Search results for "mines"

showing 10 items of 2609 documents

Cd(II) and Cu(II) coordination polymers constructed from the expanded 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene ligand: conventional and ultrasound-…

2018

Shaabani, Behrouz/0000-0001-5576-4604; Kubicki, Maciej/0000-0001-7202-9169; Grzeskiewicz, Anita M./0000-0003-0377-2260 WOS: 000447971700041 A 3D open inorganic/organic framework, {[Cd(mu-L)(mu(3)-SO4)(H2O)]center dot H2O}(n) (1) [L = 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene] was synthesized by the reaction of CdSO4 center dot 8H(2)O with L. The treatment of Cu(NO3)(2)center dot 3H(2)O with the same N,N'-donor ligand in two different solvent mixtures, methanol/ dichloromethane (2) and methanol/ chloroform (3), afforded two new ladder-like coordination polymers of formula {[Cu(mu-L)(mu-NO3)(NO3)]center dot solv}(n) [solv = CH2Cl2 (2) and CHCl3 (3)]. The non-interpenetrated ladder motifs 2 a…

Chloroform010405 organic chemistryLigand13-ButadieneGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSolventchemistry.chemical_compoundCrystallographychemistryMaterials ChemistryMoleculeLuminescenceDichloromethane
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Molecular structures of chlorophyll a aggregates: spectroscopic and molecular modeling study

1993

Molecular structures of chlorophyll a aggregates have been studied. Spectroscopic properties of these aggregates have been studied by absorption and fluorescence spectroscopy in hydrocarbon solution at various temperatures. Observed spectroscopic shifts were interpreted in terms of simple exciton theory. Exciton splittings were estimated from computer optimized models of previously suggested Chl a aggregate structures.

Chlorophyll aMolecular model010405 organic chemistryExcitonAnalytical chemistry010402 general chemistry01 natural sciencesFluorescence spectroscopy0104 chemical sciences3. Good healthchemistry.chemical_compoundchemistryChemical physicsMoleculeAbsorption (electromagnetic radiation)SpectroscopyLuminescenceSPIE Proceedings
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The toxicity of Roundup® 360 SL formulation and its main constituents: Glyphosate and isopropylamine towards non-target water photoautotrophs

2010

The toxicity of commercial formulation of Roundup® 360 SL, widely used, nonselective herbicide and its main constituents, glyphosate (PMG), equimolar (1:1) isopropylamine salt of glyphosate (GIPA) and isopropylamine (IPA) was examined towards eight aquatic microphotoautotrophs; seven cyanobacterial strains representing either saline or freshwater communities, and common eukaryotic algae Chlorella vulgaris Beijerinck. Autotrophs were cultured 21 days in their appropriate standard media supplemented with various amounts of Roundup®, glyphosate, GIPA and IPA. The determination of the growth of examined photoautotrophs was performed by time-course measurements of total chlorophyll content in ex…

ChlorophyllCyanobacteriaHealth Toxicology and MutagenesisRoundup®GlycineCyanobacteriachemistry.chemical_compoundglyphosateAquatic plantToxicity TestsBotanyIsopropylamineFood scienceAutotrophChromatography High Pressure LiquidalgaeAnalysis of VarianceDose-Response Relationship DrugPropylaminesbiologyisopropylamineHerbicidesPublic Health Environmental and Occupational HealthtoxicityGeneral Medicinebiology.organism_classificationSaline waterPollutionchemistryGlyphosateChlorophyllToxicityLinear ModelsChlorella vulgarisWater Pollutants ChemicalEcotoxicology and Environmental Safety
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A battery of toxicity tests as indicators of decontamination in composting oily waste.

2000

Heterogeneous oily waste from an old dumping site was composted in three windrows constructed from different proportions of waste, sewage sludge, and bark. The objectives of this pilot study were to examine the usefulness of composting as a treatment method for this particular waste and to study decontamination in the composting process by using a battery of toxicity tests. Five samples from the windrow having intermediate oil concentrations were tested with toxicity tests based on microbes (Pseudomonas putida growth inhibition test, ToxiChromotest, MetPLATE, and three different modifications of a luminescent bacterial test), enzyme inhibition (reverse electron transport), plants (duckweed …

ChlorophyllHealth Toxicology and MutagenesisPlant DevelopmentGerminationcomplex mixturesWindrowBioremediationPseudomonasEscherichia coliBioassayAnimalsSoil PollutantsDecontaminationSewage sludgeOrganellesPlants MedicinalEnchytraeusbiologyChemistryPublic Health Environmental and Occupational HealthFabaceaeGeneral MedicineHuman decontaminationPlantsbiology.organism_classificationPollutionInvertebratesWaste treatmentPetroleumMetalsEnvironmental chemistryToxicityLuminescent MeasurementsColorimetryDNA DamageEcotoxicology and environmental safety
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Filling the “green gap” of the major light-harvesting chlorophyll a/b complex by covalent attachment of Rhodamine Red

2009

AbstractThe major light-harvesting chlorophyll a/b complex (LHCII) greatly enhances the efficiency of photosynthesis in green plants. Recombinant LHCII can be assembled in vitro from its denatured, bacterially expressed apoprotein and plant pigments. This makes it an interesting candidate for biomimetic light-harvesting in photovoltaic applications. Due to its almost 20 pigments bound per apoprotein, LHCII absorbs efficiently in the blue and red spectral domains of visible light but less efficiently in the green domain, the so-called “green gap” in its absorption spectrum. Here we present a hybrid complex of recombinant LHCII with organic dyes that add to LHCII absorption in the green spect…

