Search results for "nmr"

showing 10 items of 1575 documents

NMR Spectroscopic and quantum chemical characterization of the (E)- and (Z)- isomers of the penta-1,3-dienyl-2-cation

2003

Dilute solutions of the (E )− and (Z )− isomers of pent-1,3-dienyl-2-cations (1) were obtained from reaction of 4-chloro-1,2-pentadiene (2) with SbF5 in SO2ClF/SO2F2 at −135 °C using high-vacuum co-condensation techniques. The experimental NMR spectra of the mixture of the two isomers were compared with quantum chemical 13C NMR chemical shift calculations at HF-SCF, MP2, CCSD and CCSD(T) levels using MP2/tzp geometries. Quantum chemical shift calculations were performed with a tzp basis (9s5p1d/5s3p1d) for carbon and a dz basis (4s/2s) for hydrogen using gauge-including atomic orbitals (GIAOs). The HF-SCF calculations deviate significantly for the positively charged carbon atoms of the ally…

NMR spectra databaseElectronic correlationCarbon-13 NMR satelliteComputational chemistryChemistryChemical shiftOrganic ChemistryAb initioPhysical chemistryNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryCarbon-13 NMRResonance (chemistry)Journal of Physical Organic Chemistry
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Preliminary study on analysis and removal of wax from a Carrara marble statue

2015

This preliminary study has mainly focused on the wax identification by nuclear magnetic resonance (NMR) and removal. Wax is used for many purposes in the field of art as protective coatings on wooden, stone or metal objects. From the comparison of the spectra H NMR and in particular with the correspondence of the resonance peaks of the samples taken from the statue and beeswax and paraffin, we can conclude that the wax applied on the statue surface is beeswax. From our data, it can be concluded that, to remove the beeswax, from any stone support, the more effective solvent is the mixture of cyclohexane/ethyl acetate. The removal percentages ranged from 19 to 99%. Lower percentages of remova…

WaxMagnetic Resonance SpectroscopyMaterials scienceEthyl acetateMineralogycleaningPlant ScienceAcetates01 natural sciencesBiochemistryBeeswaxSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliCalcium CarbonateAnalytical Chemistrychemistry.chemical_compoundPlant scienceCyclohexanesPorosityWax010405 organic chemistryOrganic Chemistryfood and beveragescultural heritageNMR0104 chemical sciencesSolvent010404 medicinal & biomolecular chemistryCalcium carbonatechemistryParaffinWaxesvisual_artSolventsvisual_art.visual_art_mediumStatuePorosityArtNuclear chemistry
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Two-dimensional single- and multiple-quantum correlation spectroscopy in zero-field nuclear magnetic resonance.

2020

We present single- and multiple-quantum correlation $J$-spectroscopy detected in zero ($<\!\!1$~$\mu$G) magnetic field using a \Rb vapor-cell magnetometer. At zero field the spectrum of ethanol appears as a mixture of \carbon isotopomers, and correlation spectroscopy is useful in separating the two composite spectra. We also identify and observe the zero-field equivalent of a double-quantum transition in ${}^{13}$C$_2$-acetic acid, and show that such transitions are of use in spectral assignment. Two-dimensional spectroscopy further improves the high resolution attained in zero-field NMR since selection rules on the coherence-transfer pathways allow for the separation of otherwise overlappi…

Nuclear and High Energy PhysicsZero field NMRMagnetometerNuclear Magnetic Resonancephysics.chem-phBiophysicsFOS: Physical sciences010402 general chemistry01 natural sciencesBiochemistryMolecular physicsSpectral line030218 nuclear medicine & medical imagingIsotopomerslaw.invention03 medical and health sciences0302 clinical medicineEngineeringquant-phlawPhysics - Chemical PhysicsJ-Spectroscopy2D NMRSpectroscopyPhysicsChemical Physics (physics.chem-ph)Quantum PhysicsCorrelation spectroscopyZero (complex analysis)Zero-field NMRCondensed Matter PhysicsMultiple-quantum NMR3. Good health0104 chemical sciencesMagnetic fieldZULF NMRPhysical SciencesQuantum Physics (quant-ph)Two-dimensional nuclear magnetic resonance spectroscopy
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Recognition of N-Alkyl- and N-Aryl-Acetamides by N-Alkyl Ammonium Resorcinarene Chlorides

