Search results for "phosphine"

showing 10 items of 618 documents

Structural and Electrochemical Studies of Copper(I) Complexes with Diethoxyphosphoryl-1,10-phenanthrolines

2014

Two series of copper(I) complexes with diethoxyphosphoryl-substituted 1,10-phenanthroline ligands were synthesized and characterized in the solid state and in solution. The first comprised mixed-ligand CuI complexes with phenanthroline and triphenylphosphine. The second series includes bis-chelates with two phenanthroline ligands. According to the X-ray data for the six complexes, the ditopic phenanthroline ligands exhibit bidentate coordination to the copper(I) atom through two nitrogen atoms in both series. Solution equilibria involving different phenanthroline copper(I) species were studied by 1H and 31P NMR spectroscopy, electrochemistry, and spectroelectrochemistry. The solution specia…

Coordination sphereDenticityLigandPhenanthrolineInorganic chemistrySubstituentchemistry.chemical_elementCopperInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistry[CHIM]Chemical SciencesSolvent effectsTriphenylphosphineComputingMilieux_MISCELLANEOUS
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[Ag67(SPhMe2)32(PPh3)8]3+: Synthesis, Total Structure, and Optical Properties of a Large Box-Shaped Silver Nanocluster

2016

Engineering the surface ligands of metal nanoparticles is critical in designing unique arrangements of metal atoms. Here, we report the synthesis and total structure determination of a large box-shaped Ag67 nanocluster (NC) protected by a mixed shell of thiolate (2,4-dimethylbenzenethiolate, SPhMe2) and phosphine (triphenylphosphine, PPh3) ligands. Single crystal X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revealed the cluster formula to be [Ag67(SPhMe2)32(PPh3)8]3+. The crystal structure shows an Ag23 metal core covered by a layer of Ag44S32P8 arranged in the shape of a box. The Ag23 core was formed through an unprecedented centered cuboctahedron, i.e.,…

CuboctahedronElectrospray ionizationnanoclusters02 engineering and technologyElectronic structureCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryTriphenylphosphinemetal nanoparticlesta116ta114ChemistryLigandGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographysurface ligandsvisual_artvisual_art.visual_art_medium0210 nano-technologySingle crystalJournal of the American Chemical Society
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CCDC 229367: Experimental Crystal Structure Determination

2005

Related Article: C.Ornelas, C.Gandum, J.Mesquita, J.Rodrigues, M.H.Garcia, N.Lopes, M.P.Robalo, K.Nattinen, K.Rissanen|2005|Inorg.Chim.Acta|358|2482|doi:10.1016/j.ica.2005.02.002

Cyano-(eta^5^-cyclopentadienyl)-bis(triphenylphosphine)-ruthenium methanol solvate hydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Cyclopentadiene with two coordinating sites: 1,5-bis(diphenylphosphino) -2,3,4-trimethylcyclopenta-1,3-diene

1997

Abstract The possibility of obtaining the new bidentate 1,2-diphenylphosphinocyclopentadienyl ligand has been studied. 1,5-bis(diphenylphosphino)-2,3,4-trimethylcyclopenta-1,3-diene can be formed from butanone and chlorodiphenylphosphine in eight steps. The results of chemical and spectroscopic studies reveal that a 1.5-sigmatropic migration of the diphenylphosphino group takes place: the 1,2-diphenylphosphino-substituted species are converted into 1.3 species.

CyclopentadieneDenticityDieneStereochemistryLigandOrganic ChemistryButanoneBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundChalcogenchemistryMaterials ChemistryChlorodiphenylphosphinePhysical and Theoretical ChemistryPhosphineJournal of Organometallic Chemistry
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Ruthenium titanocene and ruthenium titanium half-sandwich bimetallic complexes in catalytic cyclopropanation

2005

Abstract The reaction of the phosphine functionalised titanium half-sandwich complexes 7, 9 and 10 with the binuclear complex [(p-cymene)RuCl2]2 allowed the access to three new early-late bimetallic complexes (p-cymene)[(μ-η5:η1-C5H4(CH2)nPR2)TiX3]RuCl2 (11–13). The structure of 11 (n = 0, X = Cl) has been confirmed by X-ray diffraction. The ruthenium titanium half-sandwich bimetallic complexes so formed and the ruthenium titanocene analogues 4–6 catalyse the addition of ethyl diazoacetate to styrene with high selectivity toward cyclopropanation versus metathesis contrary to the monometallic complexes (p-cymene)RuCl2PR3.

CyclopropanationOrganic Chemistrychemistry.chemical_elementMetathesisBiochemistryCatalysisRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryEthyl diazoacetatePolymer chemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryBimetallic stripPhosphineTitaniumJournal of Organometallic Chemistry
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Enantiocontrol in the intermolecular cyclopropanation reaction catalyzed by dirhodium(II) complexes with ortho-metalated aryl phosphine ligands

2001

(P) and (M) dirhodium(II) complexes with ortho-metalated aryl phosphines are assessed as chiral catalysts in the enantioselective cyclopropanation of styrenes by ethyl diazoacetate; enantioselectivities up to 91% and up to 87%, respectively, for cis- and trans-2-arylcyclopropanecarboxylates are observed. Barberis, Mario, Mario.Barberis@uv.es ; Lahuerta Peña, Pascual, Pascual.lahuerta@uv.es ; Perez Prieto, Julia, Julia.Perez@uv.es ; Sanau Torrecilla, Mercedes, Mercedes.Sanau@uv.es

