Search results for "Proton NMR"

showing 10 items of 324 documents

Di-n-octyltin(IV) complexes with 5-[(E)-2-(aryl)-1-diazenyl]-2-hydroxybenzoic acid: Syntheses and assessment of solid state structures by 119Sn Mössb…

2007

Abstract Reactions of 5-[( E )-2-(aryl)-1-diazenyl]-2-hydroxybenzoic acids (LHH′, where the aryl group is an R-substituted phenyl ring such that for L 1 HH′: X = H; L 2 HH′: X=2′-OCH 3 ; L 3 HH′: X = 3′-CH 3 ; L 4 HH′: X = 4′-CH 3 ; L 5 HH′:X = 4′-Cl) with n Oct 2 SnO in 2:1 and 1:1 molar ratios have been investigated. Two types of complexes, n Oct 2 Sn(LH) 2 and {[ n Oct 2 Sn(LH)] 2 O} 2 , were isolated and they have been characterized by 1 H, 13 C, 119 Sn NMR, ESI-MS, IR and 119m Sn Mossbauer spectroscopic techniques in combination with elemental analyses. The crystal structures of n Oct 2 Sn(L 1 H) 2 ( 1 ), {[ n Oct 2 Sn(L 2 H)] 2 O} 2 ( 3 ) and {[ n Oct 2 Sn(L 3 H)] 2 O} 2 ( 4 ) were de…

ChemistryArylOrganic ChemistryAnalytical chemistryCrystal structureNuclear magnetic resonance spectroscopyBiochemistryInorganic Chemistrychemistry.chemical_compoundBipyramidCrystallographyMössbauer spectroscopyX-ray crystallographyMaterials ChemistryProton NMRMoleculePhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Multinuclear Magnetic Resonance Study of 2,4,6-Triarylpyridines, 1-Methyl-2,4,6-Triarylpyridinium, and 2,4,6-Triarylpyrylium Cations

1995

Abstract The H, 13C, 15N, and 19F NMR spectra of 2,4,6-triarylpyridines, 1-methyl-2,4,6-triarylpyridinium and 2,4,6-triarylpyrylium perchlorates have been studied. The H NMR signals of protons 3(5) in the heteroaromatic ring are deshielded due to the polarization of C-H bonds caused by delocalization of the positive charge in pyridinium and pyrylium cations. Generally, conformational and structural variations affect the 13C NMR chemical shifts of all carbons in the heteroaromatic ring. Those of carbons 3(5) can best be related to the electron-donating or electron-accepting ability of substituents. However, both electronic character of substituents and charge of heteroatom itself are needed …

ChemistryChemical shiftHeteroatomSubstituentFluorine-19 NMRCarbon-13 NMRAtomic and Molecular Physics and OpticsAnalytical Chemistrychemistry.chemical_compoundCrystallographyProton NMRMoleculeOrganic chemistryPyridiniumSpectroscopySpectroscopy Letters
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NMR spectroscopy in environmental chemistry:1H and13C NMR parameters of tricyclic polychlorinated C10 hydrocarbons and their oxy derivatives based on…

1999

Two-dimensional homo- and heteronuclear NMR chemical shift correlation techniques were applied in the characterization of five tricyclic polychlorinated C10 hydrocarbons, chlordene (1), heptachlor (2), trans-nonachlor (3), α-chlordene (4) and γ-chlordene (5), which are spread globally in the environment owing to their use as insecticides. Approximate and partly contradictory 1H and 13C NMR chemical shifts reported in the literature were corrected in this work. The chemical shift assignments of 1–5 were based on DQF COSY, HMQC and HMBC experiments. In addition, an INADEQUATE experiment was needed to ascertain the 13C chemical shifts assignment of 2. The nJ(H,H)s of 1–5 were solved by compute…

ChemistryComputational chemistryNMR spectroscopy of stereoisomersChemical shiftAnalytical chemistryProton NMRGeneral Materials SciencePhosphorus-31 NMR spectroscopyTransverse relaxation-optimized spectroscopyGeneral ChemistryNuclear magnetic resonance spectroscopyFluorine-19 NMRCarbon-13 NMRMagnetic Resonance in Chemistry
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Synthesis and 1H-NMR configurational study of δ3-thiazolines from 2-aza-1,3-dienes

1992

Abstract A [4+1] heterocyclization process involving 2-aza-1,3-dienes and elemental sulphur leading to the synthesis of Δ3-thiazolines with excellent yields is described. A 1D TOCSY and 1D NOESY study of these systems was made in order to establish the configurations of the diastereoisomeric mixture.

ChemistryComputational chemistryOrganic ChemistryDrug DiscoveryProton NMRNuclear magnetic resonance spectroscopyBiochemistryTwo-dimensional nuclear magnetic resonance spectroscopyTetrahedron
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1,6-π-Electrocyclization of 3-Vinyl-FunctionalizedN,N-Dimethyl-2,2′-Bisindolyl: Some analysis of the educt transformation process

1998

The thermally and photochemically induced 1,6-π-electrocyclization reaction of 3-vinyl-functionalized N, N'-dimethyl-2,2′-bisindolyls 4 has been analysed and some reactivity aspects are presented. On the basis of time dependent 1H nmr and uv spectroscopic measurements the educt transformations can be observed in detail. Some results of the isomerization process of the educts are also given.

