Search results for "Urea"

showing 10 items of 888 documents

CCDC 1425262: Experimental Crystal Structure Determination

2016

Related Article: T. Mäkelä, K. Rissanen|2016|Dalton Trans.|45|6481|doi:10.1039/C6DT00414H

catena-((mu2-11'-(2356891112-Octahydro-1471013-benzopentaoxacyclopentadecine-1516-diyl)bis(3-(4-nitrophenyl)urea))-sodium iodide acetone solvate hemihydrate)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1478713: Experimental Crystal Structure Determination

2016

Related Article: Toni Mäkelä, Anniina Kiesilä, Elina Kalenius and Kari Rissanen|2016|Chem.-Eur.J.|22|14264|doi:10.1002/chem.201602362

catena-[11'1''-(17-(((4-(oxy(oxido)-azanyl)phenyl)carbamoyl)amino)-679101213202123242627-dodecahydrodibenzo[bn][1471013161922]octaoxacyclotetracosine-2316-triyl)tris(3-(4-nitrophenyl)urea)-rubidium iodide chloroform solvate]Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Iron-catalyzed C(sp2)-C(sp3) cross-coupling at low catalyst loading

2019

The iron-catalyzed C(sp2)–C(sp3) cross-coupling provides a highly economical route to exceedingly valuable alkylated arenes that are widespread in medicinal chemistry and materials science. Herein, we report an operationally-simple protocol for the selective C(sp2)–C(sp3) iron-catalyzed cross-coupling of aryl chlorides with Grignard reagents at low catalyst loading. A broad range of electronically-varied aryl and heteroaryl chlorides underwent the cross-coupling using challenging alkyl organometallics possessing β-hydrogens with high efficiency up to 2000 TON. A notable feature of the protocol is the use of environmentally-friendly cyclic urea ligands. A series of guidelines to predict cros…

chemistry.chemical_classification010405 organic chemistryArylAlkylation010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryReagentElectrophileUreaOrganic chemistryReactivity (chemistry)AlkylCatalysis Science & Technology
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Thermodynamics ofN,N,N-octylpentyldimethyl-ammonium chloride in water-urea mixtures

1997

Specific conductivities, densities, heat capacities, and enthalpies of dilution at 25‡C were measured forN,N,N-octylpentyldimethylammonium chloride (OPAC) in water-urea mixtures at various urea concentrations mu as functions of the surfactant concentration ms. From conductivity data, the cmc and the degree of the counterion dissociation Β of the OPAC micelles were calculated. The cmc increases linearly with increasingm u while Βvs. mu is a smooth concave curve. From the experimental thermodynamic data, the apparentY Φ and partialY 2 molar properties (volumes, heat capacities, and relative enthalpies) are derived as functions of mu andm s . The effect of urea on the dependences of the differ…

chemistry.chemical_classificationAqueous solutionChemistryThermodynamics of micellizationEnthalpyBiophysicsThermodynamicsBiochemistryChlorideHeat capacityDissociation (chemistry)chemistry.chemical_compoundmedicineUreaPhysical and Theoretical ChemistryCounterionMolecular Biologymedicine.drugJournal of Solution Chemistry
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Thermal diffusion of dextran in aqueous solutions in the absence and the presence of urea.

2006

The Ludwig-Soret effect was studied for aqueous solutions of dextran in the temperature range 15T55 degrees C taking into account the effect of the addition of urea. In the absence of urea, the Soret coefficient S(T) changes sign; it is positive for T45.0 degrees C but negative for T45.0 degrees C. The positive sign of S(T) means that the dextran molecules migrate toward the cold side of the fluid; this behavior is typical for polymer solutions, whereas a negative sign indicates the macromolecules move toward the hot side. The addition of urea to the aqueous solution of dextran rises S(T) and reduces the inversion temperature. For 2 M urea the change in the sign of S(T) is observed at T = 2…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsChemistryHydrogen bondAnalytical chemistryTemperatureThermodynamicsWaterBioengineeringDextransPolymerAtmospheric temperature rangeThermal diffusivityBiomaterialsDiffusionSolutionschemistry.chemical_compoundDextranMaterials ChemistryUreaUreaMacromoleculeBiomacromolecules
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Structural Characterization of Glycoconjugate Polystyrene in Aqueous Solution

