Search results for "circular"

showing 10 items of 856 documents

Supramolecular chirality in organogels: a detailed spectroscopic, morphological, and rheological investigation of gels (and xerogels) derived from al…

2010

This Article addresses the formation of chiral supramolecular structures in the organogels derived from chiral organogelator 1R (or 2R), and its mixtures with its enantiomer (1S) and achiral analogue 3 by extensive circular dichroism (CD) spectroscopic measurements. Morphological analysis by atomic force microscopy (AFM) and scanning electron microscopy (SEM) were complemented by the measurements of their bulk properties by thermal stability and rheological studies. Specific molecular recognition events (1/3 vs 2/3) and solvent effects (isooctane vs dodecane) were found to be critical in the formation of chiral aggregates. Theoretical studies were also carried out to understand the interact…

chemistry.chemical_classificationCircular dichroismSupramolecular chiralitySupramolecular chemistrySurfaces and InterfacesCondensed Matter PhysicsCrystallographyMolecular recognitionchemistryElectrochemistryOrganic chemistryGeneral Materials ScienceEnantiomerSolvent effectsChirality (chemistry)SpectroscopyAlkylLangmuir : the ACS journal of surfaces and colloids
researchProduct

Enantioselektive Trifluoracetylierung mit Hilfe chiraler Polyamide

1980

(S)-Poly(2-aminobutyric acid) (1) [(S)-poly(imino-1-methyl-3-oxotrimethylene)] was transformed into its N-trifluoroacetyl derivative 4. The IR spectra and the circular dichroism of both substances were compared. In addition, (S)-poly[N-(1-phenylethyl)acrylamide] (2) ((S)-poly-[1-(1-phenylethylaminocarbonyl)ethylene]) was trifluoroacetylated leading to polymer 5. 4 was found to react as trifluoroacetylating agent with L-1-phenylethylamine (L-3) twice as fast as it reacts with D-3. Accordingly, the reaction of 4 with D,L-3 leads preferentially to the L-form of N-(1-phenylethyl)trifluoroacetamide with optical yields up to 6%. The reaction of 5 with D,L-3 affords the D-form of N-(1-phenylethyl)…

chemistry.chemical_classificationCircular dichroismchemistry.chemical_compoundEthylenechemistryAcrylamidePolymer chemistryInfrared spectroscopyPolymerDerivative (chemistry)Die Makromolekulare Chemie
researchProduct

Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion

2015

The different natures of the weakly coordinating anions – triflate or perchlorate – in the Cu2+-mediated self-assembly of cytidine monophosphate nucleotide play a fundamental role in the homochiral resolution process, yielding one-dimensional copper(II) coordination polymers of opposite helicity that can be easily inverted, in a reversible way, by changing the nature of the anion as revealed by circular dichroism experiments both in solution and in the solid state.

chemistry.chemical_classificationCytidine monophosphateCircular dichroismStereochemistryAbsolute configurationGeneral ChemistryPolymerHelicityPerchloratechemistry.chemical_compoundCrystallographychemistrySelf-assemblyTrifluoromethanesulfonateChemical Science
researchProduct

Effect of?-cyclodextrin complexation on the photohaemolitic activity induced by Ketoprofen and Naproxen sensitization

1993

Red blood cell lysis photosensitized by two non-steroidal anti-inflammatory drugs Naproxen (NAP) and Ketoprofen (KPF) was investigated in the presence of β-cyclodextrin (β-Cyd). The photohaemolysis was inhibited by the addition of β-Cyd both for NAP and, to a lesser extent, for KPF. The protective action was found only in a restricted range of concentration of β-Cyd. Higher amounts of β-Cyd interfered with the resistance of the cell to the osmotic shock induced by the photosensitization process. The complexing action of β-Cyd was ascertained through UV-vis absorption spectroscopy, induced circular dichroism and emission spectroscopy. The isolated complexes Naproxen-β-Cyd (NAP-β-Cyd) and Ket…

chemistry.chemical_classificationKetoprofenNaproxenCircular dichroismLysisCyclodextrinOsmotic shockStereochemistryGeneral ChemistryCondensed Matter PhysicsNapchemistryBiophysicsmedicinePhototoxicityFood Sciencemedicine.drugJournal of Inclusion Phenomena and Molecular Recognition in Chemistry
researchProduct

Conformational studies of hexapeptides containing two dehydroamino acid residues in positions 2 and 5 in peptide chain

2008

Conformational preferences of a group of hexapeptides containing two dehydroamino acid residues in Positions 2 and 5 in peptide chain were investigated by means of spectroscopic methods (NMR and CD) and theoretical calculations. In the case of dimethylsulfoxide (DMSO) solution, only peptide with free N-termini adopted rigid 310-helical conformation, for the rest of examined peptides extended and “zig-zag” conformers were predominant. CD measurements showed that only in chloroform solution the conformational freedom of investigated peptides was restricted. © 2008 Wiley Periodicals, Inc. Biopolymers 89: 691–699, 2008. This article was originally published online as an accepted preprint. The “…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyProtein ConformationStereochemistryCircular DichroismMolecular Sequence DataOrganic ChemistryTemperatureBiophysicsPeptideGeneral MedicineAmidesBiochemistryProtein Structure SecondaryBiomaterialschemistry.chemical_compoundChain (algebraic topology)chemistryDehydroalanineAmino Acid SequenceAmino AcidsProtonsPeptidesConformational isomerismBiopolymers
researchProduct

