Search results for "phosphine"

showing 10 items of 618 documents

Fonctionnalisation et métallisation des diamantoïdes

2015

The thesis deals with development of synthetic methods for preparation of novel carbon-metal organohybrid based on diamondoid and palladium. The vapor pressure of various diamondoids was measured from a new measurement protocol at solid-vapor thermodynamic equilibrium state. Their volatile tendency opened a possibility to do deposition from gas phase and at various pressure (ambient, primary vacuum, and high vacuum) of diamondoids on silicon or mica substrates. SEM observations have shown that depending on the type of functional groups on the diamondoid, different crystal shapes can be produced (rods, needles, triangles, truncated octahedral form).OMCVD of palladium on functionalized diaman…

Functionalized diamondoidfunctionalized diamondoidsOMCVD de palladiumChemistry & allied sciencesPd OMCVDhybrid materialair-stable phosphineAir-stable phosphineorganic self-assemblyOrganic self-assembly[CHIM.OTHE] Chemical Sciences/Other[ CHIM.OTHE ] Chemical Sciences/Otherddc:540[CHIM.OTHE]Chemical Sciences/OtherHybrid material
researchProduct

Catalytic systems based on transition metals for the carbonylation of methanol to dimethylcarbonate

1997

Abstract The results of an investigation on catalytic systems arising from the electrochemical activation of salts and complexes of several transition metals for the carbonylation of methanol to dimethylcarbonate (DMC) are reported. Metals were tested as inorganic salts or complexes with ligands such as 2,2′-bipyridine (bipy), 1,6-bis (2-oxyphenyl)-2,5-diaza-1,5-hexadiene (salen), 2,4-pentanedionate (acac), triphenylphosphine (TPP) in methanol at room temperature saturated with carbon monoxide at atmospheric pressure. Best faradic yields vs DMC were observed as follows: CuCl(bipy): 84.8%; PdCl 2 (bipy): 64.0%; CoCl 2 : 26.0%; RhCl 3 : 25.0%; AgBF 4 (bipy): 10.2%; AuCl 3 : 9.4%; Cr(acac) 3 :…

General Chemical EngineeringInorganic chemistryPrimary alcoholElectrosynthesisMedicinal chemistryCatalysischemistry.chemical_compoundTransition metalchemistryElectrochemistryMethanolTriphenylphosphineCarbonylationCarbon monoxide
researchProduct

Hydroformylation of 1-Octene in Supercritical Carbon Dioxide: Can Alkylation of Arylphosphines with tertButyl Groups Lead to Soluble and Active Catal…

2008

Abstract The possibility of increasing the solubility and activity of rhodium catalysts in the hydroformylation of 1-octene in supercritical carbon dioxide (scCO2) by attachment of tertbutyl (tBu) groups to the triarylphosphine ligand was investigated. The solubility of the parent and monoalkylated ligands in a mixture of gaseous components (CO2/CO/H2) was evaluated by visual observation in a view cell. In the case of triphenylphosphine, introduction of one tertbutyl group does not seem to affect the solubility of the phosphine. When the behaviour of (diphenyl)biphenylphosphine and (para-tertbutyldiphenyl)biphenylphosphine was compared a clear solubilising effect of the tBu group was observ…

General Chemical Engineeringchemistry.chemical_elementHomogeneous catalysisAlkylationCondensed Matter PhysicsCatalysisRhodiumchemistry.chemical_compoundchemistryOrganic chemistryPhysical and Theoretical ChemistryTriphenylphosphineSolubilityHydroformylationPhosphine
researchProduct

Progress in palladium-based catalytic systems for the sustainable synthesis of annulated heterocycles: a focus on indole backbones

2012

BIOVERT+LDJ; A survey highlighting the most recent palladium catalytic systems produced and their performances for progress in direct synthesis of indole backbones by heterocarbocyclization of reactive substrates is provided. The discussion is developed in relation with the principles of sustainable chemistry concerning atom and mass economy. In this respect, the general convergent character of the syntheses is of particular interest (one-pot, domino, cascade or tandem reactions), and the substrates accessibility and reactivity, together with the final waste production, are also important. This critical review clearly indicates that the development of ligand chemistry, mainly phosphines and…

