Search results for "Molecule"

showing 10 items of 5162 documents

Comparison of Water Adsorption Characteristics of Oligo and Polysaccharides of α-Glucose Studied by Near Infrared Spectroscopy

2014

The adsorption properties of water molecules on oligo and polysaccharides are attributed to the OH groups of the glucose rings in the molecules. The water molecules are adsorbed onto OH groups by hydrogen bond formation. Near infrared spectroscopic and gravimetric techniques were used in analysing the adsorption characteristics of malto-oligosaccharides and some polysaccharides. Near infrared spectra of the dry oligo and polysaccharides were acquired during the adsorption of water molecules at a relative humidity of 50-55%. The amounts of water adsorbed by the samples were also recorded by an analytical balance. Second derivative techniques were used in decomposing the OH combination freque…

chemistry.chemical_compoundAdsorptionProperties of waterChemistryAmyloseHydrogen bondAmylopectinInorganic chemistryGeneral EngineeringMaltotrioseOrganic chemistryGravimetric analysisMoleculeAdvanced Materials Research
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Water Adsorption Characteristics of Acyclic Oligosaccharides of α-Gluose Studied by Near Infrared Spectroscopy

2013

The adsorption properties of water molecules on maltooligosaccharides are attributed to the OH groups of the glucose rings in maltooligosaccharides. The water molecules are adsorbed onto OH groups by hydrogen bond formation. Near infrared spectroscopic and gravimetric techniques were used in analysing the adsorption characteristics of maltooligosaccharides. Near infrared spectra of the dry maltooligosaccharides were acquired during the adsorption of wa- ter molecules at a relative humidity of 50%. The amounts of water adsorbed by the samples were also recorded by an ana- lytical balance. Second derivative techniques were used in decomposing the OH combination frequency of the adsorbed water…

chemistry.chemical_compoundAdsorptionProperties of waterchemistryPeriod (periodic table)Hydrogen bondInorganic chemistryMaltotrioseMoleculeGravimetric analysisOrganic chemistryRelative humidityThe Open Spectroscopy Journal
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Sorption Kinetics of Benzene and p-Xylene on Template Supported Synthesized Gallosilicates

1993

Adsorption equilibria and kinetics of benzene and p-xylene on microporous gallosilicates (Ga-MFI) were measured piezometrically to ascertain the role of Ga in the system and to compare it with Ga-free MFI structures. The intracrystalline mobility of benzene follows a diffusional mechanism throughout the entire concentration range with an energy of activation that considerably exceeds that for the Ga-free species (78 kJmol−1 and 26 kJmol−1, respectively). For p-xylene, the kinetics indicate the existence of three sorption states. Sorbing species become highly immobile at a pore filling of ca n > 4 molecules per unit cell, i.e. in the range of concentration where isotherm hysteresis occurs. T…

chemistry.chemical_compoundAdsorptionchemistryKineticsPhysical chemistryMoleculeOrganic chemistrySorptionMicroporous materialActivation energyBenzenep-Xylene
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Formation of α-ω(4,7,10,13-pentaoxa-16-azacyclooctadecane) hexadecane micelles in aqueous solution – effect of HCl addition

2003

The structure of aggregates of a new bolaform surfactant [α-ω (4,7,10,13-pentaoxa-16-azacyclooctadecane) hexadecane] in neat aqueous solution has been investigated by small-angle neutron scattering. Preliminary data analysis unequivocally indicates that globular micelles are formed. This finding has been confirmed by the analysis of data obtained upon addition of hydrochloric acid. The observed significant reduction of micelle aggregation number has been attributed to the peculiar complexing ability of the two aza-crown ether units in the surfactant molecule; this is in line with information inferred from the complexation of ions into the non alkylated azacrown ethers. As a consequence of h…

chemistry.chemical_compoundAqueous solutionAggregation numberPulmonary surfactantChemistryInorganic chemistryPhysical chemistryMoleculeEtherHexadecaneSmall-angle neutron scatteringMicelleGeneral Biochemistry Genetics and Molecular BiologyJournal of Applied Crystallography
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Effect of Monooxygenase Inducers on the Binding of Benzo-(A)Pyrene Metabolites to Cellular Macromolecules in Perfused Rat Lungs

