Search results for "Protonation"

showing 10 items of 583 documents

1977

The investigation of electron transfer and subsequent reactions of divinylidene compounds not capable of anionic homopolymerization was extended to 1,3-bis(1-phenylvinyl)benzene (2). A new method for the preparation of this compound is described. Its reaction with Li, Na, and K as electron transfer reagents in THF as solvent results in an increasing yield in polymeric combination products of the radical anions formed primarily with increasing reducing power of the alkali metal. The main product, however, in any case is the cyclic dimeric tetra-anion of 2, which upon protonation yields 1,4,11,14-tetraphenyl[4.4]metacyclophane (3).

Solventchemistry.chemical_compoundElectron transferChemistryYield (chemistry)ReagentPolymer chemistryProtonationBenzeneAlkali metalDie Makromolekulare Chemie
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Guest-to-host proton transfer in melatonin-beta-cyclodextrin inclusion complex by ionspray, fast atom bombardment and tandem mass spectrometry.

2001

Ionspray (IS) and fast atom bombardment (FAB) positive ionization mass spectrometry (MS) of 1:1 β-cyclodextrin (β-CD)-melatonin (MLT) host-guest complex allowed the detection of gaseous protonated 1:1 β-CD-MLT. Tandem MS collision-induced dissociation (CID) of such protonated 1:1 β-CD-MLT species showed the proton (charge) to be retained to a significant extent by the host and by its cage fragmentation products, in spite of the higher proton affinity of MLT with respect to that of β-CD. This requires an endothermic guest-to-host proton transfer to occur within the gaseous association. Collisional activation could be accounted for by the promotion of such an endothermic process; however…

Spectrometry Mass Electrospray IonizationFast atom bombardmentTandem mass spectrometryAnalytical chemistryBeta-CyclodextrinsProtonationSpectrometry Mass Fast Atom BombardmentPhotochemistryTandem mass spectrometryDissociation (chemistry)Inclusion compoundchemistry.chemical_compoundFragmentation (mass spectrometry)CyclodextrinSpectroscopyβ-cyclodextrin host-guest complexeMelatoninCyclodextrinsbeta-Cyclodextrinsbeta-CyclodextrinFast atom bombardmentElectrosprayEndothermic guest-to-host proton transferAlgorithmchemistryIonsprayProton affinityAlgorithmsJournal of mass spectrometry : JMS
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Hydration/elimination reactions of trapped protonated fluoroalkyl triazines

2007

Spectrometry Mass Electrospray IonizationHydrocarbons FluorinatedTriazinesChemistryIONIZATION MASS-SPECTROMETRYWaterProtonationFLUORINATED HETEROAROMATIC-COMPOUNDS5-MEMBERED RINGSElimination reactionComputational chemistry2 HETEROATOMSProtonsHETEROCYCLESSpectroscopyJournal of Mass Spectrometry
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Entrapment of amino acids in gas phase surfactant assemblies: The case of tryptophan confined in positively charged (1R,2S)-dodecyl (2-hydroxy-1-meth…

2017

The ability of positively charged aggregates of the surfactant (1R,2S)‐dodecyl (2‐hydroxy‐1‐methyl‐2‐phenylethyl))dimethylammonium bromide (DMEB) to incorporate D-tryptophan or L-tryptophan in the gas phase has been investigated by electrospray ion mobility mass spectrometry (ESI‐IM‐MS). Strongly impacted by the pH of the electrosprayed solutions, both protonated (T+) and deprotonated (T-) tryptophan are effectively included into the aggregates, whereas, tryptophan in zwitterionic (T0) form is practically absent in singly charged DMEB aggregates but can be found in multiply charged ones. The ability to incorporate tryptophan increases with the aggregation number and charge state of aggr…

