Search results for "MR"

showing 10 items of 3001 documents

A method for measurement of spin-spin couplings with sub-mHz precision using zero- to ultralow-field nuclear magnetic resonance.

2017

We present a method which allows for the extraction of physical quantities directly from zero- to ultralow-field nuclear magnetic resonance (ZULF NMR) data. A numerical density matrix evolution is used to simulate ZULF NMR spectra of several molecules in order to fit experimental data. The method is utilized to determine the indirect spin-spin couplings ($J$-couplings) in these, which is achieved with precision of $10^{-2}$--$10^{-4}$ Hz. The simulated and measured spectra are compared to earlier research. Agreement and precision improvement for most of the $J$-coupling estimates are achieved. The availability of an efficient, flexible fitting method for ZULF NMR enables a new generation of…

Chemical Physics (physics.chem-ph)Nuclear and High Energy PhysicsZero field NMRField (physics)ChemistryBiophysicsFOS: Physical sciences010402 general chemistryCondensed Matter Physics01 natural sciences7. Clean energyBiochemistrySpectral line0104 chemical sciences3. Good healthNMR spectra databaseMatrix (mathematics)Nuclear magnetic resonancePhysics - Chemical Physics0103 physical sciencesTransverse relaxation-optimized spectroscopy010306 general physicsSpin (physics)Two-dimensional nuclear magnetic resonance spectroscopyJournal of magnetic resonance (San Diego, Calif. : 1997)
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13C NMR study on the methoxy carbon chemical shifts in chloro-substituted anisoles and guaiacols

1983

The 13C NMR chemical shifts of methoxy carbons in chlorinated anisoles and guaiacols have been measured for acetone-d6 solutions. Multiple linear regression analysis, and also ‘simple sum rule’ calculations, have been used to estimate the effects of the chlorine atoms (the position and degree of substitution) on the chemical shifts. The most important effects have shown to be due to the chlorine atoms adjacent to the methoxy and hydroxy substituents. For chlorinated guaiacols, the greatest effect is due to the chlorine atom adjacent to the methoxy group. For chlorinated anisoles, the substituents adjacent to the methoxy group (2,6-disubstitution) cause large effects. For both groups of comp…

Chemical shiftChlorine atomSubstituentchemistry.chemical_elementGeneral ChemistryCarbon-13 NMRPhotochemistryMedicinal chemistrychemistry.chemical_compoundDegree of substitutionchemistrypolycyclic compoundsChlorineGeneral Materials ScienceMultiple linear regression analysisCarbonOrganic Magnetic Resonance
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DFT calculation of structures and NMR chemical shifts of simple models of small diameter zigzag single wall carbon nanotubes (SWCNTs)

2011

Linearly conjugated benzene rings (acenes), belt-shape molecules (cyclic acenes) and model single wall carbon nanotubes (SWCNTs) were fully optimized at the unrestricted level of density functional theory (UB3LYP/6-31G*). The models of SWCNTs were selected to get some insight into the potential changes of NMR chemical shift upon systematic increase of the molecular size. The theoretical NMR chemical shifts were calculated at the B3LYP/pcS-2 level of theory using benzene as reference. In addition, the change of radial breathing mode (RBM), empirically correlated with SWCNT diameter, was directly related with the radius of cyclic acenes. Both geometrical and NMR parameters were extrapolated t…

Chemical shiftGeneral ChemistryCarbon nanotubeCarbon-13 NMRConjugated systemlaw.inventionBond lengthchemistry.chemical_compoundchemistryComputational chemistrylawMoleculePhysical chemistryGeneral Materials ScienceDensity functional theoryBenzeneMagnetic Resonance in Chemistry
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Fourier transform nmr investigations of organotin compounds

1980

Abstract NMR spectra have been obtained for fiteen title compounds, mainly with R = Me. Tin chemical shifts were found to lie within the expected ranges, but to vary little with R or, apparently, with change in ring size. While the magnitute of 1 (SnSe) was as predicted, the of 1 (SnTe) was more than twice as large as that previously observed for (Me 3 Sn) 2 Te. In compounds Me 6 Sn( 3 X 3 , 2 J(SnMSn) varied systematically with variations in x, but within relatively narrow limits (195-250 Hz); a much more drastic variation was observed for Me 6 Sn 3 X 2 , possibly due to bond angle changes at Sn and X.

