Search results for "complex"

showing 10 items of 5889 documents

Chiral α-P,N Ligands From a Diastereoselective Ph2PH Addition to (η6-Benzaldimine)tricarbonylchromium Complexes

1999

International audience; Chiral α-aminophosphane (α-P–C–N) ligands have been prepared by reversible addition of Ph2PH to tricarbonylchromium benzaldimine complexes (CO)3Cr[η6-o-C6H4(Y)(CH=NR)] (with Y, R = CH3, CH3 or CH2COOCH3; CH3O, CH3 or p-CH3OC6H4; Cl, C6H5), with complete diastereoselectivity. These complexes are stabilized in solution by electron-withdrawing group(s) on the imine.

Diastereoselective reactionsStereochemistryOrganic ChemistryImine3. Good healthP ligandschemistry.chemical_compoundChromium complexeschemistryAminophosphaneGroup (periodic table)[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryChiralityChirality (chemistry)
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Diastereoselective Synthesis of Dialkylated Bis(phosphino)ferrocenes: Their Use in Promoting Silver-Mediated Nucleophilic Fluorination of Chloroquino…

2017

International audience; The diastereoselective synthesis of dialkylated ferrocenyl bis(phosphane)s bearing aryl, alkyl, and hetero- or polycyclic substituents on the phosphino groups is reported, together with their characterization in the solid state by X-ray structure analysis and in solution by multinuclear NMR spectroscopy. Introduction of various alkyl groups on the ferrocene backbone, namely, tert-butyl, isopropyl, and trimethylsilyl, has a significant influence on the stereoselectivity of the ensuing lithiation/phosphination reactions. Only the introduction of the tert-butyl groups ensures both a high yield and perfect diastereoselectivity, which leads to the exclusive formation of t…

Diastereoselectivitybond formationTrimethylsilylfunctionalized arylone-potelectrophilic fluorinationPhosphanesAlkylationc-h fluorination[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNucleophileFluorinationOrganic chemistryAlkylpolyphosphane ligandsferrocenyl derivativeschemistry.chemical_classificationp-31 nmr010405 organic chemistryArylHalex reactiondirect arylationreductive elimination[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryNuclear magnetic resonance spectroscopySandwich complexes0104 chemical scienceschemistryFerroceneIsopropyl
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The importance of a highly active and DeltapH-regulated diatoxanthin epoxidase for the regulation of the PS II antenna function in diadinoxanthin cyc…

2005

The present study focuses on the regulation of diatoxanthin (Dtx) epoxidation in the diadinoxanthin (Ddx) cycle containing algae Phaeodactylum tricornutum, Thalassiosira pseudonana, Cyclotella meneghiniana and Prymnesium parvum and its significance for the control of the photosystem II (PS II) antenna function. Our data show that Dtx epoxidase can exhibit extremely high activities when algal cells are transferred from high light (HL) to low light (LL). Under HL conditions, Dtx epoxidation is strongly inhibited by the light-driven proton gradient. Uncoupling of the cells during HL illumination restores the high epoxidation rates observed during LL. In Ddx cycle containing algae, non-photoche…

DiatomsPhotosystem IIbiologyLightPhysiologyZeaxanthin epoxidaseAlgal ProteinsDiadinoxanthinDiatoxanthinEukaryotaPhotosystem II Protein ComplexPlant ScienceHydrogen-Ion ConcentrationXanthophyllsPhotochemistrychemistry.chemical_compoundchemistryPhotoprotectionbiology.proteinElectrochemical gradientChlorella vulgarisOxidoreductasesAgronomy and Crop ScienceChlorophyll fluorescenceViolaxanthinJournal of plant physiology
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Atom Transfer Radical Addition Catalyzed by Ruthenium–Arene Complexes Bearing a Hybrid Phosphine–Diene Ligand

