0000000001004227

AUTHOR

Naser Eltaher Eltayeb

showing 10 related works from this author

PtII versus PdII-assisted [2+3] cycloadditions of nitriles and nitrone. Synthesis of nitrile-derived arylamido platinum(II) and Δ4-1,2,4-oxadiazoline…

2019

Abstract The reactions of bis(organonitrile) platinum(II) complexes trans-[PtCl2(N CR)2] (R = C6H4(p-HC O), CH2C6H4(p-CH3)) with pyrroline N-oxide −O+N CHCH2CH2CMe2 afford arylamido platinum(II) complexes trans-[PtCl2{(O CR)N CCH2CH2CMe2NH}2] (R = C6H4(p-HC O) (1), CH2C6H4(p-CH3) (2)). The spectral data of 1 and 2 show that the oxadiazoline rings in both cases have opened by a spontaneous N O bond cleavage to form (Z)-p-formyl-N-(5,5-dimethylpyrrolidin-2-ylidene)benzamide or (Z)-N-(5,5-dimethylpyrrolidin-2-ylidene)-2-p-tolylacetamide ligands, respectively, where the N-atoms of the benzamide or acetamide moieties coordinate to platinum(II) metal centre in trans positions. However, the reacti…

platinaNitrilechemistry.chemical_elementPyrroline010402 general chemistry01 natural sciencesMedicinal chemistryNitroneInorganic ChemistryMetalchemistry.chemical_compoundN–O bond cleavageMaterials ChemistrynitrilesplatinumPhysical and Theoretical Chemistryta116Bond cleavagechemistry.chemical_classification010405 organic chemistry[2+3] cycloadditionskompleksiyhdisteetpalladium0104 chemical scienceschemistryvisual_artvisual_art.visual_art_mediumPlatinumAcetamidePalladiumPolyhedron
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Crystal and molecular structure studies of (Z)-N-methyl-C-4-substituted phenyl nitrones by XRD, DFT, FTIR and NMR methods

2017

Abstract (Z)-N-methyl-C-4-substituted phenyl nitrones –O+N(Me)=C(H)R (Z-2a R = 4-ClC6H4, Z-2b R = 4-NO2C6H4, Z-2c R = 4-CH3OC6H4) were synthesized and characterized by elemental analyses, FTIR, 1H, 13C and DEPT-135 NMR spectroscopy and also by single crystal X-ray diffraction (in the case of Z-2a and Z-2b). The geometries of the nitrone molecules Z-2a, Z-2b and Z-2c and their E-isomers; (E)-N-methyl-C-4-chlorophenyl nitrone E-2a, (E)-N-methyl-C-4-nitrophenyl nitrone E-2b and (E)-N-methyl-C-4-methoxyphenyl nitrone E-2c were optimized using density functional theory (DFT) at the B3LYP/6-311++G(d,p) level of theory. The theoretical vibrational frequencies obtained by DFT calculations are in go…

B3LYP010402 general chemistry01 natural sciencesDFTAnalytical ChemistryNitroneInorganic ChemistryComputational chemistry(Z)-N-methyl-C-4-substituted phenyl nitronessingle crystal X-rayMoleculeHOMO/LUMOta116Spectroscopychemistry.chemical_classification010405 organic chemistryChemistryChemical shiftOrganic ChemistryNuclear magnetic resonance spectroscopyNMR0104 chemical sciencesNMR spectra databaseCrystallographyDensity functional theorySingle crystalJournal of Molecular Structure
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Crystal structure oftrans-dichloridobis[N-(5,5-dimethyl-4,5-dihydro-3H-pyrrol-2-yl-κN)acetamide]palladium(II) dihydrate

2017

The title complex, [PdCl2(C8H14N2O)2]·2H2O, was obtained by N–O bond cleavage of the oxadiazoline rings of thetrans-[dichlorido-bis(2,5,5-trimethyl-5,6,7,7a-tetrahydropyrrolo[1,2-b][1,2,4]oxadiazole-N1)]palladium(II) complex. The palladium(II) atom exhibits an almost square-planar coordination provided by twotrans-arranged chloride anions and a nitrogen atom from each of the two neutral organic ligands. In the crystal, N—H...O, O—H...O and O—H...Cl hydrogen bonds link complex molecules into double layers parallel to thebcplane.

crystal structureNitrileInorganic chemistrychemistry.chemical_elementCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryNitronechemistry.chemical_compoundGeneral Materials ScienceN—O bond cleavageta116cycloadditionBond cleavagenitronechemistry.chemical_classificationCrystallographynitrileChemistryHydrogen bondGeneral Chemistrypalladiumcyclo­additionCondensed Matter PhysicsCycloaddition0104 chemical sciencesQD901-999AcetamidePalladiumActa Crystallographica Section E Crystallographic Communications
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Synthesis and characterization of ferrocene-based Schiff base and ferrocenecarboxaldehyde oxime and their adsorptive removal of methyl blue from aque…

