0000000001302003

AUTHOR

Afnan Al-hunaiti

showing 9 related works from this author

Organocatalytic Oxidation of Secondary Alcohols Using 1,2-Di(1-naphthyl)-1,2-ethanediamine (NEDA) (Eur. J. Org. Chem. 28/2014)

2014

010405 organic chemistryChemistryOrganocatalysisOrganic ChemistryKineticsOrganic chemistryPhysical and Theoretical Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesEuropean Journal of Organic Chemistry
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Solvent free oxidation of primary alcohols and diols using thymine iron(III) catalyst.

2010

In this study, we developed an efficient and selective iron-based catalyst system for the synthesis of ketones from secondary alcohols and carboxylic acids from primary alcohol. In situ generated iron catalyst of thymine-1-acetate (THA) and FeCl(3) under solvent-free condition exhibits high activity. As an example, 1-octanol and 2-octanol were oxidized to 1-octanoic acid and 2-octanone with 89% and 98% yields respectively.

Primary (chemistry)Solvent free010405 organic chemistryChemistryMetals and AlloysGeneral ChemistryPrimary alcohol010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisThyminelaw.inventionchemistry.chemical_compoundMagazinelawAlcohol oxidationMaterials ChemistryCeramics and CompositesHigh activityOrganic chemistryChemical communications (Cambridge, England)
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Organocatalytic Oxidation of Secondary Alcohols Using 1,2-Di(1-naphthyl)-1,2-ethanediamine (NEDA)

2014

Diamine, 1,2-di(1-naphthyl)-1,2-ethanediamine (NEDA), efficiently catalyzes the oxidation of alcohols by using TBHP as an oxidant. Notably, secondary benzyl alcohols are oxidized in almost quantitative yields, and the catalyst also displays high activity towards even hindered cycloaliphatic secondary alcohols. With enantiopure (R,R)-NEDA, oxidative kinetic resolution can be realized and depending on the alcohol ee up to 99 % are achieved.

010405 organic chemistryOrganic ChemistryAlcohol010402 general chemistry01 natural sciences0104 chemical sciences3. Good healthCatalysisKinetic resolutionchemistry.chemical_compoundEnantiopure drugchemistryDiamineAlcohol oxidationOrganic chemistryHigh activityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Catalytic Oxidation of Alkanes and Alkenes by H 2 O 2 with a μ‐Oxido Diiron(III) Complex as Catalyst/Catalyst Precursor

2015

A new mu-oxo diiron(III) complex of the lithium salt of the pyridine-based unsymmetrical ligand 3-[(3-{[bis(pyridin-2-ylmethyl)amino]methyl}-2-hydroxy-5-methylbenzyl)(pyridin2-ylmethyl)amino] propanoate (LiDPCPMPP), [Fe-2(mu-O)(LiDPCPMPP)(2)](ClO4)(2), has been synthesized and characterized. The ability of the complex to catalyze oxidation of several alkanes and alkenes has been investigated by using CH3COOH/H2O2 (1:1) as an oxidative system. Moderate activity in cyclohexane oxidation (TOF = 33 h(-1)) and good activity in cyclohexene oxidation (TOF = 72 h(-1)) were detected. Partial retention of configuration (RC = 53%) in cis- and trans-1,2-dimethylcyclohexane oxidation, moderate 3 degrees…

Cyclohexane010405 organic chemistryAdamantaneCyclohexeneHomogeneous catalysis010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryCatalytic oxidationlithiumPyridineSelectivityta116European Journal of Inorganic Chemistry
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Di- and Tetrairon(III) μ-Oxido Complexes of an N3S-Donor Ligand: Catalyst Precursors for Alkene Oxidations

2019

The new di- and tetranuclear Fe(III) μ-oxido complexes [Fe 4 (μ-O) 4 (PTEBIA) 4 ](CF 3 SO 3 ) 4 (CH 3 CN) 2 ] (1a), [Fe 2 (μ-O)Cl 2 (PTEBIA) 2 ](CF 3 SO 3 ) 2 (1b), and [Fe 2 (μ-O)(HCOO) 2 (PTEBIA) 2 ](ClO 4 ) 2 (MeOH) (2) were prepared from the sulfur-containing ligand (2-((2,4-dimethylphenyl)thio)-N,N-bis ((1-methyl-benzimidazol-2-yl)methyl)ethanamine (PTEBIA). The tetrairon complex 1a features four μ-oxido bridges, while in dinuclear 1b, the sulfur moiety of the ligand occupies one of the six coordination sites of each Fe(III) ion with a long Fe-S distance of 2.814(6) A. In 2, two Fe(III) centers are bridged by one oxido and two formate units, the latter likely formed by methanol oxidati…