2018

International audience; The synthesis and characterization of a series of arene ruthenium complexes bearing either (3,5-cycloheptadienyl)diphenylphosphine or (cycloheptyl)-diphenylphosphine are reported. Upon irradiation or heating, all these complexes lose their arene ligand but then exhibit a different behavior depending on the nature of the phosphine ligand. (Cycloheptadienyl)phosphine complexes 1 and 3 give a cationic dinuclear Ru complex 5 for which the two Ru atoms are bridged by three chlorido ligands and flanked by two tridendate (cycloheptadienyl)phosphines. (Cycloheptyl)-diphenylphosphine complexes 2 and 4 undergo arene exchange when toluene is used as solvent or degrade in dithlo…

Dieneeffective core potentialsprecursorchemistry.chemical_element010402 general chemistrychemistry01 natural sciencesMedicinal chemistryAdductInorganic Chemistrychemistry.chemical_compoundMoiety[CHIM.COOR]Chemical Sciences/Coordination chemistryarylationPhysical and Theoretical ChemistryDiphenylphosphine010405 organic chemistryAtom-transfer radical-polymerizationLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry[CHIM.CATA]Chemical Sciences/Catalysismolecular calculations0104 chemical sciencesRutheniumkharasch reactionatrc reactionschemistrypolymerizationpincer complexesmetathesisPhosphine
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Propyl substituted 4-arylimino-1,2,3-trihydroacridylnickel complexes: Their synthesis, characterization and catalytic behavior toward ethylene

2015

Propyl substituted 4-arylimino-1,2,3-trihydroacridylnickel dihalide complexes were designed and prepared by metal-induced template reaction with NiCl2 center dot 6H(2)O or (DME)NiBr2. They were characterized by infrared spectroscopy and elemental analysis. Single crystal X-ray crystallography of representative complex Ni3 revealed a distorted trigonal bipyramidal geometry around nickel. The catalytic activities of the title nickel complexes were negatively affected by propyl substituent on their backbone when comparing with the results by unsubstituted ones. With the activation of diethylaluminium chloride, all nickel complexes exhibited moderate activity (up to 5.10 x 10(5) g mol(-1)(Ni) h…

Diethylaluminium chlorideEthyleneStereochemistryOrganic ChemistrySubstituentchemistry.chemical_elementInfrared spectroscopyBiochemistryMedicinal chemistryCatalysis2-propyl-4-arylimino-1Inorganic ChemistryNickelchemistry.chemical_compoundTemplate reactionTrigonal bipyramidal molecular geometrychemistryMaterials Chemistry3-dihydroacridine; Nickel complex; Ethylene oligomerizationPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Achieving branched polyethylene waxes by aryliminocycloocta[b]pyridylnickel precatalysts: Synthesis, characterization, and ethylene polymerization

2017

Cycloocta[b]pyridin-10-one was prepared to form the corresponding imino derivatives, which then reacted with (DME)NiBr2 to form 10-aryliminocycloocta[b]pyridylnickel bromides (Ni1–Ni5). The new compounds were characterized by means of FT-IR spectroscopy as well as elemental analysis and the organic ligands were also analyzed by the NMR measurements. Furthermore, the molecular structure of a representative complex Ni3 was determined by the single crystal X-ray diffraction, indicating the distorted tetrahedral geometry around the nickel atom. Upon the activation with either methylaluminoxane (MAO) or diethylaluminium chloride (Et2AlCl), the title nickel complexes exhibited high activity in et…

Diethylaluminium chloridePolymers and Plastics010405 organic chemistryChemistryOrganic ChemistryDispersityMethylaluminoxaneCationic polymerizationnickel complexPolyethylene010402 general chemistryBranching (polymer chemistry)01 natural sciences0104 chemical scienceschemistry.chemical_compoundPolymerization10-aryliminocycloocta[b]pyridinePolymer chemistryMaterials ChemistryCoordination polymerizationcationic polymerizationpolyethyl-eneJournal of Polymer Science Part A-Polymer Chemistry
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Development of a new peat-based oil sorbent using peat pyrolysis

