Search results for "COORDINATION CHEMISTRY"

showing 10 items of 231 documents

Synthesis, Coordination to Rh(I), and Hydroformylation Catalysis of New β-Aminophosphines Bearing a Dangling Nitrogen Group:  An Unusual Inversion of…

2002

Variants of the beta-aminophosphine L(1) [Ph(2)PCH(2)CH(Ph)NHPh] containing additional nitrogen donor functions have been prepared. These functions are branched off the C atom adjacent to the P atom, or the P atom itself. Ligand [Ph(2)PCH(o-C(6)H(4)NMe(2))CH(Ph)NHPh] has been obtained as a mixture of two diastereomers L(3A) and L(3B) by lithiation of L(2) [Ph(2)PCH(2)(o-C(6)H(4)NMe(2))] with n-BuLi followed by PhCH=NPh addition and hydrolysis. The diastereomers have been separated by fractional crystallization from ethanol. Ligand Et(2)NCH(2)P(Ph)CH(2)CH(Ph)NHPh has been obtained as a mixture of two diastereomers L(5A) and L(5B)(starting with P-Ph reductive cleavage of L(1) by lithium and s…

DenticityStereochemistrychemistry.chemical_elementLigands010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisRhodiumInorganic Chemistrychemistry.chemical_compound[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryDiethylamine[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryLigandChemistryDiastereomer[CHIM.CATA]Chemical Sciences/CatalysisOxidative addition0104 chemical sciencesMetalsMixturesHydroformylationMolecular structureHydroformylationInorganic Chemistry
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Direct arylation of heterocycles: the performances of ferrocene-based polyphosphane ligands in palladium-catalyzed C-H bond activation

2010

International audience; The palladium-catalyzed direct arylation of alkylated- furan, thiophene, and thiazole and benzoxazole heterocycles with electronically and sterically deactivated bromoarenes was selectively and efficiently promoted by ferrocenyl polyphosphanes. In this C[BOND]H bond activation reaction of heteroaromatics, the performances of polydentate di-, tri-, and tetraphosphane ligands were compared, showing that the triphosphane 1,1′,2-tris(diphenylphosphino)-4-tert-butylferrocene 3 was the most effective for the coupling. The introduction of more electron-donating (iPr) or electron-withdrawing (furyl) groups on the phosphorus atoms did not improve the ligand performances. The …

Denticitychemistry.chemical_elementCH activation010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisThiopheneOrganic chemistryChelation[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryThiazoleheterocycles010405 organic chemistryLigandOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.CATA]Chemical Sciences/CatalysisBenzoxazolepalladiumhomogeneous catalysis0104 chemical sciencesTriphosphanechemistryligands effectsPalladium
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General route to dissymmetric heteroannular-functionalized ferrocenyl 1,2-diphosphines: selective synthesis and characterization of a new class of tr…

2006

Several monosubstituted-cyclopentadienyl anions (A-Li) and [1,2-bis(diphenylphosphino)-4-tert-butylcyclopentadienyl]lithium (B-Li) react with FeCl2 to afford a novel class of multidentate ferroceny...

Denticitysynthesis010405 organic chemistryChemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementCharacterization (mathematics)010402 general chemistryligand01 natural sciencesCombinatorial chemistry3. Good health0104 chemical sciencesInorganic Chemistryferrocenylphosphinedissymetrically functionalized ferroceneDiphosphinesmultidentarityOrganic chemistryLithium[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistrydiphosphineComputingMilieux_MISCELLANEOUS
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Chiral α-P,N Ligands From a Diastereoselective Ph2PH Addition to (η6-Benzaldimine)tricarbonylchromium Complexes

1999

International audience; Chiral α-aminophosphane (α-P–C–N) ligands have been prepared by reversible addition of Ph2PH to tricarbonylchromium benzaldimine complexes (CO)3Cr[η6-o-C6H4(Y)(CH=NR)] (with Y, R = CH3, CH3 or CH2COOCH3; CH3O, CH3 or p-CH3OC6H4; Cl, C6H5), with complete diastereoselectivity. These complexes are stabilized in solution by electron-withdrawing group(s) on the imine.

