Search results for "Spectroscopy"

showing 10 items of 10293 documents

3-(4-Fluorophenyl)-1-methyl-4-(4-pyridyl)quinolin-2(1H)-one

2007

The title compound, C21H15FN2O, was synthesized in the course of our studies of p38 mitogen-activated protein kinase inhibitors. It has been investigated by 1H and 13C NMR spectroscopy and was proven by X-ray crystallographic analysis to be the N-methyl rather than the O-methyl isomer. In the crystal structure, a three-dimensional network is formed consisting of quinolinone aromatic stacking inter­actions and weak C—H⋯O and C—H⋯N hydrogen bonds.

Crystallography13c nmr spectroscopyHydrogen bondStereochemistryChemistryStackingGeneral Materials ScienceGeneral ChemistryCrystal structureCondensed Matter PhysicsProtein kinase AActa Crystallographica Section E Structure Reports Online
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Tetranitroresorcin[4]arene: synthesis and structure of a new stereoisomer

2009

The direct reaction between 2-nitroresorcinol and acetaldehyde in alkaline medium yields tetranitro-C1-resorcin[4]arene in a moderate 8.2% overall yield which was characterized by single crystal X-ray crystallography, 1H NMR spectroscopy and electrospray ionization mass spectrometry (ESI-MS). In solution and in the solid state, the product adopts a unique, thermally stable and unprecedented rcct-boat conformation.

Crystallography1h nmr spectroscopychemistry.chemical_compoundchemistryYield (chemistry)Electrospray ionizationOrganic ChemistryDrug DiscoverySolid-stateAcetaldehydeDirect reactionBiochemistrySingle crystalTetrahedron Letters
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Decoupling the artificial special pair to slow down the rate of singlet energy transfer

2012

Trimer 2, composed of a cofacial heterobismacrocycle, octamethyl-porphyrin zinc(II) and bisarylporphyrin zinc(II) held by an anthracenyl spacer, and a flanking acceptor, bisarylporphyrin free-base ( Ar = -3,5-(t Bu )2 C 6 H 3), has been studied by means of absorption spectroscopy, "steady state and time-resolved fluorescence" and fs transient absorption spectroscopy, and density functional theory (DFT) in order to assess the effect of decoupling the chromophores' low energy MOs on the rate of the singlet, S1, energy transfer, k ET , compared to a recently reported work on a heavily coupled trimeric system, Trimer 1, [biphenylenebis(n-nonyl)porphyrin zinc(II)]-bisarylporphyrin free-base ( A…

CrystallographyAbsorption spectroscopyChemistryUltrafast laser spectroscopyTrimerDensity functional theoryGeneral ChemistrySinglet stateChromophoreAbsorption (electromagnetic radiation)PhotochemistryAcceptorJournal of Porphyrins and Phthalocyanines
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FTIR Microscopy with Polarized Radiation for the Analysis of Adsorption Processes in Molecular Sieves

1994

FTIR Microscopy with polarized light was used to study the orientation of different molecules in Silicalite I, SAPO-5 and AlPO 4 -5 molecular sieves during the adsorption process and in their equilibrium positions. While the uptake and the equilibrium positions of p-xylene are essentially not influenced by the the framework charge, large differences between AlPO 4 -5 and SAPO-5 are observed with the strongly basic p-nitroaniline molecule.

CrystallographyAdsorptionChemistryMicroscopyMoleculeFourier transform infrared spectroscopyRadiationMolecular sieve
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Formation of complex defects in Mn c Mg 1–c O and Ni c Mg 1–c O single solid solution

2005

The results of investigation of the fast neutron irradiation and thermal treatment on absorption spectra of single solid solution of MncMg1–cO, NicMg1–cO and MgO crystals are presented. It is shown that at impurity ion concentration larger than 0.1 mass.% a probability of formation of aggregate centers consisting of more than three F+- or F-centers is small. After thermal treatment of MncMg1–cO and NicMg1–cO single solid solution irradiated by fast neutrons additional wide bands are observed. We assume that these additional bands belong to complex centers of Mn3+-VMg and Ni3+-VMg. The mechanisms of bands formation are discussed. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

CrystallographyAggregate (composite)Absorption spectroscopyImpurityChemistryAnalytical chemistryThermal treatmentIrradiationNeutron temperatureSolid solutionIonphysica status solidi (c)
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Isomer spectroscopy in254No

2006

Isomeric states in No-254 were investigated using a calorimetric method. Two different isomers were found with half-lives of T-1/2 = 266 +/- 2 ms and T-1/2 = 184 +/- 3 mu s, respectively. The domin ...

CrystallographyChemistryCondensed Matter PhysicsSpectroscopyMathematical PhysicsAtomic and Molecular Physics and OpticsPhysica Scripta
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Asymmetric [N–I–N]+ halonium complexes

2020

The first asymmetric halogen-bonded iodonium complexes [I(py)(4-DMAP)]PF6 (2c) and [I(py)(4-Etpy)]PF6 (2e) were prepared via [N–Ag–N]+ → [N–I–N]+ cation exchange of their analogous 2-coordinate silver complexes. The complexes were characterised by 1H and 1H–15N HMBC NMR spectroscopy, and single crystal X-ray crystallography.

CrystallographyChemistryMaterials ChemistryMetals and AlloysCeramics and CompositesHalonium ionGeneral ChemistryNuclear magnetic resonance spectroscopySingle crystalCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical Communications
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Complete assignments of1H and13C NMR spectra of four hispanane diterpenoids

2000

An NMR study of four hispanane diterpenoids is described. In addition to conventional 1D NMR methods, 2D shift-correlated experiments [1H,1H-COSY, 1H,1H-TOCSY, 1H,13C-HSQC-1J(C,H). 1H,13C-HMBC-nJ(C,H) (n = 2 and 3)] and 2D 1H,1H-NOESY were used for the complete and unambiguous 1H and 13C chemical shift assignments of these diterpenoids. Copyright © 2000 John Wiley & Sons, Ltd.

CrystallographyChemistryNMR spectroscopy of stereoisomersAnalytical chemistryProton NMRGeneral Materials ScienceGeneral ChemistryFluorine-19 NMRCarbon-13 NMRTwo-dimensional nuclear magnetic resonance spectroscopySpectral lineMagnetic Resonance in Chemistry
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Doubly charged ions of bridged [4n] annulenes. An evaluation of diatropic ring current effects.

1985

Abstract [4n]Annulenes are transformed into doubly charged ions (dianion, dication) and characterized NMR spectroscopically. The diatropic character of the ionic (4n+2)π-systems is studied as a function of the number of π-electrons.

CrystallographyChemistryStereochemistryOrganic ChemistryDrug DiscoveryIonic bondingElectronic structureNuclear magnetic resonance spectroscopyAnnuleneBiochemistryRing currentIonDicationTetrahedron Letters
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Letter to the Editor: Backbone1H,13C and15N Resonance Assignments for the 18.7 kDa GTPase Domain of Escherichia Coli MnmE Protein

2004

CrystallographyChemistrymedicineBiophysicsResonanceGTPasemedicine.disease_causeBiochemistryEscherichia coliSpectroscopyDomain (software engineering)Journal of Biomolecular NMR
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