2013

The growing use and transport of crude oil and oil products has led to increasing numbers of oil spillages of various scales. Oil sorbents have been extensively used for remediation of the consequences of such accidents. The aim of this study is to investigate the possible use of peat and its thermal treatment products for oil sorption. Peat as an oil sorbent has poor buoyancy characteristics, relatively low oil sorption capacity and low hydrophobicity. However, thermal treatment (low-temperature pyrolysis and synthesis of peat-based activated coal) helps to significantly improve its sorptive characteristics. Peat is a potential material for oil sorption because it has such advantages as lo…

Differential Thermal AnalysisHot TemperaturePeatSorbentWaste managementEnvironmental remediationSorptionGeneral MedicinePulp and paper industrycomplex mixturesThermogravimetryKineticsSoilPetroleumSpecific surface areaSoil PollutantsEnvironmental ChemistryEnvironmental scienceAdsorptionPorosityWaste Management and DisposalPyrolysisEnvironmental Restoration and RemediationWater Science and TechnologyEnvironmental Technology
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Purification of Large Cytosolic Proteases for In Vitro Assays: 20S and 26S Proteasomes

2012

Proteasomes are the main cytosolic proteases responsible for generating peptides for antigen processing and presentation in the MHC (major histocompatibility complex) class-I pathway. Purified 20S and 26S proteasomes have been widely used to study both specificity and efficiency of antigen processing. Here, we describe the purification of active human 20S and 26S proteasomes from human erythrocytes by DEAE-ion exchange chromatography, ammonium sulfate precipitation, glycerol density gradient centrifugation, and Superose-6 size exclusion chromatography and their characterization using fluorogenic substrates and specific inhibitors.

Differential centrifugationCytosolProteasesProteasomebiologyBiochemistryAntigen processingChemistrybiology.proteinMajor histocompatibility complexPolyacrylamide gel electrophoresisAmmonium sulfate precipitation
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Nuclear DNA fractions with grossly different base ratios in the genome of the marine sponge Geodia cydonium

2008

The DNA of the marine sponge Geodia cydonium (G.c.), a member of the phylogenetically old phylum Porifera, was characterized by density gradient centrifugation and by determining its genetic complexity by reassociation kinetics. At least five subcomponents were identified by curve-fit analyses of analytical density gradient centrifugation profiles of total G.c.-DNA. Four of these subcomponents were isolated from total G.c.-DNA by preparative density gradient centrifugation. The GC-contents of the subcomponents were determined to be 36.4%, 44.0%, 58.7%, and 66.1%, respectively. To our knowledge, such an extreme heterogeneity of DNA composition has never before been observed for any organism.…

Differential centrifugationchemistry.chemical_classificationGenetic complexityBase (chemistry)Geodia cydoniumBiologybiology.organism_classificationGenomeNuclear DNASpongechemistry.chemical_compoundBiochemistrychemistryBotanyDNA
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Time multiplexing super-resolved imaging without a priori knowledge of the spatial distribution of the encoding structured illumination

2021

Time multiplexing is a super-resolution technique that sacrifices time to overcome the resolution reduction obtained because of diffraction. There are many super resolution methods based on time multiplexing, but all of them require a priori knowledge of the time changing encoding mask, which is projected on the object and used to encode and decode the high-resolution information. In this paper, we present a time multiplexing technique that does not require the a priori knowledge on the projected encoding mask. First, the theoretical concept of the technique is demonstrated; then, numerical simulations and experimental results are presented.

DiffractionComputer sciencebusiness.industryResolution (electron density)02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMultiplexingAtomic and Molecular Physics and Optics010309 opticsReduction (complexity)OpticsEncoding (memory)0103 physical sciencesA priori and a posteriori0210 nano-technologybusinessImage resolutionAlgorithmComputer Science::Information TheoryOptics Express
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