Search results for "Trim"

showing 10 items of 1942 documents

Supramolecular 2D/3D isomerism in a compound containing heterometallic Cu(II)2Co(II) nodes and dicyanamide bridges.

2014

Three new heterometallic copper(II)-cobalt(II) complexes [(CuL(2))2Co{dca}2]·H2O(1), [(CuL(1))2Co{dca}2]n (2a), and [(CuL(1))2Co{dca}2]n (2b) [dca(-) = dicyanamide = N(CN)2(-)] have been synthesized by reacting the "metallo-ligand" [CuL(1)] or [CuL(2)] with cobalt(II) perchlorate and sodium dicyanamide in methanol-water medium (where H2L(1) = N,N'-bis(salicylidene)-1,3-propanediamine and H2L(2) = N,N'-bis(α-methylsalicylidene)-1,3-propanediamine). The three complexes have been structurally and magnetically characterized. Complex 1 is a discrete trinuclear species in which two metallo-ligands coordinate to a cobalt(II) ion through the phenoxido oxygen atoms along with two terminally coordina…

ChemistryStereochemistrySupramolecular chemistrychemistry.chemical_elementTrimerCopperInorganic Chemistrychemistry.chemical_compoundPerchlorateCrystallographyOxygen atomPhysical and Theoretical ChemistryCobaltDicyanamideInorganic chemistry
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Assembly and Separation of Semiconductor Quantum Dot Dimers and Trimers

2011

Repeated precipitation of colloidal semiconductor quantum dots (QD) from a good solvent by adding a poor solvent leads to an increasing number of QD oligomers after redispersion in the good solvent. By using density gradient ultracentrifugation we have been able to separate QD monomer, dimer, and trimer fractions from higher oligomers in such solutions. In the corresponding fractions QD dimers and trimers have been enriched up to 90% and 64%, respectively. Besides directly coupled oligomers, QD dimers and trimers were also assembled by linkage with a rigid terrylene diimide dye (TDI) and separated again by ultracentrifugation. High-resolution transmission electron micrographs show that the …

ChemistrySurface PropertiesDimerAnalytical chemistryTrimerGeneral ChemistrySubstrate (electronics)PhotochemistryBiochemistryCatalysisSolventchemistry.chemical_compoundColloidColloid and Surface ChemistryMonomerSemiconductorsDiimideQuantum DotsDensity gradient ultracentrifugationParticle SizeDimerization
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Ab initio modeling of excitonic and charge-transfer states in organic semiconductors: the PTB1/PCBM low band gap system.

2013

A detailed quantum chemical simulation of the excitonic and charge-transfer (CT) states of a bulk heterojunction model containing poly(thieno[3,4-b]thiophene benzodithiophene) (PTB1)/[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) is reported. The largest molecular model contains two stacked PTB1 trimer chains interacting with C60 positioned on top of and lateral to the (PTB1)3 stack. The calculations were performed using the algebraic diagrammatic construction method to second order (ADC(2)). One main result of the calculations is that the CT states are located below the bright inter-chain excitonic state, directly accessible via internal conversion processes. The other important aspects…

Chemistrybusiness.industryBand gapAb initioTrimerCharge (physics)General ChemistryInternal conversion (chemistry)BiochemistryMolecular physicsCatalysisPolymer solar cellOrganic semiconductorDelocalized electronColloid and Surface ChemistryOptoelectronicsbusinessJournal of the American Chemical Society
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Exchange of Pigment-Binding Amino Acids in Light-Harvesting Chlorophyll a/b Protein

1999

Four amino acids in the major light-harvesting chlorophyll (Chl) a/b complex (LHCII) that are thought to coordinate Chl molecules have been exchanged with amino acids that presumably cannot bind Chl. Amino acids H68, Q131, Q197, and H212 are positioned in helixes B, C, A, and D, respectively, and, according to the LHCII crystal structure [Kühlbrandt, W., et al. (1994) Nature 367, 614-621], coordinate the Chl molecules named a(5), b(6), a(3), and b(3). Moreover, a double mutant was analyzed carrying exchanges at positions E65 and H68, presumably affecting Chls a(4) and a(5). All mutant proteins could be reconstituted in vitro with pigments, although the thermal stability of the resulting mut…

