Search results for "Palladium"

showing 10 items of 956 documents

Spontaneous growth of 2D coordination polymers on functionalized ferromagnetic surfaces

2018

2D coordination polymers grow spontaneously on reactive surfaces due to surface oxidation. The growth process is observed in real time.

BILAYERSMaterials scienceSolucions polimèriquesChemistry MultidisciplinaryCOPPERchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesMetalCrystallinitySELF-ASSEMBLED MONOLAYERSMonolayerWATERMoleculeLamellar structureDEPOSITION[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]AlkylComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationScience & TechnologyPALLADIUMGeneral ChemistryPolymerQuímica021001 nanoscience & nanotechnology0104 chemical sciencesChemistrychemistryChemical engineeringvisual_artPhysical Sciencesvisual_art.visual_art_mediumCHAIN0210 nano-technologyCobaltINTERFACESBEHAVIORChemical Science
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Thermal stability, structural properties and catalytic activity of Pd catalysts supported on Al2O3–CeO2–BaO mixed oxides prepared by sol–gel method

2003

Abstract Al2O3–CeO2–BaO oxides with constant Al/Ba mass ratio and increasing cerium content were prepared, using the sol–gel procedure, and calcined at 1000 °C for 5 h. The influence of barium oxide on the thermal stability and on the morphological and structural properties of the corresponding supports, in terms of increasing surface area of alumina and ceria dispersion, was studied. The corresponding Pd (1 wt.%) catalysts were prepared by a stepwise impregnation method with a solution of palladium acetylacetonate in benzene. Palladium was introduced in two sequential steps by impregnation 0.5 wt.% of Pd each time. The structural and textural properties of the materials were studied by X-r…

Barium oxideProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementCatalysisCatalysislaw.inventionCeriumchemistry.chemical_compoundchemistrylawThermal stabilityCalcinationPhysical and Theoretical ChemistryBET theoryPalladiumJournal of Molecular Catalysis A: Chemical
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An exclusive approach to 3,4-disubstituted cyclopentenes and alkylidene cyclopentenes via the palladium catalyzed ring opening of azabicyclic olefins…

2013

A simple and efficient method for the stereoselective ring opening of bicyclic hydrazines with various aryl halides under palladium catalysis has been elaborated. The reactions afforded trans-3,4-disubstituted cyclopentenes or alkylidene cyclopentenes in good to excellent yields. By taking advantage of multiple points of functionalization in the synthesized trans-3-phenyl-4-hydrazino-cyclopentene, we have synthesized the antidepressant Cypenamine (trans-2-phenylcyclopentylamine).

Bicyclic moleculeChemistryGeneral Chemical EngineeringArylchemistry.chemical_elementHalideGeneral ChemistryRing (chemistry)Medicinal chemistryCatalysischemistry.chemical_compoundReagentOrganic chemistryStereoselectivityta116PalladiumRSC Advances
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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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Hybrid ferrocene ligands (P, N) : synthesis, coordination to metals and applications in arylation coupling catalysis

2017

The research theme developed during this thesis concerns the development of new hybrid ferrocene hybrid (P, N) ligands with controlled conformation, robust and stable to air. These hybrid tetradent ligands comprise two types of coordinating functions with distinct steric and electronic properties. Their coordination chemistry with metals such as gold or palladium has been studied and some isolated Au (I) complexes have been used in the arylation coupling catalysis of aryl iodides.

Bis(aminométhyl)-ferrocèneN) à conformation contrôléeNitrogenCouplage C-CRMN 15NBis (aminomethyl)-ferroceneAzoteFunctionalization of ferrocenePhosphorusOrHybrid ligandsHybrid ligands (PFonctionnalisation de ferrocène[CHIM.OTHE] Chemical Sciences/OtherLigands hybridesPhosphoreLigands hybrides-(PGoldFerrocene15N NMRLigands multidentes[CHIM.OTHE]Chemical Sciences/OtherN) with controlled conformationPalladiumC-C cross Coupling
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Palladium-catalyzed formation and reactions of iodo- and bromosiloxane intermediates

