Search results for "NMR spectra"

showing 10 items of 113 documents

Design, synthesis and spectral studies of novel bile acid-arene conjugates: Trans to cis isomerization of azobenzene core controlled by bile acid hyd…

2008

Abstract Four bile acid-arene conjugates, 1,4-bis[dimethyl(3α,7α,12α-trihydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]benzene dibromide ( 1 ), 1,3,5-tris[dimethyl(3α,7α,12α-trihydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]benzene tribromide ( 2 ), bis{4-[dimethyl(3α,7α,12α-trihydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]phenyl}diazene dibromide ( 3 ), and bis{4-[dimethyl(3α-hydroxy-5β-cholan-24-amidoethyl)ammoniomethyl]phenyl}diazene dibromide ( 4 ), have been synthesized in good yields, and their structures have been characterized by 1 H, 13 C, 13 C DEPT-135, PFG 1 H, 13 C HMQC, PFG 1 H, 13 C HMBC, and PFG 1 H, 15 N HMBC NMR spectra. Their molecular weights and elemental compositions have…

StereochemistryOrganic ChemistryMedicinal chemistryp-XyleneAnalytical ChemistryInorganic ChemistryNMR spectra databasechemistry.chemical_compoundchemistryAzobenzeneMoietyTribromideMesityleneIsomerizationSpectroscopyProtic solventJournal of Molecular Structure
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"Through-space" 31P spin-spin couplings in ferrocenyl tetraphosphine coordination complexes: improvement in the determination of the distance depende…

2008

Abstract From the analysis of several nickel and palladium halide complexes of a constrained ferrocenyl tetraphosphine, the existence in solution phase of unique 31P–31P “through-space” nuclear spin–spin coupling constants (JPP) had been previously evidenced. Due to the blocked conformation of the species in solution, and based on the NMR spectra obtained for the complexes and their corresponding solid state X-ray structures, these JPP constants had been shown to clearly depend on the mutual spatial position of the corresponding phosphorus atoms. Herein, the quantitative correlation disclosed at that time (P⋯P distance dependence of coupling constants) is remarkably confirmed, and mathemati…

Stereochemistrychemistry.chemical_elementHalide010402 general chemistrySpace (mathematics)01 natural sciencesBiochemistryInorganic Chemistrychemistry.chemical_compoundMaterials Chemistryphosphorus carbon bond formation[CHIM.COOR]Chemical Sciences/Coordination chemistryspin couplingPhysical and Theoretical ChemistrySpin (physics)ComputingMilieux_MISCELLANEOUSCoupling constantaminophosphine010405 organic chemistryOrganic Chemistrythrough-spaceferrocene[ CHIM.COOR ] Chemical Sciences/Coordination chemistryNMR0104 chemical sciencesNMR spectra databaseNickelCrystallographychemistryFerrocenepolyphosphinePalladium
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Substituent effects of1H NMR parameters of chlorinated diphenyl ethers. A statistical approach

1994

The 1H NMR spectra of 64 polychlorinated diphenyl ethers (PCDEs) were measured and assigned. Multiple linear regression analysis was used to estimate the effects of chlorine atoms on the 1H NMR chemical shifts and coupling constants. The ‘simple sum rules’ were found to be inadequate for the prediction of 1H NMR chemical shifts of PCDEs. Therefore, corrective terms of two chlorine atoms were taken into account. The most important effects on chemical shifts were shown to be the steric interactions of two adjacent chlorine atoms and the intramolecular ring current effect observed in the ortho-proton of tri-ortho-substituted PCDEs. The substituent effects on J(HH) coupling constants were found…

Steric effectsChemistryStereochemistryChemical shiftSubstituentEtherGeneral ChemistryPolychlorinated diphenyl ethersNMR spectra databasechemistry.chemical_compoundComputational chemistryIntramolecular forceProton NMRGeneral Materials ScienceMagnetic Resonance in Chemistry
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Spectroscopic and conformational properties of size-fractions separated from a lignite humic acid