1999

Maltopentaose-carrying polystyrene was synthesized by the homopolymerization of vinylbenzyl maltopentaose amide. Resulted amphiphilc polymacromonomer was dissolved in 0.1 M urea aqueous solution, and its structure was characterized by small-angle X-ray scattering and molecular modeling. Maltopentaose-carrying polystyrene polymacromonomer was found to be represented by a molecular bottlebrush, composed of a large helix of polystyrene backbone and maltopentaose brushes. The molecular bottlebrush seems to be distributed randomly or many even be broken once or twice in segments with no apparent intersegmental spatial correlation. A large helix of polystyrene backbone is formed by a random seque…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsMolecular modelGlycoconjugateOrganic ChemistryRadical polymerizationInorganic Chemistrychemistry.chemical_compoundAldosechemistryAmidePolymer chemistryMaterials ChemistryUreaPolystyreneMacromolecules
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ERA-experiment “space biochemistry”

1995

Abstract The general goal of the experiment was to study the response of anhydrobiotic (metabolically dormant) microorganisms (spores of Bacillus subtilis, cells of Deinococcus radiodurans, conidia of Aspergillus species) and cellular constituents (plasmid DNA, proteins, purple membranes, amino acids, urea) to the extremely dehydrating conditions of open space, in some cases in combination with irradiation by solar UV-light. Methods of investigation included viability tests, analysis of DNA damages (strand breaks, DNA-protein cross-links) and analysis of chemical effects by spectroscopic, electrophoretic and chromatographic methods. The decrease in viability of the microorganisms was as exp…

chemistry.chemical_classificationAtmospheric SciencebiologyDNA damageChemistryMicroorganismFungal geneticsAerospace EngineeringAstronomy and AstrophysicsDeinococcus radioduransBacillus subtilisbiology.organism_classificationAmino acidchemistry.chemical_compoundGeophysicsBiochemistrySpace and Planetary ScienceUreaGeneral Earth and Planetary SciencesDNAAdvances in Space Research
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Study of peak shape and efficiency in butyl acrylate-based monolithic columns for capillary electrochromatography.

2009

Abstract The study and modelling peak shape of in capillary electrochromatography (CEC), obtained using butyl acrylate (BA)-based monolithic columns, is described in this article. A modified-Gaussian model, which is a function of conventional experimental parameters: retention time (tR), peak height (H0) and standard deviation (σ0) at the peak maximum, and left (A) and right (B) halfwidths, was used to describe the peaks of thiourea and several polyaromatic hydrocarbons compounds, which were eluted under several applied voltages. A mean relative error below 2% in the prediction of peak shape is obtained. Based on peak parameters, an easy and reliable estimation of global chromatographic per…

chemistry.chemical_classificationCapillary electrochromatographyMonolithic HPLC columnChromatographyElutionButyl acrylateOrganic ChemistryAnalytical chemistryThioureaGeneral MedicineBiochemistryAnalytical ChemistryElectrophoresischemistry.chemical_compoundHydrocarbonThioureachemistryElectrochromatographyAcrylatesCapillary ElectrochromatographyPolycyclic Aromatic HydrocarbonsJournal of chromatography. A
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Solid–liquid extraction of ω-amino acids using ditopic receptors

2008

Abstract Five heteroditopic ligands have been prepared to be used in solid–liquid extraction of ω-amino acids into DMSO solutions. The prepared ligands contain crown ethers as cation binding sites and thiourea or amide groups for anion recognition. The aliphatic zone of the 1H NMR spectra suggests that two different species related to the amino acid are present in solution. One of these species is the complexed zwitterionic form and the other seems to be free non-zwitterionic amino acid. The presence of these two species allows extraction efficiencies higher than 100%.

chemistry.chemical_classificationCation bindingChemistryOrganic ChemistryExtraction (chemistry)BiochemistryIonAmino acidchemistry.chemical_compoundThioureaAmideDrug DiscoveryPolymer chemistryProton NMROrganic chemistrySolid phase extractionTetrahedron
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Gaschromatographisch-massenspektrometrische identifizierung der durch umsetzung von aminen mit isocyanaten gebildeten harnstoffderivate

1977

Abstract Gas chromatographic-mass spectrometric identification of urea derivatives formed by the reaction of amines with isocyanates N,N′-Di- and N,N′,N′-trisubstituted ureas constitute suitable derivatives for the gas chromatographic (GC) determination of primary and secondary amines. The GC identification of N- tert. -butyl-,N′,N′-alkyl urea derivatives presented in the first communication has been succesfully confirmed by mass spectrometry (MS) and mass fragmentometry. The reproduced mass spectra of six N- tert. -butyl-,N′,N′-alkyl ureas were interpreted according to the decomposition mechanisms of less complicated alkyl ureas known from the literature. Using combined GC-MS the detection…

chemistry.chemical_classificationDetection limitChromatographyChemistryMass fragmentometryOrganic ChemistryGeneral MedicineMass spectrometryBiochemistryAnalytical ChemistryMass spectrumOrganic chemistryKovats retention indexUrea derivativesAlkylJournal of Chromatography A
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