ChlorophyllChloroplastsMacromolecular SubstancesStereochemistryMolecular Sequence DataPhotosynthetic Reaction Center Complex ProteinsPigment bindingLight-Harvesting Protein ComplexesTrimerBiochemistrychemistry.chemical_compoundAmino Acid SequenceAmino AcidsPeptide sequencePlant Proteinschemistry.chemical_classificationBinding SitesChlorophyll APeasPhotosystem II Protein Complexfood and beveragesAmino acidChloroplastB vitaminsAmino Acid SubstitutionchemistryChlorophyllThylakoidMutagenesis Site-DirectedCarrier ProteinsBiochemistry
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Localization of the N-terminal Domain in Light-harvesting Chlorophyll a/b Protein by EPR Measurements

2005

The conformational distribution of the N-terminal domain of the major light-harvesting chlorophyll a/b protein (LHCIIb) has been characterized by electron-electron double resonance yielding distances between spin labels placed in various domains of the protein. Distance distributions involving residue 3 near the N terminus turned out to be bimodal, revealing that this domain, which is involved in regulatory functions such as balancing the energy flow through photosystems (PS) I and II, exists in at least two conformational states. Models of the conformational sub-ensembles were generated on the basis of experimental distance restraints from measurements on LHCIIb monomers and then checked f…

ChlorophyllModels MolecularThreonineConformational changeTime FactorsLightMacromolecular SubstancesProtein ConformationPhotosynthetic Reaction Center Complex ProteinsLight-Harvesting Protein ComplexesElectronsTrimerCrystallography X-RayThylakoidsBiochemistryProtein Structure Secondarylaw.inventionResidue (chemistry)chemistry.chemical_compoundlawEscherichia coliAnimalsPhosphorylationAnnexin A4Electron paramagnetic resonanceMolecular BiologyPhotosystemPhotosystem I Protein ComplexChemistryChlorophyll AElectron Spin Resonance SpectroscopyPeasPhotosystem II Protein ComplexCell BiologyRecombinant ProteinsProtein Structure TertiaryOxygenN-terminusCrystallographyMonomerThylakoidMutationCattleSpin LabelsDimerizationJournal of Biological Chemistry
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A new ionic liquid dimethyldinonylammonium bromide as a flow modifier for the simultaneous determination of eight carboxylates by capillary electroph…

2005

Two new methods of capillary zone electrophoresis based on aqueous phosphate running buffers with UV spectrophotometric detection were developed and optimized for the determination of eight carboxylates as copper complexes. Metalcomplexes are negatively charged, so measurements were made as anion analyses with flow reversal in the capillary. Two flow modifiers were used: a common tetradecyltrimethylammonium bromide (TTAB) and a new ionic liquid dimethyldinonylammonium bromide (DMDNAB). The methods were compared to each other. Better separation was achieved with DMDNAB as the flow modifier. Method development was done using a fused silica capillary (61 cm x 50 microm i.d.). Optimization was …

ChromatographyAqueous solutionmedicine.diagnostic_testCapillary actionOrganic ChemistryAnalytical chemistryCarboxylic Acidschemistry.chemical_elementElectrophoresis CapillaryGeneral MedicineBiochemistryCopperTrimethyl Ammonium CompoundsAnalytical ChemistryQuaternary Ammonium Compoundschemistry.chemical_compoundElectrophoresisCapillary electrophoresischemistrySpectrophotometryIonic liquidmedicineSpectrophotometry UltravioletCarboxylateWater Pollutants ChemicalJournal of chromatography. A
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Seafood freshness determination through vapour phase Fourier transform infrared spectroscopy.

