Search results for "Coordination Chemistry"

showing 10 items of 231 documents

Templated synthesis of a rotaxane with a [Ru(diimine)3]2+ core.

2003

A rotaxane containing a ruthenium bisphenanthroline complex, acting as an axis, and a macrocycle incorporating a 2,2'-bipyridine (bpy) unit, threaded by the axis, has been synthesized. The bisphenanthroline ligand is such that its ruthenium(II) complexes possess a clearly identified axis, making such compounds ideal components of rotaxanes constructed around an octahedral ruthenium(II) center, which serves as a template. The ring is threaded by the axial ruthenium(II) precursor complex, to afford the corresponding pseudorotaxane in moderate yield. The X-ray structure analysis of this compound reveals the threaded nature of the complex. The length of the threaded ring (35 atoms in the periph…

Rotaxane010405 organic chemistryStereochemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesCatalysis0104 chemical sciencesRutheniumBipyridinechemistry.chemical_compoundCrystallographychemistryOctahedron[ CHIM.ORGA ] Chemical Sciences/Organic chemistryProton NMR[CHIM.COOR]Chemical Sciences/Coordination chemistryDiimineComputingMilieux_MISCELLANEOUSChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Phenoxyamidine Zn and Al Complexes: Synthesis, Characterization, and Use in the Ring-Opening Polymerization of Lactide

2019

International audience; Herein we report the synthesis of new ditopic ligands, which consist of a phenoxy group and N,N,N'trisubstituted amidines linked by a methylene spacer (L1-L4). Their coordination chemistry has been studied/investigated with Zn(II) and Al(III). Alkane elimination route between the phenol-amidine proligands (L1H-L4H) and Et2Zn led to dinuclear complexes [(L1-L4)ZnEt]2 (1a-4a) in which the Zn centers are chelated by phenoxyamidine ligands and bridged through the oxygen atom of the phenoxy groups. Salt metathesis reaction between two equivalents of the sodium amidine phenate L1Na and ZnCl2 led to a bis-chelate chiral spiro-complex (L12Zn) 1a'. Analogous alkane eliminatio…

STRUCTURAL-CHARACTERIZATIONchemistry.chemical_elementCATALYSTSZinc010402 general chemistryLIGANDS SYNTHESIS01 natural sciencesRing-opening polymerizationCoordination complexCatalysisInorganic Chemistrychemistry.chemical_compoundZINCIMINE LIGANDSGroup (periodic table)Polymer chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryMethyleneCYCLIC ESTERSALUMINUM COMPLEXESchemistry.chemical_classificationEPSILON-CAPROLACTONELactide010405 organic chemistryOrganic ChemistryGROUP-4 METAL-COMPLEXES[CHIM.CATA]Chemical Sciences/CatalysisImine ligands0104 chemical scienceschemistryINITIATORSGROUP-4 METAL-COMPLEXES; ALUMINUM COMPLEXES; EPSILON-CAPROLACTONE; LIGANDS SYNTHESIS; IMINE LIGANDS; STRUCTURAL-CHARACTERIZATION; CYCLIC ESTERS; ZINC; CATALYSTS; INITIATORS
researchProduct

Catalytic Functionalization of Methane and Light Alkanes in Supercritical Carbon Dioxide

2014

International audience; The development of catalytic methods for the effective functionalization of methane yet remains a challenge. The best system known to date is the so-called Catalytica Process based on the use of platinum catalysts to convert methane into methyl bisulfate with a TOF rate of 10−3 s. In this contribution, we report a series of silver complexes containing perfluorinated tris(indazolyl)borate ligands that catalyze the functionalization of methane into ethyl propionate upon reaction with ethyl diazoacetate (EDA) by using supercritical carbon dioxide (scCO2) as the reaction medium. The employment of this reaction medium has also allowed the functionalization of ethane, prop…

SilverLigands010402 general chemistry01 natural sciences7. Clean energyCatalysisCatalysischemistry.chemical_compoundEthyl propionateEthyl diazoacetateCoordination ComplexesMethyl bisulfateAlkanesOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistrySupercritical carbon dioxide010405 organic chemistryOrganic ChemistryButaneDiazonium CompoundsGeneral ChemistryCarbon Dioxide0104 chemical sciencesSolubilitychemistryIsobutaneOxidative coupling of methaneMethaneChemistry - A European Journal
researchProduct