1978

The irreversible binding of metabolically activated [3H]-benzo(a)pyrene (BP) to cellular macromolecules of isolated perfused rat lungs was studied. Lungs from differently pretreated animals were perfused in situ in a recirculating system without ventilation. BP with a specific activity of 10 mCi/μmol was added to 50 ml perfusion medium containing 40% washed bovine erythrocytes to a final concentration of 1 μM. DNA, RNA and protein fractions were isolated and assayed for irreversibly bound radioactivity.

chemistry.chemical_compoundBenzo(a)pyrenechemistryBiochemistryRNAPyreneInducerSpecific activityMonooxygenaseDNAMacromolecule
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<title>Nonlinear optical properties of some indandione-1,3 pyridinium betaine derivatives</title>

1997

In this paper nonlinear optical properties of indandione-1,3 pyridinium betaine (IPB) molecule and its novel amphiphilic derivatives have been studied. Hyper-Rayleigh scattering (HRS) has been used as a direct and accurate tool to determine effective hyperpolarizability (beta) of IPB derivatives dissolved in chloroform. Evaluation of hyperpolarizability gives an averaged values of (beta) from 140 multiplied by 10-30 to 450 multiplied by 10-30 esu. Disordering of molecular orientation for multilayer Langmuir-Blodgett films of compound C17-IPB has been studied by SHG techniques and discussed for different film thickness. It has been observed that orientation degree of the Z-type molecular str…

chemistry.chemical_compoundBetainechemistryScatteringAmphiphilePhysical chemistrySecond-harmonic generationNonlinear opticsHyperpolarizabilityMoleculeOrganic chemistryPyridiniumSPIE Proceedings
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1983

Synthese a partir de l'hexahydro-1,5,5a,6,9,9a benzodioxepinne-2,4. Polymerisation en masse en un produit incolore, cireux (Tg=−11°C)

chemistry.chemical_compoundBicyclic moleculeChemistryPolymer chemistryAcetalCationic polymerizationRing-opening polymerizationEne reactionDie Makromolekulare Chemie, Rapid Communications
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STUDIES ON BICYCLO[3.3.1]NONANES FOR SYNTHESIS OF CYCLOOCTENES

2002

This paper describes a full conformational and stereochemical study of bicylo[3.3.1]nonanes, obtained from the reaction between cinnamaldehyde and 1-morpholine 1-cyclohexene. NMR data and stereochemistry were unequivocally established and assigned by two-dimensional experiments and single-crystal X-ray analysis. The crystal structure of a minor compound, 4, is reported. Cyclooctenes, which are present in natural products with biological activities, were synthesized from the bicyclononanes via the Wharton fragmentation.

chemistry.chemical_compoundBicyclic moleculeChemistryStereochemistryOrganic ChemistryCrystal structureNmr dataCinnamaldehydeSynthetic Communications
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Synthetic studies toward natural furanosesquiterpenoids from santonin. Synthesis of (+)-1,2-dihydrotubipofuran

1994

Abstract Santonin (1) was converted into (+)-1,2-dihydrotubipofuran (13) via a synthetic pathway involving a very easy preparation of 7,11-ene-8,12-olide and 8,12-furan moieties and A-ring elaboration on the eudesmane framework.

chemistry.chemical_compoundBicyclic moleculeChemistryStereochemistryOrganic ChemistryDrug DiscoveryEnantiomerSesquiterpeneBiochemistrySantoninTetrahedron
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Iod-induzierte stereoselektive Carbocyclisierungen – Beispiele für eine breit anwendbare, neue Methode zur Synthese von Cyclohexan- und -hexen-Deriva…

1988

chemistry.chemical_compoundBicyclic moleculeIntramolecular reactionChemistryGeneral MedicineHalocarbonMedicinal chemistryAngewandte Chemie
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