Search results for "Nuclear magnetic resonance spectroscopy"

showing 10 items of 843 documents

New 2-Methoxy Acetylenic Acids and Pyrazole Alkaloids from the Marine Sponge Cinachyrella sp.

2017

Three new 2-methoxy acetylenic acids (1–3) and a known derivative (4), in addition to three new natural pyrazole alkaloids (5–7) were isolated from an Indonesian marine sponge of the genus Cinachyrella. Compounds 5 and 6 have previously been reported as synthetic compounds. The structures of the new compounds were established on the basis of one- and two-dimensional NMR spectroscopy as well as by mass spectrometric data. The absolute configuration of the new acetylenic acid derivatives (1–3) was established by ECD spectroscopy. All isolated compounds were evaluated for their cytotoxicity against L5178Y mouse lymphoma cells. Compounds 1–4 exhibited strong activity with an IC50 value of 0.3 µ…

food.ingredientLymphomaStereochemistrynatural productsCinachyrella sp.Pharmaceutical ScienceAntineoplastic AgentsPyrazole010402 general chemistry01 natural sciencesArticlepyrazole alkaloidMicechemistry.chemical_compoundAlkaloidsfoodTermészettudományokCell Line TumorDrug DiscoveryAnimalsOrganic chemistryKémiai tudományokCytotoxicitynatural products; marine sponge; Cinachyrella sp.; 2-methoxy acetylenic acid; pyrazole alkaloidPharmacology Toxicology and Pharmaceutics (miscellaneous)lcsh:QH301-705.5biology010405 organic chemistryChemistryAcetylenic acidAbsolute configurationNuclear magnetic resonance spectroscopybiology.organism_classificationMass spectrometricBiosynthetic PathwaysPorifera0104 chemical sciencesSpongelcsh:Biology (General)IndonesiaAlkynesddc:540Fatty Acids UnsaturatedPyrazolesDrug Screening Assays AntitumorCinachyrella2-methoxy acetylenic acidmarine spongeMarine Drugs
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Multinuclear and Solid State NMR of Gels

2020

Over the past six decades, nuclear magnetic resonance spectroscopy has been an integral part of synthetic organic and organometallic chemistry, as well as biochemistry. Beyond solution state experiments, increasing developments have opened new avenues to study materials in their solid state. Between two extremes (i.e., solution and solid), there exist several other forms of materials, especially soft materials such as gels and liquid crystals. Traditionally gels have been studied using solution state NMR spectroscopic methods. However, the viscosity of complex viscoelastic fluids such as gels affects the molecular tumbling, which in turn affects the chemical shift anisotropy and dipolar and…

geelitchemistry.chemical_classificationMaterials sciencekiinteän olomuodon kemiaNuclear magnetic resonance spectroscopyPolymerViscoelasticitychemistry.chemical_compoundSolid-state nuclear magnetic resonancechemistryChemical physicsLiquid crystalMagic angle spinningNMR-spektroskopiaAnisotropyOrganometallic chemistry
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Spatial patterns of, and environmental controls on, soil properties at a riparianepaddock interface

2012

Abstract Riparian zones are prominent features of agricultural landscapes because they are the last point to intercept nutrients and sediments before they enter water bodies. We investigated the soil properties, nutrient dynamics and vegetation composition at the riparian–agriculture interface. Soil physicochemical and vegetation properties were spatially heterogeneous along the transition from the grazed paddock into the un-grazed and revegetated riparian zone. Soil C stocks varied considerably across the site, with values ranging from 2% in the paddock to 5% in the riparian zone. Using Bayesian model selection, a predictive model for total soil carbon was developed. By including soil mois…

geographygeography.geographical_feature_categorySoil nutrientSettore AGR/13 - Chimica AgrariaSoil ScienceSoil scienceVegetationSoil carbonSoil respirationSoil typeMicrobiologySoil carbonSoil respirationRiparian restorationNutrientSoil waterEnvironmental scienceEcosystemNuclear magnetic resonance spectroscopy (NMR)Bayesian modellingRiparian zoneNitrogen cycling
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Diorganotin(IV) complexes ofD-galacturonic acid: solid-state and solution-phase structural study

