Search results for "polymerization"

showing 10 items of 1689 documents

Isolation of enantiomerically pure organometallic palladium compounds: synthesis of the triangles prepared from enantiopure [cis-Pd2(C6H4PPh2)2(NCCH3…

2009

Reaction of the racemic [Pd(C(6)H(4)PPh(2))Br](4) () with the silver salt of 1R-(1alpha,2beta,3alpha)]-3-methyl-2-(nitromethyl)-5-oxocyclopentaneacetate, (R)-AgO(2)CR*, results in the formation of a mixture of diastereoisomers (RRR)- and (SRR)- of the formula Pd(2)(C(6)H(4)PPh(2))(2)(O(2)CR*)(2) that were separated by standard chromatographic methods. Each diastereoisomer was readily converted into the tetrametallic stereoisomers (SS)- and (RR)-, of the formula [Pd(C(6)H(4)PPh(2))Br](4) that were isolated and characterized by X-ray crystallography. The R enantiomer of the solvated cationic species [cis-Pd(2)(C(6)H(4)PPh(2))(2)(NCCH(3))(4)](2+), obtained from (RR)-, was reacted with ammonium…

chemistry.chemical_classificationChemistryStereochemistryCationic polymerizationDiastereomerSalt (chemistry)chemistry.chemical_elementInorganic Chemistrychemistry.chemical_compoundEnantiopure drugAmmonium31p nmr spectroscopyEnantiomerPalladiumDalton Transactions
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Chiral Lanthanocene Derivatives Containing Two Linked Amido−Cyclopentadienyl Ligands:  Heterobimetallic Structure and Lactone Polymerization Activity

1997

Reaction of 2 equiv of dilithium amido−cyclopentadienide Li2(C5R4SiMe2NCH2CH2X) (C5R4 = C5Me4, C5H3tBu; X = OMe, NMe2) with anhydrous LnCl3 (Ln = Y, Lu) gave C2-symmetric complexes of the type Li[Ln(η5:η1-C5R4SiMe2NCH2CH2X)2] containing a heterobimetallic core. The molecular structure of Li[Y(η5:η1-C5Me4SiMe2NCH2CH2OMe)2] was determined by single-crystal X-ray structural analysis, which showed it to exhibit both a pseudotetrahedral yttrium as well as a tetrahedral lithium center. In accordance with a formal 20-electron configuration at the rare earth metal center Ln, the amido-nitrogen atoms are shown to be pyramidalized. In the case of Li[Y(η5:η1-C5H3tBuSiMe2NCH2CH2X)2], mixtures of the tw…

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryDiastereomerchemistry.chemical_elementYttriumInorganic ChemistryDilithiumCrystallographychemistry.chemical_compoundPolymerizationCyclopentadienyl complexMoleculeLithiumPhysical and Theoretical ChemistryLactoneOrganometallics
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Bis(oxalato)chromium(III) complexes: Versatile tectons in designing heterometallic coordination compounds

2011

Abstract The mononuclear oxalato-containing chromium(III) complexes of general formula [Cr(AA)(C2O4)2]− (AA = α-diimine type ligand) are able to produce a large variety of heterometallic complexes by acting as ligands towards either fully solvated metal ions or preformed cationic complexes with available coordination sites. This review focuses on the structural diversity of the polynuclear complexes (oligonuclear and coordination polymers) which are generated by the bis(oxalato)chromate(III) species, with a special emphasis to their magnetic properties.

chemistry.chemical_classificationChromate conversion coatingbiologyChemistryStereochemistryLigandMetal ions in aqueous solutionCationic polymerizationStructural diversitychemistry.chemical_elementASPHCoordination complexInorganic ChemistryChromiumPolymer chemistryMaterials Chemistrybiology.proteinPhysical and Theoretical ChemistryCoordination Chemistry Reviews
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Hydrophobicity of Ionizable Compounds. A Theoretical Study and Measurements of Diuretic Octanol−Water Partition Coefficients by Countercurrent Chroma…

1999

Countercurrent chromatography was used to determine the octanol−water partition coefficients (Po/w) of 23 diuretic drugs. The measured Po/w values ranged over 4 orders of magnitude from 0.05 to 550 (−1.3 < log Po/w < +2.7). All the compounds, except spironolactone, were ionizable. The Po/w values were strongly depending on the aqueous-phase pH. A theoretical model linking these values with the pH was derived for four cases:  (i) molecular acid−anionic base, (ii) cationic acid−molecular base, (iii) biprotic systems with two acidic or basic groups showing the same charge sign, and (iv) biprotic systems with ionizable groups showing different charges with special attention to the amino acid ca…

chemistry.chemical_classificationChromatographyBase (chemistry)Ammonium phosphateCarboxylic acidCationic polymerizationAnalytical chemistryAnalytical ChemistryPartition coefficientchemistry.chemical_compoundCountercurrent chromatographychemistryAmine gas treatingIonic compoundAnalytical Chemistry
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Influence of the presence of surfactants and humic acid in waters on the indophenol-type reaction method for ammonium determination.

