Search results for "phosphorus"

showing 10 items of 431 documents

CCDC 727817: Experimental Crystal Structure Determination

2009

Related Article: P.Mal, B.Breiner, K.Rissanen, J.R.Nitschke|2009|Science|324|1697|doi:10.1126/science.1175313

Space GroupCrystallographytetrakis(tetramethylammonium) hexakis(mu2-44'-bis([(pyridin-2-yl-kN)methylidene]amino-kN)biphenyl-22'-disulfonite)-tetra-iron tetraphosphorus clathrate hydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Syntheses, X-ray structures, and physicochemical properties of phenoxo-bridged dinuclear nickel(II) complexes: kinetics of transesterification of 2-h…

2009

Four dinuclear nickel(II) complexes [Ni(II)(2)(L(1))(O(2)CMe)(2)(H(2)O)(2)][PF(6)].MeOH.3H(2)O (1), [Ni(II)(2)(L(1))(O(2)CMe)(2)(NCS)] (2), [Ni(II)(2)(L(2))(O(2)CMe)(2)(MeOH)(H(2)O)][ClO(4)] (3), and [Ni(II)(2)(L(2))(O(2)CMe)(2)(MeOH)(H(2)O)][BPh(4)].3MeOH.H(2)O (4) have been synthesized [HL(1): 2,6-bis[N-methyl-N-(2-pyridylethyl)amino]-4-methylphenol; HL(2): 2,6-bis[3-(pyridin-2-yl)pyrazol-1-ylmethyl]-4-methylphenol]. Complexes 1, 3, and 4 are new while complex 2 was reported previously by Fenton and co-workers (the structure of 2 was presented but no physicochemical properties of this complex were reported; in this work such studies have been completed). X-ray crystallographic analyses of…

Spectrophotometry InfraredStereochemistryKineticschemistry.chemical_elementPyrazoleCrystallography X-RayMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMagneticsOrganophosphorus CompoundsBiomimeticsNickelOrganometallic CompoundsMoietyChelationPhysical and Theoretical ChemistryEsterificationHydrolysisX-rayTitrimetryEstersTransesterificationHydrogen-Ion ConcentrationOrganophosphatesNickelKineticschemistryPotentiometryEthylamineOxidation-ReductionInorganic chemistry
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Estimating aggregated nutrient fluxes in four Finnish rivers via Gaussian state space models

2013

Reliable estimates of the nutrient fluxes carried by rivers from land-based sources to the sea are needed for efficient abatement of marine eutrophication. Although nutrient concentrations in rivers generally display large temporal variation, sampling and analysis for nutrients, unlike flow measurements, are rarely performed on a daily basis. The infrequent data calls for ways to reliably estimate the nutrient concentrations of the missing days. Here, we use the Gaussian state space models with daily water flow as a predictor variable to predict missing nutrient concentrations for four agriculturally impacted Finnish rivers. Via simulation of Gaussian state space models, we are able to esti…

Statistics and ProbabilityHydrologyWater flowEcological ModelingGaussianPhosphorusMonte Carlo methodSampling (statistics)chemistry.chemical_elementsymbols.namesakeNutrientchemistrysymbolsState spaceEnvironmental scienceEutrophicationEnvironmetrics
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Process understanding of a wastewater batch reactor with block-wise PLS

2007

In this work a systematic methodology ‘block-wise PLS’ has been applied to thoroughly analyse data from a sequencing batch reactor (SBR) operated for biological phosphorus removal from wastewater. The aim of this study was to diagnose process variables (collected by the inexpensive and low-maintenance sensors installed in the SBR) likely related to the main key indicator of process performance: the phosphorus removal efficiency (PRE), determined off-line in the quality control laboratory. In this way, it is intended to aid the process operators in the detection of abnormal values of these critical variables which would indicate undesirable process performance, so that, they could act on the…

Statistics and Probabilitybusiness.industryComputer scienceProcess (engineering)Ecological Modelingmedia_common.quotation_subjectBatch reactorSequencing batch reactorEnhanced biological phosphorus removalWastewaterQuality (business)Process engineeringbusinessBlock (data storage)media_commonEnvironmetrics
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Reaction Rate Modeling in Cryoconcentrated Solutions: Alkaline Phosphatase Catalyzed DNPP Hydrolysis

2000

The hydrolysis of disodium p-nitrophenyl phosphate catalyzed by alkaline phosphatase was chosen as a model to study the kinetics of changes in frozen food products. The initial reaction rate was determined in concentrated sucrose solutions down to -24 degrees C, and the enzymatic characteristics K(M) and V(max) were calculated. The experimental data were compared to the kinetics predicted by assuming that the reaction was viscosity dependent. Indeed, an analysis of the enzymatic reaction demonstrated that both the diffusion of the substrate and the flexibility of the enzyme segments were controlled by the high viscosity of the media. When the temperature was too low for the viscosity to be …

StereochemistryChemistryHydrolysisDiffusionInorganic chemistryKineticsTemperatureSubstrate (chemistry)Concentration effectGeneral ChemistryAlkaline PhosphataseCatalysisCatalysisNitrophenolsSolutionsReaction rateViscosityOrganophosphorus CompoundsGeneral Agricultural and Biological SciencesGlass transitionJournal of Agricultural and Food Chemistry
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"Through-space" 31P spin-spin couplings in ferrocenyl tetraphosphine coordination complexes: improvement in the determination of the distance depende…