2003

Three diorganotin(IV) complexes of D-galacturonic acid (H2GalA; R = Me, n-Bu, Ph), two of which are new derivatives (R = Me, Ph), have been synthesized and their solid-state and solution-phase investigated by IR, Mossbauer, 1H, 13C and 119Sn NMR spectroscopy. The FTIR data suggest that H2GalA, in the dialkyltin derivatives, behaves as a dianionic ligand, coordinating the tin(IV) atom through an ester-type carboxylate and deprotonated alcoholic hydroxo groups, whereas a bridging carboxylate occurs in the diphenyltin(IV) complex. Octahedral and trigonal bipyramidal local geometries on tin(IV) atoms are proposed for dialkyltin(IV)GalA and diphenyltin(IV)GalA complexes respectively on the basis…

geometryalpha pyranosidesynthesisStereochemistryMossbauer spectroscopychemistry.chemical_elementproton nuclear magnetic resonanceMedicinal chemistrystructure analysiInorganic Chemistrychemistry.chemical_compoundDeprotonationcomplex formationMoleculegalacturonic acidorganotin compoundCarboxylateDiorganotininfrared spectroscopybeta furanosidic acidbeta pyranosidedecompositiondiphenyltin galacturonic acid complexLigandarticlecarboxyl groupsolid stateGeneral ChemistryNuclear magnetic resonance spectroscopycarbon nuclear magnetic resonanceNMRdiphenyltin complexunclassified drugTrigonal bipyramidal molecular geometrychemistryOctahedronChemistry (miscellaneous)Settore CHIM/03 - Chimica Generale E InorganicaMössbauerTinApplied Organometallic Chemistry
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Iodine(I) and Silver(I) Complexes of Benzoimidazole and Pyridylcarbazole Derivatives

2021

The synthesis of iodine(I) complexes with either benzoimidazole or carbazole-derived sp 2 N -containing Lewis bases is described, as well as their corresponding silver(I) complexes. The addition of elemental iodine to the linear two-coordinate Ag(I) complexes produces iodine(I) complexes with a three-center four-electron (3c-4e) [N — I — N] + bond. The 1 H and 1 H- 15 N HMBC NMR studies unambiguously confirm the formation of the complexes in all cases via the [N — Ag — N] + → [N — I — N] + cation exchange, with the 15 N NMR chemical shift change between 94 to 111 ppm when compared to the free ligand. The single crystal X-ray crystallographic studies on four I + complexes revealed highly sym…

halogeenitLigandChemical shiftOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyhalogen(I)kompleksiyhdisteetIodineCatalysissupramolecular chemistryNMRCrystallographykemialliset sidoksetchemistryX-ray crystallographysupramolekulaarinen kemiahalogen bondLewis acids and basesNMR-spektroskopiaSingle crystalröntgenkristallografiaX-ray crystallography
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Preparation of 2,3-seco-5α-cholestane-2,3-diol and 4α-methyl-2,3-seco-5α-cholestane-2,3-diol and its reactions with o-nitrophenyl selenocyanate

1984

The reaction of 2,3-seco-5 alpha-cholestane-2,3-diol and 4 alpha-methyl-2,3-seco-5 alpha-cholestane-2,3-diol with o-nitrophenyl selenocyanate was studied. The diols were synthesized from cholesterol.

inorganic chemicalsMagnetic Resonance SpectroscopyChemical PhenomenaOptical RotationSpectrophotometry InfraredClinical BiochemistryDiolBiochemistrychemistry.chemical_compoundEndocrinologySpectrophotometryNitrilespolycyclic compoundsmedicineSecosteroidsOrganic chemistryMolecular BiologyPharmacologyintegumentary systemmedicine.diagnostic_testorganic chemicalsOrganic ChemistryNuclear magnetic resonance spectroscopyChemistrychemistryIndicators and ReagentsCholestaneCholestanolshormones hormone substitutes and hormone antagonistsSteroids
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From Mono- to Poly-Substituted Frameworks: A Way of Tuning the Acidic Character of C-c-H in o-Carborane Derivatives

2009

[EN] The incorporation of iodine atoms onto the boron vertices of the o-carborane framework causes, according to spectroscopic data, a uniform increase in the acidic character of the C-c-H (C-c= cluster carbon) vertices, whereas the incorporation of methyl groups onto the boron vertices of the o-carborane framework reduces their acidity. Methyl groups when attached to boron are electron-withdrawing in boron clusters, whereas iodine atoms bonded to boron act as electron donors. This has been proven on B-methyl and B-iodinated o-carboranes with NMR spectroscopy measurements and DFT calculations of natural bond orbital (NBO) charges. which show a Cumulative buildup of positive cluster only tot…

inorganic chemicalsNatural bond orbital chargesInorganic chemistrychemistry.chemical_elementElectron010402 general chemistryIodine01 natural sciencesCatalysisQUIMICA ANALITICACluster (physics)BoronCarboranesBoron010405 organic chemistryOrganic ChemistryGeneral ChemistryNuclear magnetic resonance spectroscopy3. Good health0104 chemical sciencesCrystallographyDensity functional calculationschemistryCarboraneCarbonNatural bond orbitalIodine
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Nano-sized I12L6 Molecular Capsules Based on the [N⋅⋅⋅I+⋅⋅⋅N] Halogen Bond