Forever Young: Structural Stability of Telomeric Guanine-Quadruplexes in Presence of Oxidative DNA Lesions

2020

AbstractHuman telomeric DNA (h-Telo), in G-quadruplex (G4) conformation, is characterized by a remarkable structural stability that confers it the capacity to resist to oxidative stress producing one or even clustered 8-oxoguanine lesions. We present a combined experimental/computational investigation, by using circular dichroism in aqueous solutions, cellular immunofluorescence assays and molecular dynamics (MD) simulations, that identifies the crucial role of the stability of G4s to oxidative lesions, related also to their biological role as inhibitors of telomerase, an enzyme overexpressed in most cancers associated to oxidative stress.

chemistry.chemical_classificationTelomeraseCircular dichroismmedicine.diagnostic_testOxidative phosphorylationImmunofluorescencemedicine.disease_causeMolecular dynamicschemistry.chemical_compoundEnzymechemistrymedicineBiophysicsDNAOxidative stress
researchProduct

Transition metal–saccharide chemistry: synthesis, characterization and solution stability studies of cis-dioxomolybdenum saccharide complexes

1998

Six cis-dioxomolybdenum(VI) complexes of simple monosaccharides (D-glucose, D-fructose, D-galactose, D-mannose, D-ribose and D-xylose) have been synthesized and characterized by a variety of analytical and spectral methods. Both the solution and solid-state studies have supported the presence of dimeric structures, formed through the cis-MoO2 moieties and the bridging saccharide units. Solution stability of these complexes as a function of time has also been addressed.

chemistry.chemical_classificationThermal AnalysisCircular dichroismSpectrometersStereochemistryCircular DichroismOrganic ChemistryMannoseFructoseGeneral MedicineXyloseBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryTransition metalGalactoseRiboseOrganic chemistryMonosaccharideCyclic VoltammetryIndraStra Global
researchProduct

Predicted secondary structure of hydroperoxide lyase from green bell pepper cloned in the yeast Yarrowia lipolytica

2010

International audience; Fatty acid hydroperoxide lyase (HPL) is a member of the cytochrome P450 family acting on fatty acid hydroperoxides in many organisms. The active green bell pepper HPL, cloned and expressed in the yeast Yarrowia lipolytica, was purified by immobilized metal-ion affinity chromatography (IMAC) in the presence of 2% of Triton X-100R. The secondary structure prediction by bioinformatics servers of HPL was realized by ANTHEPROT software, using the GOR, DPM and Predator methods. The theoretical results which are average values obtained from three different calculation methods showed 33% α-helix, 18% β-sheet, 7% turn and 42% coil. On the other hand, the secondary structure a…

chemistry.chemical_classificationYarrowia lipolyticaCircular dichroismChromatographybiologyProcess Chemistry and Technology[SDV]Life Sciences [q-bio]Circular dichroism spectroscopyBioengineeringYarrowiabiology.organism_classificationBiochemistryCatalysisYeastRandom coilHydroperoxide lyaseEnzymeAffinity chromatographyBiochemistrychemistrySecondary structureSpecific activityPredictionProtein secondary structure
researchProduct

Modification of Chiral Properties Due to Interaction of Polymers and Small Molecules or Ions

1979

The first part of this report deals with changes in the optical rotatory dispersion and circular dichroism resulting from the chemical modification of optically active polymers. Amylose derivatives have very different chiroptical properties compared with cellulose derivatives. Variations in glucosidic bonds and differing secondary structures are described and suggested as causes for this. The N-chlorination of synthetic optically active polyamides is also described, which in all probability proceeds without changing the configuration at the asymmetric C atoms. Reactions of inactive polymers with low molecular weight chiral reagents usually give optical rotation values proportional to the de…

chemistry.chemical_classificationchemistry.chemical_compoundCircular dichroismChemistryComputational chemistryTacticityEnantioselective synthesisChemical modificationsense organsPolymerOptical rotationOptical rotatory dispersionInclusion compound
researchProduct

Conformational studies of hexapeptides containing two dehydroamino acid residues in positions 3 and 5 in peptide chain

2008

Abstract Synthesis and structural studies of hexapeptides containing two dehydroamino acid residues in positions 3 and 5 in a peptide chain were performed. All the investigated peptides adopted bent conformations, stabilized by intramolecular hydrogen bonding, and could exist as two different conformers in solution. Only in the case of the peptide containing ΔAla residues, expected 3 10 -helical conformation was found.

chemistry.chemical_classificationconformationCircular dichroismStereochemistryHydrogen bondOrganic ChemistryBent molecular geometryCD spectroscopyPeptidedehydroalanineNMRAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryChain (algebraic topology)DehydroalanineIntramolecular forceisomers of dehydrophenylalanineConformational isomerismSpectroscopyJournal of Molecular Structure
researchProduct