Search results for "ALK"

showing 10 items of 4314 documents

Enantioselective addition of Et2Zn to seven‐membered cyclic imines catalyzed by a (R)-VAPOL-Zn(II) complex

2017

Various substituted dibenzo[b,f][1,4]oxazepines underwent an enantioselective alkylation with Et2Zn catalyzed by a (R)-VAPOL-Zn(II) complex. The corresponding chiral 11-ethyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine derivatives were obtained with good yields and moderate enantioselectivities. This represents the first example of enantioselective addition of Et2Zn to cyclic aldimines.

chemistry.chemical_classificationAldimine010405 organic chemistryChemistryStereochemistryOrganic ChemistryEnantioselective synthesischemistry.chemical_elementZincAlkylation010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesCatalysischemistry.chemical_compoundCatàlisiDrug DiscoveryOxazepineQuímica orgànicaTetrahedron Letters
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Asymmetric Synthesis of Fluorinated Monoterpenic Alkaloid Derivatives from Chiral Fluoroalkyl Aldimines via the Pauson‐Khand Reaction

2020

chemistry.chemical_classificationAldiminechemistry.chemical_compoundchemistryPauson–Khand reactionAlkaloidEnantioselective synthesisOrganic chemistryGeneral ChemistryN-tert-butanesulfinyl imineOrganofluorine chemistryAdvanced Synthesis & Catalysis
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ChemInform Abstract: Calixcrowns : Synthesis and Properties

2009

The synthesis and properties of calix[n]crowns (n = 4–8), calix[n]biscrowns and their related compounds, resorcinarene crowns, have been discussed and reviewed. These macrocycles exhibit remarkable ionophoric properties toward alkali and alkaline earth metal cations, as well as, to tertiary amines. The selectivity and efficiency of calixcrowns in binding cations have been attributed to their structural features, which include substituent effects and size of the crown ether moiety and, conformation of the parent calixarene.

chemistry.chemical_classificationAlkaline earth metalChemistrySubstituentGeneral MedicineResorcinareneAlkali metalstomatognathic diseaseschemistry.chemical_compoundstomatognathic systemCalixarenePolymer chemistryMoietySelectivityCrown etherChemInform
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Behavior of Actinium, Alkaline, and Rare Earth Elements in Sr-Resin/Mineral Acid Systems

2015

In this work, the interactions between the divalent alkaline earth elements (AEE) (Sr, Ba, Ra), the trivalent rare earth elements (REE) (Ce-Lu, Y), and Ac(III) with Sr-resin were investigated in the presence of HNO3, HCl, HBr, HClO4, and HPF6. Distribution coefficients of these ions on the Sr-resin were determined under batch-loading conditions. Lastly, online column separations were performed to demonstrate the utility of these systems. Substantial differences in the behavior of the ions in solutions comprised of the five different acids were observed. These differences can partly be explained by a combination of ion exchange (primary) and extraction (solvation) mechanisms. From a practica…

chemistry.chemical_classificationAlkaline earth metalIon exchangeGeneral Chemical EngineeringExtraction (chemistry)Inorganic chemistrySolvationchemistry.chemical_elementMineral acidGeneral ChemistryDivalentIonActiniumchemistrySolvent Extraction and Ion Exchange
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Pseudopeptidic ligands: exploring the self-assembly of isophthaloylbisglycine (H2IBG) and divalent metal ions.

2012

We present a systematic study of the complexation of the new pseudopeptidic ligand isophthaloylbisglycine (H(2)IBG) with divalent metal ions of varying ionic radius. This work represents the initial employment of H(2)IBG in the coordination chemistry of alkaline earth, 3d transition, Zn(II) and Cd(II) metal elements. Infrared, NMR, thermal, magnetic, adsorption and theoretical studies of these compounds are also discussed.

chemistry.chemical_classificationAlkaline earth metalIonic radiusMagnetic Resonance SpectroscopySpectrophotometry InfraredInfraredLigandChemistryInorganic chemistryGlycineMolecular ConformationLigandsCoordination complexInorganic ChemistryMetalAdsorptionX-Ray DiffractionCoordination ComplexesMetalsDivalent metal ionsvisual_artvisual_art.visual_art_mediumQD0146ta116OligopeptidesDalton transactions (Cambridge, England : 2003)
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Crystal structure analysis of supramolecular arrangements in bis(1-isoquinolinecarboxamide)alkanes and their Ag(i) complexes

