Search results for " Structures"

showing 10 items of 4162 documents

Functionalization of aliphatic polyesters by nitroxide radical coupling

2014

Functionalized poly(butylene succinate) (PBS) samples were prepared by a post-polymerization method based on the coupling reaction between TEMPO derivatives bearing different functionalities and PBS macroradicals generated by H-abstraction using a peroxide. 4-Benzoyloxy-2,2,6,6-tetramethylpiperidine-1- oxyl (BzO-TEMPO) and 4-(1-naphthoate)-2,2,6,6-tetramethylpiperidine-1-oxyl (NfO-TEMPO), a pro-fluorescent nitroxide, were successfully grafted on PBS, as revealed by MALDI TOF MS and UV-Vis spectroscopy. The functionalization degrees were accurately determined by UV-Vis analysis and confirmed by 1H-NMR spectroscopy. The grafting site was identified by combining theoretical calculations with e…

chemistry.chemical_classificationNitroxide mediated radical polymerizationgenetic structuresPolymers and PlasticsOrganic ChemistrySide reactionBioengineeringPolymerBiochemistryPeroxideCoupling reactionlaw.inventionPolyesterchemistry.chemical_compoundaliphatic polyesterchemistrylawPolymer chemistrySurface modificationElectron paramagnetic resonancenitroxide radicalpolymer functionalizationPolymer Chemistry
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Spectroscopic and structural characterization of pure and FeCl3-containing tri-n-butyl phosphate

2014

The spectroscopic properties and liquid structure of pure tri-n-butyl phosphate (TBP) and FeCl3/TBP solutions have been investigated by Uv–Vis and Raman spectroscopies, X-ray diffraction and conductometry. Uv–Vis and Raman spectra, supported by conductometric measurements, consistently indicate that the solubilized salt is present mostly as TBP n [FeCl3 − n ] n+ and FeCl4 − complex ions due to specific interaction with the TBP phosphate group. Thanks to this interaction, a high amount of salt (up to 13 % w/w) can be dissolved despite the relatively low dielectric constant of TBP. The X-ray diffractogram of pure TBP has been interpreted in terms of three main contributions which can be attri…

chemistry.chemical_classificationPolymers and PlasticsConductometryChemistryInorganic chemistryTri-N-butyl PhosphateFeCl3 . Tri-n-butyl phosphate . Self-assembling . Local structures .Amphiphilic solventsNanoparticleSalt (chemistry)Ionic bondingTri-n-butyl phosphatePhosphatesymbols.namesakechemistry.chemical_compoundColloid and Surface ChemistryFeCl3Materials ChemistrysymbolsMoleculeSelf-assemblingAmphiphilic solventsPhysical and Theoretical ChemistryLocal structuresRaman spectroscopy
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Manganese(III)-mediated oxidative carbon-carbon bond cleavage of the 1,10-phenanthroline-5,6-dione ligand

1999

[EN] A new manganese(III)-1,10-phenanthroline-5,6-dione (phendione) complex possessing a putative Mn-2(mu-O) (mu-O2CMe)(2) core has been found to undergo a Ligand-based oxidative cleavage of the C(5)-C(6) bond in weak acid aqueous MeOH under aerobic conditions at room temperature to yield 2,2'-bipyridyl-3,3'-dicarboxylate with co-reduction to the corresponding Mn-II-phendione species.

chemistry.chemical_classificationQuinone complexesPolynuclear complexesAqueous solutionLigandCarboxylato complexesPhenanthrolinechemistry.chemical_elementCrystal structureManganesePhotochemistryCleavage (embryo)Medicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryCarbon–carbon bondYield (chemistry)FISICA APLICADACrystal structuresOxidationMaterials ChemistryPhysical and Theoretical ChemistryManganese complexes
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B-DNA Structure and Stability as Function of Nucleic Acid Composition. Dispersion-Corrected DFT Study of Dinucleoside-Monophosphate Single and Double…

