Ibrahim Mohamed

Prof. Dr. Ibrahim Mohamed

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2010 in Carbohydrate Polymers
Verified
Journal Article
Closed access
NINabil A. Ibrahim
Nabil A. Ibrahim
AEA.R. El-Gamal
A.R. El-Gamal
Mohamed GoudaMohamed Gouda
Mohamed Gouda
FMF. Mahrous
F. Mahrous

25 April 2018 in ACS Biomaterials Science & Engineering
Verified
Journal Article
Closed access
HMHamouda Mousa
Hamouda Mousa
Abdalla Abdal-hayAbdalla Abdal-hay
Abdalla Abdal-hay
MBMichal Bartnikowski
Michal Bartnikowski
IMIbrahim M. A. Mohamed
Ibrahim M. A. Mohamed
AYAhmed S. Yasin
Ahmed S. Yasin
CKCheol Sang Kim
Cheol Sang Kim

1 January 2020 in Chemosphere
Verified
Journal Article
Closed access
Noha ElessawyNoha Elessawy
Noha Elessawy
MEMohamed Elnouby
Mohamed Elnouby
Mohamed GoudaMohamed Gouda
Mohamed Gouda
HHHesham A. Hamad
Hesham A. Hamad
NTNahla A. Taha
Nahla A. Taha
MEMohamed S. Mohy Eldin
Mohamed S. Mohy Eldin

1 March 2020 in Journal of Alloys and Compounds
Verified
Journal Article
Closed access
IMIbrahim M.A. Mohamed
Ibrahim M.A. Mohamed
PKPalsamy Kanagaraj
Palsamy Kanagaraj
AYAhmed S. Yasin
Ahmed S. Yasin
WIWaheed Iqbal
Waheed Iqbal
Changkun LiuChangkun Liu
Changkun Liu

1 October 2016 in Separation and Purification Technology
Verified
Journal Article
Closed access
AYAhmed S. Yasin
Ahmed S. Yasin
HMHend Omar Mohamed
Hend Omar Mohamed
IMIbrahim M.A. Mohamed
Ibrahim M.A. Mohamed
HMHamouda Mousa
Hamouda Mousa
NBNasser A.M. Barakat
Nasser A.M. Barakat

17 January 2023 in Materials
Verified
Journal Article
Open access
PDF file
MAMohamed Ali Ibrahim Al-Gaber
Mohamed Ali Ibrahim Al-Gaber
Hany M. Abd El-LateefHany M. Abd El-Lateef
Hany M. Abd El-Lateef
MKMai Khalaf
Mai Khalaf
SSSaad Shaaban
Saad Shaaban
MSMohamed Shawky
Mohamed Shawky
Ahmed Abu-Dief MohammedAhmed Abu-Dief Mohammed
Ahmed Abu-Dief Mohammed
A new heterocyclic azo dye ligand (L) was synthesized by the combination of 4-amino antipyrine with 4-aminophenol. The new Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Cu(II), Zn(II), and Cd(II) complexes were synthesized in excellent yields. The metal chelate structures were elucidated using elemental analyses, FT-IR, 1H-NMR, mass, magnetic moment, diffused reflectance spectral and thermal analysis (TG-DTG), and molar conductivity measurement. According to the FT-IR study, the azo dye ligand exhibited neutral tri-dentate behavior, binding to the metal ions with the azo N, carbonyl O, and protonated phenolic OH. The 1H-NMR spectral study of the Zn(II) complex supported the coordination of the zo dye ligand without proton displacement of the phenolic OH. Diffused reflectance and magnetic moment studies revealed the octahedral geometry of the complexes, as well as their good electrolytic nature, excepting the Zn(II) and Cd(II) complexes, which were nonelectrolytes, as deduced from the molar conductivity study. The theoretical calculations of optimized HOMO–LUMO energies, geometrical parameters, electronic spectra, natural atomic charges, 3D-plots of MEP, and vibrational wavenumbers were computed and elucidated using LANL2DZ and 6-311G (d, p) basis sets of density functional theory (DFT) with the approach of B3LYP DFT and TD-DFT methods. The ligand and complexes have been assayed for their antimicrobial activity and compared with the standard drugs. Most of the complexes have manifested excellent antimicrobial activity against various microbial strains. A molecular docking investigation was also performed, to acquire more information about the binding mode and energy of the ligand and its metal complexes to the Escherichia coli receptor using molecular docking. Altogether, the newly created ligand and complexes showed positive antibacterial effects and are worth future study.