Search results for "RESONANCE"

showing 10 items of 6625 documents

A Simple Complex on the Verge of Breakdown: Isolation of the Elusive Cyanoformate Ion

2014

Cyanide Hitches a Ride Cyanide is a by-product of the biosynthesis of ethylene in plants and it has been somewhat puzzling how the ion is safely removed before it can shut down enzymatic pathways by coordination to catalytic iron centers. A proposed mechanism has implicated the cyanoformate ion—essentially, a weak adduct of cyanide and carbon dioxide—as the initial product, although its lifetime was uncertain. Murphy et al. (p. 75 ; see the Perspective by Alabugin and Mohamed ) crystallized this previously elusive adduct and found that its solution-phase stability varies inversely with the dielectric properties of the medium. The results bolster a picture in which the adduct shuttles the cy…

crystal structureEthyleneMagnetic Resonance SpectroscopyFormateskemiallinen sitoutuminenCyanideMineralogykiderakenneMedicinal chemistryIonCatalysisAdductchemistry.chemical_compoundsyanoformaattiX-Ray DiffractionCatalytic DomainNitrilesta116MultidisciplinaryAqueous solutionCyanidesMolecular StructureChemistrychemical bondingCarbon DioxideEthylenesThermodynamicsAmino Acid OxidoreductasescyanofrmateCrystallizationShut downScience
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A Gadolinium(III) Complex Based on the Thymine Nucleobase with Properties Suitable for Magnetic Resonance Imaging

2021

The paramagnetic gadolinium(III) ion is used as contrast agent in magnetic resonance (MR) imaging to improve the lesion detection and characterization. It generates a signal by changing the relaxivity of protons from associated water molecules and creates a clearer physical distinction between the molecule and the surrounding tissues. New gadolinium-based contrast agents displaying larger relaxivity values and specifically targeted might provide higher resolution and better functional images. We have synthesized the gadolinium(III) complex of formula [Gd(thy)2(H2O)6](ClO4)3·2H2O (1) [thy = 5-methyl-1H-pyrimidine-2,4-dione or thymine], which is the first reported compound based on gadolinium…

crystal structureMaterials scienceMagnetometerQH301-705.5GadoliniumContrast Mediachemistry.chemical_elementmetal complexesCrystallography X-Ray010402 general chemistry01 natural sciencesArticleCatalysisIonNucleobaselaw.inventionInorganic Chemistrymagnetic resonanceMagneticsParamagnetismchemistry.chemical_compoundNuclear magnetic resonanceHeterocyclic CompoundslawthyminemedicineMoleculePhysical and Theoretical ChemistryBiology (General)Molecular BiologyQD1-999SpectroscopyMolecular Structuremedicine.diagnostic_test010405 organic chemistryOrganic ChemistryWaterMagnetic resonance imagingGeneral Medicinecontrast agentMagnetic Resonance Imaging0104 chemical sciencesComputer Science ApplicationsThymineChemistrychemistryrelaxivityProtonsgadolinium
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Novel 2,6-disubstituted phenylboronic compounds - Synthesis, crystal structures, solution behaviour and reactivity

2015

Abstract 2,6-Diformylphenylboronic acid has been synthesized and characterized both in the solid state as well as in solution. In crystal, an unusual structural pattern has been found with the formation of intermolecular hydrogen bonds by B(OH) 2 and CHO groups as well as water molecules. In solution tautomeric equilibrium with the formation of oxaborole ring by one of the formyl groups was proved on the basis of multinuclear NMR spectroscopy. The title compound reacts with secondary mono- and diamines to form various types of substituted benzoxaboroles, which have been characterized by XRD and spectroscopic methods.