2013

actions of the sugar-phosphate skeleton with water; (6) hydrophobic interactions of the DNA cylindrical core, made up by the hydrogen-bonded and stacked nitrogen bases, with the water solvent. Recently, there has been increasing effort in developing and applying quantum chemical methods able to reproduce the structure of native B-DNA and to correctly describe the energy involved in the intrastrand and interstrand noncovalent interactions between the nucleotide monomers. This topic has been approached by both wave function methods and density functional theory. [2] Water solvent and sodium counterions also play an important role in the formation and relative stabilization of the double-helic…

chemistry.chemical_classificationStereochemistryChemistryBase pairHydrogen bondStackingGeneral ChemistryCrystal structureFull Papersstacking interactionsNucleobaseHydrophobic effectCrystallographyDNA structuresSettore CHIM/03 - Chimica Generale E Inorganicadensity functional calculationshydrogen bondsNon-covalent interactionsDNA DFT calculations structure stabilityDensity functional theoryWatson–Crick base pairsTheoretical ChemistryGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)
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Eye Cataract Simulation Using Polymer Dispersed Liquid Crystal Scattering Obstacles

2004

Polymer dispersed liquid crystals with electrically induced variations of light scattering extent similar to that of transparent PLZT ceramics are used for simulation of different development stages of eye cataract. Wavelength dependencies of scattering are determined in the visible spectral range, and human visual response looking through the scattering obstacle to the onset of various spatial frequency stimuli is determined psychophysically and electrophysiologically in order to find correlation between the scattering extent, visual acuity and visual evoked potential VEP chromatic characteristics.

chemistry.chemical_classificationVisual acuityMaterials sciencegenetic structuresbusiness.industryScatteringPolymerCondensed Matter Physicseye diseasesLight scatteringElectronic Optical and Magnetic MaterialsWavelengthOpticschemistryLiquid crystalmedicineChromatic scaleSpatial frequencymedicine.symptombusinessFerroelectrics
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Interaction of Dimethyltin(IV)2+ Cation with Gly-Gly, Gly-His, and Some Related Ligands. A New Case of a Metal Ion Able To Promote Peptide Nitrogen D…

1999

Equilibrium (pH-metric) and spectroscopic (1H,13C, and 119Sn NMR and 119Sn Mossbauer) studies were performed to characterize the interaction of the dimethyltin(IV) cation with glycine, glycyl-glycine (Gly-Gly), imidazole-4-acetic acid, histamine, histidine, glycyl-histamine, glycyl-histidine (Gly-His), and β-alanyl-histidine (carnosine). For histamine and glycyl-histamine (having only nitrogen donor atoms) no complex formation was detected. The hydrolyzed species of the dimethyltin(IV) cation are always dominant over the complexes formed with the other ligands, except with Gly-Gly and Gly-His. For these two ligands, {COO-,N-,NH2} coordinated complexes are dominant in the neutral pH range wi…

chemistry.chemical_classificationanimal structuresAqueous solutionintegumentary systemInorganic chemistryPeptideMedicinal chemistryInorganic ChemistryMetalchemistry.chemical_compoundTrigonal bipyramidal molecular geometryDeprotonationchemistryvisual_artembryonic structuresvisual_art.visual_art_mediumChelationCarboxylatePhysical and Theoretical ChemistryHistidineInorganic Chemistry
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ChemInform Abstract: Convenient High Yielding Gram Scale Solution Synthesis of Methionine-Enkephalin.

