Search results for "Solvent"

showing 10 items of 1395 documents

Syntheses and properties of gel chromatography materials

1970

Abstract The effect of the mode of synthesis on the characteristics of cross-linked polymers is examined for cross-linked copolymers of ethylvinylbenzene-divinylbenzene and vinyl acetate-divinyl adipate. For homogenously cross-linked gels the amount of cross-linking agent determines the “pore size” of these gels in the swollen state. Decreasing the amount of the divinyl component results in gels with an increase in the excluded molecular weight. The mechanical stability sets the experimental limit of their usage, so this type of gel is mostly suited for the separation of oligomers; polymers, however, may be separated by use of heterogenously cross-linked gels. The latter type of gel is prep…

chemistry.chemical_classificationInertChromatographyMolecular massChemistryOrganic ChemistryGeneral MedicinePolymerBiochemistryAnalytical ChemistrySolventGel permeation chromatographyPolymerizationAdipatePolymer chemistryCopolymerJournal of Chromatography A
researchProduct

1979

The kinetics of the anionic polymerization of styrene were investigated under pressure (1≤p/bar < 1800) with Na+ as counter ion in tetrahydropyran (THP) as solvent and with Cs+ as counter ion in 1,2-dimethoxyethane (DME) as solvent. The results yielded the activation volume of the contact ion pair ΔV and the sum (ΔV + ΔVcs) of the activation volume of the solvent separated ion pair ΔV and the volume change upon formation of solvent separated ion pairs from contact ion pairs ΔVcs. The numerical values are negative. The activation volume of the solvent separated ion pairs could be estimated.

chemistry.chemical_classificationInorganic chemistryKineticsAnalytical chemistryTetrahydropyranStyreneSolventchemistry.chemical_compoundAnionic addition polymerizationchemistryVolume (thermodynamics)Polymer chemistryCounterionBar (unit)Die Makromolekulare Chemie
researchProduct

Progress in Understanding of the Interactions between Functionalized Polyolefins and Organo-Layered Double Hydroxides

2013

The dispersion of organo-layered double hydroxides (O-LDH) in functionalized polyolefins (POs) is investigated. Two different polyethylene matrices (maleic anhydride (MAH) and diethyl maleate functionalized) are tested and a hydrogenated fatty acid modified LDH is used. The attention is focused on evidencing the interaction between the functional groups of the polymer and the O-LDH through FT-IR. Moreover, a combination of solvent fractionation, morphological, and rheological characterizations enables to gain a deeper insight into the structure of these composites. In particular, the formation of bridging bonds between the particles and MAH functionalized macromolecules is assumed, possibly…

chemistry.chemical_classificationIonic clustersPolymers and PlasticsChemistryGeneral Chemical EngineeringLayered double hydroxidesMaleic anhydrideGeneral ChemistryPolymerengineering.materialPolyethylenechemistry.chemical_compoundPolymer chemistrySolvent fractionationengineeringDispersion (chemistry)MacromoleculeMacromolecular Reaction Engineering
researchProduct

The ionic liquid effect on the Boulton-Katritzky reaction: a comparison between substrates of different structure

2015

The mononuclear rearrangement of heterocycles, also called Boulton–Katritzky reaction, was studied in ionic liquid solution using N-(5-phenyl-1,2,4-oxadiazol-3-yl)-N′-(4-nitrophenyl)-formamidine as substrate. The investigation was carried out using piperidine as basic catalyst and several ionic liquids differing in both cation and anion structure. Kinetic data collected were compared with the ones previously reported using (Z)-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole to have information about the effect due to the different structure of the alkyl chain borne on the substrate. Furthermore, data were analysed on the grounds of polarity, Kamlet–Taft solvent parameters, but taking…

chemistry.chemical_classificationIonic liquids MRH reaction base catalysisPolarity (physics)Organic ChemistryInorganic chemistrySubstrate (chemistry)Settore CHIM/06 - Chimica OrganicaBiochemistryIonCatalysisSolventchemistry.chemical_compoundchemistryDrug DiscoveryIonic liquidPhysical chemistryPiperidineAlkyl
researchProduct

Aggregation processes of perylene bisimide diimidazolium salts

2015

The supramolecular aggregation of three diimidazolium- functionalized perylene bisimides, differing in the alkyl chain length was investigated. These salts form aggregates in solvents like chloroform, dichloromethane, and glycerol. Solvent-, concentration-, and temperature-dependent spectroscopic studies were carried out, evidencing the occurrence of an isodesmic, enthalpy-driven aggregation process, underpinned by p–p stacking and hydrogen bonding. Moreover, dynamic light scattering (DLS) measurements and SEM images revealed that these salts aggregate in chloroform into elongated structures.

chemistry.chemical_classificationIsodesmic reactionChloroformOrganic ChemistrySupramolecular chemistryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaCatalysisSolventchemistry.chemical_compoundchemistryDynamic light scatteringPolymer chemistryOrganic chemistrydiimidazolium salts perylene bisimide self-assemblyAlkylPeryleneDichloromethaneSettore CHIM/02 - Chimica Fisica
researchProduct

Distance Matters: Biasing Mechanism, Transfer of Asymmetry, and Stereomutation in N-Annulated Perylene Bisimide Supramolecular Polymers