crystal structureboronic acidsChemistryHydrogen bondOrganic ChemistryCrystal structureNuclear magnetic resonance spectroscopyRing (chemistry)BiochemistryTautomerreductive aminationtautomeric equilibriaInorganic ChemistryCrystalbenzoxaborolesPolymer chemistryMaterials ChemistryMoleculeReactivity (chemistry)Physical and Theoretical ChemistryJournal of Organometallic Chemistry
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Spontaneous Resolution of an Electron‐Deficient Tetrahedral Fe4L4cage

2015

A highly electron-deficient C3-symmetric tris(bipyridyl) ligand was prepared in four steps and used for the coordination of Fe(OTf)2, thereby resulting in the homochiral assembly of a new family of robust tetrahedral M4L4 cages. This homochiral T-symmetric cage containing a relatively large cavity of 330 A(3) is capable of encapsulating an anionic guest, as was determined by mass spectrometry, (19)F NMR spectroscopy, and finally shown from its crystal structure. Moreover, crystallization of the cage from CH3CN led to crystals containing both (ΔΔΔΔ and ΛΛΛΛ) enantiomers, while crystallization from CH3 OH resulted in crystals containing only the right-handed (ΔΔΔΔ) cage. The difference in the…

crystallization010405 organic chemistryChemistryLigandelectron-deficient tetrahedral Fe4L4Supramolecular chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyCrystal structureGeneral Medicine010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceslaw.inventionCrystalCrystallographylawX-ray crystallographyCrystallizationChirality (chemistry)ta116Angewandte Chemie
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A new member of the fusaricidin family – structure elucidation and synthesis of fusaricidin E

2017

Two hitherto unknown fusaricidins were obtained from fermentation broths of three Paenibacillus strains. After structure elucidation based on tandem mass spectrometry and NMR spectroscopy, fusaricidin E was synthesized to confirm the structure and the suggested stereochemistry. The synthesis was based on a new strategy which includes an efficient access to the 15-guanidino-3-hydroxypentadecanoyl (GHPD) side chain from erucamide.

cyclodepsipeptidesStereochemistry010402 general chemistryTandem mass spectrometry01 natural sciencesFull Research Paperlcsh:QD241-441Paenibacilluslcsh:Organic chemistrySide chaintotal synthesislcsh:Sciencebiology010405 organic chemistryChemistryFamily structureOrganic Chemistrystructure elucidationTotal synthesisNuclear magnetic resonance spectroscopyfusaricidinsbiology.organism_classificationlipopeptides0104 chemical sciencesChemistryFermentationlcsh:QBeilstein Journal of Organic Chemistry
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Resolution Characterizations of JetRIS in Mainz Using 164Dy

2022

Atoms 10(2), 57 (2022). doi:10.3390/atoms10020057

de Laval nozzlenobeliumNuclear and High Energy PhysicsScience & TechnologyRESONANCE IONIZATION SPECTROSCOPYPhysicsJetRIS; fluorescence spectroscopy; gas-jet; de Laval nozzle; nobeliumPhysics Atomic Molecular & Chemicalfluorescence spectroscopyCondensed Matter Physics530Atomic and Molecular Physics and OpticsJetRISPhysical SciencesELEMENTSgas-jetddc:530Physics::Atomic PhysicsNuclear ExperimentLASER SPECTROSCOPYAtoms
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Enhancing the luminescence efficiency of silicon-nanocrystals by interaction with H+ions

2018

The emission of silicon nanocrystals (Si-NCs), synthesized by pulsed laser ablation in water, was investigated on varying the pH of the solution. These samples emit μs decaying orange photoluminescence (PL) associated with radiative recombination of quantum-confined excitons. Time-resolved spectra reveal that both the PL intensity and the lifetime increase by a factor of ∼20 when the pH decreases from 10 to 1 thus indicating that the emission quantum efficiency increases by inhibiting nonradiative decay rates. Infrared (IR) absorption and electron paramagnetic resonance (EPR) experiments allow addressing the origin of defects on which the excitons nonradiatively recombine. The linear correl…

