Search results for "Phosphine"

showing 10 items of 618 documents

Synthesis, reactivity, and computational analysis of halophosphines supported by dianionic guanidinate ligands.

2012

The reported chemistry and reactivity of guanidinate supported group 15 elements in the +3 oxidation state, particularly phosphorus, is limited when compared to their ubiquity in supporting metallic elements across the periodic table. We have synthesized a series of chlorophosphines utilizing homo- and heteroleptic (dianionic)guanidinates and have completed a comprehensive study of their reactivity. Most notable is the reluctancy of these four-membered rings to form the corresponding N-heterocyclic phosphenium cations, the tendency to chemically and thermally eliminate carbodiimide, and the scarcely observed ring expansion by insertion of a chloro(imino)phosphine into a P-N bond of the P-N-…

AnionsModels MolecularPhosphinesRing (chemistry)Crystallography X-RayLigandsBiochemistryGuanidinesCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryGroup (periodic table)Oxidation statePolymer chemistryOrganic chemistryMoleculeReactivity (chemistry)ta116chemistry.chemical_classificationMolecular StructureChemistryGeneral ChemistryElectron acceptorvisual_artvisual_art.visual_art_mediumQuantum TheoryPhosphineJournal of the American Chemical Society
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Inhibitoren der Korrosion (11). Nachweis der auf Eisengrenzflächen gebildeten Sekundärinhibitoren durch UV-Absorptions- und Fluoreszenzspektroskopie

1972

Aus Triphenylbenzylphosphoniumchlorid bildet sich in saurer Losung auf der Eisenoberflache eine Schicht, die aufgrund der UV-Reflexionsspektroskopie mit Triphenylphosphin identisch sein durfte. Auch das Mono- und Bis-Phosphoniumsalz wird an der Eisengrenzflache reduktiv abgebaut; die dabei entstehenden Anthracenderivate werden auf dieselbe Weise identifiziert. Es handelt sich um Methylanthracen. Die zur weiteren Aufgliederung der Reaktionsprodukte vorgenommene dunnschicht-chromatografische Auftrennung (Untersuchung des Extrakts in Cyclohexanol und Methanol) ergibt kein sich deutlich unterscheidenden Fluoreszenzspektren. Identification, by UV absorption and fluorescence spectroscopy, of the …

AnthraceneMechanical EngineeringMetals and AlloysCyclohexanolGeneral MedicineChlorideFluorescence spectroscopyThin-layer chromatographySurfaces Coatings and Filmschemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMaterials ChemistrymedicineEnvironmental ChemistryMethanolSpectroscopyPhosphinemedicine.drugMaterials and Corrosion/Werkstoffe und Korrosion
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Synthesis and characterization of complexes of trialkyl- and triarylphosphine gold(I) with thiolated purines and pyrimidines. A class of bifunctional…

1991

Abstract New complexes of the type R 3 PAuL or (R 3 PAu) 2 (μ-L) where R=ethyl or phenyl and L=6-thioguanine, 2, 6- dithioxanthine, 2, 4-dithiouracil and/or dithioerythritol have been prepared. These complexes have been identified by using elemental analysis, 1 H, 13 C and 31 P NMR spectroscopy. The structures have been proposed based on these spectroscopic studies. Sulfur appears to be the binding site in disubstituted complexes of 2, 4-dithiouracil and 1, 4-dithioerythritol, while the phosphine gold( I ) moieties appear to be S and N bonded in 2, 6-dithioxanthine and 6-thioguanine. The potential use of these complexes as antitumor drugs is discussed.

Antitumor activityBicyclic moleculeDithioerythritolStereochemistryChemistrychemistry.chemical_elementBiological activityNuclear magnetic resonance spectroscopySulfurBiochemistryCombinatorial chemistryInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryPhysical and Theoretical ChemistryBinding sitePurine metabolismBifunctionalPhosphineJournal of Inorganic Biochemistry
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ChemInform Abstract: Efficient Synthesis of Racemic and Chiral Alkenyl Sulfoxides by Palladium-Catalyzed Suzuki Coupling.

