Search results for "31P NMR"

showing 10 items of 15 documents

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
researchProduct

Coordination abilities of N-methyl alkylaminomethane-1,1-diphosphonic acids towards zinc(II), magnesium(II) and calcium(II) metal ions. Equilibrium s…

2017

Abstract Complex-formation abilities of a series of N-methyl alkylaminomethane-1,1-diphosphonic acids (1–7) with a common tertiary nitrogen atom (CH3−N−R) bearing linear or branched alkyl, cycloheptyl or phenylalkyl R substituents towards zinc(II), magnesium(II) and calcium(II) in aqueous solution have been studied by means of pH-potentiometry, ESI-MS spectrometry, 1H NMR and 31P NMR methods. The obtained results indicate that in the all presented systems mononuclear protonated equimolar and bis complexes are formed. In acidic and neutral solution, the formation of the protonated dinuclear species has been confirmed. The comparative analysis of the potentiometric and NMR data reveal that th…

1H and 31P NMRMetal ions in aqueous solutionInorganic chemistrychemistry.chemical_elementProtonationpH potentiometryZinc010402 general chemistry01 natural sciencesMedicinal chemistrymagnesium(II) and calcium(II) complexesInorganic Chemistrychemistry.chemical_compoundaminomethane-1Materials ChemistryPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationAqueous solutionzinc(II)010405 organic chemistryMagnesiumESI-MSPhosphonate0104 chemical scienceschemistryProton NMR1-diphosphonic acidsPolyhedron
researchProduct

Phosphonate degradation by Spirulina strains: cyanobacterial biofilters for the removal of anticorrosive polyphosphonates from wastewater

2011

The ability of Spirulina spp. to metabolize the recalcitrant xenobiotic Dequest 2054(®) [hexamethylenediamine-N,N,N',N'-tetrakis(methylphosphonic acid)], a CaSO(4) inhibitor used for boiler treatment and reverse osmosis desalination, was investigated. The compound served as sole source of phosphorus, but not of nitrogen, for cyanobacterial growth. In vivo utilization was followed by (31)P NMR analysis. The disappearance of the polyphosphonate proceeded only with actively dividing cells, and no release of inorganic phosphate was evident. However, no difference was found between P-starved and P-fed cultures. Maximal utilization reached 1.0 ± 0.2 mmoll(-1), corresponding to 0.56 ± 0.11 mmol g(…

Magnetic Resonance SpectroscopyOrganophosphonatesBioengineeringBiologyCyanobacteriaApplied Microbiology and BiotechnologyBiochemistryWaste Disposal FluidXenobioticschemistry.chemical_compoundBioremediationOrganophosphorus CompoundsbioremediationSpirulina31P NMR31 P NMRpolyphosphonateSpirulina spp.Methylphosphonic acidChromatographySpirulina sppBiodegradationwastewater treatmentBiodegradation Environmentalxenobiotic biodegradationchemistryBiochemistryWastewaterBiofilterpolyphosphonate; xenobiotic biodegradation; 31P NMR; Spirulina spp.; wastewater treatment; bioremediationSewage treatmentXenobioticFiltrationBiotechnologyWaste disposal
researchProduct

Dinuclear Palladium(II) and -(III) Compounds with O,O-Chelating Ligands. Room-Temperature Direct 2-Phenylation of 1-Methylindole

2012

New dinuclear palladium(III) compounds of general formula Pd2[(C6H4)PPh2]2[O–O]2Cl2, O–O being chelating phenolates C6H4OC(O)R (R = CH3, 3a; R = C2H5, 3b; R = OPh, 3c) or acetylacetonates RC(O)CHC(O)R (R = CH3, 4a; R = CF3, 4b; R = C(CH3)3, 4c), have been obtained by oxidation with PhICl2 of the corresponding palladium(II) compounds. The stability of the new compounds has been studied by 31P NMR spectroscopy from 200 to 298 K. DFT calculations of the stability of the complexes have also been performed. In agreement with these calculations, only compound Pd2[(C6H4)PPh2]2[(CF3C(O)CHC(O)CF3]2Cl2, 6b, showed the highest thermal stability. 6b was characterized by X-ray diffraction methods, prese…