2021

International audience; The synthesis of two series of N-annulated perylene bisimides (PBIs), compounds 1 and 2, is reported, and their self-assembling features are thoroughly investigated by a complete set of spectroscopic measurements and theoretical calculations. The study corroborates the enormous influence that the distance between the PBI core and the peripheral groups exerts on the chiroptical properties and the supramolecular polymerization mechanism. Compounds 1, with the peripheral groups separated from the central PBI core by two methylenes and an ester group, form J-type supramolecular polymers in a cooperative manner but exhibit negligible chiroptical properties. The lack of cl…

chemistry.chemical_classificationIsodesmic reactionQuenching (fluorescence)010405 organic chemistrySupramolecular chemistryQuímica orgánicaGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryArticleCatalysis0104 chemical sciencesSupramolecular polymersSolventchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryPolymerization[CHIM]Chemical SciencesMethylcyclohexanePerylene
researchProduct

Isoniazid cocrystallisation with dicarboxylic acids: vapochemical, mechanochemical and thermal methods

2016

Cocrystallisation with a series of related compounds allows for the exploration of trends and limitations set by structural differences between these compounds. In this work, we investigate how the length of a dicarboxylic acid influences the outcome of cocrystallisation with isoniazid. We have performed a systematic study on the mechanochemical, thermal and solvent vapour-assisted cocrystallisation of aliphatic dicarboxylic acids (C3–C10) with isoniazid. Our results demonstrate that the rate of mechanochemical and vapour-assisted cocrystallisation depends on the acid chain length and shows alternation between odd- and even-chain acids. The results of thermal cocrystallisation showed that t…

chemistry.chemical_classificationIsoniazid02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesSolventChain lengthDicarboxylic acidchemistryMelting pointmedicineOrganic chemistryGeneral Materials Science0210 nano-technologyEutectic systemThermal methodsmedicine.drugCrystEngComm
researchProduct

Highly Enantioselective Protonation of the 3,4-Dihydro-2- methylnaphthalen-1(2H)-one Li-Enolate by TADDOLs

2000

A series of nine TADDOLs (=α,α,α′,α′-tetraaryl-1,3-dioxolane-4,5-dimethanols) 1a – 1i, have been tested as proton sources for the enantioselective protonation of the Li-enolate of 2-methyl-1-tetralone (=3,4-dihydro-2-methylnaphthalen-1(2H)-one). The enolate was generated directly from the ketone (with LiN(i-Pr)2 (LDA)/MeLi) or from the enol acetate (with 2 MeLi) or from the silyl enol ether (with MeLi) in CH2Cl2 or Et2O as the solvent (Scheme). The Li-enolate (associated with LiBr/LDA, or LiBr alone) was combined with 1.5 – 3.0 equiv. of the TADDOL at −78° by addition of the latter or by inverse addition. 2-Methyl-1-tetralone of (S)-configuration is formed (≤80% yield) with up to 99.5% sele…

chemistry.chemical_classificationKetoneOrganic ChemistryEnantioselective synthesisProtonationSilyl enol etherBiochemistryMedicinal chemistryEnolCatalysisInorganic ChemistrySolventchemistry.chemical_compoundchemistryYield (chemistry)Drug DiscoveryPhysical and Theoretical ChemistrySelectivityHelvetica Chimica Acta
researchProduct

Impact of ultrasound-assisted extraction and solvent composition on bioactive compounds and in vitro biological activities of thyme and rosemary

2020

Mediterranean herbs, specially thyme and rosemary, are important ingredients in food preparation and more recently have been studied as natural sources of bioactive compounds. This study aimed to study the effect of matrix (thyme vs. rosemary), and extraction protocol (conventional extraction vs. ultrasound assisted extraction) solvent composition (water vs. 50:50 ethanol:water solution) on the extraction of high value compounds (phenolic compounds, flavonoids and carotenoids) and also explore the antioxidant, antimicrobial (Listeria innocua, Staphylococcus aureus, and Salmonella enterica), probiotic (Lactobacillus casei and Bifidobacterium lactis), and anti-inflammatory activities. The phe…

chemistry.chemical_classificationLactobacillus caseiAntioxidantbiologyListeriaPlant Extractsmedicine.medical_treatmentExtraction (chemistry)Flavonoidfood and beveragesAntimicrobialbiology.organism_classificationRosmarinusThymus Plantchemistry.chemical_compoundchemistryPolyphenolSolventsmedicineFood scienceKaempferolCarotenoidFood ScienceFood Research International
researchProduct

Effects of solvent-free microwave extraction on the chemical composition of essential oil of Calamintha nepeta (L.) Savi compared with the convention…

2008

The essential oil of Calamintha nepeta has been obtained by solvent-free microwave extraction (SFME) and by classical hydrodistillation (HD). A comparative qualitative-quantitative study on the composition of the oils was carried out. A total of 38 compounds, constituting 97.6% of the oil, were identified in the oil obtained by SFME, whereas 46 compounds, representing 95.4% of the oil, were characterized in the HD oil. SFME-distilled oil is richer in lightly oxygenated monoterpenes (LOM) than HD oil. It also has a higher amount of sesquiterpenes and a lower quantity of hydrocarbon monoterpenes. HD oil seems to be affected by chemical changes more than SFME oil.

chemistry.chemical_classificationLamiaceaeChromatographybiologyPlant ExtractsExtraction (chemistry)TemperatureFiltration and SeparationSettore CHIM/06 - Chimica Organicabiology.organism_classificationCalamintha nepeta essential oil hydrodistillation solvent-free microwave extractionCalaminthaAnalytical Chemistrylaw.inventionSteam distillationHydrocarbonchemistrylawNepetaOils VolatileSolventsLamiaceaeMicrowavesChemical compositionEssential oil
researchProduct