2010

Alkenyl sulfoxide derivatives are obtained in high yields through a palladium-catalyzed Suzuki/Miyaura cross-coupling reaction of racemic and chiral 1-halo sulfoxides with aryl and alkenyl boronic acids. Chiral substrates react with no loss of optical purity and high optical yields. The reaction takes place with different palladium catalysts, such as Pd(PPh 3 ) 4 or Pd(OAc) 2 /DABCO. Although nitrogen ligands like DABCO lead to an active palladium catalyst, they are less effective than the phosphine ones.

Arylchemistry.chemical_elementSulfoxideGeneral MedicineDABCOMedicinal chemistryCatalysischemistry.chemical_compoundchemistrySuzuki reactionOrganic chemistryEnantiomeric excessPhosphinePalladiumChemInform
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Propriétés et performances de phosphines ferrocéniques dans le couplage C-O, C-S et C-N : nouvelles méthodologies de synthèse au palladium

2012

Multidentate ligands usually show great activities in low loading organometallic catalysis in palladium. Among these ligands, the use of ferrocenyl polyphosphane ligands give interesting results. Robust palladium-ferrocenyl triphosphane catalytic systems have permitted to obtain biarylamines and aryl-heteroaryl ethers in the presence of low catalytic loadings. DFT studies on catalytic cycle during formation of aryl-heteroaryl ethers were carried out. The presence of third phosphino group stabilizes a transition state which enhances the rate of the reductive elimination. Triarylamines were obtained with ferrocenyl diphosphane in the presence of 2 mol% of palladium loading. Moderate to excell…

Aryl-heteroaryl sulfidesThioéthers d'aryle et d'hétéroaryleLiaison carbone-hétéroatomeÉthers d'aryle et d'hétéroarylePolyphosphines ferrocéniquesCarbon-heteroatom bondHomogeneous catalysisFerrocenyl polyphosphanesAryl-heteroaryl ethersDiarylaminesBiarylaminesCatalyse homogène[CHIM.OTHE] Chemical Sciences/Other[ CHIM.OTHE ] Chemical Sciences/Other[CHIM.OTHE]Chemical Sciences/OtherTriarylaminesPalladium
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Phosphine-diène and Salicylamidines ligands : coordination chemistry, catalysis and therapy

2017

The subject of this thesis concerns the development of new ligands, their coordination chemistry, and the synthesis of the corresponding metal complexes for catalysis and therapy.The first part of this work relates to the synthesis of diene-phosphine ligands, their saturated analogs, and the corresponding arene-ruthenium complexes. Arene decoordination allows the formation of a cationic bimetallic complex where the ligand is diène-η4/κ-P coordinated to the ruthenium. These complexes have been applied to atom transfer radical addition (ATRA) of CCl4 to styrene. When harsh reaction conditions are used, the superiority of the “diene” complexes is highlighted comparing to saturated analogs.The …

Arène-ruthéniumCatalyse[CHIM.COOR] Chemical Sciences/Coordination chemistryCatalysisAmidineROPChimie de coordinationDièneCoordination chemistrySchiff baseBase de SchiffArene-rutheniumDieneAza-dipyrromethenePLAThérapie[CHIM.COOR]Chemical Sciences/Coordination chemistryTherapyATRAAza-dipyrrométhènePhosphine
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2020

Abstract. Aerosol mass spectrometers (AMS) are frequently applied in atmospheric aerosol research in connection with climate, environmental or health-related projects. This is also true for the measurement of the organic fraction of particulate matter, still the least understood group of components contributing to atmospheric aerosols. While quantification of the organic and/or inorganic aerosol fractions is feasible, more detailed information about individual organic compounds or compound classes can usually not be provided by AMS measurements. In this study, we present a new method to detect organic peroxides in the particle phase in real-time using an AMS. Peroxides (ROOR') are of high i…

Atmospheric ScienceOzone010504 meteorology & atmospheric sciencesAnalytical chemistryrespiratory system010501 environmental sciencesParticulatesMass spectrometrycomplex mixtures01 natural sciencesAerosolchemistry.chemical_compoundTime of flightchemistryParticleAerosol mass spectrometryTriphenylphosphine oxide0105 earth and related environmental sciencesAtmospheric Measurement Techniques
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Preparation and Characterization of P2 BCh Ring Systems (Ch=S, Se) and Their Reactivity with N-Heterocyclic Carbenes