Chelating ligandsStereochemistryOrganic Chemistrychemistry.chemical_elementMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryThermal stabilityChelation1-Methylindole31p nmr spectroscopyPhysical and Theoretical ChemistryPalladiumOrganometallics
researchProduct

Ruthenium Metallodendrimers Based on Nitrile‐Functionalized Poly(alkylidene imine)s

2005

The preparation of the first- and second-generation of nitrile-functionalized poly(alkylidene imine) dendrimers with the organometallic ruthenium complex [Ru(η5-C5H5)(PPh3)2Cl] peripherally attached is described. The reaction of N,N′-bis(cyanomethyl)piperazine (1), N,N′-bis[N′′,N′′′-bis(cyanoethyl)aminoethyl]piperazine (2), or N,N,N′,N′-tetrakis(cyanoethyl)ethylenediamine (3) with [Ru(η5-C5H5)(PPh3)2Cl] (4) in the presence of TlPF6 gives the new air-stable ruthenium metallodendrimers 5, 6, and 7, respectively. These stable metallodendrimers are easily prepared and represent a novel quantitative method to solidify and chromatographically purify the otherwise semi-liquid nitrile-functionalize…

DendrimersNitrileIminechemistry.chemical_elementEthylenediamineSandwich complexes.Mass spectrometryRutheniumRutheniumInorganic ChemistryFaculdade de Ciências Exatas e da Engenhariachemistry.chemical_compoundPiperazineN ligandschemistryDendrimerPolymer chemistryOrganic chemistry31p nmr spectroscopyEuropean Journal of Inorganic Chemistry
researchProduct

Phosphonates as Unique Components of Plant Seeds—A Promising Approach to Use Phosphorus Profiles in Plant Chemotaxonomy

2021

Phosphorus is one of the most important elements essential for all living beings. Plants accumulate and store phosphorous in various forms that have diverse physiological and biochemical functions. In this study, we determine and then examine the phosphorus profiles of seeds of plants belonging to different taxa based on extractable inorganic phosphates and organic forms of phosphorus. We paid particular attention to the presence of natural phosphonates in the tested materials. The inorganic phosphates were determined colorimetrically, whereas phosphorus profiles were created by using 31P NMR spectroscopy. Our study on phosphorus profiles revealed that the obtainedsets of data vary signific…

Magnetic Resonance SpectroscopyQH301-705.5Organophosphonateschemistry.chemical_elementArticleCatalysisInorganic ChemistryBotany31P NMRBiology (General)Physical and Theoretical ChemistryQD1-999Molecular BiologySpectroscopyphosphorus profileChemistryPhosphorusOrganic Chemistryphosphonatesfood and beveragesPhosphorusGeneral MedicinePlantsPlant taxonomyComputer Science Applications<sup>31</sup>P NMRChemistryChemotaxonomySeeds31p nmr spectroscopyInternational Journal of Molecular Sciences
researchProduct

The influence of phase transitions in phosphatidylethanolamine models on the activity of violaxanthin de-epoxidase

2008

In the present study, the influence of the phospholipid phase state on the activity of the xanthophyll cycle enzyme violaxanthin de-epoxidase (VDE) was analyzed using different phosphatidylethanolamine species as model lipids. By using (31)P NMR spectroscopy, differential scanning calorimetry and temperature dependent enzyme assays, VDE activity could directly be related to the lipid structures the protein is associated with. Our results show that the gel (L beta) to liquid-crystalline (L alpha) phase transition in these single lipid component systems strongly enhances both the solubilization of the xanthophyll cycle pigment violaxanthin in the membrane and the activity of the VDE. This pha…

