Search results for "COORDINATION CHEMISTRY"

showing 10 items of 231 documents

Photochemical intermediates of trans-Rh(CO)L2Cl where L=PMe3, PBu3, and i-Pr2HN and cis-Rh(CO)2(i-Pr2HN)Cl in frozen organic glasses

2002

International audience; The Nujol glass matrix photolyses of Rh(CO)(PMe3)2Cl (1), Rh(CO)(PBu3)2Cl (2), Rh(CO)2(i-Pr2HN)Cl (3), and Rh(CO)(i-Pr2HN)2Cl (4), have been examined. Phototolysis of 1 (λirr>400 nm) and 2 (350<λirr<400 nm) give new species, A, with carbonyl stretching bands slightly below the parent bands. In the case of 1 this species appears to give rise to a second product, C, upon either extended photolysis or annealing. High-energy photolysis of 1, 2, and 4, result in loss of CO and formation of an IR silent species, RhL2Cl. In the case of 1 a new carbonyl species, B, is observed upon high-energy photolysis or annealing of a matrix containing CO and Rh(PMe3)2Cl. B may be conver…

Photolysis010405 organic chemistryChemistryAnnealing (metallurgy)Organic ChemistryPhotodissociationAmine derivatives010402 general chemistryPhotochemistryGlass matrix01 natural sciencesBiochemistry0104 chemical sciencesInorganic ChemistryDFT analysischemistry.chemical_compoundNujolExcited stateMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryPhosphineAmine derivativesJournal of Organometallic Chemistry
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Carboranyl Substituted Siloxanes and Octasilsesquioxanes: Synthesis, Characterization, and Reactivity

2008

Carboranyl-containing disiloxane, cyclic-siloxane and cage-like silsesquioxane have been prepared in high yields. Two routes are compared for their preparation, a classical hydrolytic process based on hydrolysis and condensation of the freshly prepared carboranylalkylchlorosilane and ethoxysilane precursors and a nonhydrolytic route based on the specific reactivity of chorosilane toward DMSO. Based on the typical reactivity of the carboranyl group toward nucleophiles, dianionic disiloxanes and octaanionic silsesquioxanes were obtained without modification of the siloxane bond. Products are fully characterized by FTIR, NMR and MALDI-TOF methods.

Polymers and Plastics010405 organic chemistryOrganic ChemistryChemical modification[CHIM.MATE]Chemical Sciences/Material chemistryDisiloxane010402 general chemistry01 natural sciencesSilsesquioxane0104 chemical sciencesInorganic Chemistrychemistry.chemical_compound[CHIM.POLY]Chemical Sciences/PolymersNucleophilechemistrySiloxanePolymer chemistryMaterials ChemistryCarboraneOrganic chemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)ComputingMilieux_MISCELLANEOUSMacromolecules
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Highly trans-stereospecific Isoprene Polymerization by Neodymium Borohydrido Catalysts

2005

Highly stereospecific polymerization of isoprene was achieved using borohydridoneodymium complexes. In combination with stoichiometric amounts of dialkylmagnesium, Nd(BH4)3(THF)3 (1) and Cp*‘Nd(BH4)2(THF)2 (2) (Cp*‘ = C5Me4nPr) afford very efficient catalysts. The activity reaches 37300 (g of polyisoprene/mol of Nd)/h. Half-lanthanidocene 2 gives rise to polyisoprene, 98.5% trans-regular, the highest content yet described for a homogeneous organometallic catalyst. NMR experiments argue for the formation of bimetallic Nd(μ-BH4)Mg active species.

Polymers and Plasticschemistry.chemical_element010402 general chemistry01 natural sciencesNeodymiumCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundStereospecificityPolymer chemistryMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryBimetallic stripIsoprene010405 organic chemistryChemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[ CHIM.POLY ] Chemical Sciences/Polymers[CHIM.POLY]Chemical Sciences/PolymersPolymerizationHomogeneousStoichiometry
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Chimie de coordination du phosphore aux métaux du groupe 11 : progrès en catalyse de couplage C-N au Cu(I) et nouveaux complexes polyphosphines de l'…