2017

A homologous series of bis(1-isoquinolinecarboxamide)alkane derivatives (3a–f) with two to seven carbon atoms in the alkyl bridge and their Ag(I) complexes (4a–f) have been synthesized. Four ligand and five Ag(I) complex crystal structures were obtained by single crystal X-ray diffraction and analyzed in terms of: a) their structural patterns based on intra- and intermolecular hydrogen bonds which were compared to those of bis(2-quinolinecarboxamide)alkanes (1n) and bis(6-quinolinecarboxamide)alkanes (2n) attending to specific geometrical parameters and b) the Ag(I) coordinate bond effect on these patterns and the amide-to-amide hydrogen bonds. The crystal structures of the ligands 3a, 3c, …

chemistry.chemical_classificationAlkane010405 organic chemistryLigandHydrogen bondStereochemistrySupramolecular chemistryGeneral ChemistryCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundHomologous seriesCrystallographychemistryAmideGeneral Materials ScienceAlkylCrystEngComm
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Continuum-uniform approach calculations of the solubility of hydrocarbons in water

1993

Abstract The ransfer free energies from gas phase to water for some hydrocarbons are calculated by means of a continuum-uniform model of the solvent. For the calculation of the cavitation energy a model based on the surface tension is proposed. The calculated values are compared with the experimental free energies obtained with and without a corrective factor that accounts for the difference in the solute—solvent sizes. Good agreement between the theoretical free energies and the corrected experimental data is obtained. Our calculations seem to show that the hydrophobic effect is directly related to the molecular surface area.

chemistry.chemical_classificationAlkaneAqueous solutionGeneral Physics and AstronomyThermodynamicsMineralogySolventHydrophobic effectSurface tensionHydrocarbonchemistryCavitationPhysical and Theoretical ChemistrySolubilityChemical Physics Letters
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Spin Transition of 1D, 2D and 3D Iron(II) Complex Polymers The Tug-of-War between Elastic Interaction and a Shock-Absorber Effect

2003

The structures of linear chain Fe(II) spin-crossover compounds of α,β- and α,ω-bis (tetrazol-1-yl)alkane type ligands are described in relation to their magnetic properties. The first threefold interlocked 3-D catenane Fe(II) spin-transition system, [μ-tris(1,4-bis(tetrazol-1-yl)butane-N1,N1′) iron(II)] bis(perchlorate), will be discussed. An analysis is made among the structures and the cooperativity of the spin-crossover behaviour of polynuclear Fe(II) spin-transition materials.

chemistry.chemical_classificationAlkaneCatenaneInorganic chemistrySpin transitionCooperativityGeneral ChemistryPolymerPerchloratechemistry.chemical_compoundCrystallographychemistrySpin crossoverTetrazoleMonatshefte f�r Chemie / Chemical Monthly
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1986

Poly(methylmethacrylate) (PMMA), poly(butylmethacrylate) (PBMA), and poly(decylmethacrylate) (PDMA) are completely miscible with toluene at normal pressure from room temperature up to the boiling point of the solvent. In alkanes (C6 to C10) and 1-pentanol the solubility increases with the length of the side chain of the polymer: PMMA always exhibits a solubility gap within the above temperature range, PBMA shows upper critical solution temperatures (except n-hexane, which is a non-solvent), and PDMA mixes completely with all alkanes under consideration. Alcohols (up to C4) are non-solvents for PMMA but theta solvents for PBMA and PDMA (except ethanol which is a non-solvent for the latter). …

chemistry.chemical_classificationAlkaneChemistryTheta solventPolymerTolueneSolventchemistry.chemical_compoundHydrocarbonChemical engineeringPolymer chemistrySide chainGeneral Materials ScienceSolubilityAngewandte Makromolekulare Chemie
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Preparation and characterisation of Na 2 S and ZnSO 4 nanoparticles in water/sodium bis(2-ethylhexyl)sulphosuccinate/ n -heptane microemulsions

2001

The preparation procedure for nanoparticles of the water-soluble salts Na2S and ZnSO4, two commonly used reagents to synthesise ZnS nanoparticles, by evaporation of volatile components of salt-containing water-in-oil microemulsions is described. In suitable conditions, the evaporation leads to the formation of dry salt–surfactant composites and to the formation of Na2S or ZnSO4 nanoparticles. It was found that the salt–surfactant composites can be totally redissolved in a dry apolar organic solvent allowing the formation of virtually water-free solutions containing a considerable amount of the water-soluble salts. The presence of nanoparticles in these solutions and in the composites has be…

chemistry.chemical_classificationAlkaneHeptanePolymers and PlasticsChemistryInorganic chemistryNanoparticleEvaporation (deposition)chemistry.chemical_compoundColloid and Surface ChemistryHydrocarbonChemical engineeringTernary compoundReagentMaterials ChemistryMicroemulsionPhysical and Theoretical ChemistryColloid & Polymer Science
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