Green chemistryIndole testIndolesPhosphines010405 organic chemistryLigandchemistry.chemical_elementChemistry Techniques Synthetic[CHIM.CATA]Chemical Sciences/CatalysisGeneral ChemistryLigands010402 general chemistry[SDE.ES]Environmental Sciences/Environmental and Society01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistryWaste productionAlkynesOrganic chemistryReactivity (chemistry)MethanePalladiumPalladiumChemical Society Reviews
researchProduct

Ultra-Low Catalyst Loading as a Concept in Economical and Sustainable Modern Chemistry: The Contribution of Ferrocenylpolyphosphane Ligands

2007

The challenge of sustainability in modern chemistry will be met with new technologies and processes provided significant progress is made in several key research areas, such as the expansion of chemistry from renewable feedstock, the design of environmentally benign chemicals and solvents, the minimization of depletive resources, and the development of high-performance catalysis. In this prospect, ligand chemistry is a pivotal science that links modern-organic,-inorganic, -organometallic, and -coordination chemistry through a vast number of valuable applications, precisely associated to catalysis. We review in this article our recent work on catalysis promoted by original ferrocenyl tetra-,…

Green chemistryaminesSonogashira couplingHomogeneous catalysisvinylation catalystsultra-low010402 general chemistry01 natural sciencesCatalysisCoordination complexInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundcross-couplingferrocenylpolyphosphineOrganic chemistrycatalyzedDiphosphaneReactivity (chemistry)ComputingMilieux_MISCELLANEOUSAminationchemistry.chemical_classificationalkynylationligands010405 organic chemistryChemistryLigandSonogashira[CHIM.CATA]Chemical Sciences/CatalysisGeneral MedicinepalladiumCombinatorial chemistry0104 chemical sciencesHeckcoupling reactionChemInform
researchProduct

First donor stabilized-phosphenium rhodium complexes

2008

Abstract The coordination properties of a donor stabilized-phosphenium adduct have been examined in rhodium chemistry. The preparation as well as the characterization of the first examples of donor stabilized-phosphenium rhodium(I) complexes is reported in this paper. Indeed, mono- and di-cationic rhodium complexes were obtained in quantitative yield by the direct addition of this imidazolium P(III)-ligand to [RhCl(1,5-COD)] 2 in CH 2 Cl 2 solution with a 1:1 P/Rh ratio under argon and 2:1 P/Rh ratio under CO atmosphere, respectively. Crystal structure of the bis-cationic donor stabilized-phosphenium rhodium(I) complex has been obtained from an acetone/pentane mixture. Its molecular structu…

Halidechemistry.chemical_elementCrystal structure010402 general chemistryPhotochemistry01 natural sciencesAdductRhodiumInorganic Chemistrychemistry.chemical_compounddonor–acceptor ligandPolymer chemistryMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryphospheniumPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS010405 organic chemistryChemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryphosphine3. Good health0104 chemical sciencesPentaneYield (chemistry)rhodiumelectronic propertiesPhosphine
researchProduct

P-chirogenic secondary phosphine oxides : new synthesis and applications

2015

A new stereoselective synthesis of phosphinous acid boranes is described by hydrolysis of aminophosphines boranes prepared by reaction of the oxazaphospholidine complex derived from ephedrine with organolithium reagents.By reaction with a strong acid, the phosphinous acid boranes lead to the corresponding P-chirogenic secondary phosphine oxides in very good yields (90%) and with complete retention of the configuration at the phosphorus atom. The secondary phosphine oxides have been used in asymmetric hydrogenation and intramolecular Heck cyclisation using rhodium and palladium complexes, respectively. In a second part, a new synthesis of P-chirogenic ortho-halogenophenyl phosphine oxides is…

HomocouplingAcide phosphineux-boranePhosphinous acid boraneAsymmertric catalysisHomocouplage[CHIM.ORGA]Chemical Sciences/Organic chemistryP-chirogenic ligandOxyde de phosphine secondaire[CHIM.ORGA] Chemical Sciences/Organic chemistryO-halogénophosphineHétérocouplageCluster chiraux[ CHIM.ORGA ] Chemical Sciences/Organic chemistryCatalyse asymétriqueSecondary phosphine oxideHeterocouplingLigand P-chirogéniqueChiral cluster
researchProduct

