Search results for "alkali"

showing 10 items of 566 documents

Kinetics of alkaline phosphatase from pig kidney. Influence of complexing agents on stability and activity

1976

Metal ion-complexing agents, like KCN, EDTA etc., inactivate alkaline phosphatase of pig kidney. This inactivation is reversible at low concentrations of the complexing agents and irreversible at high concentrations. The reversible inhibition is probably due to removal of Zn2+ ions from the active site, where they are necessary for catalytic action, whereas the irreversible inhibition results from the removal of Zn2+ ions necessary for preservation of the structure. The inactivation is pseudo-first order. It depends on the concentration, size and charge of the complexing agents. β-Glycerophosphate and Mg2+ ions protect the enzyme from inactivation by complexing agents. Quantitative examinat…

chemistry.chemical_classificationbiologyDimerInorganic chemistryAllosteric regulationKineticsSubstrate (chemistry)Active siteCell BiologyCombinatorial chemistryBiochemistrychemistry.chemical_compoundEnzymechemistrybiology.proteinAlkaline phosphataseChelationMolecular BiologyBiochemical Journal
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Organometallic complexes with biological molecules. XV. Effects of tributyltin(IV)chloride on enzyme activity, Ca2+, and biomolecule and synthesis in…

2001

Considerable attention has been given in recent years to the possibility that xenobiotics in the environment may affect reproduction in animals. In this study, the relative impact of tributyltin(IV) (TBT) chloride, one of the most toxic environmental pollutants, was investigated using Ciona intestinalis ovary as a model system. The pleiotropic effects of TBT exposure are concentration dependent and include a decrease of ATP levels, lipid content and nucleic acid content and synthesis. In contrast, a marked increase in calcium (Ca2+) and glucose content is observed. Furthermore, TBT alters enzymatic activity, inhibiting creatine kinase and stimulating alkaline phosphatase and cholinesterase …

chemistry.chemical_classificationbiologychemistry.chemical_elementGeneral ChemistryCalciumbiology.organism_classificationEnzyme assayInorganic Chemistrychemistry.chemical_compoundEnzymechemistryBiochemistryNucleic acidTributyltinbiology.proteinAlkaline phosphataseCiona intestinalisXenobioticApplied Organometallic Chemistry
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Decomposition of organic matter with molten alkali: determination of arsenic and antimony in organic compounds

1982

Decomposition of organic matter with molten alkali has been examined as a method of opening out organic matrices for elemental detection and/or determination. The fusion product is readily soluble. Arsenic and antimony in organic compounds can be determined iodimetrically after mineralization by this fusion method.

chemistry.chemical_classificationchemistryAntimonyInorganic chemistrychemistry.chemical_elementOrganic matterMineralization (soil science)Alkali metalDecompositionArsenicAnalytical ChemistryTalanta
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ChemInform Abstract: Synthesis, Structures and DFT Calculations on Alkaline-Earth Metal Azide-Crown Ether Complexes.

2008

The first examples of azide complexes of calcium, strontium or barium with crown ethers have been prepared and fully characterised, notably [Ba([18]crown-6)(N3)2(MeOH)], [Sr([15]crown-5)(N3)2(H2O)], [Ca([15]crown-5)(N3)2(H2O)] and [Sr([15]crown-5)(N3)(NO3)]. Crystal structures reveal the presence of a variety of coordination modes for the azide groups including 1-, -1,3- and linkages via H-bonded water molecules, in addition to azide ions. The [Ba([18]crown-6)(N3)2(MeOH)]1/3 MeOH contains dinuclear cations with three -1,3-NNN bridges, the first example of this type in main group chemistry. The structures obtained have been compared with molecular structures computed by density functional th…

chemistry.chemical_classificationchemistry.chemical_compoundCrystallographychemistryCoordination numberMoleculeIonic bondingEtherGeneral MedicineCrystal structureAzideAlkali metalCrown etherChemInform
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Über die möglichkeit der bildung makrocyclischer polyoxyniethylene. 29. mitt über polyoxymethylene1

1966

Bei der kationischen Polymerisation von 1,3,5-Trioxan in Cyclohexan entstehen Polyoxymethylene, welche partiell thermisch stabil und alkalibestandig sind, ohne das irgendwelche bekamiten stabilen Endgruppen nachgewiesen werden konnten. Moglicberweise handelt es sich hierbei um Makrocyclen. Cationic polymerization of 1,3,5-trioxan in cyclohexane yields polyoxymethylene which is partially stable to heat and to alkali but does not contain any of the known stable endgroups. These polymers possibly have a macrocyclic structure.

chemistry.chemical_classificationchemistry.chemical_compoundPolyoxymethylenePolymerizationCyclohexaneChemistryPolymer chemistryCationic polymerizationPolymerAlkali metalDie Makromolekulare Chemie
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Kronenethersubstituierte 1,4-Distyrylbenzole und ihre Komplexierung mit Alkalipikraten

