Search results for "BOX"

showing 10 items of 2676 documents

Polymerization of vinylidene fluoride with perfluoropolyether surfactants in supercritical carbon dioxide as a dispersing medium

2006

The heterogeneous polymerization of vinylidene fluoride (VDF) was investigated at 50 °C with supercritical carbon dioxide (scCO 2 ) as a dispersing medium and diethylperoxidicarbonate as an initiator in the presence of different perfluoropolyether surfactants. When FLK 7004A ammonium carboxylate salts were used at a 5% (w/w) concentration with respect to VDF, with an initial pressure of 31-45 MPa and with an olefin concentration of about 5.5 mol/L, monomer conversions up to 63% were obtained, corresponding to a final solid content higher than 200 g/L, and the polymer was collected at the end of the process in the form of a white powder completely composed of microspheres. The effects of the…

chemistry.chemical_classificationDispersion polymerizationSupercritical carbon dioxidePolymers and PlasticsfluoropolymerOrganic ChemistryRadical polymerizationPolymerradical polymerizationchemistry.chemical_compoundMonomersupercritical carbon dioxidechemistryPolymerizationChemical engineeringPolymer chemistryMaterials ChemistrydispersionCarboxylateFluorideJournal of Polymer Science Part A: Polymer Chemistry
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CO2 as a C1-organic building block: Electrocarboxylation of aromatic ketones. A quantitative study of the effect of the concentration of substrate an…

2006

The purpose of this work is to establish and discuss quantitative relationships between the selectivity in preparative scale electrolysis and intrinsic and operational parameters for the electrocarboxylation of aromatic ketones. For the investigated ketones, under appopriate experimental conditions the selectivity of the process is mainly determined by the competition between carboxylation and protonation, de-halogenation reactions (when an halogenated ketone is involved), and possibly dimerizations involving the electrogenerated radical anion. A simple model was proposed to account for these unwanted side paths which allows to predict the dependence of the selectivity as a function of the …

chemistry.chemical_classificationElectrolysisKetoneGeneral Chemical EngineeringInorganic chemistryProtonationSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryElectrocarboxylation Electrochemistry Aromatic ketonesCarbon dioxide Concentration profileAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistryCarboxylationlawElectrochemistryBenzophenoneOrganic chemistrySelectivityAcetophenoneJournal of Electroanalytical Chemistry
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Approaching an experimental electron density model of the biologically active trans ‐epoxysuccinyl amide group—Substituent effects vs. crystal packing

2017

The trans-epoxysuccinyl amide group as a biologically active moiety in cysteine protease inhibitors such as loxistatin acid E64c has been used as a benchmark system for theoretical studies of environmental effects on the electron density of small active ingredients in relation to their biological activity. Here, the synthesis and the electronic properties of the smallest possible active site model compound are reported to close the gap between the unknown experimental electron density of trans-epoxysuccinyl amides and the well-known function of related drugs. Intramolecular substituent effects are separated from intermolecular crystal packing effects on the electron density, which allows us…

chemistry.chemical_classificationElectron densitybiology010405 organic chemistryChemistryCarboxylic acidOrganic ChemistryIntermolecular forceSubstituentActive siteContext (language use)010402 general chemistry01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundAmideIntramolecular forcebiology.proteinPhysical and Theoretical ChemistryJournal of Physical Organic Chemistry
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Aromatic Ketones as Photocatalysts: Combined Action as Triplet Photosensitiser and Ground State Electron Acceptor

2006

chemistry.chemical_classificationElectron transferKetonechemistryCarboxylic acidPhotocatalysisPhysical and Theoretical ChemistryTriplet stateElectron acceptorGround statePhotochemistryAcceptorAtomic and Molecular Physics and OpticsChemPhysChem
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Computer-Aided Rational Design of Catalytic Antibodies: The 1F7 Case.

2007

chemistry.chemical_classificationEngineering drawingCyclohexanecarboxylic AcidsMolecular StructureRotationbiologyStereochemistryChemistryChorismic AcidRational designAntibodies CatalyticStereoisomerismCatalytic antibodyGeneral ChemistryGeneral MedicineCatalysisCatalysisStructure-Activity RelationshipEnzymeCyclohexenesbiology.proteinComputer-aidedComputer SimulationAntibodyChemInform
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The Catalytic Mechanism of Carboxylesterases: A Computational Study