2005

Abstract This work has evaluated the influence of humic acid and/or surfactants in the quantification of ammonium in waters with the indophenol-type reaction method. Thymol has been employed with the colorimetric method for sample ammonium concentrations between 0.25 and 1 mg L −1 . In addition, SPE/diffuse reflectance method has been used for quantification of ammonium at low concentrations (between 0.025 and 0.25 mg L −1 ). Matrix effect owing to humic substances were observed with the colorimetric method when the concentration was equal or higher than 25 mg L −1 . Lower concentrations of humic compounds produced matrix effects with the more sensitive SPE/diffuse reflectance method. Gener…

chemistry.chemical_classificationChromatographyCationic polymerizationcomplex mixturesColorimetry (chemical method)Analytical Chemistrychemistry.chemical_compoundchemistryStandard additionHumic acidAmmoniumSolid phase extractionIndophenolDerivatizationTalanta
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Influence of Thermal Annealing on the Thermodynamic and Mass-Transfer Kinetic Properties of d- and l-Phenylalanine Anilide on Imprinted Polymeric Sta…

1999

An investigation of the material, chromatographic, thermodynamic, and kinetic properties of thermally treated (i.e., annealed) polymeric stationary phases imprinted with l-phenylalanine anilide (l-PA) was carried out. The imprinting procedure of the solid phase used in this study was the same as for the untreated imprinted stationary phase studied previously. However, after polymerization, these new stationary phases were treated at elevated temperatures (50, 120, 140, and 160 °C) for 24 h. The treatment at 120 and 140 °C led to a larger decrease in the retention of l-PA than that of d-PA. The polymer treated at 160 °C could no longer resolve the d,l-PA racemate. The heat treatments were ac…

chemistry.chemical_classificationChromatographyChemistryKineticsThermal treatmentPolymerAnalytical ChemistryAdsorptionPolymerizationChemical engineeringMass transfermedicineMoleculeSwellingmedicine.symptomAnalytical chemistry
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Development of a semiautomated procedure for the synthesis and evaluation of molecularly imprinted polymers applied to the search for functional mono…

2001

Abstract A previously described scaled-down version of the established monolith procedure, where molecularly imprinted polymers (MIPs) are prepared on the bottom surface of chromatographic vials [Anal. Chem. 71 (1999) 2092] has been here further optimised with respect to its full automation. The protocol results in savings of time and reagents compared to the monolith procedure, allowing ca. 60 polymers (∼50 mg each) to be synthesised in parallel. Both blank and imprinted polymers are then evaluated in situ by equilibrium batch rebinding tests. Each step in the synthesis and evaluation was considered with the aim of achieving an automated method with wide applicability with regards to templ…

chemistry.chemical_classificationChromatographyMolecularly imprinted polymerPolymerBiochemistryDissociation (chemistry)Analytical Chemistrychemistry.chemical_compoundMonomerTemplatechemistryPolymerizationEnvironmental ChemistryMoleculeSelectivitySpectroscopyAnalytica Chimica Acta
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Preparation of monodisperse polyethylene oxides by gel permeation chromatography of discontinuous polymer-homologous series

1970

Abstract Starting from triethylene glycol, monodisperse polyethylene oxides of a molecular weight (MW) up to 2000 (degree of polymerisation (DP) During the first step the ditosylate of triethylene glycol is reacted with the sodium alkoxide of the same diol at room temperature. The condesation product (polymer homologues of triethylene glycol) was separated by molecular distillation and yielded the pure oligomers nonaethylene glycol (DP = 9, MW 414) and pentadecaethylene glycol (DP = 15, MW = 678), as proved by gel chromatography. During the next step the polymer homologues of nonaethylene glycol were synthesised in a similar way. The pure oligomers hepteicosa (DP = 27, MW = 1207) and pentat…

chemistry.chemical_classificationChromatographyOrganic ChemistryDispersityDiolGeneral MedicinePolymerDivinylbenzeneBiochemistryAnalytical ChemistryGel permeation chromatographychemistry.chemical_compoundchemistryPolymerizationPolymer chemistryPolystyreneTriethylene glycolJournal of Chromatography A
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Determination of cationic surfactants by capillary zone electrophoresis and micellar electrokinetic chromatography with deoxycholate micelles in the …

2000

Mixtures of the cationic surfactants benzalkonium chloride (BKC) and cetylpyridinium chloride (CPC) were quickly resolved and reproducibly and reliably determined by using background electrolytes (BGEs) containing 80 mM borate, pH 8.5, bile salts and large concentrations of an organic solvent. When the bile salt is present, the separation mechanism changes from capillary zone electrophoresis (CZE) to a mixed micellar electrokinetic chromatography (MEKC)-CZE, with predominant MEKC interactions, which lead to an excellent resolution of all the solutes, including the C12-C18 homologues of BKC and CPC. A BGE containing 50 mM sodium deoxycholate and 30% ethanol for an extreme resolution, or 20% …

chemistry.chemical_classificationChromatographyResolution (mass spectrometry)Organic ChemistryCationic polymerizationSalt (chemistry)General MedicineCetylpyridinium chlorideBiochemistryMicelleMicellar electrokinetic chromatographyAnalytical Chemistrychemistry.chemical_compoundBenzalkonium chlorideSurface-Active AgentsCapillary electrophoresischemistryCationsmedicineSolventsMicellesmedicine.drugChromatography Micellar Electrokinetic CapillaryDeoxycholic AcidJournal of chromatography. A
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Non-Centrosymmetric Homochiral Supramolecular Polymers of Tetrahedral Subphthalocyanine Molecules

2015

This is the peer reviewed version of the following article: Angewandte Chemie - International Edition 54.8 (2015): 2543-2547, which has been published in final form at http://dx.doi.org/10.1002/anie.201411272. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving

chemistry.chemical_classificationCircular dichroismMaterials scienceSubphthalocyanineSupramolecular chemistryStackingPorphyrinoidsGeneral MedicineGeneral ChemistrySelf-assemblyQuímicaCatalysisSupramolecular polymersCrystallographychemistryPolymerizationPolymer chemistryMoleculeSelf-assemblyChirality (chemistry)Homochiral aggregatesSupramolecular polymerization
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