2017

Summary Self-assembly of pre-organized subunits with a concave overall shape is an effective strategy for the synthesis of supramolecular capsules. We report the synthesis of a cavitand-based hexameric capsule held together solely by 12 robust [N⋅⋅⋅I + ⋅⋅⋅N] halogen bonds and its characterization in solution and in the gas phase via 1 H NMR spectroscopy, diffusion-ordered nuclear magnetic resonance spectroscopy (DOSY), and electrospray ionization mass spectrometry. The [N⋅⋅⋅I + ⋅⋅⋅N] halogen-bonded hexameric capsule was efficiently synthesized from the isolobal metallosupramolecular Ag + capsule by application of the [N⋅⋅⋅Ag + ⋅⋅⋅N] → [N⋅⋅⋅I + ⋅⋅⋅N] cation-exchange reaction.

inorganic chemicalsStereochemistrycapsuleGeneral Chemical EngineeringElectrospray ionizationSupramolecular chemistrysupramolecular capsule010402 general chemistry01 natural sciencesBiochemistrysupramolecular chemistryresorcinarene cavitandMaterials ChemistryEnvironmental ChemistryHalonium ionhalonium-ion-based nanotechnologyta116silver-to-iodine cation exchangeHalogen bond010405 organic chemistryChemistryBiochemistry (medical)CavitandIsolobal principleself-assemblyGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesCrystallographyhalonium ionProton NMRhalogen bondChem
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The effect of the cation p-surface area on the 3D organization and catalytic ability of imidazolium-based ionic liquids

2011

The dichotomic nature of ionic liquids (ILs, simple solvents or supramolecular fluids) induced us to carry out a structural investigation of some mono-and dicationic ionic liquids using 1D and 2D NMR, resonance light scattering, and UV/Vis spectroscopy. Ionic liquids with different cation π-surface areas were used, namely [bmim][NTf2], [Bzmim][NTf 2], [Bzbim][NTf2], [p-Xyl-(bim)2][NTf 2]2, and [m-Xyl-(bim)2][NTf2] 2 [bmim = 1-butyl-3-methylimidazolium, Bzmim = 1-benzyl-3- methylimidazolium, Bzbim = 1-benzyl-3-butylimidazolium, NTf2 = bis(trifluoromethansulfonyl)imide]. In order to verify to what extent the structural investigation, coupled with the determination of solvent parameters, could…

ionic liquids structural investigation MRH reaction.Organic ChemistrySupramolecular chemistrySettore CHIM/06 - Chimica OrganicaResonance (chemistry)CatalysisSolventchemistry.chemical_compoundchemistryIonic liquidPhysical chemistryOrganic chemistryPhysical and Theoretical ChemistrySpectroscopyImideTwo-dimensional nuclear magnetic resonance spectroscopy
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Direct detection of 17O NMR in [Gd(DOTA)]- by NMR Spectroscopy

2015

The 17O NMR spectrum of the non-coordinated carboxyl oxygen in the GdIII-DOTA (DOTA = tetraazacyclododecanetetraacetic acid) complex has been observed experimentally. Its line width is essentially unaffected by paramagnetic relaxation due to gadolinium, and is only affected by the quadrupole pathway. The results are supported by the relevant parameters (hyperfine and quadrupole coupling constants) calculated by relativistic DFT methods. This finding opens up new avenues for investigating the structure and reactivity of paramagnetic GdIII complexes used as contrast agents in magnetic resonance imaging.

lanthanide complexesLanthanideGadoliniumchemistry.chemical_elementImaging agentsCatalysisNMR spectroscopy; Density functional calculations; lanthanide complexes; gadolinium; O-17 nmrParamagnetismchemistry.chemical_compoundNMR spectroscopyNuclear magnetic resonanceLanthanidesDOTAHyperfine structureChemistryOrganic ChemistryRelaxation (NMR)General ChemistryNuclear magnetic resonance spectroscopyDensity functional calculationsSettore CHIM/03 - Chimica Generale E InorganicaQuadrupole17O NMR Lanthanides DFTCondensed Matter::Strongly Correlated ElectronsgadoliniumO-17 nmr
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