ChemistryComputational chemistryScientific methodOrganic ChemistryProton NMRReactivity (chemistry)IsomerizationTransformation (music)Journal of Heterocyclic Chemistry
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Cooperatively Enhanced Ion Pair Binding with a Hybrid Receptor

2015

A simple 18-crown-6-based bis-urea receptor R(1) was synthesized in three steps from a commercial starting material. The receptor's behavior toward anions, cations, and ion pairs was studied in solution with (1)H NMR, in solid state with single-crystal X-ray diffraction, and in gas phase with mass spectrometry. In 4:1 CDCl3/dimethyl sulfoxide solution the receptor's binding preference of halide anions is I(-) < Br(-) < Cl(-) following the trend of the hydrogen-bonding acceptor ability of the anions. The receptor shows a remarkable positive cooperativity toward halide anions Cl(-), Br(-), and I(-) when complexed with Na(+), K(+), or Rb(+). The solid-state binding modes of R(1) with alkali an…

ChemistryElectrospray ionizationion pair bindingHalideCooperative bindingAlkali metalMass spectrometryAcceptorIonInorganic ChemistryCrystallographyProton NMROrganic chemistryPhysical and Theoretical Chemistryta116hybrid receptorsInorganic Chemistry
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Binding Modes of Nonspherical Anions to N-Alkylammonium Resorcinarenes in the Solid State

2012

A series of hydrogen bond stabilized N-alkylammonium resorcinarene salts with nitrate, triflate, and picrate as the counteranions were synthesized and characterized with 1H NMR and electrospray ionization (ESI) mass spectrometry. Together with electrostatic interactions, the binding of the anions with several hydrogen bond donor sites proceeds through a complex array of intra- and intermolecular hydrogen bonds, evidenced by single crystal X-ray diffraction analysis. These N-alkyl ammonium resorcinarenes bind the larger nonspherical anions into deformed cavitand-like structures and enforce a transformation of the resorcinarene conformation from almost symmetrical to extremely distorted.

ChemistryHydrogen bondPicrateElectrospray ionizationIntermolecular forceInorganic chemistryGeneral ChemistryResorcinareneCondensed Matter PhysicsMass spectrometrychemistry.chemical_compoundCrystallographyProton NMRGeneral Materials ScienceTrifluoromethanesulfonateta116resorcinarenes; non-spherical anions; hydrogen bonding; X-ray structureCRYSTAL CROWTH & DESIGN
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Low-temperature methyl group dynamics of hexamethylbenzene in crystalline and glassy matrices as studied by 2H NMR

1991

Abstract 2 H NMR spectra of hexamethylbenzene (HMB) in protonated crystalline and amorphous matrices at low temperatures are presented. All spectra reveal lineshape changes which can be attributed to methyl group tunnelling. Compared to neat HMB, a drastic increase of the tunnelling frequency is found for all systems. This indicates that the hindering potential originates predominantly from intermolecular forces. We studied the temperature dependence of these spectra and the spin-lattice relaxation in order to exclude a distribution of motional correlation times describing a thermally activated process. In addition, we find a distortion of the methyl tetrahedron.

ChemistryIntermolecular forceRelaxation (NMR)Spin–lattice relaxationGeneral Physics and AstronomyNuclear magnetic resonance spectroscopyAmorphous solidchemistry.chemical_compoundNuclear magnetic resonanceProton NMRHexamethylbenzenePhysical chemistryPhysical and Theoretical ChemistryMethyl groupChemical Physics Letters
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Efficient synthesis of copillar[5]arenes and their host–guest properties with dibromoalkanes

2011

An efficient method for the synthesis of copillar[5]arenes was developed with FeCl(3) as catalyst and different 1,4-dialkoxybenzenes and paraformaldehyde as reactants (yields: 50-85%). The host-guest property of (co)pillar[5]arenes and terminal dibromoalkanes was investigated by (1)H NMR measurements and an X-ray study. The complexation behavior of the copillar[5]arenes can be tuned by changing the substituents on the host. A complete complexation selectivity was found between pillar[5]- and pillar[6]arenes, which is an interesting aspect for sensor techniques.

ChemistryOrganic ChemistryPillarProton NMROrganic chemistryPhysical and Theoretical ChemistrySelectivityBiochemistryCombinatorial chemistryCatalysisOrganic &amp; Biomolecular Chemistry
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ChemInform Abstract: 1,6-π-Electrocyclization of 3-Vinyl-Functionalized N,N′-Dimethyl-2,2′-bisindolyl: Some Analysis of the Educt Transformation Proc…

2010

The thermally and photochemically induced 1,6-π-electrocyclization reaction of 3-vinyl-functionalized N, N'-dimethyl-2,2′-bisindolyls 4 has been analysed and some reactivity aspects are presented. On the basis of time dependent 1H nmr and uv spectroscopic measurements the educt transformations can be observed in detail. Some results of the isomerization process of the educts are also given.

ChemistryScientific methodProton NMRNanotechnologyReactivity (chemistry)General MedicinePhotochemistryIsomerizationTransformation (music)ChemInform
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