2007

Abstract A lignite humic acid (HA) was fractionated by preparative high performance size-exclusion chromatography (HPSEC) in seven different size-fractions. The size-fractions were characterized by cross polarization (CP) magic angle spinning (MAS) 13 C NMR spectroscopy and a further analytical HPSEC elution under UV and fluorescence detection. The alkyl hydrophobic components mainly distributed in the largest molecular-size-fraction, whereas the amount of oxidized carbons increased with decreasing size of fractions. Cross polarization time ( T CH ) and proton spin-lattice relaxation time in the rotating frame ( T 1 ρ (H)) were measured from variable contact time (VCT) experiments. The bulk…

Steric effectsMagnetic Resonance SpectroscopyEnvironmental EngineeringHealth Toxicology and MutagenesisSettore AGR/13 - Chimica AgrariaAnalytical chemistryFractionationLigninFluorescence spectroscopyMagic angle spinningEnvironmental ChemistryHumic acidParticle SizeHumic SubstancesAlkylchemistry.chemical_classificationChemistrySpectrum AnalysisPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryCarbon-13 NMRPollutionNMR spectra databaseHumic substancesSize-fractionationHPSECCPMAS-13C NMRUV and fluorescence spectrophotometryEnvironmental PollutantsEnvironmental MonitoringChemosphere
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2-Methyl-4-phenyl-3,4-dihydro­quinazoline

2011

The title compound, C15H14N2, was formed during the lithiation of 2-methylquinazoline with phenyllithium followed by hydrolysis of the intermediate lithium 2-methyl-4-phenyl-4H-quinazolin-3-ide. NMR spectra as well as single-crystal X-ray structural data indicate that the reaction product to have the same structure in chloroform solution as in the crystalline state. The phenyl substituent is twisted out of the plane of the 3,4-dihydroquinazoline ring system by 86.47 (7)°. In the crystal, intermolecular N—H...N interactions connect the molecules into infinite chains.

Substituentchemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic PapersReaction productlcsh:ChemistryNMR spectra databaseCrystalHydrolysischemistry.chemical_compoundCrystallographylcsh:QD1-999chemistryQuinazolineGeneral Materials ScienceLithiumta116Acta Crystallographica Section E: Structure Reports Online
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Syntheses and properties of some exo,exo-bis(isodicyclopentadienyl)titanium low-valent complexes

2002

Abstract The paramagnetic compounds exo,exo-bis(η5-isodicyclopentadienyl)chlorotitanium(III) (3) and its analogue with trimethylsilyl-substituted isodicyclopentadienide (isodiCp) ligand (4), and the similar pair of diamagnetic exo,exo-bis(isodicyclopentadienyl)[η2-bis(trimethylsilyl)ethyne]titanium(II) complexes 5 and 6 were obtained by common reduction procedures from exo,exo-bis(isodicyclopentadienyl)titanium(IV) dichloride (1) and exo,exo-bis[η5-2-(trimethylsilyl)isodicyclopentadienyl]titanium(IV) dichloride (2), respectively. As indicated by ESR spectroscopy compound 3 is a dimer in the solid state and in frozen toluene glass but monomeric in toluene solution. Compound 4 is monomeric in…

TrimethylsilylStereochemistryLigandDimerOrganic Chemistrychemistry.chemical_elementCrystal structureBiochemistryTolueneMedicinal chemistryInorganic ChemistryNMR spectra databasechemistry.chemical_compoundMonomerchemistryMaterials ChemistryPhysical and Theoretical ChemistryTitaniumJournal of Organometallic Chemistry
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Peptide synthesis with 5-amino-1-methyl-1H-[1,2,4]triazole-3-carboxylic acid