2006

Abstract A new vapour-phase manifold has been developed to determine trimethylamine (TMA) in fish and cephalopod samples by Fourier transform infrared (FT-IR) spectroscopy. Samples were treated off-line for 1 h with trichloroacetic acid (TCA), filtered and washed. The obtained extracts were aspirated and alkalinized with NaOH 2.0 M, in an on-line system. TMA was separated from the solution in a gas phase separator and then transported by means of a nitrogen carrier into a home made 10 cm pathlength IR gas cell, where the corresponding FT-IR spectra were acquired by accumulating 30 scans per spectrum with 2 cm−1 nominal resolution. The method was applied to the determination of TMA in natura…

ChromatographyChemistryInfraredAnalytical chemistrySeparator (oil production)chemistry.chemical_elementTrimethylamineBiochemistryNitrogenAnalytical Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformsymbolsEnvironmental ChemistryGas chromatographyFourier transform infrared spectroscopySpectroscopySpectroscopyAnalytica chimica acta
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Identification of diterpenes in canvas painting varnishes by gas chromatography-mass spectrometry with combined derivatisation.

2004

A derivatisation method that combines the formation of ethyl esters from the carboxylic groups and trimethylsilyl ethers from hydroxyl groups of the components of diterpenic resins is presented in this paper. This methodology involves two experimental steps: (1) formation of ethyl esters using ethyl chloroformate; and (2) the esterified compounds are lead to react with trimethylsilylimidazole to form the corresponding trimethylsilyl ethers. The main advantage of the proposed method is the possibility of performing simultaneously the analysis of amino acids from proteins, fatty acids from drying oils, and diterpenic compounds from natural resins usually found in works of art. This methodolog…

ChromatographySilylationTrimethylsilylChemistryOrganic ChemistryVarnishGeneral Medicineengineering.materialReference StandardsBiochemistryAnalytical Chemistrychemistry.chemical_compoundCanada balsamvisual_artPaintvisual_art.visual_art_mediumengineeringOrganic chemistryEthyl chloroformatePaintingsGas chromatographyGas chromatography–mass spectrometryDiterpenesAbietic acidJournal of chromatography. A
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Simultaneous dissolution profiles of two drugs in pharmaceutical formulations by an FIA manifold

2002

Abstract This article deals with the simultaneous determination of dissolution profiles of two drugs with overlapped spectra, present in the same pharmaceutical formulation. The official procedure for the dissolution profile is adapted to the continuous-flow methodology; the dissolution vessel is connected to an FIA manifold, in which the sample aliquots from the dissolution vessel are treated in order to adjust to the suitable pH and dilution degree to be monitored. The resulting solution is injected into the carrier stream, an acetic acid–acetate buffer at pH 4.3 and forced to the flow-cell of the spectrophotometer. The simultaneous determination of both profiles is based on the first der…

ChromatographySulfamethoxazoleChemistryClinical BiochemistryPharmaceutical SciencePharmaceutical formulationTrimethoprimDosage formAnalytical Chemistrylaw.inventionDilutionAnti-Infective AgentsSolubilitylawFlow Injection AnalysisDrug DiscoveryManifold (fluid mechanics)Quantitative analysis (chemistry)DissolutionSpectroscopyAnalysis methodJournal of Pharmaceutical and Biomedical Analysis
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Enantioseparation of phenotiazines by affinity electrokinetic chromatography using human serum albumin as chiral selector

2007

Nowadays, there is a special interest within the pharmaceutical laboratories to develop single enantiomer formulations and consequently a need for analytical methods to determine the enantiomeric purity of drugs. The present paper deals with the enantiomeric separation of promethazine and trimeprazine enantiomers by affinity electrokinetic chromatography (AEKC)-partial filling technique using human serum albumin (HSA) as chiral selector. A multivariate optimization of the most critical experimental variables in enantioresolution, running pH, HSA concentration and plug length, is carried out to obtain enantioresolution of promethazine and trimeprazine. The estimated maximum and optimum resol…

ChromatographybiologyResolution (mass spectrometry)TrimeprazineSerum albuminHuman serum albuminBiochemistryAnalytical ChemistryPromethazinechemistry.chemical_compoundAffinity chromatographychemistryPhenothiazinebiology.proteinmedicineEnvironmental ChemistryEnantiomerSpectroscopymedicine.drugAnalytica Chimica Acta
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