2014

Nowadays, sustainable development encourages chemists to develop new economic and ecologic synthesis, because natural ressources are reducing. Most exploited ressources are gas and petroleum, but precious metals are also essential. This thesis is focusing on the enhancement of gold and copper complexes, obtained in our laboratory from phosphorous-based ligands. In the first part, we will develop a new system for the N-arylation of pyrazoles from a copper complexe coordinated by a new hybrid phosphinoalkene ligand. In the second part, coordination properties of gold to different ferrocenic polyphosphine will be studied. Several new innovative complexes will be isolated, and could be used in …

Polyphosphine ferrocéniqueAurophilicity[CHIM.ORGA]Chemical Sciences/Organic chemistryOrHybrid ligandLigand hybrideCatalyse[CHIM.ORGA] Chemical Sciences/Organic chemistryFerrocenic polyphosphineCatalysisChimie de coordinationCoordination chemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryCuivreGoldAurophilieCopper
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Regioselective C–H amination of free base porphyrins via electrogenerated pyridinium-porphyrins and stabilization of easily oxidized amino-porphyrins…

2020

Four free base aminoporphyrins were synthesized in two steps via regioselective anodic nucleophilic substitution with pyridine followed by ring opening of the electrogenerated pyridinium with piperidine. The X-ray crystallographic structure of the unstable 2-aminotetraphenylporphyrin was solved. Protonation of this latter compound leads to the stable diiminium porphyrin salt.

Protonation010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryPyridinePolymer chemistryMaterials ChemistryNucleophilic substitution[CHIM.COOR]Chemical Sciences/Coordination chemistryAmination[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryMetals and AlloysFree base[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryPorphyrin0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesPyridiniumPiperidineChemical Communications
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Synergetic effect of host-guest chemistry and spin crossover in 3D Hofmann-like metal-organic frameworks [Fe(bpac)M(CN)4] (M=Pt, Pd, Ni).

2012

The synthesis and characterization of a series of three-dimensional (3D) Hofmann-like clathrate porous metal-organic framework (MOF) materials [Fe(bpac)M(CN) 4] (M=Pt, Pd, and Ni; bpac=bis(4-pyridyl)acetylene) that exhibit spin-crossover behavior is reported. The rigid bpac ligand is longer than the previously used azopyridine and pyrazine and has been selected with the aim to improve both the spin-crossover properties and the porosity of the corresponding porous coordination polymers (PCPs). The 3D network is composed of successive {Fe[M(CN) 4]} n planar layers bridged by the bis-monodentate bpac ligand linked in the apical positions of the iron center. The large void between the layers, w…

Pyrazine010405 organic chemistryChemistryStereochemistrymicroporous materialsTransition temperatureOrganic Chemistryhost–guest systemsStackingSpin transitionGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographymetal–organic frameworksspin crossoverSpin crossoveradsorptionMoleculeMetal-organic framework[CHIM.COOR]Chemical Sciences/Coordination chemistryHost–guest chemistryChemistry (Weinheim an der Bergstrasse, Germany)
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Unveiling the Effect of Magnetic Noise in the Coherence of Single-Molecule Quantum Processors.

2019

Quantum bits (qubits) constitute the most elementary building-blocks of any quantum technology, where information is stored and processed in the form of quantum superpositions between discrete energy levels. In particular, the fabrication of quantum processors is a key long-term goal that will allow us conducting specific tasks much more efficiently than the most powerful classical computers can do. Motivated by recent experiments in which three addressable spin qubits are defined on a potential single-molecule quantum processor, namely the [Gd(H2O)P5W30O110]12− polyoxometalate, we investigate the decohering effect of magnetic noise on the encoded quantum information. Our state-of-the-art m…

Quantum decoherenceDephasingmolecular magnetism02 engineering and technology010402 general chemistry01 natural scienceslcsh:Chemistryquantum algorithmQuantum mechanicspolyoxometalateQuantum informationdecoherenceQuantumscalabilityQuantum computerOriginal ResearchPhysicsmolecular spin qubitsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesQuantum technologyChemistrymolecular nanomagnetlcsh:QD1-999Qubitcoordination chemistryQuantum algorithm0210 nano-technologyFrontiers in chemistry
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An Experimental and Computational Study on the Effect of Al(OiPr)3 on Atom-Transfer Radical Polymerization and on the Catalyst-Dormant Chain Halogen …

