Search results for "Protonation"

showing 10 items of 583 documents

Fluorescence enhancement of quinolines by protonation.

2020

A study of the fluorescence enhancement of isoquinoline, acridine (benzo[b]quinoline) and benzo[h]quinoline is reported with six organic acids of different pKa values. Protonation was found to be an effective tool in the fluorescence enhancement of quinolines. A significant increase in the fluorescence intensity is observed only when strong acids are used, resulting in an over 50-fold increase in fluorescence with trifluoroacetic or benzenesulfonic acid and isoquinoline in a 1.5 : 1 ratio. The benzenesulfonic acid was found to be the most effective in the protonation of the bases despite its higher pKa value compared to trifluoro- and trichloroacetic acid. The X-ray crystal structures of 14…

aromaattiset yhdisteet010405 organic chemistryHydrogen bondprotonationGeneral Chemical Engineering116 Chemical sciencesQuinolinefluoresenssifluorescence enhancementProtonationGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryFluorescence3. Good health0104 chemical scienceschemistry.chemical_compoundBenzenesulfonic acidchemistryAcridineTrichloroacetic acidIsoquinolineRSC advances
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Proton‐Gated Ring‐Closure of a Negative Photochromic Azulene‐Based Diarylethene

2020

Abstract Proton‐responsive photochromic molecules are attractive for their ability to react on non‐invasive rapid optical stimuli and the importance of protonation/deprotonation processes in various fields. Conventionally, their acidic/basic sites are on hetero‐atoms, which are orthogonal to the photo‐active π‐center. Here, we incorporate azulene, an acid‐sensitive pure hydrocarbon, into the skeleton of a diarylethene‐type photoswitch. The latter exhibits a novel proton‐gated negative photochromic ring‐closure and its optical response upon protonation in both open and closed forms is much more pronounced than those of diarylethene photoswitches with hetero‐atom based acidic/basic moieties. …

azulenenegative photochromismProtonation010402 general chemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compoundPhotochromismDeprotonationDiaryletheneMoleculeMolecular switchphotochemistryPhotoswitch010405 organic chemistryCommunicationPhotoswitchesGeneral ChemistryAzuleneCommunications3. Good health0104 chemical sciences540 Chemie und zugeordnete Wissenschaftenchemistryacid-base equilibriaddc:540diarylethene
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[Et4N][7-Me2S-nido-B11H12]

2003

Tetraethylammonium 7-dimethylsulfanyl-nido-dodecahydroundecaborate, [Et(4)N][7-Me(2)S-nido-B(11)H(12)] or C(8)H(20)N(+).C(2)H(18)B(11)S(-), is a product of the deprotonation of [7-Me(2)S-nido-B(11)H(13)] with KHBEt(3) and precipitation with tetraethylammonium chloride. The effect of removing one endo-terminal H atom is to cause a general contraction of the open-face B-B distances.

biology010405 organic chemistryPrecipitation (chemistry)ChemistryInorganic chemistryGeneral MedicineCrystal structure010402 general chemistry01 natural sciencesChlorideMedicinal chemistryGeneral Biochemistry Genetics and Molecular Biology0104 chemical sciencesDeprotonationmedicinebiology.proteinMoleculemedicine.drugOrganic anionActa Crystallographica Section C Crystal Structure Communications
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Cluster and Periodic Calculations of the Ethene Protonation Reaction Catalyzed by theta-1 Zeolite: Influence of Method, Model Size, and Structural Co…

2001

The protonation of ethene by three different acid sites of theta-1 zeolite was theoretically studied to analyze the extent and relevance of the following aspects of heterogeneous catalysis: the local geometry of the Bronsted acid site in a particular zeolite, the size of the cluster used to model the catalyst, the degree of geometry relaxation around the active site, and the effects related to medium- and long-range interactions between the reaction site and its environment. It has been found that while the reaction energy is very sensitive to the local geometry of the site, the activation energy is mainly affected by the methodology used and by electrostatic effects on account of the carbo…

biologyChemistryOrganic ChemistryActive siteProtonationGeneral ChemistryActivation energyHeterogeneous catalysisCatalysisCatalysisAb initio quantum chemistry methodsComputational chemistryChemical physicsbiology.proteinBrønsted–Lowry acid–base theoryZeoliteChemistry
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Azide and chloride binding to carboxypeptidase A in the presence of L-phenylalanine

1990

The interaction of chloride with native and cobalt (Co)-substituted carboxypeptidase-A (CPD) has been investigated by 35Cl nuclear magnetic resonance (NMR) spectroscopy in the presence and absence of L-Phe. The affinity constants of azide and chloride toward the Co(II)CPD·L-Phe complex have been measured by electronic spectroscopy. The correlation times determining T1 and T2 for the 35Cl nuclei are related to movements inside the cavity. In the presence of L-Phe, the anions bind to the metal with a relatively high affinity at pH values below 6. Anion binding to the Co enzyme can be analyzed in terms of the three protonation state model for the enzyme (EH2 α EH α E). In the presence of L-Phe…

biologyInorganic chemistryActive sitePhenylalanineProtonationBiochemistryChlorideMedicinal chemistryInorganic ChemistryMetalchemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumbiology.proteinmedicineCarboxypeptidase AAzideAnion bindingmedicine.drugJournal of Inorganic Biochemistry
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Computational Modeling of Biological Systems: The LDH Story

