Search results for "Chemical shift"

showing 10 items of 205 documents

ChemInform Abstract: Tetraarylmethane Analogues in Group 14. Part 2. Ph4-nSi(p-Tol)n and Ph4-nSn(p-Tol)n (n = 0-4): Effect of the p-Tolyl Substituent…

2010

ChemistryGroup (periodic table)StereochemistryChemical shiftGeneral MedicineChemInform
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Predominance of inductive over resonance substituent effect on33S NMR chemical shifts of 4-substituted phenyl-4′-methylphenacyl sulfones

1999

33S NMR chemical shifts have been determined for the first time for a series of 10 substituted phenacyl sulfones. Electron-withdrawing and electron-releasing substituents in 4-substituted phenyl-4′-methylphenacyl sulfones, p-MeC6H4COCH2SO2C6H4R-p, cause a ‘reverse’ substituent effect on the 33S NMR resonance. Dual-substituent parameter (DSP) analysis of δ(33S) values revealed that the inductive effect of the substituent predominates over its resonance effect. This finding shows that the 33S NMR chemical shifts are of importance in estimating the electronic properties of sulfur-containing compounds. The 13C and 17O NMR chemical shifts of the title compounds are also discussed. Copyright © 19…

ChemistryStereochemistryCarbon-13 NMR satelliteChemical shiftSubstituentGeneral ChemistryCarbon-13 NMRResonance (chemistry)PhenacylMedicinal chemistrychemistry.chemical_compoundGeneral Materials ScienceInductive effectResonance effectMagnetic Resonance in Chemistry
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A statistical study of the additivities of substituent effects in the13C NMR chemical shifts of hydroxy- and chloro-substituted benzenes

1980

The 13C NMR spectra of six hydroxybenzenes, all chlorobenzenes, all chlorophenols and eight chlorocatechols are measured and assigned. The additivity of the substituent effects and the usefulness of some corrective parameters are studied with regression analysis. The order of the chemical shifts is most efficiently predicted by the simplest substituent effect model, containing only the direct effects of the substituents, although the 95% confidence limits of the calculated shifts are as high as 5.6 ppm. If the chemical shifts need to be predicted within the measuring errors (approximately 0.05–0.10 ppm, in the present data), the number of necessary corrections is very impractical. The corre…

ChemistryStereochemistryChemical shiftDirect effectsSubstituentGeneral ChemistryCarbon-13 NMRSpectral lineSolventchemistry.chemical_compoundChlorobenzeneComputational chemistryAdditive functionGeneral Materials ScienceOrganic Magnetic Resonance
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Determination of the Relative Stereochemistry of Flexible Organic Compounds by Ab Initio Methods: Conformational Analysis and Boltzmann-Averaged GIAO…

2002

Ab initio calculations at the Hartree-Fock level with full-geometry optimization using the 6-31G(d) basis set, and GIAO (gauge including atomic orbitals) 1 3 C NMR chemical shifts, are presented here as a support in the study of the stereochemistry of low-polar organic compounds having an openchain structure. Four linear stereoisomers, fragments of a natural product previously characterized by experimental 1 3 C NMR spectra, which possesses three stereogenic centers, 11 carbon atoms, and 38 atoms in total, were considered. Conformational searches, by empirical force-field molecular dynamics, pointed out the existence of 8-13 relevant conformers per stereoisomer. Thermochemical calculations …

ChemistryStereochemistryChemical shiftOrganic ChemistryAb initioGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRCatalysisAb initio quantum chemistry methodsComputational chemistryAtomConformational isomerismBasis setChemistry - A European Journal
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Tautomerism and the Protonation/Deprotonation of Isocytosine in Liquid- and Solid-States Studied by NMR Spectroscopy and Theoretical Calculations

2011

Isocytosine crystallizes as a 1:1 ratio of two tautomers in a manner similar to that of the guanine and cytosine pairs in DNA. The solid-state NMR chemical shifts of crystalline neutral isocytosine, the sodium salt of isocytosine, and those of isocytosine hydrochloride were measured and related to the NMR parameters in aqueous and organic solutions. The experimental chemical shifts were compared with those calculated by three different methods: (1) calculations on isolated molecules, (2) calculations on isocytosine clusters of various sizes, and (3) infinite crystal calculations, that is, the gauge-including projector-augmented wave (GIPAW) method. The data obtained with the GIPAW method we…