2012

Polysiloxanes are useful materials because of their functionality, such as high thermal stability, electrical resistance, and hydrophobicity. In this regard, we studied palladium-catalyzed formation of iodo-and bromopolysiloxanes from two types of hydrosiloxanes, alpha,omega-dihydropoly(dimethylsiloxane) (1) and cyclotetra(hydromethylsiloxane) (2), and their reactions. Treatment of 1 with mixtures of cyclic ethers or lactones and MeI or allylBr in the presence of a catalytic amount of PdCl2 gave the corresponding alpha,omega-bis(haloalkoxy and haloalkanoyloxy) poly(dimethylsiloxane)s in good yields, via iodo-and bromopoly(dimethylsiloxane) intermediates. Transformation of the iodobutoxy-ter…

BoromosilaneIodosilanechemistry.chemical_element430BiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryThermal stabilityPhysical and Theoretical Chemistrychemistry.chemical_classification430Quenching (fluorescence)EthanolOrganic ChemistryPolysiloxanePolymerLactonechemistryCyclic etherPalladium catalystCyclic etherLactonePalladiumJournal of Organometallic Chemistry
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Highly-fluorescent BODIPY-functionalised metallacages as drug delivery systems

2022

With the aim of designing new metallosupramolecular architectures for drug delivery, research has focused on porous 3-dimensional (3D)-metallacages able to encapsulate cytotoxic agents protecting them from metabolism while targeting them to cancer sites. Here, two self-assembled [Pd2L4]4+ cages (CG1 and CG2) featuring 3,5-bis(3-ethynylpyridine)phenyl ligands (L) exo-functionalised with dipyrromethene (BODIPY) groups have been synthesised and characterised by different methods, including NMR spectroscopy and mass spectrometry. 1H NMR spectroscopy studies shows that the cages are able to encapsulate the anticancer drug cisplatin in their hydrophobic cavity, as evidenced by electrostatic poten…

Boron CompoundsInorganic ChemistryDrug Delivery SystemsCell Line TumorHumansCisplatinPalladiumDalton Transactions
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Synthesis and coordinating ability of an anionic cobaltabisdicarbollide ligand geometrically analogous to BINAP.

2004

The anionic chelating ligand [1,1'-(PPh 2 ) 2 -3,3'-Co(1,2-C 2 B 9 H 1 0 ) 2 ] - has been synthesized from [3,3'-Co(1,2-C 2 B 4 H 1 1 ) 2 ] - in very good yield in a one-pot process with an easy work-up procedure. The coordinating ability of this ligand has been studied with Group 11 metal ions (Ag, Au) and with transition-metal ions (Pd, Rh). The two dicarbollide halves of the [1,1'-(PPh 2 ) 2 -3,3'-Co(1,2-C 2 B 9 H 1 0 ) 2 ] - ligand can swing about one axis in a manner analogous to the constituent parts of BINAP and ferrocenyl phosphine derivatives. All these ligands function as hinges, with the most important property in relation to the coordination requirements of the metal being the P…

Boron CompoundsModels MolecularMagnetic Resonance SpectroscopySilverStereochemistryMetal ions in aqueous solutionMolecular ConformationHomogeneous catalysisBoranesNaphthalenes010402 general chemistryCrystallography X-Ray01 natural sciencesCatalysischemistry.chemical_compoundOrganometallic CompoundsChelationRhodiumBINAPChelating AgentsAtropisomerMolecular Structure010405 organic chemistryChemistryLigandOrganic ChemistryGeneral ChemistryCations Monovalent0104 chemical sciencesCrystallographySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationGoldPhosphinePalladiumChemistry (Weinheim an der Bergstrasse, Germany)
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Front Cover Picture: SBA‐15/POSS‐Imidazolium Hybrid as Catalytic Nanoreactor: the role of the Support in the Stabilization of Palladium Species for C…

2019

C c couplingFront coverchemistryHeck reactionPolymer chemistrychemistry.chemical_elementGeneral ChemistryNanoreactorHeterogeneous catalysisCoupling reactionPalladiumCatalysisAdvanced Synthesis & Catalysis
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Synthese substituierter 1,4-Divinylbenzole durch doppelte Heck-Reaktion mit Ethen unter Druck

1999

Substituted 1,4-divinylbenzenes 3a–i were synthesized by twofold Heck coupling from the corresponding 1,4-dibromo) (electron withdrawing substituents) or 1,4-di-iododialkoxybenzenes 1a–i and ethene. Oligomerizations could be suppressed by increasing the pressure of ethene to 30 bar, simultaneously improving the yields of the title compounds.

C c couplingchemistry.chemical_compoundchemistryHeck reactionPolymer chemistryPolar effectchemistry.chemical_elementDivinylbenzenePalladiumBar (unit)Journal für praktische Chemie
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