Search results for "Anion"

showing 10 items of 488 documents

Divergent reactivity of nucleophilic 1-bora-7a-azaindenide anions

2017

The reactions of 1-bora-7a-azaindenide anions, prepared in moderate to excellent yields by reduction of the appropriate 1-bora-7a-azaindenyl chlorides with KC8 in THF, with alkyl halides and carbon dioxide were studied. With alkyl halides (CH2Cl2, CH3I and BrCH(D)CH(D)tBu), the anions behave as boron anions, alkylating the boron centre via a classic SN2 mechanism. This was established with DFT methods and via experiments utilizing the neo-hexyl stereoprobe BrCH(D)CH(D)tBu. These reactions were in part driven by a re-aromatization of the six membered pyridyl ring upon formation of the product. Conversely, in the reaction of the 1-bora-7a-azaindenide anions with CO2, a novel carboxylation of …

inorganic chemicalschemistry.chemical_classificationanionit010405 organic chemistryHalidechemistry.chemical_element010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic ChemistryNucleophilechemistryCarboxylation13. Climate actionbooriSN2 reactionReactivity (chemistry)Boronboronta116anionsAlkyl
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Bifunctional Acid-Base Catalysis

2011

Acid-base catalysis with bifunctional catalysts is a very prominent catalytic strategy in both small-molecule organocatalysts as well as enzyme catalysis. In both worlds, small-molecule catalysts and enzymatic catalysis, a variety of different general acids or hydrogen bond donors are used. In this chapter, important parallels between small molecule catalysts and enzymes are discussed, and a comparison is also made to the emerging field of frustrated Lewis pair catalysis.

inorganic chemicalschemistry.chemical_compoundchemistryHydrogen bondTetrahedral carbonyl addition compoundOxyanion holeBifunctionalCombinatorial chemistryFrustrated Lewis pairBifunctional catalystCatalysisEnzyme catalysis
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Ion pair recognition by ditopic crown ether based bis-urea and uranyl salophen receptors

2016

ionition pair bindingcrown ethersuranyl salophensureatitraussupramolecular chemistryditopic receptorsionisidosanion bindinguranyylisalofeenitkemialliset sidoksetkruunueetteritsupramolekyylikemia¹H NMR titrationsNMR-spektroskopiaorgaaniset yhdisteetröntgenkristallografiaX-ray crystallography
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Kompanjonu izīrēšanas fenomens Japānā

2018

Maģistra darbā „Kompanjonu izīrēšanas fenomens Japānā” tiek pētīta Japānas kompānijas izīrēšanas industrija, tās aizsākumi, līdzīgie modeļi, sabiedriskie un kulturālie cēloņi un ietekme uz Japānas sabiedrību. Mūsdienu Japānas sabiedrība cieš no vientulības un darba kultūras saistītām problēmām. Tāpēc izīrējamā kompanjona jautājums, īpaši jautājums par tā cēloņiem un ietekmi uz sabiedrību Japānai šobrīd ir ļoti aktuāls. Darba mērķi ir: Atrast izīrējama kompanjona vēsturiskos precedentus Noteikt profesijas veidošanas cēloņus un iemeslus popularitātei mūsdienās; Aprakstīt un kategorizēt izīrējamo kompanjonu veidus; Noskaidrot, kāda attieksme pret tāda veida profesijām pastāv Japānā. Tika secin…

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Anion Responsive Molecular Switch Based on a Doubly‐Strapped Calix[4]pyrrole

2022

A calix[4]pyrrole receptor bearing two proximally meso - meso linking isophthaloyl straps displays open and closed states depending on the calix[4]pyrrole conformation. In the crystal structures and in non-polar solvent, the calix[4]pyrrole adopts open 1,3-alternate conformation with straps on the sides. Anion binding triggers a closed state of the receptor providing two types of interactions with an aromatic benzoate guest: hydrogen bonds from the pyrrolic groups and π ··· π interactions from the phenyl groups of the straps. Slow exchange dynamics was observed on the NMR timescale indicating that benzoate, acetate and chloride anions, which bind with relatively low affinity get kinetically…

kemialliset sidoksetNMR spectroscopyvetysidoksetanionitcalix[4]pyrrolessupramolekulaarinen kemiaNMR-spektroskopiaheterosykliset yhdisteetanionssupramolecular chemistrymolecular switch
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LFER and the Effect of Temperature on Oxyanion Adsorption by Goethite

2019

A linear relationship between the Gibbs free energy, ΔGr,H+, of the aqueous complex deprotonation reaction, and the Gibbs free energy, ΔGr,ads, of bidentate surface complexation reaction of oxyanions was derived from modelling of temperature dependent batch equilibrium adsorption experiments. As exemplified in this study, this relationship may be exploited to predict temperature-dependent adsorption behavior of oxyanions not yet known such as pertechnetate.

lcsh:GE1-350DenticityGoethiteAqueous solutionInorganic chemistryOxyanionGibbs free energysymbols.namesakechemistry.chemical_compoundAdsorptionDeprotonationchemistryvisual_artvisual_art.visual_art_mediumsymbolsTaft equationPhysics::Chemical Physicslcsh:Environmental sciencesE3S Web of Conferences
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Chiral hemicucurbit[8]uril as an anion receptor: selectivity to size, shape and charge distribution