Magnetic Resonance SpectroscopyBiophysicsAnalytical chemistryPhospholipidMonogalactosyldiacylglycerolXanthophyllsBiochemistryViolaxanthin de-epoxidaseModels BiologicalPhase Transitionchemistry.chemical_compoundDifferential scanning calorimetrySpinacia oleraceaPhase (matter)31P NMRInverted hexagonal phaseDe-epoxidationchemistry.chemical_classificationPhosphatidylethanolaminePhospholipid structuresChemistryPhosphatidylethanolaminesTemperatureCell BiologyNuclear magnetic resonance spectroscopyLipid MetabolismSolubilityArrheniusXanthophyllBiophysicsOxidoreductasesViolaxanthinBiochimica et Biophysica Acta (BBA) - Biomembranes
researchProduct

Further orthometalated dinuclear palladium(iii) compounds with bridging N,S-donor ligands

2013

New dinuclear palladium(III) compounds of general formula Pd2[(C6H4)PPh2]2[N-S]2Cl2, N-S being 2-mercaptopyridinate, 3a; 2-mercapto-6-methylpyridinate, 3b; 2-quinolinethiolate, 3c; 2-mercaptopyrimidinate, 3d; 1-methyl-1H-imidazole-2-thiolate, 3e; 1-methyl-1H-benzimidazole-2-thiolate, 3f; 2-mercaptobenzothiazolate, 3g and 5-mercapto-1-methyltetrazolate, 3h have been obtained by oxidation with PhICl2 of the corresponding palladium(II) counterparts. The stability of the new compounds has been studied by (31)P NMR spectroscopy from 200 to 298 K. Compounds 3f-h were relatively stable until room temperature and they have been synthesized and characterized by (31)P, (1)H and (13)C NMR spectroscopy…

Inorganic ChemistryCrystallography13c nmr spectroscopychemistryAtomic orbitalInorganic chemistryDensity analysischemistry.chemical_element31p nmr spectroscopySulfurPalladiumDalton Trans.
researchProduct

On the mechanistic behavior of highly efficient palladium-tetraphosphine catalytic systems for cross-coupling reactions: first spectroscopic and elec…

2008

Electrochemical studies carried out in conjunction with 31P NMR spectroscopy on the palladium(II)/palladium(0) halogeno complexes of the tetraphosphine 1,1′,2,2′-tetrakis(diphenylphosphino)-4,4′-di...

crystal structureDenticityredox reactionoxidative additiontetraphosphinechemistry.chemical_elementmechanism010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCoupling reactionCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysiscross-coupling reactionsferrocenylpolyphosphine complexesPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSelectrochemical studies010405 organic chemistryChemistryOrganic Chemistry[CHIM.CATA]Chemical Sciences/CatalysispalladiumCombinatorial chemistryOxidative addition0104 chemical sciences3. Good healthcatalytic systemsreaction kinetics31p nmr spectroscopyPalladium
researchProduct

Efficient Nucleophilic Degradation of an Organophosphorus Pesticide “Diazinon” Mediated by Green Solvents and Microwave Heating

2019

An efficient strategy for the degradation of organophosphate pesticide Diazinon was investigated. In this work, ionic liquids, bio-based solvents, and two conventional organic solvents were used as reaction media. Kinetics studies by means of half-life (t1/2,h) were followed by 31P NMR and the products analyzed by GC-MS, HPLC-MS and NMR techniques. These results have shown that t1/2 values in ionic liquids were the lowest and also they were able to activate two electrophilic centers in Diazinon, whilst degradation in bio-based solvents occurred slowly by only an aromatic pathway. In addition, a study to estimate the influence of green activation techniques was carried out by using Ultrasoun…

DiazinonKinetics02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesmicrowaveslcsh:Chemistryionic liquidschemistry.chemical_compoundNucleophile31P NMRorganophosphate pesticidesOriginal ResearchultrasoundGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSolventChemistrylcsh:QD1-999chemistrygreener solventsIonic liquidDegradation (geology)Piperidine0210 nano-technologyMicrowaveFrontiers in Chemistry
researchProduct