2007

Abstract In the search for the peptide synthesis of new potential lexitropsins, starting with methyl 5‐amino‐1‐methyl‐1H‐[1,2,4]triazole‐3‐carboxylate 1a, we synthesized the chloroacetyl derivative of 2a, which was hydrolyzed to acid 2b and ammonolyzed to the peptide 2c. A more effective route was the use of (t‐butoxycarbonyl)glycyl‐benzotriazolide 3 to the acylation 1a, which leads the N/C protected peptide 4. This peptide was selectively N‐deprotected to be the useful segment 5 for further peptide syntheses to the N‐terminus. It was also C‐deprotected, that is hydrolyzed to give peptide 2c for further C‐extension. To the best of our knowledge, this is the first peptide that is a derivativ…

chemistry.chemical_classification4]triazole-3-carboxylic acidStereochemistryNMR spectraLexitropsinCarboxylic acidAcylationOrganic Chemistry2124-TriazolePeptideGeneral MedicineCombinatorial chemistry5-amino-1-methyl-1H-[1Acylationchemistry.chemical_compoundHydrolysisPeptide synthesischemistryFTIR spectraHetareneamino acidPeptide synthesisBenzotriazolideDerivative (chemistry)Synthetic Communications
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Insights into catanionic vesicles thermal transition by NMR spectroscopy

2012

Oppositely charged ionic surfactants can self-assemble into hollow structures, called catanionic vesicles, where the anionic-cationic surfactant pair assumes a double-tailed zwitterionic attitude. In the present work, multilamellar- to-unilamellar thermal transition of a mixed aqueous system of sodium dodecyl sulphate (SDS) and cetyl trimethyl ammonium bromide (CTAB), with a slight excess of the anionic one, has been investigated by 1H, 2H, 14N NMR spectra and 23Na transverse relaxation measurements. It has been inferred that an increase of the temperature enhances the SDS counterion dissociation, which can be considered as one of the driving forces of the mentioned transition. Moreover, in…

chemistry.chemical_classificationAmmonium bromideAqueous solutionVesicleIonic bondingNuclear magnetic resonance spectroscopyDissociation (chemistry)NMR spectra databasechemistry.chemical_compoundchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPhysical chemistrylipids (amino acids peptides and proteins)Catanionic Vesicles NMR PGSTE Thermal TransitionCounterion
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Iron(II) Complexes with Scorpiand-Like Macrocyclic Polyamines: Kinetico-Mechanistic Aspects of Complex Formation and Oxidative Dehydrogenation of Coo…

2017

The Fe(II) coordination chemistry of a pyridinophane tren-derived scorpiand type ligand containing a pyridine ring in the pendant arm is explored by potentiometry, X-ray, NMR, and kinetics methods. Equilibrium studies in water show the formation of a stable [FeL]2+ complex that converts to monoprotonated and monohydroxylated species when the pH is changed. A [Fe(H–2L)]2+ complex containing an hexacoordinated dehydrogenated ligand has been isolated, and its crystal structure shows the formation of an imine bond involving the aliphatic nitrogen of the pendant arm. This complex is low spin Fe(II) both in the solid state and in solution, as revealed by the Fe–N bond lengths and by the NMR spect…

chemistry.chemical_classificationAqueous solution010405 organic chemistryLigandImineInorganic chemistryCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesCoordination complexInorganic ChemistryNMR spectra databasechemistry.chemical_compoundchemistryPolymer chemistryPyridineDehydrogenationPhysical and Theoretical ChemistryInorganic chemistry
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Historical and current progress in understanding the origin and structure of humic substances

2010

Research into humic substances (HS) has focused selectively on the search for aromatic structures. All aromatic compounds are regarded as eligible HS constituents, whereas aliphatic, polysaccharide structural constituents are considered non-HS. Wet chemical methods for analysing HS produce 2–5% aromatic compounds from the original starting material. Only those compounds in the hydrophobic extraction phases are studied carefully. Compounds in the hydrophilic extraction phases, containing mainly aliphatics, are discarded. Solid-state NMR spectra from HS show 30–40% of carbon–carbon unsaturation, which is selectively interpreted as ‘aromatic’. No recognition is given to the fact that NMR spect…

chemistry.chemical_classificationDegree of unsaturationEcologyExtraction (chemistry)Nuclear magnetic resonance spectroscopyPolysaccharideNMR spectra databasechemistry.chemical_compoundchemistryGeneral Earth and Planetary SciencesLigninOrganic chemistryMoleculeEcology Evolution Behavior and SystematicsGeneral Environmental ScienceChemistry and Ecology
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