Spectrometry Mass Electrospray IonizationSurfactant aggregateCollision-induced dissociationIon mobilityMolecular ConformationProtonationRandom hexamerGas-phase self-assembly010402 general chemistryPhotochemistry01 natural sciencesGas‐phase self‐assemblychemistry.chemical_compoundSurface-Active AgentsDeprotonationBromideCationsOrganic chemistryMoietyDMEBSpectroscopyAggregation number010401 analytical chemistryTryptophanTryptophanStereoisomerism0104 chemical sciencesQuaternary Ammonium CompoundschemistryGasesJournal of mass spectrometry : JMS
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Infrared Difference Spectroscopy of Proteins: From Bands to Bonds

2020

Infrared difference spectroscopy probes vibrational changes of proteins upon their perturbation. Compared with other spectroscopic methods, it stands out by its sensitivity to the protonation state, H-bonding, and the conformation of different groups in proteins, including the peptide backbone, amino acid side chains, internal water molecules, or cofactors. In particular, the detection of protonation and H-bonding changes in a time-resolved manner, not easily obtained by other techniques, is one of the most successful applications of IR difference spectroscopy. The present review deals with the use of perturbations designed to specifically change the protein between two (or more) functional…

Spectrophotometry Infrared010405 organic chemistryInfraredChemistryMembrane ProteinsWaterHydrogen BondingProtonationGeneral ChemistryNanosecond010402 general chemistryVibration01 natural sciences0104 chemical sciencesIsotopic labelingChemical physicsMutagenesis Site-DirectedSide chainAnimalsHumansMoleculeAmino AcidsSpectroscopyRotational–vibrational couplingChemical Reviews
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Metal complexes of the carbonic anhydrase inhibitor methazolamide (Hmacm). Crystal structure of the Zn(macm)2 (NH3)2. Anticonvulsant properties of th…

1995

Complexes of Co(II), Cu(II), and Zn(II) with deprotonated methazolamide and ammonia are synthesized and characterized. The complex Zn(macm)2(NH3)2 crystallizes in the monoclinic C2/c space group with a = 13.468(1), b = 6.759(1), c = 23.014(2) A, beta = 90.27(1), and Z = 4. The structure was refined to R = 0.049 (Rw = 0.053). The Zn(II) ion is coordinated to two deprotonated sulfonamido nitrogen atoms of the macm- ligand and two nitrogen atoms of the ammonia ligands in a distorted tetrahedron. The Zn(macm)2(NH3)2 complex is shown to be a simple model for the methazolamide inhibition of CA. EHMO calculations applied to fractional coordinates of the Zn(macm)2(NH3)2 complex indicate that the at…

Spectrophotometry InfraredCations DivalentInorganic chemistryMethazolamidechemistry.chemical_elementCrystal structureZincCrystallography X-RayBiochemistryInorganic ChemistryMetalDeprotonationmedicineAnimalsMethazolamideHOMO/LUMOMolecular StructureChemistryLigandElectron Spin Resonance SpectroscopyCobaltZincCrystallographyvisual_artvisual_art.visual_art_mediumAnticonvulsantsCoppermedicine.drugMonoclinic crystal systemJournal of Inorganic Biochemistry
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Rhenium(I) and platinum(II) complexes with diimine ligands bearing acidic phenol substituents: hydrogen-bonding, acid-base chemistry and optical prop…

2010

Tricarbonylchloro-rhenium(i) (1-4) and catecholato-platinum(ii) complexes (6, 7) of diimine ligands bearing phenol and O-protected phenol substituents have been prepared and fully characterised including single crystal structure analyses of 1, 4 and 7. The redox behaviour of the catecholato platinum(ii) complexes 6 and 7 has been probed by cyclic voltammetry, preparative oxidation and EPR spectroscopy (6˙(+), 7˙(+)). Reversible deprotonation of the hydroxy substituted complexes 1, 3 and 6 to 1(-), 3(-) and 6(-) resulted in significant changes in their electronic spectra. The luminescence properties of the diamagnetic complexes have been investigated using emission spectroscopy. DFT and TD-D…