Diastereoselective reactionsStereochemistryOrganic ChemistryImine3. Good healthP ligandschemistry.chemical_compoundChromium complexeschemistryAminophosphaneGroup (periodic table)[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryChiralityChirality (chemistry)
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Dialkyl(butadiene)cyclopentadienylmolybdenum(III) Complexes. Synthesis, Characterization, and Reactivity

2000

International audience; Treatment of CpMo(η4-diene)Cl2 (diene = 1,3-butadiene, C4H6, 1‘; isoprene, C5H8, 1‘ ‘; 2,3-dimethyl-1,3-butadiene, C6H10, 1‘ ‘) in diethyl ether at low temperature with 2 equiv of alkylmagnesium RMgX reagents affords the corresponding dialkyl complexes CpMo(η4-1,3-diene)R2 (2, 2‘, 2‘ ‘, R = CH3, a; CH2Ph, b; CH2SiMe3, c). These species are isolable in moderate yields and have been fully characterized by EPR, elemental analyses, and cyclic voltammetry. They all show a reversible reduction process at relatively low potentials and an irreversible oxidation. The structure of 2‘ ‘a was confirmed by single-crystal X-ray diffraction. The mixed complex CpMo(η4-C4H6)Cl(CH3), …

DieneStereochemistryReaction productsLigands010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compound[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryRedistribution (chemistry)Redox reactionsPhysical and Theoretical ChemistryIsoprene010405 organic chemistryLigandArylOrganic ChemistryAlkyls0104 chemical scienceschemistryReagentCyclic voltammetryDiethyl etherElectron paramagnetic resonance spectroscopyOrganometallics
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Atom Transfer Radical Addition Catalyzed by Ruthenium–Arene Complexes Bearing a Hybrid Phosphine–Diene Ligand

2018

International audience; The synthesis and characterization of a series of arene ruthenium complexes bearing either (3,5-cycloheptadienyl)diphenylphosphine or (cycloheptyl)-diphenylphosphine are reported. Upon irradiation or heating, all these complexes lose their arene ligand but then exhibit a different behavior depending on the nature of the phosphine ligand. (Cycloheptadienyl)phosphine complexes 1 and 3 give a cationic dinuclear Ru complex 5 for which the two Ru atoms are bridged by three chlorido ligands and flanked by two tridendate (cycloheptadienyl)phosphines. (Cycloheptyl)-diphenylphosphine complexes 2 and 4 undergo arene exchange when toluene is used as solvent or degrade in dithlo…

Dieneeffective core potentialsprecursorchemistry.chemical_element010402 general chemistrychemistry01 natural sciencesMedicinal chemistryAdductInorganic Chemistrychemistry.chemical_compoundMoiety[CHIM.COOR]Chemical Sciences/Coordination chemistryarylationPhysical and Theoretical ChemistryDiphenylphosphine010405 organic chemistryAtom-transfer radical-polymerizationLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry[CHIM.CATA]Chemical Sciences/Catalysismolecular calculations0104 chemical sciencesRutheniumkharasch reactionatrc reactionschemistrypolymerizationpincer complexesmetathesisPhosphine
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Antiferromagnetic Interactions in Copper(II) µ-Oxalato Dinuclear Complexes: The Role of the Counterion

