Search results for "HIF"

showing 10 items of 1515 documents

Study of the Density and Temperature Dependences of the Vibrational Raman Transition in Compressed Liquid N2

1991

0021-9606; Accurate values of linewidth and line shift in the isotropic vibrational Raman spectrum of compressed liquid N2 have been obtained by using inverse Raman spectroscopy. Experiments have been performed for eight isotherms, from the normal boiling point to the critical point temperatures of N2, the number density varying between the value on the coexistence line, and the maximum value of 2.1 x 10^22 cm-3. Minima of the linewidth have been observed above 86 K, showing the increasing influence of vibration-rotation coupling (motional narrowing) competing with the broadening due to pure vibrational dephasing. Moreover, for the first time, maxima of the red line shifts have been found, …

NITROGENMEDIASPECTROSCOPYENERGY RELAXATIONN2TRANSITIONSSCATTERING SPECTRAMOLECULAR-DYNAMICS SIMULATIONFREQUENCY-SHIFT MEASUREMENTSQ-BRANCHREGION
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A New Entry to the Substituted Pyrrolo[3,2-c]quinoline Derivatives of Biological Interest by Intramolecular Heteroannulation of Internal Imines.

2004

New 1,3,4-substituted pyrrolo[3,2-c]quinoline derivatives were synthesised in good yields by oxidative heteroannulation of internal imines starting from easily prepared substituted 5-(2-aminophenyl)pyrroles and commercially available aryl and heteroaryl aldehydes. The reaction occurs as a one-pot process involving an intramolecular acid catalysed reaction.

NMR chemical shiftsArylOrganic ChemistryQuinolineGeneral MedicineBiochemistryInternal iminesCombinatorial chemistry2-c]quinoline derivativeschemistry.chemical_compoundchemistryIntramolecular forceDrug DiscoveryOrganic chemistryPyrrolo[3Intramolecular heteroannulationChemInform
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1H,13C,17O NMR and IR spectroscopic study of all methyl chloropropanoates

1994

1 H, 13 C and 17 O NMR chemical shifts, n J(H,H) and n J(C,H) spin-spin coupling constants and IR absorption maxima and intensities for the most characteristic bands of methyl propanoate and all eleven chloropropanoic acid methyl esters are reported

NMR spectra databaseCoupling constantOxygen-17Ir absorptionStereochemistryChemistryChemical shiftHydrogen-1Carbon-13Physical chemistryInfrared spectroscopyGeneral Materials ScienceGeneral ChemistryMagnetic Resonance in Chemistry
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ChemInform Abstract: The Tautomerism of Nitraminopyridines

2010

1H, 13C and 15N NMR data for nitraminopyridines are discussed in terms of tautomeric equilibria in these compounds. The favoured tautomer is determined mainly from 15N NMR spectroscopy. The chemical shift of the nitrogen atom of the nitro group in nitraminopyridines and N-nitroanilines which cannot tautomerize vary from 28·0 to 35·4 ppm in DMSO solution. 3-Nitraminopyridine and 2-nitramino-3- and -5-nitropyridines behave similarly. In the 15N NMR spectra of nitrimino-1-methyldihydropyridines, used as models, an upfield shift of that atom, different from that observed for 2-nitraminopyridine, indicates the significance of the nitrimino tautomer. In contrast, a downfield shift of the ring nit…

NMR spectra databaseCrystallographyProtonChemistryChemical shiftAtomNitroGeneral MedicineNuclear magnetic resonance spectroscopyRing (chemistry)TautomerChemInform
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The tautomerism of nitraminopyridines

1995

1H, 13C and 15N NMR data for nitraminopyridines are discussed in terms of tautomeric equilibria in these compounds. The favoured tautomer is determined mainly from 15N NMR spectroscopy. The chemical shift of the nitrogen atom of the nitro group in nitraminopyridines and N-nitroanilines which cannot tautomerize vary from 28·0 to 35·4 ppm in DMSO solution. 3-Nitraminopyridine and 2-nitramino-3- and -5-nitropyridines behave similarly. In the 15N NMR spectra of nitrimino-1-methyldihydropyridines, used as models, an upfield shift of that atom, different from that observed for 2-nitraminopyridine, indicates the significance of the nitrimino tautomer. In contrast, a downfield shift of the ring nit…

NMR spectra databaseCrystallographyProtonChemistryStereochemistryChemical shiftOrganic ChemistryAtomNitroNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryRing (chemistry)TautomerJournal of Physical Organic Chemistry
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Structure Validation of Natural Products by Quantum-Mechanical GIAO Calculations of 13C NMR Chemical Shifts GIAO=gauge including atomic orbitals.

2002

Geometry optimization and GIAO (gauge including atomic orbitals) 1 3 C NMR chemical shift calculations at Hartree-Fock level, using the 6-31G(d) basis set, are proposed as a tool to be applied in the structural characterization of new organic compounds, thus providing useful support in the interpretation of experimental NMR data. Parameters related to linear correlation plots of computed versus experimental 1 3 C NMR chemical shifts for fourteen low-polar natural products, containing 10-20 carbon atoms, were employed to assess the reliability of the proposed structures. A comparison with the hybrid B3LYP method was carried out to evaluate electron correlation contributions to the calculatio…

NMR spectra databaseElectronic correlationAb initio quantum chemistry methodsComputational chemistryChemistryChemical shiftOrganic ChemistryStructure validationGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRCatalysisBasis setChemistry - A European Journal
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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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Symmetry: Friend or foe?

1999

While symmetry in molecules or supramolecular complexes is desirable from the design point of view and affords simpler NMR spectra, the study of symmetrical species by NMR is often subject to ambiguities resulting from signal degeneracy. In this paper we shall discuss different ways of breaking symmetry in order to obtain additional structural information by NMR.

NMR spectra databasePhysicsTheoretical physicsIsotopic shiftSupramolecular chemistrySymmetry (geometry)Degeneracy (mathematics)
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The combined effects of two chlorine substituents and the non-additivities of chemical shifts in aliphatic dichloro esters

1982

Carbon-13 NMR spectra were measured for 25 methyl esters of aliphatic dichlorocarboxylic acids for substituted propanoic to hexanoic acids. Observed 13C shifts are compared with calculated shift values obtained from the shifts of the corresponding monochloro esters by applying a simple sum method. The greatest failures from additivity are observed for αβ and αα substituted carbons. The combined effects of two chlorine substituents were determined, and compared with those obtained from chlorine substituent effects in monochloro esters by assuming additivity. The trends displayed by the combined effects, and also by the non-additivity effects, are discussed.

NMR spectra databasechemistryComputational chemistryChemical shiftChlorinechemistry.chemical_elementOrganic chemistryGeneral Materials ScienceGeneral ChemistryChlorine substituentOrganic Magnetic Resonance
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ChemInform Abstract: 4-Fluoroanilines: Synthesis and Decomposition.

2010

Abstract Fourteen N- and/or 2-substituted 4-fluoroanilines were prepared (the series includes N–C2-bridged compounds). Some of them were found to be thermally unstable when dissolved in chloroform. Both 19 F NMR spectra and comparison of GIAO-DFT calculated and experimental 13 C chemical shifts were used to suggest decomposition products of 4-fluoroanilines.

NMR spectra databasechemistry.chemical_compoundChloroformchemistryComputational chemistryChemical shiftOrganic chemistryGeneral MedicineDecompositionPyrrole derivativesChemInform
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