2000

Crown Ether Substituted 1,4-Distyrylbenzenes and their Complexation with Alkali Picrates The 1,4-distyrylbenzenes 8 and 9, which contain two crown ether units, each, were prepared by Wittig—Horner reactions. Their complexation tendencies with alkali picrates (Li—Cs) in water/dichloromethane were investigated. Potas sium ions give the strongest complexes. Generally monomo-lecular 1:1-complexes are formed; however, [K-8] + [Pik]—, [K-9]+ [Pik]— and [Rb-8] + [Pik]— generate aggregates, for which a stairway structure is proposed.

chemistry.chemical_classificationchemistry.chemical_compoundchemistryOrganic chemistryAlkali metalMedicinal chemistryCrown CompoundsCrown etherDichloromethaneJournal für praktische Chemie
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Lithium Ion Recognition with Nanofluidic Diodes through Host-Guest Complexation in Confined Geometries

2018

[EN] The lithium ion recognition is receiving significant attention because of its application in pharmaceuticals, lubricants and, especially, in energy technology. We present a nanofluidic device for specific lithium ion recognition via host guest complexation in a confined environment. A lithium-selective receptor molecule, the aminoethyl-benzo-12-crown-4 (BC12C4-NH2), is designed and functionalized on single conical nanopores in polyethylene terephthalate (PET) membranes. The native carboxylic acid groups on the pore walls are covalently linked with the crown ether moieties and the process is monitored from the changes in the current voltage (I-V) curves. The B12-crown-4 moieties are kno…

chemistry.chemical_classificationchemistry.chemical_elementIon current02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryAlkali metal01 natural sciencesChloride0104 chemical sciencesAnalytical ChemistryIonchemistry.chemical_compoundMembranechemistryFISICA APLICADAmedicineLithium chlorideLithium0210 nano-technologyCrown ethermedicine.drug
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Untersuchungen zum oxidativen Abbau nativer Cellulose, 2. Einfluß der Alkalibehandlung auf die Viskositäts-Molekulargewichts-Beziehungen

1974

Um die Kinetik des oxidativen Abbaus nativer Cellulose viskosimetrisch verfolgen zu konnen, mussen neue [η]-M-Eichbeziehungen aufgestellt werden, da die Behandlung der Cellulose mit konzentriertem Alkali den Staudingerindex [η] erniedrigt, ohne das Molekulargewicht M zu verandern. Es wurden zwei Reihen oxidativ abgebauter, verschieden lange mit Alkali vorbehandelter Cellulosen hergestellt und an diesen die Konstanten der Kuhn-Mark-Houwink-Gleichung fur die Cellulosenitrate in Aceton und die Cellulosen in Cuoxam (Cu(NH3)4(OH)2) durch Vergleich mit Lichtstreuungsmessungen bestimmt. For kinetic studies of cellulose degradation by molecular oxygen it is necessary to establish new [η]-M-relation…

chemistry.chemical_compoundCellulose degradationChemistrySodium hydroxideIntrinsic viscosityPolymer chemistryAcetoneMolecular oxygenCelluloseAlkali metalDie Makromolekulare Chemie
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Die herstellung molekulareinheitlicher leiteroligomerer und einer molekulareinheitlichen hexaacrylsäure. IV. Mitt.: Modelle für matrizenreaktionen

1968

Die phenolischen Hydroxylgruppen molekulareinheitlicher Mehrkernverbindungen mit vier und funf pKresolbausteinen je Molekul konnten vollstandig mit Acrylsaurechlorid in Gegenwart von Triathylamin verestert werden. Lies man auf die in siedendem Benzol stark verdunnten mehrafachen Acrylsaureester einen Uberschus an Radikalen aus α.α′-Azoisobutyrodinitril einwirken, so bildeten sich mit guter Ausbeute molekulareinheitliche, dunnschichtchromatographisch reine Leiteroligomere. Die alkalische Verseifung des Leiteroilgomeren mit vier p-Kresolbausteinen gab eine molekulareinheitliche Hexaacrylsaure, die als Hexamethylester durch Elementaranalyse und Molekulargewicht charakterisiert wurde; die gefun…

chemistry.chemical_compoundChemistryHomogeneousRadicalPolymer chemistryReaction pathAlkaline hydrolysis (body disposal)Normal limitOligomerTriethylamineDie Makromolekulare Chemie
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Calix Crowns Derived from para-Bridged Calix[4]arenes

2000

Two calix[4]arenes, bridged by aliphatic chains of five and eight carbon atoms spanning two opposite para positions, have been converted into their 1,3-crown ether derivatives by reaction with tetraethylene and pentaethylene glycol ditosylates. Of the two possible 1,3-crown derivatives, only the formation of those isomers is observed in which the phenolic units connected at the para positions are etherified. This has been established in one case by a single-crystal X-ray analysis. Preliminary results for the extraction of selected alkali and alkaline-earth metals are reported.

chemistry.chemical_compoundChemistryOrganic ChemistryExtraction (chemistry)Organic chemistrychemistry.chemical_elementEtherPhysical and Theoretical ChemistryAlkali metalBiochemistryCarbonOrganic Letters
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