2018

Four-membered rings with a P2BCh core (Ch = S, Se) have been synthesized via reaction of phosphinidene chalcogenide (Ar*P=Ch) and phosphaborene (Mes*P=BNR2). The mechanistic pathways towards these rings are explained by detailed computational work that confirmed the preference for the formation of P–P, not P–B, bonded systems, which seems counterintuitive given that both phosphorus atoms contain bulky ligands. The reactivity of the newly synthesized heterocycles, as well as that of the known (RPCh)n rings (n = 2, 3), was probed by the addition of Nheterocyclic carbenes, which revealed that all investigated compounds can act as sources of low-coordinate phosphorus species. peerReviewed

BOND COVALENT RADIIChalcogenidePHOSPHINIDENE ADDUCTSSULFURchemistry.chemical_element010402 general chemistryRing (chemistry)ION ABSTRACTION01 natural sciencesMedicinal chemistryCatalysischemistry.chemical_compoundELEMENTSmain-group heterocyclesReactivity (chemistry)N-heterocyclic carbenesMETHYLENEPHOSPHINEta116epäorgaaniset yhdisteetphosphinidene chalcogenidesheterocycleskemiallinen synteesiphosphaborenes010405 organic chemistryPhosphorusOrganic ChemistryGeneral ChemistryREAGENT0104 chemical sciencesCharacterization (materials science)PHOSPHORUSchemistryPhosphinideneinorganic compoundsSULFURIZATIONchemical synthesisX-RAY-STRUCTUREChemistry - A European Journal
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Novel heterobimetallic radiotheranostic: preparation, activity, and biodistribution.

2014

A novel Ru(II) (arene) theranostic complex is presented. It is based on a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid macrocycle bearing a triarylphosphine and can be tracked in vivo by using the γ emission of (153) Sm atoms. Notably, the heteroditopic ligand can be selectively metalated with ruthenium at the phosphorus atom despite the presence of other functionalities that are prone to metal coordination. Subsequent labeling with radionuclides such as (153) Sm can then be performed easily. The resulting heterobimetallic complex exhibits favorable solubility and stability properties in biologically relevant media. It also shows in vitro cytotoxicity in line with that expected …

BiodistributionStereochemistryCell SurvivalPhosphinesIn vitro cytotoxicitychemistry.chemical_elementBiochemistryRutheniumMetalHeterocyclic Compounds 1-RingMiceIn vivoCoordination ComplexesCell Line TumorDrug DiscoveryAnimalsHumansTissue DistributionGeneral Pharmacology Toxicology and PharmaceuticsSolubilityPharmacologyChemistryLigandOrganic ChemistryWaterRutheniumvisual_artPhosphorus atomIsotope Labelingvisual_art.visual_art_mediumMolecular MedicineRadiopharmaceuticalsChemMedChem
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Palladium-Catalyzed Arylation of Linear and Cyclic Polyamines.

2005

Synthetic protocols for the palladium-catalyzed arylation of various linear and cyclic polyamines and polyoxapolyamines has been worked out. Pd(0) and Pd(II) complexes with such phosphine ligands as dppf, BINAP, PPF-OMe, P(tBu) 3 , 2-ditert-butylphosphino- 1,1'-biphenyl have been explored in the catalytic amination reactions. Monoamination of chloro-, bromo-, and iodoarenes with di-, tri-, and tetraamines have been carried out, condi- tions for di- and polyarylation of linear polyamines have been elaborated. Successful aryla- tion of 1,4,7,10-tetraazacyclododecane (cyclene) and 1,4,8,11-tetraazacyclotetradecane (cy- clam) have been conducted. Intramolecular diamination of dihaloarenes such …

BiphenylAnthraceneOrganic Chemistrychemistry.chemical_elementHomogeneous catalysisGeneral MedicineElectrophilic aromatic substitutionMedicinal chemistryQuinonechemistry.chemical_compoundchemistryIntramolecular forceOrganic chemistryPhysical and Theoretical ChemistryAminationPhosphinePalladiumBINAPChemInform
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