Reinvestigation of the Pd-catalysed bis(silylation) of alkynes with 1,1,2,2-tetramethyl-1,2-bis(phenylthiomethyl)disilane: Unexpected formation of th…

2013

International audience; The bis(silylated) alkenes Z-(PhSCH2)Me2SiC(H)=C(Fc)SiMe2(CH2SPh) (2) and Z-(PhSCH2)Me2SiC(H)=C(bipheny)SiMe2(CH2SPh) (3) have been prepared by Pd-catalysed double silylation of ethynylferrocene and 4-ethynyl-1,1'-biphenyl in the presence of 1,1,2,2-tetramethyl-1,2-bis(phenylthiomethyl)disilane (1). A reinvestigation on the interaction of 1 with [PdCl2(PhCN)2] in technical-grade CH2Cl2 as solvent revealed competition between reduction to elemental palladium (due to oxidative addition of the Si-Si bond across Pd(II) and subsequent reductive elimination) and formation of an unusual eight-membered chelate complex cis-[PdCl2{(PhSCH2SiMe2)2O}] (4), which is fluxional in s…

SilylationStereochemistryEthynylferrocene[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryDFTReductive eliminationInorganic Chemistrychemistry.chemical_compound[ CHIM.CRIS ] Chemical Sciences/Cristallography[ CHIM.ORGA ] Chemical Sciences/Organic chemistryDisilaneMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryConformational isomerismComputingMilieux_MISCELLANEOUSThioether complexesSiloxane010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryDisiloxaneOxidative addition0104 chemical scienceschemistrySiloxaneDisilanePalladium
researchProduct

Spin forbidden chemical reactions of transition metal compounds. New ideas and new computational challenges.

2003

International audience; Many reactions of transition metal compounds involve a change in spin. These reactions may proceed faster, slower—or at the same rate as—otherwise equivalent processes in which spin is conserved. For example, ligand substitution in [CpMo(Cl)2(PR3)2] is faster than expected, whereas addition of dinitrogen to [Cp*Mo(Cl)(PMe3)2] is slow. Spin-forbidden oxidative addition of ethylene to [Cp*Ir(PMe3)] occurs competitively with ligand association. To explain these observations, we discuss the shape of the different potential energy surfaces (PESs) involved, and the energy of the minimum energy crossing points (MECPs) between them. This computational approach is of great he…

Spin states010405 organic chemistryChemistry02 engineering and technologyGeneral MedicineGeneral Chemistry021001 nanoscience & nanotechnology010402 general chemistryPhotochemistry01 natural sciencesChemical reactionPotential energyOxidative addition0104 chemical sciencesHybrid functional[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryTransition metalChemical physics[CHIM.COOR]Chemical Sciences/Coordination chemistryDensity functional theory0210 nano-technologySpin-½Chemical Society reviews
researchProduct

Ligand dissociation accelerated by spin state change: locating the minimum energy crossing point for phosphine exchange in CpMoCl2(PR3)2 complexes

2000

International audience; The minimum energy crossing point between the doublet and quartet potential energy surfaces of CpMoCl2(PH3)2 is calculated to lie 4.8 kcal mol−1 lower in energy than the doublet dissociative intermediate CpMoCl2(PH3). Implications for the influence of spin state changes on the rates of organometallic reactions are discussed.

Spin states010405 organic chemistryChemistryGeneral Chemistry010402 general chemistry01 natural sciencesPotential energyCatalysisDissociation (chemistry)3. Good health0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundComputational chemistryMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryAtomic physicsPhosphineNew Journal of Chemistry
researchProduct

Very Long-Lived Photogenerated High-Spin Phase of a Multistable Spin-Crossover Molecular Material

2018

The spin-crossover compound [Fe(n-Bu-im)3(tren)](PF6)2 shows an unusual long relaxation time of 20 h after light-induced excited spin state trapping when irradiating at 80 K. This is more than 40 times longer than when irradiating at 10 K. Optical absorption spectroscopy, magnetometry, and X-ray diffraction using synchrotron radiation were used to characterize and explain the different relaxation behaviors of this compound after irradiation below and above 70 K. Rearrangement of the butyl chains of the ligands occurring during the relaxation after irradiation above 70 K is thought to be responsible for the unusually long relaxation time at this temperature.

