Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drug

The vibrational, electronic and charge transfer studies on 2-bromo-6-methoxynaphthalene (2BMN) were done using DFT method with B3LYP/6-311++G(d,p) theory using GAUSSIAN 09W software. Theoretical and experimental investigations on FT-IR and FT Raman were executed on 2BMN. The calculated vibrational w...

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Main Authors: Rinnu Sara Saji, Johanan Christian Prasana, S. Muthu, Jacob George
Format: Article
Language:English
Published: Elsevier 2021-06-01
Series:Heliyon
Subjects:
NBO
ELF
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844021013165
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spelling doaj-c5d287b3c26a4ec69f4a274aa0d03b972021-07-05T16:34:17ZengElsevierHeliyon2405-84402021-06-0176e07213Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drugRinnu Sara Saji0Johanan Christian Prasana1S. Muthu2Jacob George3Department of Physics, Madras Christian College, East Tambaram 600059, Tamil Nadu, India; University of Madras, Chennai, 600005, Tamil Nadu, IndiaDepartment of Physics, Madras Christian College, East Tambaram 600059, Tamil Nadu, India; Corresponding author.Department of Physics, Arignar Anna Government Arts College, Cheyyar, 604407, Tamil Nadu, India; Department of Physics, Puratchi Thalaivar Dr. M. G. R Govt. Arts and Science College, Uthiramerur, 603406, Tamil Nadu, India; Corresponding author.Department of Physics, Madras Christian College, East Tambaram 600059, Tamil Nadu, India; University of Madras, Chennai, 600005, Tamil Nadu, IndiaThe vibrational, electronic and charge transfer studies on 2-bromo-6-methoxynaphthalene (2BMN) were done using DFT method with B3LYP/6-311++G(d,p) theory using GAUSSIAN 09W software. Theoretical and experimental investigations on FT-IR and FT Raman were executed on 2BMN. The calculated vibrational wavenumbers were scaled using suitable scaling factors and vibrational assignments were done to all modes of vibrations using Potential Energy Distribution (PED). Frontier Molecular Orbitals were calculated using TD-DFT method and the HOMO-LUMO energy gap was also obtained. Other electronic properties and global parameters for 2BMN were found using the HOMO-LUMO energy values. An energy gap of 4.208 eV shows the stability of the molecule. The reactive sites were predicted using Molecular Electrostatic Potential (MEP), Electron Localization Function (ELF) and Fukui calculations. Hence all electrophilic sites and nucleophilic areas of the molecule were determined. The delocalization of electron density was studied using NBO calculations. The intramolecular transitions and stability of structure were explained using in detail using the former. As the compound satisfies drug-like properties and has a softness value (indicating its less toxic nature), it may be used as a pharmaceutical product. Molecular docking studies were made and the protein-ligand binding properties were discussed. It was found out that title compound exhibits anti-cancer activities. The low binding energy predicts that the compound may be modified as a drug for treating Cancer.http://www.sciencedirect.com/science/article/pii/S2405844021013165FT-IRFT RamanMolecular dockingNBOELF
collection DOAJ
language English
format Article
sources DOAJ
author Rinnu Sara Saji
Johanan Christian Prasana
S. Muthu
Jacob George
spellingShingle Rinnu Sara Saji
Johanan Christian Prasana
S. Muthu
Jacob George
Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drug
Heliyon
FT-IR
FT Raman
Molecular docking
NBO
ELF
author_facet Rinnu Sara Saji
Johanan Christian Prasana
S. Muthu
Jacob George
author_sort Rinnu Sara Saji
title Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drug
title_short Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drug
title_full Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drug
title_fullStr Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drug
title_full_unstemmed Experimental and theoretical spectroscopic (FT-IR, FT-Raman, UV-VIS) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: A potential anti-cancer drug
title_sort experimental and theoretical spectroscopic (ft-ir, ft-raman, uv-vis) analysis, natural bonding orbitals and molecular docking studies on 2-bromo-6-methoxynaphthalene: a potential anti-cancer drug
publisher Elsevier
series Heliyon
issn 2405-8440
publishDate 2021-06-01
description The vibrational, electronic and charge transfer studies on 2-bromo-6-methoxynaphthalene (2BMN) were done using DFT method with B3LYP/6-311++G(d,p) theory using GAUSSIAN 09W software. Theoretical and experimental investigations on FT-IR and FT Raman were executed on 2BMN. The calculated vibrational wavenumbers were scaled using suitable scaling factors and vibrational assignments were done to all modes of vibrations using Potential Energy Distribution (PED). Frontier Molecular Orbitals were calculated using TD-DFT method and the HOMO-LUMO energy gap was also obtained. Other electronic properties and global parameters for 2BMN were found using the HOMO-LUMO energy values. An energy gap of 4.208 eV shows the stability of the molecule. The reactive sites were predicted using Molecular Electrostatic Potential (MEP), Electron Localization Function (ELF) and Fukui calculations. Hence all electrophilic sites and nucleophilic areas of the molecule were determined. The delocalization of electron density was studied using NBO calculations. The intramolecular transitions and stability of structure were explained using in detail using the former. As the compound satisfies drug-like properties and has a softness value (indicating its less toxic nature), it may be used as a pharmaceutical product. Molecular docking studies were made and the protein-ligand binding properties were discussed. It was found out that title compound exhibits anti-cancer activities. The low binding energy predicts that the compound may be modified as a drug for treating Cancer.
topic FT-IR
FT Raman
Molecular docking
NBO
ELF
url http://www.sciencedirect.com/science/article/pii/S2405844021013165
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