2010

A simple, large-scale synthesis of a cytokine, methionine-enkephalin, Tyr-Gly-Gly-Phe-Met, has been elaborated. Classical solution peptide chemistry methods without protection of amino acid side-chain functions and 1+(2+2) segment condensation were used. A nine-step synthesis from commercial amino acid derivatives was developed with yields ranging from 86% to 99%, averaging 92%. The purity of all intermediates was found to be 99.0-100% by HPLC. The process has been used to prepare greater than 150 g quantities of the pentapeptide as a monohydrate of 100% purity. Hydantoin formation was observed during saponification of Boc-Tyr-Gly-Gly-Phe-Met-OMe and minimised.

chemistry.chemical_classificationanimal structuresChromatographyintegumentary systemChemistryCondensationHydantoinGeneral MedicineSolution synthesisPentapeptide repeatHigh-performance liquid chromatographyAmino acidchemistry.chemical_compoundSaponificationGramChemInform
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ChemInform Abstract: Oligosaccharide Synthesis via Electrophile-Induced Activation of Glycosyl-N-allylcarbamates.

2010

Abstract Glycosyl-N-allyl carbamates, obtained by reaction of anomerically unprotected saccharides with allyl isocyanate, can be activated by an electrophile-induced cyclisation and reacted with glycosyl acceptors to form the corresponding oligosaccharides By this method the mucin core 2 trisaccharide2 has successfully been synthesized. Due to the mild glycosylation conditions even 1-O-acetyl protected glycosyl acceptors can be used. This was demonstrated in the synthesis of a 1,6-linked glucosyl trisaccharide whereby a reptitious glycosylation strategy could be applied. 1. Dedicated to the memory of Professor Akira Hasegawa.

chemistry.chemical_classificationanimal structuresGlycosylationStereochemistryMucinfood and beveragesmacromolecular substancesGeneral Medicinecarbohydrates (lipids)chemistry.chemical_compoundchemistryElectrophilelipids (amino acids peptides and proteins)GlycosylTrisaccharideAllyl isocyanateOligosaccharide synthesisChemInform
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Biochemical identification and tissue-specific expression patterns of keratins in the zebrafish Danio rerio

1998

We have identified a number of type I and type II keratins in the zebrafish Danio rerio by two-dimensional polyacrylamide gel electrophoresis, complementary keratin blot-binding assay and immunoblotting. These keratins range from 56 kDa to 46 kDa in molecular mass and from pH 6.6 to pH 5.2 in isoelectric point. Type II zebrafish keratins exhibit significantly higher molecular masses (56-52 kDa) compared with the type I keratins (50-48 kDa), but the isoelectric points show no significant difference between the two keratin subclasses (type II: pH 6.0-5.5; type I: pH 6.1-5.2). According to their occurrence in various zebrafish tissues, the identified keratins can be classified into "E" (epider…

chemistry.chemical_classificationanimal structuresHistologyintegumentary systembiologyMolecular massCellular differentiationDanioCell Biologybiology.organism_classificationMolecular biologyPathology and Forensic MedicineIsoelectric pointMicroscopy FluorescenceBiochemistrychemistryGenetic modelKeratinAnimalsKeratinsTissue DistributionPolyacrylamide gel electrophoresisZebrafishCytoskeletonZebrafishCell and Tissue Research
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Changes in cell wall pectin and pectinase activity in apple and tomato fruits duringPenicillium expansum infection

2006

Cell wall pectin degradation in apple and tomato fruit during infection by Penicillium expansum was investigated. In infected apple fruit, a significant decrease in the average molecular mass was observed in pectins extracted with CDTA and also in pectins extracted with Na2CO3. In tomato fruits, depolymerisation was also observed in both pectic fractions during infection, the major change being in the pectins extracted with Na2CO3. This pectin depolymerisation associated with P. expansum infection can be attributed to the action of pectinases; in apple fruit, a significant increase in polygalacturonase and pectin methylesterase was observed in infected fruits, although in tomato fruit the o…

chemistry.chemical_classificationanimal structuresNutrition and Dieteticsfood.ingredientbiologyPectinfungifood and beveragesFungi imperfectibiology.organism_classificationPolysaccharidecomplex mixturesCell wallfoodchemistryBotanyFood sciencePenicillium expansumPectinaseAgronomy and Crop ScienceSolanaceaeLegumeFood ScienceBiotechnologyJournal of the Science of Food and Agriculture
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