Spectrophotometry InfraredMolecular Conformationchemistry.chemical_elementPhotochemistryCrystallography X-RayLigandsRedoxlaw.inventionInorganic ChemistryDeprotonationlawCoordination ComplexesPolymer chemistryElectron paramagnetic resonanceDiiminePlatinumPhenolHydrogen bondHydrogen BondingRheniumRheniumchemistryQuantum TheorySpectrophotometry UltravioletIminesCyclic voltammetryPlatinumDalton transactions (Cambridge, England : 2003)
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Single-Molecule-Magnet Fe Fe and Antiferromagnetic Fe Coordination Clusters

2019

Supported by endogenous (part of the ligand, in-built) phenoxo bridges provided by the ligand 2,6-bis[{{(5-bromo-2-hydroxybenzyl)}{(2-(pyridylethyl)}amino}methyl]-4-methylphenol) (H3L), in its deprotonated form, exogenous (not part of the ligand, externally added or generated) oxo-/hydroxo- and acetato-bridged [FeII4FeIII2(O)2(O2CMe)4(L)2]·4Et2O (1) and [FeIII4(OH)2(O2CMe)3(L)2](ClO4)·3MeCN·2H2O (2) coordination clusters have been synthesized and structurally characterized. Complexes 1 and 2 have μ4-O and μ3-OH bridges, respectively. Magnetic studies on 1 reveal slow magnetic relaxation below 2 K. Both in-phase ( χ'M) and out-of-phase (χ″M) magnetic susceptibility were found to be frequency…

Spin states010405 organic chemistryChemistryLigand010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryCrystallographyDeprotonationMagnetAntiferromagnetismMagnetic relaxationSingle-molecule magnetPhysical and Theoretical Chemistry
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Spin Trapping of Carbon-Centered Ferrocenyl Radicals with Nitrosobenzene

2015

In contrast to metal centered 17 valence electron radicals, such as [Mn(CO)5]•, ferrocenium ions [Fe(C5H5)2]+ (1+), [Fe(C5Me5)2]+ (2+), [Fe(C5H5)(C5H4Et)]+ (3+), [Fe(C5H5)(C5H4NHC(O)Me)]+ (4+), and [Fe(C5H5)(C5H4NHC(S)Me)]+ (5+) do not add to nitrosobenzene PhNO to give metal-coordinated stable nitroxyl radicals. In the presence of the strong and oxidatively stable phosphazene base tert-butylimino-tris(dimethylamino)phosphorane, the quite acidic ferrocenium ions 1+–5+ are deprotonated to give a pool of transient and persistent radicals with different deprotonation sites [1–Hx]•–[5–Hx]•. One rather persistent iron-centered radical [4–HN]•, deprotonated at the nitrogen atom, has been detected…

Spin trappingRadicalOrganic ChemistryPhotochemistryPhosphoranelaw.inventionInorganic ChemistryMetalNitrosobenzenechemistry.chemical_compoundDeprotonationchemistrylawvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryElectron paramagnetic resonancePhosphazeneOrganometallics
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Correlation between the molecular structure and the kinetics of decomposition of azamacrocyclic copper(II) complexes

2015

The formation of copper(II) complexes with symmetrical dinucleating macrocyclic ligands containing two either monomethylated (L1) or trimethylated (L2) diethylenetriamine (Medien or Me3dien) subunits linked by pyridine spacers has been studied by potentiometry. Potentiometric studies show that L1 has larger basicity than L2 as well as higher stability of its mono- and binuclear complexes. The crystal structures of L1·6HCl (1), [Cu2(L1)Cl2](CF3SO3)2 (2), [Cu2(L1)(OH)](ClO4)3·3H2O (3) and [Cu(L1)](ClO4)2 (4) show that L1 adopts different coordination modes when bound to copper(II). Whereas in 2, each copper(II) is bound to one Medien subunit and to one pyridine group, in 3 each metal center i…

StereochemistryChemistryLigandchemistry.chemical_elementProtonationCrystal structureCopperDecompositionInorganic Chemistrychemistry.chemical_compoundCrystallographyPyridineDiethylenetriamineMolecule
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