Search results for "Catalysis"

showing 10 items of 5944 documents

Polymetallic oxalate-based 2D magnets: Soluble molecular precursors for the nanostructuration of magnetic oxides

2010

Here we describe the synthesis and magnetic characterization of a family of 2D polymetallic oxalate-bridged polymeric networks with general formula [M(II)(H(2)O)(2)](3)[M(III)(ox)(3)](2)(18-crown-6)(2) (M(III) = Cr, Fe; M(II) = Mn, Fe, Co, Ni; 18-crown-6 = C(12)H(24)O(6)). Depending on the nature of the trivalent metal ion, they exhibit ferro- (Cr(3+)) or ferrimagnetic (Fe(3+)) ordering in the 3.6-20 K interval. In contrast with most of the oxalate-bridged CPs reported so far, these complexes do not need any additional templating cation for their assembly and represent the first series of oxalate-based polymeric networks which can be considered intrinsically neutral. As previously observed …

Decomposition processInorganic chemistryGeneral ChemistryCoordination PolymersMolecular precursorBiochemistryCatalysisOxalateMagnetic oxideschemistry.chemical_compoundColloid and Surface ChemistrychemistryMagnetMixed oxide
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Synthesis of quadruped-shaped polyfunctionalized o-carborane synthons

2011

[EN] o-Carborane derivatives with precisely defined patterns of substitution have been prepared from 8,9,10,12-I-4-1,2-closo-C2B10H8 by replacing the iodine atoms, bonded to four adjacent boron vertices in the cluster, with allyl, and subsequently 3-hydroxypropyl groups. The resulting structures, comprising four pendant arms and two reactive vertices located on opposite sides of a central o-carborane core, can be envisaged as versatile precursors for dendritic growth

DendrimersIcosahedral CarboranesStereochemistryMolecular ConformationNeutron-Capture TherapySupramolecular Assemblieschemistry.chemical_elementBoranesCrystallography X-Ray010402 general chemistry01 natural sciencesCatalysisMolecular conformationDendrimerQUIMICA ANALITICAMaterials ChemistryCluster (physics)BoranesBoronta116CancerIodination010405 organic chemistryChemistryPolysubstituted FrameworksSynthonMetals and AlloysHalogenationGeneral Chemistry3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsC-HChemistryCrystallographyCeramics and CompositesCarboraneDerivativesIodineChemical Communications
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Design and photophysical properties of zinc(II) porphyrin-containing dendrons linked to a central artificial special pair.

2011

The click chemistry synthesis and photophysical properties, notably photo-induced energy and electron transfers between the central core and the peripheral chromophores of a series of artificial special pair-dendron systems (dendron = G1, G2, G3; Gx = zinc(II) tetra-meso-arylporphyrin-containing polyimides) built upon a central core of dimethylxanthenebis(metal(II) porphyrin) (metal = zinc, copper), are reported. The dendrons act as singlet and triplet energy acceptors or donors, depending on the dendrimeric systems. The presence of the paramagnetic d(9) copper(II) in the dendrimers promotes singlet-triplet energy transfer from the zinc(II) tetra-meso-arylporphyrin to the bis(copper(II) por…

DendrimersMolecular StructureChemistryMetalloporphyrinsOrganic Chemistrychemistry.chemical_elementGeneral ChemistryZincChromophorePhotochemistryCopperPorphyrinCatalysisElectron transferchemistry.chemical_compoundZincEnergy TransferDendrimerClick ChemistrySinglet statePhosphorescenceCopperChemistry (Weinheim an der Bergstrasse, Germany)
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Amphiphilic Dendrimers Control Protein Binding and Corona Formation on Liposome Nanocarriers

2020

Amphiphilic polyphenylene dendrimers (PPDs) with distinct lipophilic and positively or negatively charged surface groups were adsorbed onto liposomes and their impact on protein adsorption in blood plasma was studied. The PPD corona reduced binding of specific opsonins and increased the adsorption of proteins controlling cellular uptake based on their surface patches.