2018

Abstract The ferrocene-based Schiff base 3 was synthetized by reaction of ferrocenecarboxaldehyde 1 with 4-aminoantipyrine 2. However, the reaction of 1 with hydroxylamine affords ferrocenecarboxaldehyde oxime 4. Compounds 3 and 4 were fully characterized by IR, 1H, 13C and DEPT-135 NMR spectroscopy, elemental analyses and also by single crystal X-ray diffraction. Compounds 3 and 4 were used to remove anionic methyl blue dye from wastewater. The results established that both compounds have high adsorption capacity towards methyl blue. Langmuir adsorption capacity of compound 4 (464 mmol/g) is much higher than that of compound 3 (193 mmol/g) at 25 °C. The kinetics data was fitted well pseudo…

methyl blue dyeLangmuirMethyl blue02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundAdsorptionHydroxylamineMaterials ChemistryPhysical and Theoretical Chemistryferrocenecarboxaldehyde oximeta116single crystal X-ray diffractionAqueous solutionSchiff baseOrganic Chemistry021001 nanoscience & nanotechnologyOximeferrocene-based Schiff base0104 chemical sciencesFerrocenechemistryadsorption0210 nano-technologyNuclear chemistryJournal of Organometallic Chemistry
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Synthesis and characterization of ferrocene-based Schiff base and ferrocenecarboxaldehyde oxime and their adsorptive removal of methyl blue from aque…

2018

The ferrocene-based Schiff base 3 was synthetized by reaction of ferrocenecarboxaldehyde 1 with 4-aminoantipyrine 2. However, the reaction of 1 with hydroxylamine affords ferrocenecarboxaldehyde oxime 4. Compounds 3 and 4 were fully characterized by IR, 1H, 13C and DEPT-135 NMR spectroscopy, elemental analyses and also by single crystal X-ray diffraction. Compounds 3 and 4 were used to remove anionic methyl blue dye from wastewater. The results established that both compounds have high adsorption capacity towards methyl blue. Langmuir adsorption capacity of compound 4 (464 mmol/g) is much higher than that of compound 3 (193 mmol/g) at 25 °C. The kinetics data was fitted well pseudo-second-o…

methyl blue dyeferrocenecarboxaldehyde oximeadsorptioferrocene-based Schiff basesingle crystal X-ray diffraction
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CCDC 1482397: Experimental Crystal Structure Determination

2016

Related Article: Jamal Lasri, Naser Eltaher Eltayeb, Matti Haukka, Yousef Alghamdi|2017|J.Mol.Struct.|1128|70|doi:10.1016/j.molstruc.2016.08.058

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersN-methyl-N-(4-nitrobenzylidene)imine oxideExperimental 3D Coordinates
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CCDC 1482396: Experimental Crystal Structure Determination

2016

Related Article: Jamal Lasri, Naser Eltaher Eltayeb, Matti Haukka, Yousef Alghamdi|2017|J.Mol.Struct.|1128|70|doi:10.1016/j.molstruc.2016.08.058

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersN-(4-chlorobenzylidene)-N-methylimine oxideExperimental 3D Coordinates
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CCDC 1864425: Experimental Crystal Structure Determination

2018

Related Article: Jamal Lasri, Naser Eltaher Eltayeb, Matti Haukka, Bandar A. Babgi|2019|Polyhedron|158|65|doi:10.1016/j.poly.2018.10.057

Space GroupCrystallographybis(N-(55-dimethylpyrrolidin-2-ylidene)-4-formylbenzamide)-dichloro-platinum 4-formylbenzonitrile chloroform solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1812970: Experimental Crystal Structure Determination

2018

Related Article: Jamal Lasri, Abeer S. Elsherbiny, Naser Eltaher Eltayeb, Matti Haukka, Mohamed E. El-Hefnawy|2018|J.Organomet.Chem.|866|21|doi:10.1016/j.jorganchem.2018.04.004

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters((hydroxyimino)methyl)ferroceneExperimental 3D Coordinates
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CCDC 1812968: Experimental Crystal Structure Determination

2018

Related Article: Jamal Lasri, Abeer S. Elsherbiny, Naser Eltaher Eltayeb, Matti Haukka, Mohamed E. El-Hefnawy|2018|J.Organomet.Chem.|866|21|doi:10.1016/j.jorganchem.2018.04.004

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters1-([(15-dimethyl-3-oxo-2-phenyl-23-dihydro-1H-pyrazol-4-yl)imino]methyl)ferroceneExperimental 3D Coordinates
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