0000000001305554

AUTHOR

Samir M. El-medani

showing 12 related works from this author

Thiophene based imino-pyridyl palladium(II) complexes : Synthesis, molecular structures and Heck coupling reactions

2017

Abstract The new compounds (5-methyl-2-thiophene-2-pyridyl(R))imine [R = methyl (L1); R = ethyl (L2)] and (5-bromo-2-thiophene-2-pyridyl(R)imine [R = methyl (L3); R = ethyl (L4)] were successfully synthesized via Schiff base condensation reaction and obtained in good yields. These potential ligands were reacted with [PdCl2(COD)] and [PdClMe(COD)] to give the corresponding complexes [PdCl2(L)] (L = L1-L4; 1–4) and [PdClMe(L)] (L = L1-L4; 5–8). All compounds were characterized by IR, 1H and 13C NMR spectroscopy, elemental analysis and mass spectrometry. The molecular structures of 1, 2, 6 and 8 were confirmed by X-ray crystallography. The complexes were evaluated as catalyst precursors for st…

Steric effectssynthesisStereochemistryIminechemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryCatalysismolecular structuresInorganic Chemistrychemistry.chemical_compoundHeck reactionMaterials ChemistryThiophenePhysical and Theoretical Chemistryta116heck reactionsSchiff base010405 organic chemistryOrganic ChemistryCondensation reactionpalladium0104 chemical sciencesimino-pyridylchemistryPalladiumJournal of Organometallic Chemistry
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Spectroscopic, density functional theory, nonlinear optical properties and in vitro biological studies of Co(II), Ni(II), and Cu(II) complexes of hyd…

2021

Inorganic Chemistrychemistry.chemical_compoundNonlinear opticalSchiff baseBiological studieschemistryComputational chemistryBiological activityDensity functional theoryGeneral ChemistryHydrazideX ray analysisIn vitroApplied Organometallic Chemistry
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Spectroscopic, crystal structural, theoretical and biological studies of phenylacetohydrazide Schiff base derivatives and their copper complexes

2020

Two phenylacetohydrazide Schiff base derivatives: N’-(1-(2-hydroxyphenyl)ethylidene)-2-phenylacetohydrazide, HL1, and N’-((1-hydroxynaphthalen-2-yl)methylene)-2-phenylacetohydrazide, HL2, were synthesized. HL1 dimerizes in presence of HCl, probably via radical mechanism to give (2,2’-((1E)-hydrazine-1,2-diylidenebis(ethan-1-yl-1-ylidene))diphenol (DIM). Thermal reactions of Cu(II) ions with the two Schiff base ligands resulted in formation of the binuclear complexes [(CuL1)2] and [(CuL2)2]. The stoichiometry and structures of the reported compounds were investigated by several spectroscopic and analytical techniques. The structure of the HL1 ligand and its complex [(CuL1)2] as well as the D…

CT-DNA bindingantioxidant activitychemistry.chemical_elementkupari010402 general chemistry01 natural sciencesAnalytical ChemistryInorganic Chemistrykemialliset sidoksetchemistry.chemical_compoundDFT studiesReactivity (chemistry)copper complexesMethyleneSpectroscopyantioksidantitSchiff base010405 organic chemistryLigandtiheysfunktionaaliteoriaOrganic Chemistrymolecular dockingkompleksiyhdisteetCopper0104 chemical sciencesCrystallographyMolecular geometrychemistrySingle crystalröntgenkristallografiaStoichiometryX-ray analysisJournal of Molecular Structure
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Thiophene based imino-pyridyl palladium(II) complexes : Synthesis, molecular structures and Heck coupling reactions

2017

The new compounds (5-methyl-2-thiophene-2-pyridyl(R))imine [R = methyl (L1); R = ethyl (L2)] and (5-bromo-2-thiophene-2-pyridyl(R)imine [R = methyl (L3); R = ethyl (L4)] were successfully synthesized via Schiff base condensation reaction and obtained in good yields. These potential ligands were reacted with [PdCl2(COD)] and [PdClMe(COD)] to give the corresponding complexes [PdCl2(L)] (L = L1-L4; 1–4) and [PdClMe(L)] (L = L1-L4; 5–8). All compounds were characterized by IR, 1H and 13C NMR spectroscopy, elemental analysis and mass spectrometry. The molecular structures of 1, 2, 6 and 8 were confirmed by X-ray crystallography. The complexes were evaluated as catalyst precursors for standard He…

synteesipalladiumheck reactionsimino-pyridylmolecular structures
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CCDC 1908713: Experimental Crystal Structure Determination

2020

Related Article: Samir M. El-Medani, Abdelmoneim A. Makhlouf, Hussein Moustafa, Manal A. Afifi, Matti Haukka, Ramadan M. Ramadan|2020|J.Mol.Struct.|1208|127860|doi:10.1016/j.molstruc.2020.127860

Space GroupCrystallographyCrystal SystemN'-[1-(2-hydroxyphenyl)ethylidene]-2-phenylacetohydrazide monohydrateCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1525885: Experimental Crystal Structure Determination

2017

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterschloro-methyl-(1-(5-methyl-2-thienyl)-N-(2-(pyridin-2-yl)ethyl)methanimine)-palladium(ii)Experimental 3D Coordinates
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CCDC 971206: Experimental Crystal Structure Determination

2017

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterschloro-methyl-(1-(5-methyl-2-thienyl)-N-(2-(pyridin-2-yl)ethyl)methanimine)-palladium(ii)Experimental 3D Coordinates
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CCDC 1940696: Experimental Crystal Structure Determination

2020

Related Article: Samir M. El-Medani, Abdelmoneim A. Makhlouf, Hussein Moustafa, Manal A. Afifi, Matti Haukka, Ramadan M. Ramadan|2020|J.Mol.Struct.|1208|127860|doi:10.1016/j.molstruc.2020.127860

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters22'-[hydrazinediylidenebis(eth-1-yl-1-ylidene)]diphenolExperimental 3D Coordinates
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CCDC 971205: Experimental Crystal Structure Determination

2017

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

Space GroupCrystallography(1-(5-bromo-2-thienyl)-N-(2-(pyridin-2-yl)ethyl)methanimine)-chloro-methyl-palladium(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1880656: Experimental Crystal Structure Determination

2020

Related Article: Ramadan M. Ramadan, Samir M. El���Medani, Abdelmoneim Makhlouf, Hussein Moustafa, Manal A. Afifi, Matti Haukka, Ayman Abdel Aziz|2021|Appl.Organomet.Chem.|35|e6246|doi:10.1002/aoc.6246

Space GroupCrystallographyCrystal SystemCrystal Structurebis{mu-[N-{1-[2-oxyphenyl]ethylidene}-2-phenylethanehydrazonato]}-di-copperCell ParametersExperimental 3D Coordinates
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CCDC 1510203: Experimental Crystal Structure Determination

2017

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

Space GroupCrystallographydichloro-(1-(5-methyl-2-thienyl)-N-((pyridin-2-yl)methyl)methanimine)-palladium(ii) dichloromethane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1510204: Experimental Crystal Structure Determination

2017

Related Article: Fatma M. Elantabli, Mduduzi P. Radebe, William M. Motswainyana, Bernard O. Owaga, Samir M. El-Medani, Erik Ekengard, Matti Haukka, Ebbe Nordlander, Martin O. Onani|2017|J.Organomet.Chem.|843|40|doi:10.1016/j.jorganchem.2017.04.022

Space GroupCrystallographydichloro-(1-(5-methyl-2-thienyl)-N-(2-(pyridin-2-yl)ethyl)methanimine)-palladium(ii)Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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