2014

N-alkyl ammonium resorcinarene chlorides are stabilized by an intricate array of intra- and intermolecular hydrogen bonds that leads to cavitand-like structures. Depending on the upper-rim substituents, self-inclusion was observed in solution and in the solid state. The self-inclusion can be disrupted at higher temperatures, whereas in the presence of small guests the self-included dimers spontaneously reorganize to 1:1 host-guest complexes. These host compounds show an interesting ability to bind a series of N-alkyl acetamide guests through intermolecular hydrogen bonds involving the carbonyl oxygen (C=O) atoms and the amide (NH) groups of the guests, the chloride anions (Cl(-)) and ammoni…

chemistry.chemical_classificationHydrogen bondStereochemistryArylOrganic ChemistryIntermolecular forceGeneral Chemistrymacromolecular substancesResorcinareneMedicinal chemistryCatalysischemistry.chemical_compoundchemistryAmideAmmoniumresorcinarenes; NMR titration; amides; host-guest complexes; X-ray crystallographyta116AlkylAcetamide
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Structure of a polysaccharide from the lipopolysaccharide of Vibrio vulnificus CECT4602 containing 2-acetamido-2,3,6-trideoxy-3-[(S)- and (R)-3-hydro…

2008

A polysaccharide was isolated by GPC after mild acid treatment of the lipopolysaccharide of Vibrio vulnificus CECT4602 and found to contain L-Rha, D-GlcpNAc and 2-acetamido-2,3,6-trideoxy-3-(3-hydroxybutanoylamino)-L-mannose (L-RhaNAc3NHb). GLC analysis of the trifluoroacetylated (S)-2-octyl esters derived by full acid hydrolysis of the polysaccharide showed that approximately 80% of the 3-hydroxybutanoic acid has the S configuration and approximately 20% the R configuration. The following structure of the polysaccharide was established by (1)H and (13)C NMR spectroscopies, including 2D ROESY and (1)H/(13)C HMBC experiments: [carbohydrate sequence see in text].

Lipopolysaccharideschemistry.chemical_classificationMagnetic Resonance SpectroscopybiologyLipopolysaccharideStereochemistryMolecular Sequence DataPolysaccharides BacterialOrganic ChemistryMannoseGeneral MedicineVibrio vulnificusCarbon-13 NMRbiology.organism_classificationPolysaccharideBiochemistryAnalytical Chemistrychemistry.chemical_compoundCarbohydrate SequencechemistryAcid hydrolysisAcid treatmentMannoseVibrio vulnificusCarbohydrate Research
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A CNDO/2 study on the additivity and the nature of the non-additivity of the substituent effects on13C NMR shifts in chlorobenzenes and chlorophenols

1980

The general correlation between the electron densities and the 13C NMR chemical shifts is found to be quite poor in the cases discussed. The non-additivities of the substituent effects on the chemical shifts and the CNDO/2 electron densities correlate only weakly. However, when the electron densities are made specific to different types of atomic orbitals, the s electrons have a pronounced effect in all the models tested. This is explained by an indirect effect on the 〈1/r3〉 term of the p electrons. Good correlations are found between the sums of the chemical shifts and the corresponding sums of the substituent charge excesses. The different behaviour of OH and Cl substituents in the additi…

CNDO/2chemistry.chemical_compoundAtomic orbitalComputational chemistryChemistryChlorobenzeneChemical shiftAdditive functionSubstituentGeneral Materials ScienceGeneral ChemistryElectronCarbon-13 NMROrganic Magnetic Resonance
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Surface Relaxivity of Cement Hydrates

2014

Numerous aspects of the physical chemistry of colloidal systems are conditioned by the solid–liquid interface, and this is also the case for hydrated cement systems. Estimating the surface area is thus essential for studying the kinetics of cement hydration and admixture adsorption. Proton nuclear magnetic resonance (NMR) relaxation techniques have already proven useful for this objective, but, for hydrating cements at early ages, it is necessary to know the surface relaxivities of all of the individual phases present to correctly interpret the relaxation data. This paper reports the results of a comparison of NMR relaxometry and Brunauer–Emmett–Teller gas adsorption measurements on various…