2005

International audience; Compound Al(OiPr)3 is shown to catalyze the halide-exchange process leading from [Mo(Cp)Cl2(iPrN=CH-CH=NiPr)] and CH3CH(X)COOEt (X=Br, I) to the mixed-halide complexes [Mo(Cp)ClX(iPrN=CH-CH=NiPr)]. On the other hand, no significant acceleration is observed for the related exchange between [MoX3(PMe3)3] (X=Cl, I) and PhCH(Br)CH3, by analogy to a previous report dealing with the RuII complex [RuCl2(PPh3)3]. A DFT computation study, carried out on the model complexes [Mo(Cp)Cl2(PH3)2], [MoCl3(PH3)3], and [RuCl2(PH3)3], and on the model initiators CH3CH(Cl)COOCH3, CH3Cl, and CH3Br, reveals that the 16-electron RuII complex is able to coordinate the organic halide RX in a…

Radical polymerizationHalide010402 general chemistryPhotochemistry01 natural sciencesCatalysisAdductLewis acid catalysisNucleophilic substitution[CHIM.COOR]Chemical Sciences/Coordination chemistryLewis acids and bases010405 organic chemistryAtom-transfer radical-polymerizationChemistryOrganic ChemistryGeneral ChemistryHalide exchange[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciencesLewis acid catalysis[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallography[CHIM.POLY]Chemical Sciences/PolymersDensity functional theoryDensity functional theoryHalogen atom transfer
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From CO2 to dimethyl carbonate with dialkyldimethoxystannanes: the key role of monomeric species.

2011

International audience; The formation of dimethyl carbonate (DMC) from CO(2) and methanol with the dimer [n-Bu(2)Sn(OCH(3))(2)](2) was investigated by experimental kinetics in support of DFT calculations. Under the reaction conditions (357-423 K, 10-20 MPa), identical initial rates are observed with three different reacting mixtures, CO(2)/toluene, supercritical CO(2), and CO(2)/methanol, and are consistent with the formation of monomeric di-n-butyltin(iv) species. An intramolecular mechanism is, therefore, proposed with an Arrhenius activation energy amounting to 104 ± 10 kJ mol(-1) for DMC synthesis. DFT calculations on the [(CH(3))(2)Sn(OCH(3))(2)](2)/CO(2) system show that the exothermi…

Reaction mechanismDimerInorganic chemistryGeneral Physics and AstronomyCATALYSTSActivation energy010402 general chemistry01 natural sciencesMedicinal chemistryHOMOGENEOUS HYDROGENATIONCatalysischemistry.chemical_compoundsymbols.namesake[CHIM.ANAL]Chemical Sciences/Analytical chemistryReactivity (chemistry)Physical and Theoretical ChemistryCOORDINATION CHEMISTRYCOPOLYMERIZATIONCHALLENGES010405 organic chemistryOXIDEREACTIVITY0104 chemical sciencesGibbs free energy[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryIntramolecular force[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrysymbols[ CHIM.ANAL ] Chemical Sciences/Analytical chemistryMETAL-COMPLEXESDimethyl carbonateEPOXIDESDIOXIDE
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Copper(II)-dipicolinate-mediated clickable azide–alkyne cycloaddition in water as solvent

2018

Copper(II)-dipicolinate complex [CuIIL(H2O)2] (1) (H2L = dipicolinic acid (H2dipic)) was synthesized via oxidation of copper(I) iodide and pyridine-2,6-dicarboxylic acid in water and acetonitrile in the presence of glycine. Complex 1 was characterized by FT-IR and elemental analysis and its structure confirmed by single crystal X-ray analysis. This complex is an efficient precatalyst that mediates azide-alkyne cycloaddition reactions in water at room temperature either in the absence or presence of a reducing agent. Compound 1-mediated azide-alkyne cycloaddition affords alkyl/aryl substituted 1,2,3-triazole heterocycles in a regioselective manner and excellent yields under very mild reactio…

Reducing agent3-TriazolesIodide12Alkyne010402 general chemistry01 natural scienceschemistry.chemical_compoundPolymer chemistryMaterials Chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryAcetonitrilechemistry.chemical_classification010405 organic chemistryChemistryClick chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryAryl[CHIM.CATA]Chemical Sciences/CatalysisAzide-alkyne cycloadditionCycloaddition0104 chemical sciencesDipicolinic acidClick chemistryAzideCopperHomogenous catalysis
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