2014

The catalytic mechanism of carboxylesterases (CEs, EC 3.1.1.1) is explored by computational means. CEs hydrolyze ester, amide, and carbamate bonds found in xenobiotics and endobiotics. They can also perform transesterification, a reaction important, for instance, in cholesterol homeostasis. The catalytic mechanisms with three different substrates (ester, thioester, and amide) have been established at the M06-2X/6-311++G**//B3LYP/6-31G* level of theory. It was found that the reactions proceed through a mechanism involving four steps instead of two as is generally proposed: (i) nucleophilic attack of serine to the substrate, forming the first tetrahedral intermediate, (ii) formation of the ac…

chemistry.chemical_classificationEsterificationStereochemistrycomputational studiesHydrolysisSubstrate (chemistry)AlcoholTransesterificationcatalytic mechanismCrystallography X-RayThioesterBiochemistryCatalysischemistry.chemical_compoundcarboxylesterasesNucleophilechemistryhydrolysisTetrahedral carbonyl addition compoundAmideBiocatalysisCarboxylic Ester Hydrolases
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Tailoring the anionic function and the side chains of comb-like superplasticizers to improve their adsorption

2015

Nowadays admixtures and especially superplasticizers are unavoidable components of the concrete formulation. The high fluidizing efficiency of the comb-like superplasticizers must not overshadow their high costs. This study aims to determine the PCE structure parameters which influence their adsorption in order to enhance their resistance to sulfate competitive adsorption and thus minimize their dosage. The PCE adsorption has been studied on calcite and ettringite which are both surfaces representative of early hydrating cement. The effect of the POE side chain length and density and also of the PCE anionic function i.e. carboxylate, dicarboxylate or phosphate on the adsorption has been ana…

chemistry.chemical_classificationEttringiteMaterials scienceInorganic chemistrySuperplasticizerCharge densityBuilding and ConstructionPolymerchemistry.chemical_compoundAdsorptionchemistrySide chainGeneral Materials ScienceCarboxylateSulfateCement and Concrete Research
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Synthesis of 1,3,5-Trisubstituted Hydantoins by Regiospecific Domino Condensation/Aza-Michael/O→N Acyl Migration of Carbodiimides with Activated α,β-…

2005

[reaction: see text] Carbodiimides and suitably activated alpha,beta-unsaturated carboxylic acids react effectively to afford a vast array of 1,3,5-trisubstituted hydantoins by means of a regiospecific domino condensation/aza-Michael/N--O acyl migration. The reaction works well in very mild conditions (20 degrees C, dichloromethane) with fumaric acid derivatives bearing an electron-withdrawing group in the beta position. Good results have been obtained also with less activated substrates bearing only one electron-withdrawing group in the beta position, using more polar solvents (acetonitrile, DMF), and in the presence of a base (2,4,6-trimethylpyridine). Reactions with asymmetric carbodiimi…

chemistry.chemical_classificationFumaric acidKetoneMolecular StructureBase (chemistry)ChemistryHydantoinsCarboxylic acidArylOrganic ChemistryCarboxylic AcidsRegioselectivityHydantoinStereoisomerismGeneral MedicineCondensation reactionMedicinal chemistryCarbodiimideschemistry.chemical_compoundMichael reactionOrganic chemistryChemoselectivityAcetonitrileAlkylDichloromethaneChemInform
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High Yield Syntheses of Stable, Singly Bonded Pd26+ Compounds

2006

A general method for the syntheses of dipalladium compounds having a singly bonded Pd26+ core and the formula R,S-cis-Pd2(C6H4PPh2)2(O2CR)2Cl2 is described. When the alkyl group in the carboxylate ligands is an electron donating group, the compounds are stable and the yields high. The Pd-Pd distances for the diamagnetic compounds with R = CF3 and CMe3 are 2.5434(4) and 2.5241(9) A, respectively. Calculations at the DFT level suggest that the electronic configuration is sigma2pi4delta2delta*2pi*4. These represent rare examples of palladium(III) compounds.

chemistry.chemical_classificationGeneral methodStereochemistrychemistry.chemical_elementGeneral ChemistryBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistrychemistryGroup (periodic table)Yield (chemistry)DiamagnetismCarboxylateElectron configurationAlkylPalladiumJournal of the American Chemical Society
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High efficiency joint CZE determination of sugars and acids in vegetables and fruits

2012

In this work, an improved CE method for the medium-throughput determination of main organic acids (oxalate, malate, citrate), the amino acid glutamate and the sugars fructose, glucose and sucrose in several food matrices is described. These compounds have been identified as key components in the taste intensity of fruit and vegetable crops. Using a running buffer with 20 mM 2,6-pyridine dicarboxylic acid pH 12.1 and 0.1% hexadimethrine bromide, replacing it every 5 h to avoid pH decrease, and optimizing capillary conditioning between runs with 58 mM SDS during 2 min at 20 psi, it is possible to effectively quantify these compounds while increasing medium throughput repeatability. This proce…

chemistry.chemical_classificationHexadimethrine bromideSucroseChromatographyChemistryClinical BiochemistryFructoseOrange (colour)RepeatabilityBiochemistryOxalateAnalytical Chemistrychemistry.chemical_compoundDicarboxylic acidPepperELECTROPHORESIS
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