ChlorophyllLHCIIProtein FoldingFRET (Förster resonance energy transfer)Chlorophyll aAbsorption spectroscopyBiophysicsPhotosynthesisPhotochemistryBiochemistryRhodamineLight-harvesting complexchemistry.chemical_compoundPhotosynthesisFluorescent DyesRhodaminesChlorophyll Afood and beveragesSite-specific labelingCell BiologyMaleimide dyeB vitaminsSolar spectrumchemistryChlorophyllVisible spectrumBiochimica et Biophysica Acta (BBA) - Bioenergetics
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Gaining insight in the behaviour of imidazolium-based ionic liquids as additives in reversed-phase liquid chromatography for the analysis of basic co…

2015

In reversed-phase liquid chromatography in the absence of additives, cationic basic compounds give rise to broad and asymmetrical peaks as a result of ionic interactions with residual free silanols on silica-based stationary phases. Ionic liquids (ILs), added to the mobile phase, have been suggested as alternatives to amines to block the activity of silanols. However, the dual character of ILs should be considered: both cation and anion may be adsorbed on the stationary phase, thereby creating a double asymmetrical layer positively or negatively charged, depending on the relative adsorption of both ions. In this work, a study of the performance of six imidazolium-based ILs (the chlorides an…

Chromatography Reverse-PhaseChromatographyTetrafluoroborateOrganic ChemistryCationic polymerizationImidazolesIonic bondingIonic LiquidsGeneral MedicineReversed-phase chromatographyBiochemistryAdrenergic beta-1 Receptor AntagonistsAnalytical Chemistrychemistry.chemical_compoundAdsorptionchemistryChloridesPhase (matter)Ionic liquidBoratesOrganic chemistryAminesTriethylamineChromatography High Pressure LiquidJournal of chromatography. A
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Chiral determination of amphetamine and related compounds using chloroformates for derivatization and high-performance liquid chromatography

1999

The enantiomeric determination of amphetamine and various amphetamine-type compounds by liquid chromatography after chiral derivatization with 9-fluorenylmethyl chloroformate-L-proline (FMOC-L-Pro) is reported. The results obtained were compared with those achieved after achiral derivatization with 9-fluorenylmethyl chloroformate and subsequent separation of the derivatives on a beta-cyclodextrin chiral stationary phase. Conditions for the derivatization of amphetamines with FMOC-L-Pro were investigated, including the effect of the derivatization reagent concentration, pH and reaction time, using amphetamine, ephedrine and pseudoephedrine as model compounds. On the basis of these studies, p…

ChromatographyAmphetaminesStereoisomerismChloroformatePseudoephedrineSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundchemistryReagentElectrochemistrymedicineEnvironmental ChemistryOrganic chemistryCentral Nervous System StimulantsEnantiomerEphedrineDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidSpectroscopymedicine.drugThe Analyst
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Indirect determination of paracetamol in pharmaceutical formulations by inhibition of the system luminol–H2O2–Fe(CN)63− chemiluminescence

1999

After a large drug scanning, the system Luminol-H2O2-Fe(CN)6(3-) is proposed for first time for the indirect determination of paracetamol. The method is based on the oxidation of paracetamol by hexacyanoferrate (III) and the subsequent inhibitory effect on the reaction between luminol and hydrogen peroxide. The procedure resulted in a linear calibration graph over the range 2.5-12.5 microg ml(-1) of paracetamol with a sample throughput of 87 samples h(-1). The influence of foreign compounds was studied and, the method was applied to determination of the drug in three different pharmaceutical formulations.

ChromatographyCalibration curveClinical BiochemistryAnalgesicAnalytical chemistryPharmaceutical ScienceDosage formAnalytical ChemistryLuminollaw.inventionchemistry.chemical_compoundchemistrylawDrug DiscoveryFerricyanideHydrogen peroxideQuantitative analysis (chemistry)SpectroscopyChemiluminescenceJournal of Pharmaceutical and Biomedical Analysis
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Determination of the flavor enhancer maltol through a FIA — direct chemiluminescence procedure

2001

Abstract A new FIA — direct chemiluminescence method is proposed for the determination of maltol, based upon the oxidation of the food additive by KMnO 4 in sulfuric acid medium at 80°C enhanced by hexadecylpyridinium chloride (HD) and formic acid (HCOOH). The calibration graph is linear over the range 0.5–4.0 mg l −1 of maltol, with a R.S.D. ( n =50, 0.5 mg l −1 ) of 2.9%, LOD ( s / n =3) of 10 mg l −1 and sample throughput of 153 h −1 .

ChromatographyCalibration curveFormic acidStereochemistryMaltolSulfuric acidBiochemistryChlorideAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistrylawmedicineEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyFlavorChemiluminescencemedicine.drugAnalytica Chimica Acta
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Simple high-performance liquid chromatographic assay for polyamines and their monoacetyl derivatives.

1993

A rapid reversed-phase high-performance liquid chromatographic method, using pre-column derivatization with benzoyl chloride and ultraviolet detection at 254 nm, was developed for the simultaneous measurement of polyamines and their monoacetyl derivatives. Calibration curves were linear for concentrations from 1.25 to 25 nmol/ml. The method was employed to assay these compounds in chick embryo retina explants using organic solvent extraction and 1,7-diaminoheptane as an internal standard. This simple and sensitive method can be applied to routine determinations of these compounds in various biological samples.

ChromatographyCalibration curveOrganic solventExtraction (chemistry)Reproducibility of ResultsAcetylationGeneral ChemistryChick EmbryoDiaminesHigh-performance liquid chromatographyRetinachemistry.chemical_compoundBenzoyl chloridechemistryPolyaminesAnimalsSpectrophotometry UltravioletDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidJournal of chromatography
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