Chemical shiftOrganic ChemistryAnalytical chemistrychemistry.chemical_elementBiochemistryInorganic ChemistryRing sizeNMR spectra databasesymbols.namesakeMolecular geometryFourier transformchemistryMaterials ChemistrysymbolsPhysical and Theoretical ChemistryTinJournal of Organometallic Chemistry
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Comparative NMR and IR spectral, X-ray structural and theoretical studies of eight 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxides

2007

Abstract Eight 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxides are characterized by NMR and IR spectroscopy. Single crystal X-ray structures for three congeners are reported. In addition, the transmission of substituent effects in conjugated double bond system of 6-arylidenedibenzo[b,e]thiepin-11-one-5,5-dioxide framework has been evaluated by calculating the correlations between selected 13C NMR chemical shifts and IR stretching wave numbers and Hammett constants of the substituents locating in the phenyl ring of the arylidene moiety.

Chemical shiftOrganic ChemistrySubstituentInfrared spectroscopyCarbon-13 NMRRing (chemistry)Analytical ChemistryInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryComputational chemistryProton NMRMoietySingle crystalSpectroscopyJournal of Molecular Structure
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Nitrogen-15 NMR Studies on Hydrazines. 2— Substituent Effect Analysis inortho-Substituted Phenylhydrazines and Anilines

1996

15N and 13C NMR spectra of some ortho-substituted phenylhydrazines were measured at natural isotope abundance in DMSO-d6 solutions. The substituent present exerts a larger effect on the chemical shift of the nitrogen atom directly bound to the aromatic ring (N-1), the second one (N-2) showing an attenuated trend of similar sign. Contrary to what observed for para and meta isomers, the cross-correlation between N-1 and N-2 SCS values of ortho-substituted phenylhydrazines is not satisfactory; on the other hand, N-1 SCSs show a reasonably good linear regression with the σR− constants. As expected, no correlation was found between N-1 and C-1 or H-1 SCS values. Correlations between 13C and 15N …

Chemical shiftPhenylhydrazinesSubstituentchemistry.chemical_elementNatural abundanceGeneral ChemistryCarbon-13 NMRRing (chemistry)PhotochemistryNitrogenMedicinal chemistrySpectral linechemistry.chemical_compoundchemistryGeneral Materials ScienceMagnetic Resonance in Chemistry
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NMR studies of benzoannulation in lithium, sodium and potassium ortho-formylphenolates

2010

Abstract Lithium, sodium and potassium derivatives of (benzo)salicylaldehydes have been prepared and characterized by 1 H and 13 C NMR in order to see how the metal cation and benzoannulation affect spectral parameters. There is no qualitative effect of the alkali metal atom in the compounds studied (from this point of view salicylaldehydes remind β-diketones). On the other hand, 1 H chemical shifts of the hydroxyl and formyl protons and 13 C chemical shifts of C2 (bearing OX, X = H, Li, Na or K) and of that the formyl carbon show the most significant variations being the best indicators of aromatic character of the six-membered quasi-ring of salicylaldehyde. In contrast, C1 (bearing formyl…

Chemical shiftSodiumPotassiumOrganic ChemistryInorganic chemistrychemistry.chemical_elementCarbon-13 NMRAlkali metalMedicinal chemistryAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundSalicylaldehydechemistryMoietyLithiumSpectroscopyJournal of Molecular Structure
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Effects of substitutions on cyclopentadienyl rings in complexes with molybdenum-mercury bonds. 95Mo and 199Hg NMR studies