DendrimersPolymersSurface PropertiesPlasma protein bindingCatalysisCorona (optical phenomenon)AdsorptionDendrimerAmphiphileMaterials ChemistryHumansLiposomeChemistryMetals and AlloysBlood ProteinsGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsLiposomesCeramics and CompositesBiophysicsNanoparticlesProtein CoronaAdsorptionNanocarriersPalladiumProtein BindingProtein adsorption
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2020

Skeletal muscle atrophy is characterized by a decrease in muscle fiber size as a result of a decreased protein synthesis, which leads to degradation of contractile muscle fibers. It can occur after denervation and immobilization, and glucocorticoids (GCs) may also increase protein breakdown contributing to the loss of muscle mass and myofibrillar proteins. GCs are already used in vitro to induce atrophic conditions, but until now no studies with primary human skeletal muscle existed. Therefore, this study deals with the effects of the GC dexamethasone (dex) on primary human myoblasts and myotubes. After incubation with 1, 10, and 100 µM dex for 48 and 72 h, gene and protein expression analy…

DenervationChemistryMyogenesisOrganic ChemistrySkeletal muscleGeneral MedicineProtein degradationCatalysisComputer Science ApplicationsCell biologyInorganic Chemistrymedicine.anatomical_structureMyosinGene expressionmedicineMyocytePhysical and Theoretical ChemistryMyofibrilMolecular Biologyhormones hormone substitutes and hormone antagonistsSpectroscopyInternational Journal of Molecular Sciences
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Reversible pH-induced fluorescence colour change of gold nanoclusters based on pH-regulated surface interactions.

2019

To prepare water-dispersible, biocompatible, ratiometric pH nanosensors is challenging. We report here for the first time that the emission colour of NAD+-capped AuNCs responds to the mono-/bidentate anchoring of the phosphoric groups of the ligand. The AuNCs exhibit a high luminescence (21% quantum yield) and an outstanding performance as fluorescent ratiometric pH sensors over a broad pH range.

Denticity010405 organic chemistryLigandChemistryMetals and AlloysQuantum yieldGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesFluorescenceCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanoclustersNanosensorMaterials ChemistryCeramics and CompositesNAD+ kinaseLuminescenceChemical communications (Cambridge, England)
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Ultra‐Low Catalyst Loading as a Concept in Economical and Sustainable Modern Chemistry: The Contribution of Ferrocenylpolyphosphane Ligands (Eur. J. …

2007

The cover picture shows an X-ray illustration of the multidentate ferrocenylpolyphosphane 1,1′,2,2′-tetrakis(diphenylphosphanyl)-4,4′-di-tert-butylferrocene. The cisoid conformation of the molecule, evidenced at the solid state, is conserved in solution; the phosphorus arrangement led to a rarely demonstrated multiple-coordination behaviour towards palladium, possibly useful in ultra-low catalyst loading reactions due to an improved stabilization of the metal atom. The multiple phosphane arms and their orientation resemble the elegant and intelligent creature that is the Giant Pacific Octopus (specimen from the Alaska SeaLife Centre in Seward, photo published with the kind permission of Mol…

Denticity010405 organic chemistrySolid-statechemistry.chemical_element010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisInorganic ChemistryMetalchemistryvisual_artPolymer chemistryvisual_art.visual_art_mediumMoleculePalladiumEuropean Journal of Inorganic Chemistry
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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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Syntheses, crystal structures and magnetic properties of new oxalato-, croconato- and squarato-containing copper(ii) complexesElectronic supplementar…

2003

The preparation and magnetic investigation of five mononuclear copper(II) complexes of formula [Cu(pyim)(C2O4)(H2O)]·2H2O (1), [Cu(pyim)(C4O4)(H2O)2]·2H2O (2), Cu(pyim)(C5O5)·2.5H2O (3), [Cu(H2bim)(C2O4)(H2O)]·H2O (4) and [Cu(bpz)(C5O5)(H2O)] (5) [pyim=2-(2-pyridyl)imidazole, H2bim=2,2′-biimidazole, bpz=2,2′-bipyrazine, C2O42−=dianion of oxalic acid, C4O42−=dianion of squaric acid and C5O52−=dianion of croconic acid] are reported. The crystal structures of 1, 2, 4 and 5 have been determined. The copper atom has a distorted square pyramidal geometry in this family of complexes: two nitrogen atoms from the bidentate nitrogen donor [pyim (1 and 2), H2bim (4) and bpz (5)] and two oxygen atoms e…

DenticityChemistryCroconic acidInorganic chemistryGeneral ChemistryCrystal structureSquaric acidCatalysisSquare pyramidal molecular geometryOxalatechemistry.chemical_compoundCrystallographyMaterials ChemistryMoleculeImidazoleNew Journal of Chemistry
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