Dergi Adı: JOURNAL OF MOLECULAR LIQUIDS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chemical Abstracts Core, Chimica, Compendex, INSPEC
  • Anahtar Kelimeler: DFT, Graphene, Benzopyran, Molecular docking, IMIDAZOLE DERIVATIVES, MOLECULAR-STRUCTURE, RAMAN-SPECTRA, LUMO ANALYSIS, DOCKING, HOMO, FLAVONOIDS, REACTIVITY, PRINCIPLE, PYRIDINE
  • Sivas Cumhuriyet Üniversitesi Adresli: Evet

Özet

Spectroscopic analysis and different quantum mechanical studies of four phramaceutically active flavanoid compounds, 5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one (genistein) (F1), 5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one (apigenin) (F2), 5,6,7-trihydroxy-2-phenyl-4H-chromen-4-one (baicalein) (F3) and 2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4H-chromen-4-one (fisetin) (F4) are reported in this manuscript using DFT/B3LYP/6-311++G(d,p) level of theory. Simulated IR spectrum of these compounds was compared with experimentally available data, and essential functional group assignments were made. NBO studies helped to study the various intramolecular electron delocalisation possible in the molecule. We also report the frontier orbital properties and other derived local energy descriptors which talks about the relative stability and reactivity of the compounds. The photovoltaic efficiency of the compounds was studied from the simulated electronic spectra. The compound was found to interact with graphene, to form molecular self-assembly. These self-assemblies showed tremendous enhancement in various physicochemical properties when compared with its constituents. Biological activity of the compounds were predicted using molecular docking studies. (C) 2020 Elsevier B.V. All rights reserved.