defectMaterials sciencePhotoluminescenceExcitonGeneral Physics and Astronomy02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesIonlaw.inventionlawluminescenceSpontaneous emissionQuantum confinementPhysical and Theoretical ChemistryElectron paramagnetic resonanceSilicon nanocrystalsilicon021001 nanoscience & nanotechnologyphotoluminescence efficiencysilicon nanoparticles luminescence0104 chemical sciencesAmorphous solidlaser ablationQuantum efficiencynanoparticles0210 nano-technologyLuminescence
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Utility of 3 Tesla diffusion-weighted magnetic resonance (DWMR) imaging for the characterisation of small solid renal tumours

2012

Purpose: To determine the utility of apparent diffusion coefficients (ADCs) for the characterisation of small solid renal lesions. Methods and Materials: 26 patients (GFR 30-60 mL/min) with 39 small (1-3 cm) solid renal masses [16 RCCs (10 clear cell types; 6 other types); 18 AMLs (10 fat-containing; 8 minimal-fat) and 5 oncocytomas] were examined on a 3 T system using DW-SS-EPI (b-values 0, 1000 s/mm2). The ADC of the lesions and the ADC of kidney were evaluated. Receiver operator characteristic analysis was performed to evaluate the diagnostic value of ADC for differentiating clear cell RCCs from other type RCCs, AMLs and oncocytomas. Results: The mean ADC of the lesions [1.22± 0.27 28 mm…

diffusion-weighted magnetic resonance imagingsmall solid renal tumours
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Dissociable Functional Brain Networks Associated With Apathy in Subcortical Ischemic Vascular Disease and Alzheimer’s Disease

2021

Few studies have investigated differences in functional connectivity (FC) between patients with subcortical ischemic vascular disease (SIVD) and Alzheimer’s disease (AD), especially in relation to apathy. Therefore, the aim of this study was to compare apathy-related FC changes among patients with SIVD, AD, and cognitively normal subjects. The SIVD group had the highest level of apathy as measured using the Apathy Evaluation Scale-clinician version (AES). Dementia staging, volume of white matter hyperintensities (WMH), and the Beck Depression Inventory were the most significant clinical predictors for apathy. Group-wise comparisons revealed that the SIVD patients had the worst level of “Ini…

disconnection syndromeAgingsubcortical ischemic vascular diseaseAlzheirmer’s diseaseCognitive Neuroscienceresting-state functional connectivityapathyNeurosciences. Biological psychiatry. Neuropsychiatryfunctional magnetic resonance imagingRC321-571Frontiers in Aging Neuroscience
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Preparation and physico-chemical study of inclusion complexes between idebenone and modified beta-cyclodextrins

1996

The inclusion properties of modifiedβ-cyclodextrins (trimethyl-β-cyclodextrin, dimethyl-β-cyclodextrin and hydroxypropyl-β-cyclodextrin) towards idebenone were compared with naturalβ-cyclodextrin. The inclusion complexes were prepared by different methods (coprecipitation, kneading, and freeze-drying) and characterized by differential scanning calorimetry, X-ray diffractometry, UV, CD and NMR spectroscopy. The results obtained by CD and NMR spectroscopy indicate a different orientation of idebenone in dimethyl-β-cyclodextrin with respect to other cyclodextrins. Stability constants of the complexes were determined in water at various temperatures and consequently thermodynamic parameters wer…

dissolution studyAqueous solutioncyclodextrinsChemistryCoprecipitationtechnology industry and agricultureGeneral ChemistryNuclear magnetic resonance spectroscopyCondensed Matter Physicscyclodextrins; idebenone; characterization of complexes; dissolution studycarbohydrates (lipids)idebenonecharacterization of complexesDifferential scanning calorimetrypolycyclic compoundsmedicineIdebenoneOrganic chemistrylipids (amino acids peptides and proteins)Free drugInclusion (mineral)DissolutionFood Sciencemedicine.drugNuclear chemistry
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