Search results for "Proton"

showing 10 items of 5886 documents

Bis(triorganometal) and diorganometal 1,3-dithiolates (R3M)2(C6H3XS2) and R2M(C6H3XS2) (M = Sn, Pb; X= H, Cl)

1984

Abstract Bis(triorganometal) and diorganometal 1,3-dithiolates (R3M)2(C6H3XS2) (C6H5XS2 1,3-dithiobenzene (for X = H) or 1,3-dithio-4-chlorobenzene (for X = Cl); M = Sn, X = Cl, R = CH3, C6H5; M = Pb, X = H, Cl, R = CH3, C2H5) and R2M(C6H3XS2) (R = CH3, C2H5, C6H5; M = Sn, X = Cl; M = Pb, X = H, Cl) have been prepared as the first organometal IVB derivatives of 1,3-dithiols, and investigated by vibrational, 1H NMR, and (in the case of organotin compounds) Mossbauer spectroscopy. The triorganometal derivatives are monomeric and the diorganometal derivatives dimeric in solution (37° C). For the latter a twelve-membered ring structure is proposed for both solution and the solid state.

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryDithiolNuclear magnetic resonance spectroscopyRing (chemistry)BiochemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerMössbauer spectroscopyMaterials ChemistryProton NMRMoleculePhysical and Theoretical ChemistryInorganic compoundJournal of Organometallic Chemistry
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Synthesis and protonation behaviour of the macrocycle 2,6,10,13,17,21-hexaaza[22]metacyclophane. Thermodynamic and NMR studies on the interaction of …

1996

Abstract The novel cyclophane receptor 2,6,10,13,17,21-hexaaza[22]metacyclophane (L) has been synthesised and characterised. The acid-base behaviour and interaction with ATP, ADP and AMP have been studied by potentiometry in 0.15 mol dm−3 at 298.1 K and multinuclear NMR. L presents in its protonated forms a molecular organization which enables its multipoint binding with nucleotides. Salt-bridge formation occur between the polyammonium sites of L and the phosphate chain of the nucleotides while π-stacking between the meta-phenylene subunit incorporated in the receptor and the adenine ring of the nucleotides.

chemistry.chemical_classificationChemistryStereochemistryProtein subunitProtonationRing (chemistry)Inorganic Chemistrychemistry.chemical_compoundDiamineMaterials ChemistryNucleotideATP–ADP translocasePhysical and Theoretical ChemistryPolyamineCyclophaneInorganica Chimica Acta
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ChemInform Abstract: Enantioselective Synthesis of α-Quaternary Amino Acids by Alkylation of Deprotonated α-Aminonitriles.

2015

An α-alkylation of deprotonated α-amino nitriles, prepared from chiral phenyldioxanamine (I) by Strecker reaction, leads to α-quaternary arylglycines with high optical purity after hydrolysis and oxidative cleavage of the chiral auxiliary.

chemistry.chemical_classificationChiral auxiliarychemistry.chemical_compoundHydrolysisDeprotonationchemistryStrecker amino acid synthesisEnantioselective synthesisGeneral MedicineAlkylationEnantiomeric excessMedicinal chemistryAmino acidChemInform
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Hydrophobic and cation exchange mechanisms in the retention of basic compounds in a polymeric column.

2004

A cation exchange retention mechanism concomitant with the well-known hydrophobic partition mechanism in a polymeric column has been observed and investigated. This exchange process is attributed to ionization of some acidic sites present in the polymer column at basic mobile phase pH values. Several drugs of different basicity have been chromatographed on a polymeric PLRP-S column with methanol-water and acetonitrile-water mobile phases. The cation exchange between the protonated basic drug and the buffer cations (Na+, K+ and BuNH4+) is observed at the pH range where the protonated drug and the ionized sites of the column coexist. This process produces a shift of the retention versus pH pl…

chemistry.chemical_classificationChromatographyBase (chemistry)ChemistryPolymersOrganic ChemistryProtonationGeneral MedicinePolymerHydrogen-Ion ConcentrationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHydrophobic effectIonizationPhase (matter)Cation Exchange ResinsColumn (data store)Journal of chromatography. A
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Spectrophotometric Determination of Cystine with O-Phthalaldehyde in the Absence of Thiol

1988

Abstract A spectrophotometric method for the determination of cystine with o-phthalaldehyde (OPA) in the absence of thiol is described. When cystine is heated at 60[ddot]C for 30 min in a low excess of OPA (pH 9.5), a very stable derivative with 1:2 stoichiometry (cystine:OPA) and an absorption maximum at 335 nm (E = 4600) is formed. At pH < 1 the derivative is protonated (protonation constants: log K1 = 5.88 and log K2 = 3.70 at I = 0.1 and 20[ddot]C) and another absorption band at 440 nm (E = 3800) appears, which allows the determination of cystine in the presence of other amino acids.

chemistry.chemical_classificationChromatographyBiochemistry (medical)Clinical BiochemistryCystineProtonationBiochemistryAnalytical ChemistryAmino acidchemistry.chemical_compoundO-PhthalaldehydechemistryElectrochemistryThiolAbsorption (chemistry)SpectroscopyDerivative (chemistry)StoichiometryNuclear chemistryAnalytical Letters
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Electrospray Ionization Mass Spectrometry of Non-Covalent Complexes Formed between N-Alkylimidazolium-Containing Zwitterionic Sulfonates and Protonat…