1995

NMR data for 95Mo and 199Hg nuclei have been obtained for new di- and trimetallic complexes Cp′(CO)3MoHgX containing molybdenum-mercury bonds and bulky and/or potentially bifunctional substituted cyclopentadienyl ligands; Cp′=C5HMe2Ph2, C5Me4Bz, C5Bz5, C5H4PPh2 and C5Me4PPh2 (Bz=CH2C6H5; Me =CH3; Ph=C6H5); X=Cp′(CO)3Mo, Cl, Br, 1, SCN. They are discussed within the context of our earlier results reported for analogous complexes with the cyclopentadienyl ligands bearing methyl groups. With the exception of phenyl substituted rings, a rather narrow range of 95Mo chemical shifts is found for the compounds with the same number of different substituents on cyclopentadienyl ligands. An outstandin…

Chemical shiftchemistry.chemical_elementPhotochemistryMedicinal chemistryNmr dataMercury (element)Inorganic Chemistrychemistry.chemical_compoundchemistryCyclopentadienyl complexMolybdenumIntramolecular forceMaterials ChemistryNarrow rangePhysical and Theoretical ChemistryBifunctionalInorganica Chimica Acta
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Chemical Reaction Monitoring Using Zero-Field Nuclear Magnetic Resonance Enables Study of Heterogeneous Samples in Metal Containers

2020

Abstract We demonstrate that heterogeneous/biphasic chemical reactions can be monitored with high spectroscopic resolution using zero‐field nuclear magnetic resonance spectroscopy. This is possible because magnetic susceptibility broadening is negligible at ultralow magnetic fields. We show the two‐step hydrogenation of dimethyl acetylenedicarboxylate with para‐enriched hydrogen gas in conventional glass NMR tubes, as well as in a titanium tube. The low frequency zero‐field NMR signals ensure that there is no significant signal attenuation arising from shielding by the electrically conductive sample container. This method paves the way for in situ monitoring of reactions in complex heteroge…

Chemical substanceMaterials scienceHydrogenAnalytical chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesChemical reaction7. Clean energyCatalysisNMR spectroscopyHyperpolarization (physics)Research Articleshyperpolarization010405 organic chemistryReaction MonitoringGeneral MedicineGeneral ChemistryNuclear magnetic resonance spectroscopyequipment and suppliesMagnetic susceptibility0104 chemical sciencesMagnetic fieldzero-fieldchemistryddc:540Electromagnetic shieldingResearch Article
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CoIILnIII dinuclear complexes (LnIII = Gd, Tb, Dy, Ho and Er) as platforms for 1,5-dicyanamide-bridged tetranuclear CoII2LnIII2 complexes: A magneto-…

2012

Five acetate-diphenoxo triply-bridged Co-II-Ln(III) complexes (Ln(I) = Gd, Tb, Dy, Ho, Er) of formula [Co(mu-L)(mu-Ac)Ln(NO3)(2)] and two diphenoxo doubly-bridged Co-II-Ln(III) complexes (Ln(III) = Gd, Tb) of formula [Co(H2O)(mu-L)Ln(NO3)(3)]center dot S (S = H2O or MeOH), were prepared in one pot reaction from the compartmental ligand N,N',N ''-trimethyl-N,N ''-bis(2-hydroxy3-methoxy-5-methylbenzyl)diethylene triamine (H2L). The diphenoxo doubly-bridged Co-II-Ln(III) complexes were used as platforms to obtain 1,5-dicyanamide-bridged tetranuclear Co-II-Ln(III) complexes (Ln(III) = Gd, Tb, Dy, Ho, Er). All exhibit ferromagnetic interactions between the Co-II and Ln(III) ions and in the case …

Chemistry(all)LigandGeneral Chemical EngineeringRelaxation (NMR)MineralogyGeneral ChemistryDiethylene triamineIonchemistry.chemical_compoundMagnetizationCrystallography/dk/atira/pure/subjectarea/asjc/1500chemistryFerromagnetismOne pot reactionChemical Engineering(all)/dk/atira/pure/subjectarea/asjc/1600Dicyanamideta116Comptes Rendus Chimie
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