Mono- and di-bridged heterobimetallic systems from group 5 hydride phosphido and hydride phosphino metalloligands. Crystal structure of Cp2Ta(H)( μ-H…

1997

Abstract The trihydrides Cp2MH3 (M  Nb, Ta) react with chlorophosphines PR2Cl (R  Me, Ph) affording phosphonium salts [Cp2MH2(PR2H)]+, Cl− (2 (a, b) 2′ (a, b)). Depending on the metal (Nb or Ta) and on the nature of the phosphine substituent (Me or Ph), deprotonation of these salts leads to hydride phosphino Cp2MH(PR2H) (3 (a, b) 3′a) or hydrided phosphido Cp2 TaH2(PPh2) (4′b) metalloligands. These two kinds of complexes are able to bind [M′(CO)5] or [M′(CO)4] (M′  Cr, Mo, W) organometallic fragments to give mono- or di-bridged heterobimetallic systems. The crystallographic analysis of Cp2Ta(H)(μ-H)(μ-PMe2)Cr(CO)4 (7′aCr) is reported and discussed.

HydrideStereochemistryOrganic ChemistrySubstituentCrystal structureBiochemistryMedicinal chemistryInorganic ChemistryMetalchemistry.chemical_compoundDeprotonationchemistryGroup (periodic table)visual_artMaterials Chemistryvisual_art.visual_art_mediumPhosphoniumPhysical and Theoretical ChemistryPhosphineJournal of Organometallic Chemistry
researchProduct

Hydrogen bonding and proton transfer involving the trihydride complexes Cp*M(dppe)H 3 (M = Mo, W) and fluorinated alcohols: the competitive role of t…

2003

International audience; The protonation of complexes Cp*M(dppe)H3 (dppe is ethylenebis(diphenylphosphine), M = Mo (1), W (2)) by a variety of fluorinated alcohols of different acid strength (FCH2CH2OH, CF3CH2OH, (CF3)2CHOH, and (CF3)3COH) was investigated experimentally by the variable temperature spectroscopic methods (IR, NMR) and stopped-flow technique (UV-Vis). The structures of the hydrogen-bonded and proton transfer products were studied by DFT calculations. In agreement with the calculation results, the IR data suggest that the initial hydrogen bond is established with a hydride site for complex 1 and with the metal site for complex 2. However, no intermediate dihydrogen complex foun…

Hydrogen bondingTheoretical studyUv-vis NMR spectroscopyInorganic chemistryTransition metal polyhydridesInfrared spectroscopyProtonation010402 general chemistry01 natural sciencesProton transferMetalchemistry.chemical_compound[CHIM.COOR]Chemical Sciences/Coordination chemistrychemistry.chemical_classificationDiphenylphosphine010405 organic chemistryHydrogen bondChemistryHydrideGeneral Chemistry0104 chemical sciencesCrystallographyAcid strengthvisual_artvisual_art.visual_art_mediumIRDihydrogen complex
researchProduct

Resolution of β-aminophosphines with chiral cyclopalladated complexes

2005

Abstract Resolution of the racemic chiral β-aminophosphines Ph 2 PCH 2 CH(Ph)NH(Ar) ( L 1 for Ar = C 6 H 5 and L 2 for Ar = 2,6-C 6 H 3 i Pr 2 ) has been investigated by use of different cyclopalladated complexes as chiral agents. The resulting complexes afford diastereomeric adducts in a 1:1 ratio. After successive crystallizations from ethanol, a d.e. of 98% was achieved for one aminophosphine palladium complex, while no significant d.e. was obtained after crystallizations from chlorinated solvents. The X-ray structure analysis has pointed out intermolecular hydrogen interactions N–H⋯Cl between the P,N ligand and the chloride ion, which are responsible for the formation and stabilization …

HydrogenAminophosphinesStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryChlorideMedicinal chemistryAdductInorganic ChemistryMaterials Chemistrymedicine[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistry010405 organic chemistryLigandOrganic ChemistryIntermolecular forceDiastereomerAbsolute configuration0104 chemical scienceschemistryPN ligandsRacemic resolutionChiral palladium complexesX-ray structuresPalladiummedicine.drugJournal of Organometallic Chemistry
researchProduct