2015

This paper describes non-covalent complexes between zwitterionic 3-(1-alkyl-3 N-imidazolio)-propane-1-sulfonates and different amines. Electrospray ionization (ESI) mass spectrometry and collision-induced dissociation were used to measure the stability of such complexes in solution and in the gas phase. Generally, zwitterionic sulfonates formed more abundant complexes with protonated 5-methylcytosine (5-MCH) than with aliphatic amines. The results show that the association constants and half-dissociation threshold energies of these complexes nonlinearly depend on the alkyl chain length of the zwitterion. It is shown that the complexes with the lowest stability exist in acetonitrile solutio…

chemistry.chemical_classificationCollision-induced dissociationHydrogen bondElectrospray ionizationProtonationGeneral MedicineMass spectrometryAtomic and Molecular Physics and OpticsDissociation (chemistry)chemistry.chemical_compoundchemistryComputational chemistryZwitterionSpectroscopyAlkylEuropean Journal of Mass Spectrometry
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Impedance spectroscopy characterization of functionalized alumina membranes

2005

Abstract Anodic alumina membranes have been impregnated with a protonic conductor either by immersion or by vacuum permeation of a saturated aqueous solution of CsHSO4 for different times. Synthetized salt, obtained through the reaction of cesium carbonate with sulphuric acid (in excess), contained a small quantity of Cs2SO4. Unmodified membranes consist of amorphous Al2O3 with a regular distribution of pores (average diameter: 200 nm) and are stable up to 850 °C. Long impregnation times caused partial dissolution of alumina, with formation of Al(HSO4)3 on the front surfaces as well as into pore walls. From the frequency dispersion of the impedance, the “macroscopic conductivity” of membran…

chemistry.chemical_classificationConductivityMaterials scienceAnalytical chemistrychemistry.chemical_elementSalt (chemistry)Impedance spectroscopyAlumina membraneGeneral ChemistryConductivityPermeationCondensed Matter PhysicsDielectric spectroscopyAmorphous solidProtonic conductorMembranechemistryCaesiumGeneral Materials ScienceDissolution
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Weak non-covalent interactions control the relative molecular orientation in the crystals of N-pentafluorobenzyl aniline derivatives

2010

The crystal structures of N-pentafluorobenzyl aniline derivatives are controlled by versatile aromatic–aromatic interactions between the electron deficient and electron rich aromatics; the parent compound (1) possesses an L shape while protonation (2–5) induces a conformational change resulting in a planar arrangement of molecules which pack in layer type structures with different molecular orientations.

chemistry.chemical_classificationConformational changeChemistryChemieProtonationGeneral ChemistryCrystal structureElectronCondensed Matter PhysicsCrystallographychemistry.chemical_compoundAnilineNon-covalent interactionsMoleculeGeneral Materials ScienceLayer (electronics)CrystEngComm
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Synthesis, Protonation and Cu II Complexes of Two Novel Isomeric Pentaazacyclophane Ligands: Potentiometric, DFT, Kinetic and AMP Recognition Studies

2008

The synthesis and coordination chemistry of two novel ligands, 2,6,9,12,16-pentaaza[17]metacyclophane (L1) and 2,6,9,12,16-pentaaza[17]paracyclophane (L2), is described. Potentiometric studies indicate that L1 and L2 form a variety of mononuclear complexes the stability constants of which reveal a change in the denticity of the ligand when moving from L1 to L2, a behaviour that can be qualitatively explained by the inability of the paracyclophanes to simultaneously use both benzylic nitrogen atoms for coordination to a single metal centre. In contrast, the formation of dinuclear hydroxylated complexes is more favoured for the paraL2 ligand. DFT calculations have been carried out to compare …

chemistry.chemical_classificationCoordination sphereDenticityLigandChemistryStereochemistryPotentiometric titrationProtonationCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographyMoleculeCyclophaneEuropean Journal of Inorganic Chemistry
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1H,13C and17O NMR study of chlorovanillins and some related compounds

1992

1H, 13C and 17O NMR chemical shifts and nJ(H,H), 1J(C,H) and 3J(C-6, H-formyl) spin—spin coupling constants of chlorinated vanillins (3-methoxy-4-hydroxybenzaldehydes) were determined. The variation in the long-range 4J(H,H) value between the formyl proton and an ortho-proton suggests that the ortho-substituent strongly forces the formyl group out of the aromatic plane. This can also be observed by considering the 3J(C-6,H-formyl) values and the 13C and 17O NMR chemical shifts. The 17O NMR chemical shifts show a linear correlation with the torsion angle of the formyl group calculated by molecular mechanics. The 13C and 17O NMR chemical shifts of the methoxyl group also possess strong predic…

chemistry.chemical_classificationCoupling constantProtonCarbon-13 NMR satelliteStereochemistryChemical shiftGeneral ChemistryNuclear magnetic resonance spectroscopyDihedral angleAldehydeCrystallographychemistryGroup (periodic table)General Materials ScienceMagnetic Resonance in Chemistry
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