CyclopropanationUNESCO::QUÍMICAMedicinal chemistry:QUÍMICA [UNESCO]CatalysisCatalysischemistry.chemical_compoundEthyl diazoacetateMaterials ChemistryOrganic chemistryPhosphine ligandsEnantiocontrol ; Intermolecular cyclopropanation ; Catalyst ; Phosphine ligandsArylIntermolecular forceMetals and AlloysEnantioselective synthesisGeneral ChemistryUNESCO::QUÍMICA::Química macromolecularSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnantiocontrolchemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]CatalystIntermolecular cyclopropanationPhosphine
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Enantio- and diastereocontrol in intermolecular cyclopropanation reaction of styrene catalyzed by dirhodium(II) complexes with bulky ortho-metalated …

2004

Enantiomerically pure dirhodium(II) complexes with ortho-metalated p-substituted aryl phosphines have been shown to be enantio- and diastereoselective in the cyclopropanation of styrene by ethyl diazoacetate. Enantioselectivities up to 91% and diastereoselectivities up to 90% are observed for ethyl cis-2-phenylcyclopropanecarboxylate. Estevan Estevan, Francisco, Francisco.Estevan@uv.es ; Lahuerta Peña, Pascual, Pascual.lahuerta@uv.es ; Lloret Fillol, Julio, Julio.Lloret@uv.es ; Sanau Torrecilla, Mercedes, Mercedes.Sanau@uv.es ; Ubeda Picot, M Angeles, Angeles.Ubeda@uv.es ; Vila Gomez, Jaume Llorenc, Jaume.Vila@uv.es

CyclopropanesModels MolecularReactionPhosphinesCyclopropanationUNESCO::QUÍMICAIntermolecularCrystallography X-RayMedicinal chemistryHydrocarbons Aromatic:QUÍMICA [UNESCO]CatalysisStyrenesCatalysisStyrenechemistry.chemical_compoundEthyl diazoacetateOrganometallic CompoundsMaterials ChemistryOrganic chemistryRhodiumIntermolecular ; Reaction ; Dirhodium ; Phosphines ; CyclopropanationMolecular StructureCyclopropanationArylIntermolecular forceUNESCO::QUÍMICA::Química analíticaMetals and AlloysStereoisomerismGeneral MedicineGeneral ChemistryDirhodiumSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCyclization:QUÍMICA::Química analítica [UNESCO]Ceramics and Composites
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Phosphine Ligands Based on the Ferrocenyl Platform: Advances in Catalytic Cross-Couplings

2023

Ferrocenyl skeletons tagged with a variety of donor atoms (metalloligands) have become popular in modern metal-catalyzed organic transformations, broadening the applications. Ferrocenylphosphines, such as 1′-bis(diphenylphosphino)ferrocene (dppf), have been widely used as metalloligands in academic and industrial research, motivating further investigation into novel ferrocenylphosphine ligands. The current review concentrated non-exhaustively on emblematic applications of different ferrocenylphosphine ligands in transition metal-catalyzed cross-coupling strategies. Initially, the stereochemical aspects of the ferrocenyl skeleton, nomenclature, and applications of chiral ferrocenyl phosphine…

C–C cross-couplingTransition metal catalysisC– heteroelement bond formationStructure[CHIM.CATA] Chemical Sciences/Catalysis[CHIM.COOR] Chemical Sciences/Coordination chemistryFerrocenylphosphine
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Template-controlled assembly of ditopic catechol phosphines: a strategy for the generation of complexes of bidentate phosphines with different bite a…

2008

A rational approach to the synthesis of heterobi- or -trimetallic complexes based upon self-assembly of a flexible ditopic catechol-phosphine ligand with [(cod)PdCl(2)] and simple metal halides such as GaCl(3), BiCl(3), SnCl(4), or ZrCl(4) is described. All products were characterized by spectroscopic and analytical data and single-crystal X-ray diffraction studies. The molecular structures can be described in terms of cis-configured palladium complexes with supramolecular bisphosphine ligands that are formed by the assembly of two phosphine catecholate fragments on a main group/transition metal template. Of particular interest are the distinct decreases in P-Pd-P bite angles and P...P dist…

Denticity010405 organic chemistryStereochemistryLigandOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographyMetal halideschemistryTransition metalCovalent radiusPhosphinePalladiumChemistry (Weinheim an der Bergstrasse, Germany)
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Catalytic Efficiency of a New Tridentate Ferrocenyl Phosphine Auxiliary: Sonogashira Cross-Coupling Reactions of Alkynes with Aryl Bromides and Chlor…

2005

[structure: see text] The catalytic activity in Sonogashira cross-coupling reactions of alkynes with a variety of aryl halides (including chlorides) using a multidentate ferrocenyl phosphine is presented. The novel mixed ferrocenyl aryl/alkyl triphosphine is thermally stable and insensitive to air or moisture, and its robustness allows aryl alkynylation at 10(-1) to 10(-4) mol % catalyst loadings with TONs up to 250,000. Copper-free coupling using phenylacetylene is also accessible in good yield.

DenticityArylOrganic ChemistrySonogashira couplingHalideGeneral MedicineBiochemistryCoupling reactionCatalysischemistry.chemical_compoundchemistryPolymer chemistryOrganic chemistryPhysical and Theoretical ChemistryCatalytic efficiencyPhosphineChemInform
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