2010

Lactate dehydrogenases, LDH, catalyzed reaction has been used in this chapter as a conductor wire to present the evolution and difficulties on computing methods to model chemical reactions in enzymes, since the early calculations based at semiempirical level carried out in gas phase to the recent sophisticated simulations based on hybrid Quantum Mechanical/Molecular Mechanics Dynamics (QM/MM MD) schemes. LDH catalyzes the reversible transformation of pyruvate into lactate. The chemical step consists in a hydride and a proton transfer from the cofactor (NADH) and a protonated histidine (His195), respectively. This fact has generated a lot of controversy about the timing of both transfers in …

biologyProtonChemistryHydridebiology.proteinActive siteThermodynamicsProtonationPotential of mean forceChemical reactionQuantumEnzyme catalysis
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Dehydrochlorination of Hexachlorocyclohexanes Catalyzed by the LinA Dehydrohalogenase. A QM/MM Study

2015

The elucidation of the catalytic role of LinA dehydrohalogenase in the degradation processes of hexachlorocyclohexane (HCH) isomers is extremely important to further studies on the bioremediation of HCH polluted areas. Herein, QM/MM free energy simulations are employed to provide the details of the dehydrochlorination reaction of two HCH isomers (γ and β). In particular, the role of the protonation state of one of the catalytic residues-His73-is explored. Based on our calculations, two distinct minimum free energy pathways (concerted and stepwise) were found for γ-HCH and β-HCH. The choice of the reaction channel for the dehydrochlorination reactions of γ- and β-HCH was shown to depend on t…

biologyProtonConcerted reactionStereochemistryHexachlorocyclohexaneActive siteProtonationSurfaces Coatings and FilmsCatalysisQM/MMchemistry.chemical_compoundchemistryComputational chemistryMaterials Chemistrybiology.proteinDegradation (geology)Physical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Potential ATPase mimics by polyammonium macrocycles: Criteria for catalytic activity

1992

Abstract A series of polyammonium macrocycles, ranging in size from the 18-membered ring [18]aneN6 to the 36-membered [36]aneN12 were examined as potential ATPase mimics. The rates of hydrolysis of ATP were followed at pH 3.0 and 7.0 using 31P NMR and HPLC techniques. Stability constants as a function of degree of protonation, distribution curves for the ligands as a function of pH, and distribution curves for the mixed species of nucleotides, inorganic phosphate, and macrocycle were also determined. All of the macrocycles catalyzed the hydrolysis of ATP to some extent compared to noncatalyzed hydrolysis. A critical dependence on macrocyclic ring size was observed, with [21]aneN7 being the …

biologyStereochemistryATPaseOrganic ChemistryProtonationCrystal structureRing (chemistry)PhosphateBiochemistryRing sizeHydrolysisCrystallographychemistry.chemical_compoundchemistryATP hydrolysisDrug Discoverybiology.proteinMolecular BiologyBioorganic Chemistry
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Effect of buffer nature and concentration on the chromatographic performance of basic compounds in the absence and presence of 1-hexyl-3-methylimidaz…

2019

Abstract In reversed-phase liquid chromatography, the performance for basic compounds is affected by the interaction of the protonated (cationic) species with the anionic free silanols on the alkyl-bonded stationary phases. Using aqueous-organic mobile phases in the absence of additives, the retention may be too high, and the peaks be broad and asymmetric. The performance is improved by addition to the mobile phase of ionic liquids, from which 1-hexyl-3-methylimidazolium chloride ([C6MIm][Cl]) has especially good characteristics. A recent report has also revealed that the use of the phosphate system as buffer, at varying concentration and pH, may have a significant role in the chromatograph…

buffer systemsAcetonitrilesAdrenergic beta-AntagonistsIonic LiquidsProtonationBuffers010402 general chemistry01 natural sciencesBiochemistryChlorideAnalytical Chemistryionic liquidschemistry.chemical_compoundreversed-phase liquid chromatographyBoratesmedicineFormateβ-Adrenoceptor antagonistsChromatography High Pressure LiquidChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryCationic polymerizationImidazolesWatersilanol effectGeneral MedicineReversed-phase chromatographyHydrogen-Ion ConcentrationPhosphate0104 chemical sciencesSilanolchemistryIonic liquidSolventsmedicine.drug
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Polyaminocyclodextrin nanosponges: synthesis, characterization and pH-responsive sequestration abilities

2016

New pH-responsive nanosponges were obtained by reacting four different polyaminocyclodextrins with heptakis-(6-bromo)-(6-deoxy)-β-cyclodextrin. The materials obtained were characterized by various techniques (FT-IR, potentiometric titration, differential scanning calorimetry (DSC), porosimetry (BET), 13C{1H} CP-MAS NMR). Their adsorption abilities at different pH values were verified towards a suitable set of model guests, and seem mainly controlled by electrostatic interactions, as a function of the protonation/charge status of the polymer matrix. By contrast, data positively point out a lesser importance assumed by the induced-fit effect, important in affecting the formation of host–guest…

chemistry.chemical_classification010405 organic chemistryChemistryGeneral Chemical EngineeringPotentiometric titrationInorganic chemistryAnalytical chemistryProtonationGeneral ChemistryPolymerPorosimetrySettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciences0104 chemical sciencesMatrix (chemical analysis)Differential scanning calorimetryAdsorptionCyclodextrin Polyamine Nanosponge Polymer Supramolecular ChemistryHeteronuclear moleculeSettore CHIM/02 - Chimica Fisica
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