MECHANISMFe-S interactionoxidation116 Chemical sciencesThio-rautaSULFURHomogeneous catalysis02 engineering and technology010402 general chemistry01 natural sciencesMedicinal chemistrythioetherCatalysislcsh:Chemistrychemistry.chemical_compoundThioetheriron-oxo complexAcetonitrileta116Fe-S interaction; homogeneous catalysis; iron-oxo complex; oxidation; thioetherOriginal Researchchemistry.chemical_classificationeetteritFUNCTIONAL-MODELCOORDINATIONPEROXIDEAlkeneLigandACTIVE-SITEhapettuminenGeneral Chemistrykompleksiyhdisteet021001 nanoscience & nanotechnology540COPPER-COMPLEXEShomogeneous catalysis0104 chemical sciencesChemistrychemistrylcsh:QD1-999katalyysiACIDOXO0210 nano-technologySelectivityNONHEME IRON CATALYSTSFrontiers in Chemistry
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CCDC 1874713: Experimental Crystal Structure Determination

2019

Related Article: Biswanath Das, Afnan Al-Hunaiti, Brenda N. S��nchez-Egu��a, Erica Zeglio, Serhiy Demeshko, Sebastian Dechert, Steffen Braunger, Matti Haukka, Timo Repo, Ivan Castillo, Ebbe Nordlander|2019|Frontiers in Chemistry|7|97|doi:10.3389/fchem.2019.00097

Space GroupCrystallographyCrystal SystemCrystal Structure(mu-oxo)-bis(2-[(24-dimethylphenyl)sulfanyl]-NN-bis[(1-methyl-1H-benzimidazol-2-yl)methyl]ethan-1-amine)-dichloro-di-iron(iii) bis(trifluoromethanesulfonate)Cell ParametersExperimental 3D Coordinates
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CCDC 1874714: Experimental Crystal Structure Determination

2019

Related Article: Biswanath Das, Afnan Al-Hunaiti, Brenda N. S��nchez-Egu��a, Erica Zeglio, Serhiy Demeshko, Sebastian Dechert, Steffen Braunger, Matti Haukka, Timo Repo, Ivan Castillo, Ebbe Nordlander|2019|Frontiers in Chemistry|7|97|doi:10.3389/fchem.2019.00097

(mu-oxo)-bis(mu-formato)-bis(2-[(24-dimethylphenyl)sulfanyl]-NN-bis[(1-methyl-1H-benzimidazol-2-yl)methyl]ethan-1-amine)-di-iron(iii) bis(perchlorate) methanol unknown solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1403038: Experimental Crystal Structure Determination

2015

Related Article: Biswanath Das, Afnan Al-Hunaiti, Matti Haukka, Serhiy Demeshko, Steffen Meyer, Albert A. Shteinman, Franc Meyer, Timo Repo, Ebbe Nordlander|2015|Eur.J.Inorg.Chem.||3590|doi:10.1002/ejic.201500576

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parametersbis(mu-N-(3-((bis(pyridin-2-ylmethyl)amino)methyl)-2-oxy-5-methylbenzyl)-N-(pyridin-2-ylmethyl)-beta-alaninato)-(mu-oxo)-di-iron-di-lithium tetrachloro-iron acetonitrile solvateExperimental 3D Coordinates
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CCDC 1874712: Experimental Crystal Structure Determination

2019

Related Article: Biswanath Das, Afnan Al-Hunaiti, Brenda N. S��nchez-Egu��a, Erica Zeglio, Serhiy Demeshko, Sebastian Dechert, Steffen Braunger, Matti Haukka, Timo Repo, Ivan Castillo, Ebbe Nordlander|2019|Frontiers in Chemistry|7|97|doi:10.3389/fchem.2019.00097

Space GroupCrystallographytetrakis(mu-oxo)-tetrakis(2-[(24-dimethylphenyl)sulfanyl]-NN-bis[(1-methyl-1H-benzimidazol-2-yl)methyl]ethan-1-amine)-tetra-iron(iii) tetrakis(trifluoromethanesulfonate) acetonitrile solvate hydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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