2017

A novel eight-membered macrocycle of the hemicucurbit[n]uril family, chiral (all-R)-cyclohexanohemicucurbit[8]uril (cycHC[8]) binds anions in a purely protic solvent with remarkable selectivity. The cycHC[8] portals open and close to fully encapsulate anions in a 1 : 1 ratio, resembling a molecular Pac-Man™. Comprehensive gas, solution and solid phase studies prove that the binding is governed by the size, shape and charge distribution of the bound anion. Gas phase studies show an order of SbF6− ≈ PF6− > ReO4− > ClO4− > SCN− > BF4− > HSO4− > CF3SO3− for anion complexation strength. An extensive crystallographic study reveals the preferred orientations of the anions within the octahedral cav…

macrocyclesanion receptorsvalikoivuushemicucurbituril
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Micelles in Mixtures of Sodium Dodecyl Sulfate and a Bolaform Surfactant

2006

Mixtures composed of water, sodium dodecyl sulfate (SDS), and a bolaform surfactant with two aza-crown ethers as polar headgroups (termed Bola C-16) were investigated by modulating the mole ratios between the components. The two surfactants have ionic and nonionic, but ionizable, headgroups, respectively. The ionization is due to the complexation of alkali ions by the aza-crown ether unit(s). Structural, thermodynamic, and transport properties of the above mixtures were investigated. Results from surface tension, translational self-diffusion, and small angle neutron scattering ( SANS) are reported and discussed. Interactions between the two surfactants to form mixed micelles result in a com…

mixed micellesIonic bondingEtherANGLE NEUTRON-SCATTERINGMicelleanionic surfactants; mixed micelles; neutron scatteringSurface tensionSurface-Active Agentschemistry.chemical_compoundPulmonary surfactantAQUEOUS-SOLUTIONSSodium sulfateanionic surfactantsElectrochemistrySurface TensionGeneral Materials ScienceSodium dodecyl sulfateSANS surfactant mixtures micellesMicellesSpectroscopyHYDROCARBON SURFACTANTSPHASE SEPARATION MODELChromatographyneutron scatteringSodium Dodecyl SulfateSurfaces and InterfacesCondensed Matter PhysicsSmall-angle neutron scatteringchemistryChemical engineeringLangmuir
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Polymorphism and Metallic Behavior in BEDT-TTF Radical Salts with Polycyano Anions

2012

Up to five different crystalline radical salts have been prepared with the organic donor BEDT-TTF and three different polynitrile anions. With the polynitrile dianion tcpd2− (=C[C(CN)2]32−), two closely related radical salts: α'-(ET)4tcpd·THF (1) (THF = tetrahydrofurane) and α'-(ET)4tcpd·H2O (2) have been prepared, depending on the solvent used in the synthesis. With the mono-anion tcnoetOH− (=[(NC)2CC(OCH2CH2OH)C(CN)2]−) two polymorphs with similar physical properties but different crystal packings have been synthesized: θ-(ET)2(tcnoetOH) (3) and β''-(ET)2(tcnoetOH) (4). Finally, with the mono-anion tcnoprOH− (=[(NC)2CC(OCH2CH2CH2OH)C(CN)2]−) we have prepared a metallic…

molecular conductorsGeneral Chemical EngineeringInorganic chemistrybis(ethylenedithio)tetrathiafulvalene; polycyano anions; molecular conductors; synthetic metals02 engineering and technology010402 general chemistry01 natural sciencesMedicinal chemistrysynthetic metalsInorganic ChemistryMetalCrystalbis(ethylenedithio)tetrathiafulvalenelcsh:QD901-999[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical SciencesGeneral Materials Sciencepolycyano anionsChemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSolventPolymorphism (materials science)visual_artvisual_art.visual_art_mediumlcsh:Crystallography0210 nano-technology
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Adsorption of methotrexate and calcium leucovorin onto cholestyramine in vitro.

2003

Abstract Methotrexate (MTX), an antimetabolite of folic acid, is a drug widely used in the treatment of different types of cancer. When high doses are administered, it is necessary to interrupt its action by administering calcium leucovorin (CaL). The main pathway of MTX and CaL elimination in humans occurs through the kidney, but about 10% is excreted in the faeces via the bile. Drugs, foods and sorbents in intestinal lumen modify MTX and CaL reabsorption. Individual and simultaneous studies on the adsorption of MTX and CaL from aqueous phosphate buffer by cholestyramine were carried out in order to calculate the adsorption process of MTX and CaL to cholestyramine, and to characterize the …

musculoskeletal diseasesDrugAntimetabolites Antineoplasticmedicine.drug_classmedia_common.quotation_subjectCholestyramine ResinLeucovorinPharmaceutical SciencePharmacologyAntimetabolitechemistry.chemical_compoundmedicineIon-exchange resinAnion Exchange Resinsmedia_commonLeucovorin CalciumKidneyCholestyramineChromatographyChemistryHydrogen-Ion Concentrationstomatognathic diseasesmedicine.anatomical_structureMethotrexateAntifolateMethotrexateAdsorptionmedicine.drugInternational journal of pharmaceutics
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