2018

We report the preparation, crystal structure determination, magnetic properties and DFT calculations of five oxalato-bridged dicopper(II) complexes of formula [Cu-2(bpy)(2-)(H2O)(2)(C2O4)](CF3SO3)(2) (1), [Cu-2(bpy)(2)(C2O4)](PF6)(2) (2), [Cu-2(bpy)(2)(C2O4)](ClO4)(2) (3), [Cu-2(bpy)(2)Cl-2(C2O4)]center dot H2O (4) and [Cu-2(bpy)(2)(NO2)(2)(C2O4)] (5) (bpy = 2,2'-bipyridine and C2O42-= oxalate). Compounds 1, 2, 4 and 5 crystallize in the monoclinic system and 3 crystallizes in the triclinic system. The oxalate ligands in 1-5 adopt the bis-bidentate coordination mode and the two bpy molecules act as terminal ligands. The coordination of the counterions and the surroundings of the copper(II) …

Dinuclear complexesMatériauxFerromagnetismechemistry.chemical_elementCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistryTriclinic crystal system010402 general chemistry01 natural sciencesOxalateInorganic Chemistrychemistry.chemical_compoundOxalatoMagnetic propertiesAntiferromagnetismMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryGénie des procédéschemistry.chemical_classificationCoure010405 organic chemistryPropietats magnètiquesCopper0104 chemical sciences3. Good healthCrystallographyDensity functional calculationschemistryFerromagnetismCounterionCopperMonoclinic crystal system
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Theoretical Study of the 15- and 17-Electron Structures of Cyclopentadienylchromium(III) and Cyclopentadienylmolybdenum(III) Complexes. Dichloride an…

1997

International audience; The structure and the energetics of the model systems CpMX2(PH3) + PH3 ⇄ CpMX2(PH3)2 (Cp = cyclopentadienyl; M = Cr, Mo; X = Cl, CH3) are studied by performing Møller−Plesset second order (MP2) and density functional theory (DFT) calculations. Extended basis sets are employed in the geometry optimizations. The results indicate that the structural preference can be traced back to the competition between electron pairing stabilization and M−P bond dissociation energy along the spin doublet surface. At all levels of calculation, the energy splitting, a measure of the cost of pairing the electron during the promotion process from the quartet ground state to the excited d…

Electron pairEnergy010405 organic chemistryChemistryElectrical energy010402 general chemistryLigands01 natural sciencesBond-dissociation energyQuantum mechanics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyCyclopentadienyl complexComputational chemistryMetalsExcited statePairingDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryGround stateDoublet state
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Spin State and Ligand Dissociation in [CpCoL2] Complexes (L = PH3, H2C=CH2): A Computational Study

1999

International audience; The relative energies of [CpCoL] compounds (L = PH3, H2C=CH2) were calculated at the DFT/B3LYP level of theory. The triplet spin state was found to be favored over the singlet by between 33.0 and 21.0 kcal mol−1 for both fixed and optimized geometries. The basis set size was found to be important for the energy calculations, particularly when the energetics of ligand dissociation was examined. The role of the triplet spin state in facilitating the ligand dissociation process is discussed.

Electronic structureSpin statesChemistryCobaltElectronic structureDissociation (chemistry)Ligand effects[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryInorganic ChemistryDensity functional calculationsComputational chemistrySpin statePhysics::Atomic and Molecular Clusters[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet statePhysics::Chemical PhysicsTriplet stateBasis setEuropean Journal of Inorganic Chemistry
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New Microbe Killers: Self-Assembled Silver(I) Coordination Polymers Driven by a Cagelike Aminophosphine

2019

New Ag(I) coordination polymers, formulated as [Ag(&micro

Electrospray ionizationInfrared spectroscopymetal-organic frameworks (mofs)02 engineering and technologyCrystal structure010402 general chemistry01 natural scienceslcsh:TechnologyArticleCoordination complexantimicrobial materialsGeneral Materials Sciencesilver135-triaza-7-phospaadamantanelcsh:Microscopylcsh:QC120-168.85chemistry.chemical_classificationlcsh:QH201-278.5ChemistryHydrogen bondlcsh:TPolymer021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographycoordination polymersMicrocrystallinelcsh:TA1-2040coordination chemistrylcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineering0210 nano-technologylcsh:Engineering (General). Civil engineering (General)lcsh:TK1-9971Powder diffractionMaterials
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