Spin statesAbsorption spectroscopy010405 organic chemistryChemistryRelaxation (NMR)General Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesBiochemistryMolecular physicsCatalysis0104 chemical sciencesColloid and Surface ChemistrySpin crossoverPhase (matter)Excited state[CHIM.COOR]Chemical Sciences/Coordination chemistryIrradiationSpin (physics)ComputingMilieux_MISCELLANEOUSJournal of the American Chemical Society
researchProduct

A Computational Study of Two-State Conformational Changes in 16-Electron [CpW(NO)(L)] Complexes (L=PH3, CO, CH2, HCCH, H2CCH2)

1999

International audience; High-spin and low-spin [CpW(NO) (L)] complexes are calculated to be remarkably close in energy. Several critical conformational changes in the singlet compounds are predicted to proceed more readily by spin crossover to the triplet hypersurface. The relationships between spin state, π bonding, ligand orientation, and geometry at W are explored.

Spin statesChemistryLigandOrganic ChemistryGeneral ChemistryState (functional analysis)ElectronSpin crossoverCatalysisTungstenLigand effects[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyDensity functional calculationsHypersurfaceSpin crossoverComputational chemistryPi interactionsPi interactionCondensed Matter::Strongly Correlated Electrons[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet state
researchProduct

Density Functional Study of Spin State in CpM(NO)X2 (M = Mo, Cr; X = Cl, NH2, CH3):  Spectrochemical and Nephelauxetic Effects in Organometallic Comp…

1998

International audience; The relationship between spin state and metal−ligand bonding interactions in CpM(NO)X2 species was investigated using density functional computational techniques. The geometries of CpM(NO)Cl2 (M = Cr, Mo), CpCr(NO)(NH2)X, and CpCr(NO)(CH3)X (X = Cl, CH3) were optimized at the DFT-B3LYP level for both the diamagnetic (S = 0) and paramagnetic (S = 1) electronic configurations. While the geometric parameters of the singlet compounds matched well with structures determined experimentally, the Cr−NO bond lengths in the triplet species exceeded the experimentally observed range by a significant margin, thereby indicating a propensity for nitrosyl-ligand dissociation from t…

Spin statesElectrical energyLigands010402 general chemistryQuantum mechanics01 natural sciencesDissociation (chemistry)Inorganic ChemistryParamagnetismchemistry.chemical_compoundMathematical methodsComputational chemistryAmide[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet statePhysical and Theoretical Chemistry010405 organic chemistryChemistryOrganic ChemistryAmides0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryBond lengthCrystallographyDiamagnetismElectron configurationOrganometallics
researchProduct

Electronic Structure Modulation in an Exceptionally Stable Non-Heme Nitrosyl Iron(II) Spin-Crossover Complex

2016

The highly stable nitrosyl iron(II) mononuclear complex [Fe(bztpen)(NO)](PF6)(2) (bztpen=N-benzyl-N,N',N'-tris(2-pyridylmethyl)ethylenediamine) displays an S=1/2 S=3/2 spin crossover (SCO) behavior (T-1/2=370 K, Delta H= 12.48 kJmol(-1), Delta S=33 JK(-1) mol(-1)) stemming from strong magnetic coupling between the NO radical (S=1/2) and thermally interconverted (S=0 S=2) ferrous spin states. The crystal structure of this robust complex has been investigated in the temperature range 120-420 K affording a detailed picture of how the electronic distribution of the t(2g)-e(g) orbitals modulates the structure of the {FeNO}(7) bond, providing valuable magneto-structural and spectroscopic correlat…

Spin statesIronInorganic chemistryAntiferromagnetic couplingEthylenediamineCrystal structureElectronic structure010402 general chemistry01 natural sciencesCatalysisFerrouschemistry.chemical_compoundAtomic orbitalSpin crossover[CHIM.COOR]Chemical Sciences/Coordination chemistryMolecular structures010405 organic chemistryEstructura molecularOrganic ChemistryNitric oxideGeneral ChemistryAtmospheric temperature rangeSpin crossoverÒxid nítric0104 chemical sciences3. Good healthCrystallographychemistryFISICA APLICADANitrosyl complexesMolecular structureFerroChemistry - A European Journal
researchProduct