2008

Abstract From the analysis of several nickel and palladium halide complexes of a constrained ferrocenyl tetraphosphine, the existence in solution phase of unique 31P–31P “through-space” nuclear spin–spin coupling constants (JPP) had been previously evidenced. Due to the blocked conformation of the species in solution, and based on the NMR spectra obtained for the complexes and their corresponding solid state X-ray structures, these JPP constants had been shown to clearly depend on the mutual spatial position of the corresponding phosphorus atoms. Herein, the quantitative correlation disclosed at that time (P⋯P distance dependence of coupling constants) is remarkably confirmed, and mathemati…

Stereochemistrychemistry.chemical_elementHalide010402 general chemistrySpace (mathematics)01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundMaterials Chemistryphosphorus carbon bond formation[CHIM.COOR]Chemical Sciences/Coordination chemistryspin couplingPhysical and Theoretical ChemistrySpin (physics)ComputingMilieux_MISCELLANEOUSCoupling constantaminophosphine010405 organic chemistryOrganic Chemistrythrough-spaceferrocene[ CHIM.COOR ] Chemical Sciences/Coordination chemistryNMR0104 chemical sciencesNMR spectra databaseNickelCrystallographychemistryFerrocenepolyphosphinePalladium
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N-Benzyl Residues as the P1′ Substituents in Phosphorus-Containing Extended Transition State Analog Inhibitors of Metalloaminopeptidases

2020

Peptidyl enzyme inhibitors containing an internal aminomethylphosphinic bond system (P(O)(OH)-CH2-NH) can be termed extended transition state analogs by similarity to the corresponding phosphonamidates (P(O)(OH)-NH). Phosphonamidate pseudopeptides are broadly recognized as competitive mechanism-based inhibitors of metalloenzymes, mainly hydrolases. Their practical use is, however, limited by hydrolytic instability, which is particularly restricting for dipeptide analogs. Extension of phosphonamidates by addition of the methylene group produces a P-C-N system fully resistant in water conditions. In the current work, we present a versatile synthetic approach to such modified dipeptides, based…

Stereochemistryenzyme inhibitorsPharmaceutical Scienceorganophosphorus compoundsPhosphinateArticleAnalytical Chemistrylcsh:QD241-44103 medical and health scienceschemistry.chemical_compoundHydrolysis0302 clinical medicinelcsh:Organic chemistryTransition state analogpeptide analogsDrug DiscoveryCarboxylatePhysical and Theoretical ChemistryMethylene030304 developmental biologychemistry.chemical_classification0303 health sciencesDipeptideOrganic Chemistryligand-enzyme interactionsmolecular modeling and dockingEnzymechemistryChemistry (miscellaneous)030220 oncology & carcinogenesisMolecular MedicineLeucineMolecules
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ChemInform Abstract: nBuLi-Mediated Hydrophosphination: A Simple Route to Valuable Organophosphorus Compounds.

2010

A straightforward synthesis of homoallyl- and allylphosphanes has been developed using nBuLi-mediated hydrophosphination of conjugated dienes. In all the cases the phosphorus atom of the reacting phosphane attacked the sterically less demanding side of the diene exclusively. In addition, high regioselectivities towards 1,2- or 1,4-addition products were observed depending on the nature of the dienes. This hydrophosphination reaction was extended to a variety of substrates such as styrene derivatives, alkynes and 1,3,5-cycloheptatriene. The structures of three hydrophosphination products were confirmed by X-ray diffraction studies.

Steric effectschemistry.chemical_compoundDienechemistryPhosphorus atomHydrophosphinationGeneral MedicineConjugated systemCombinatorial chemistryStyreneChemInform
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nBuLi-Mediated hydrophosphination: a simple route to valuable organophosphorus compounds

2010

A straightforward synthesis of homoallyl- and allylphosphanes has been developed using nBuLi-mediated hydrophosphination of conjugated dienes. In all the cases the phosphorus atom of the reacting phosphane attacked the sterically less demanding side of the diene exclusively. In addition, high regioselectivities towards 1,2- or 1,4-addition products were observed depending on the nature of the dienes. This hydrophosphination reaction was extended to a variety of substrates such as styrene derivatives, alkynes and 1,3,5-cycloheptatriene. The structures of three hydrophosphination products were confirmed by X-ray diffraction studies.

Steric effectsligand designDieneAlkyneConjugated system010402 general chemistryalkynes01 natural sciencesChemical synthesisStyrenechemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryhydrophosphinationOrganic chemistryPhysical and Theoretical ChemistryphosphorusComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationalkenes010405 organic chemistryAlkene[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryRegioselectivity0104 chemical scienceschemistry
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Prospects of in vivo 31P NMR method in glyphosate degradation studies in whole cell system

2009

Abstract The degradation of the phosphonate herbicide glyphosate ( N -phosphonomethylglycine) by four taxonomically distinct microorganisms was studied in vivo in whole cell system using phosphorus nuclear magnetic spectroscopy ( 31 P NMR). The time-course of glyphosate metabolization in dense cell cultures was followed by means of 31 P NMR up to 21 days after the addition. The results obtained by this non-invasive way confirmed that the cells of Spirulina platensis and Streptomyces lusitanus biodegrade herbicide. Moreover, phosphorus starvation influenced the rate of glyphosate degradation by S. platensis . On the other hand, the results of similar measurements in the cultures of green alg…

Streptomyces lusitanusMicroorganismChlorella vulgarischemistry.chemical_elementBioengineeringBiologyApplied Microbiology and BiotechnologyBiochemistrybiodegradationchemistry.chemical_compoundglyphosatein vivo31P NMRBotanyFusarium dimerumspirulina platensisPhosphorusBiodegradationbiology.organism_classificationStreptomyces lusitanusPhosphonatexenobiotic metabolismchemistryBiochemistryGlyphosateGreen algaeChlorella vulgarisBiotechnologyEnzyme and Microbial Technology
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