CementEttringiteRelaxometryMaterials scienceRelaxation (NMR)Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsColloidchemistry.chemical_compoundParamagnetismGeneral EnergyAdsorptionChemical engineeringchemistryProton NMRPhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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On the blue phase structure of hydrogen-bonded liquid crystals via 19F NMR

2018

Abstract 19 F NMR spectra are simulated for blue phase I of FPHG( St 1.5 ∗ Ap 1.5 ) based on a model of a double-twisted substructure inside cylinders that form a body-centred cubic lattice. A kinetic matrix is included to describe jump processes over quarter pitch lengths. Though the lines in the NMR spectra are broad and featureless, changes in the widths and positions with temperature are well described by the blue phase model structure. The spectra in the chiral nematic N∗ phase are also simulated. Dynamics in the BP I are found to be slower than in the N∗ phase.

Materials scienceHydrogenSpectral simulationChemieGeneral Physics and Astronomychemistry.chemical_elementBlue phase IDouble-twisted substructure02 engineering and technologyFluorine-19 NMR010402 general chemistryKinetic energy01 natural sciencesMolecular physicsSpectral lineDiffusion rateLiquid crystalLattice (order)Physical and Theoretical Chemistry021001 nanoscience & nanotechnologyFluorine NMR0104 chemical sciencesNMR spectra databasechemistrySubstructureSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyChiral nematic
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Diastereoselective Synthesis of Dialkylated Bis(phosphino)ferrocenes: Their Use in Promoting Silver-Mediated Nucleophilic Fluorination of Chloroquino…

2017

International audience; The diastereoselective synthesis of dialkylated ferrocenyl bis(phosphane)s bearing aryl, alkyl, and hetero- or polycyclic substituents on the phosphino groups is reported, together with their characterization in the solid state by X-ray structure analysis and in solution by multinuclear NMR spectroscopy. Introduction of various alkyl groups on the ferrocene backbone, namely, tert-butyl, isopropyl, and trimethylsilyl, has a significant influence on the stereoselectivity of the ensuing lithiation/phosphination reactions. Only the introduction of the tert-butyl groups ensures both a high yield and perfect diastereoselectivity, which leads to the exclusive formation of t…

Diastereoselectivitybond formationTrimethylsilylfunctionalized arylone-potelectrophilic fluorinationPhosphanesAlkylationc-h fluorination[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNucleophileFluorinationOrganic chemistryAlkylpolyphosphane ligandsferrocenyl derivativeschemistry.chemical_classificationp-31 nmr010405 organic chemistryArylHalex reactiondirect arylationreductive elimination[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryNuclear magnetic resonance spectroscopySandwich complexes0104 chemical scienceschemistryFerroceneIsopropyl
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Dihydrophenanthrenes from a Sicilian Accession of Himantoglossum robertianum (Loisel.) P. Delforge Showed Antioxidant, Antimicrobial, and Antiprolife…

2021

The peculiar aspect that emerges from the study of Orchidaceae is the presence of various molecules, which are particularly interesting for pharmaceutical chemistry due to their wide range of biological resources. The aim of our study was to investigate the properties of two dihydrophenanthrenes, isolated, for the first time, from Himantoglossum robertianum (Loisel.) P. Delforge (Orchidaceae) bulbs and roots. Chemical and spectroscopic study of the bulbs and roots of Himantoglossumrobertianum (Loisel.) P. Delforge resulted in the isolation of two known dihydrophenanthrenes—loroglossol and hircinol—never isolated from this plant species. The structures were evaluated based on 1H-NMR, 13C-NMR…

dihydrophenanthrenes; <i>Himantoglossum robertianum</i>; NMR; antioxidant enzymes; antimicrobial activity; anti-proliferative activity; proapoptotic activityantimicrobial activityantioxidant enzymeEcologyproapoptotic activityBotany<i>Himantoglossum robertianum</i>Plant SciencedihydrophenanthreneNMRHimantoglossum robertianumQK1-989anti-proliferative activityAntioxidant enzymesEcology Evolution Behavior and SystematicsDihydrophenanthrenesPlants
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