ChemistryStereochemistryChemical shiftOrganic ChemistryProtonationNuclear magnetic resonance spectroscopyCrystal structureTautomerchemistry.chemical_compoundDeprotonationMoleculePhysical chemistryIsocytosinePhysical and Theoretical Chemistryta116European Journal of Organic Chemistry
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1H,13C and17O NMR study of aromatic ring-substituted monochloro- and monobromo-(E)-3-phenylpropenals

1991

Trans-Cinnamaldehydes (CAs) or o-, m- and p-X-(E)-3-phenylpropenals; (X = Cl or Br) were synthesized and their 1H, 13C and 17O NMR spectra were measured, assigned and analysed. The long-range benzylic couplings are discussed in terms of the conformational characteristics of the related styrene systems. The 1H, 13C and 17O NMR substituent chemical shifts of the CA derivatives were compared with those of styrene and explained by the π-electron delocalization in the conjugated CCCO bond system of CA.

ChemistryStereochemistryChemical shiftSubstituentGeneral ChemistryNuclear magnetic resonance spectroscopyConjugated systemRing (chemistry)Medicinal chemistryStyrenechemistry.chemical_compoundDelocalized electronGeneral Materials ScienceSolvent effectsMagnetic Resonance in Chemistry
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(1Z,3Z)-3-[Quinolin-2(1H)-ylidene]-1-(quinolin-2-yl)prop-1-en-2-ol: An unexpected most stable tautomer of 1,3-bis(quinolin-2-yl)acetone

2009

Abstract 1 H, 13 C and 15 N NMR spectra reveal that CDCl 3 solution of 1,3-bis(quinolin-2-yl)acetone contains only ( 1Z , 3Z )-3-[quinolin-2(1 H )-ylidene]-1-(quinolin-2-yl)prop-1-en-2-ol. The proton transfer takes place between two basic centers of the molecule, which means that the process is an identity reaction by character. The situation is completely different from that detected in chloroform solution of 1,3-bis(pyridin-2-yl)acetone where three different tautomers are in equilibrium with each other. Although the proton transfers in both ( 1Z , 3Z )-3-[quinolin-2(1 H )-ylidene]-1-(quinolin-2-yl)prop-1-en-2-ol and ( 1Z , 3Z )-3-hydroxy-1-[quinolin-2(1 H )-ylidene-4-quinolin-2-yl]but-3-e…

ChloroformStereochemistryChemical shiftOrganic ChemistryConjugated systemTautomerMedicinal chemistryAnalytical ChemistryInorganic ChemistryNMR spectra databasechemistry.chemical_compoundchemistryAb initio quantum chemistry methodsAcetoneMoleculeSpectroscopyJournal of Molecular Structure
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Ab initio study of halogenated diphenyl ethers. NMR chemical shift prediction

2000

Computational chemistryChemistryChemical shiftProton NMRAb initioGeneral Materials ScienceGeneral ChemistryCarbon-13 NMRHalogenated Diphenyl EthersMagnetic Resonance in Chemistry
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Analytic second derivatives for general coupled-cluster and configuration-interaction models.

2004

Analytic second derivatives of energy for general coupled-cluster (CC) and configuration-interaction (CI) methods have been implemented using string-based many-body algorithms. Wave functions truncated at an arbitrary excitation level are considered. The presented method is applied to the calculation of CC and CI harmonic frequencies and nuclear magnetic resonance chemical shifts up to the full CI level for some selected systems. The present benchmarks underline the importance of higher excitations in high-accuracy calculations.

Coupled clusterChemistryChemical shiftMathematical analysisC++ string handlingGeneral Physics and AstronomyPhysical and Theoretical ChemistryAtomic physicsConfiguration interactionWave functionEnergy (signal processing)ExcitationSecond derivativeThe Journal of chemical physics
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1H and13C NMR spectroscopy of brominated diphenyl ethers. A multiple linear regression analysis

2000

The 1H and 13C NMR chemical shifts and 1H, 1H coupling constants of 27 brominated diphenyl ethers are reported. The increment models for the bromine substituent effects on the 1H and 13C NMR chemical shifts were constructed based on a multiple linear regression analysis. In addition to the single substituent effects, two particle increments and corrective terms for conformational effects are included in these models in order to obtain a reliable prediction of chemical shifts. Copyright © 2000 John Wiley & Sons, Ltd.

Coupling constantBromineChemical shiftSubstituentAnalytical chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRchemistry.chemical_compoundchemistryComputational chemistryProton NMRGeneral Materials ScienceMultiple linear regression analysisMagnetic Resonance in Chemistry
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