Search results for "Ethylene"

showing 10 items of 2589 documents

Regioselective synthesis of calixcrowns derived from p-tert-butylcalix[5]arene

1993

Abstract Alkylation of p-tert-butylcalix[5]arene with oligoethylene glycol-ditosylates in the presence of CsF affords the 1,3-bridged calix[5]crowns 1a–c in 51 to 72% yield. In the case of hexaethylene glycol the isomeric 1,2-bridged calix[5]crown-7 2c was obtained additionally. The calixcrowns were further modified by alkylation of the remaining hydroxyl groups.

chemistry.chemical_classificationStereochemistryOrganic ChemistryRegioselectivityAlkylationBiochemistryMedicinal chemistrychemistry.chemical_compoundPolycyclic compoundchemistryYield (chemistry)Drug DiscoveryCalixareneHexaethylene glycolCyclophaneTetrahedron
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Diastereoselective Functionalization of a Spherand‐Type Calixarene

1994

Condensation of 5,5'-di-tert-butyl-2,2'-dihydroxybiphenyl (1) with formaldehyde yields a cyclic trimer 2 (and tetramer 3) having three (four) methylene groups less than a calix[6]arene (calix[8]arene). Alkylation of the (flexible) trimer with ethyl bromoacetate gives exclusively the stereoisomer 4 with C 2 symmetry, while the isomer with D 3 symmetry is not observed. Two isomers 6a and 6b (C 2 and C 1 symmetry) are obtained by treatment with tert-butyl bromoacetate which both are converted by transesterification with methanol into the same hexamethyl ester 5 having C 2 symmetry. These results are rationalized by restricted rotation around Ar-Ar bonds for larger O-alkyl groups also around Ar…

chemistry.chemical_classificationStereochemistryTrimerCrystal structureCondensation reactionMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundEthyl bromoacetatePolycyclic compoundchemistryCalixareneMethyleneCyclophaneChemische Berichte
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Synthesis and Reactivity of New Chelate-N-Heterocyclic Biscarbene Complexes of Ruthenium

2004

The carbene-ligand precursors methylenebis(N-alkylimidazolium) iodide (alkyl = methyl, neo-pentyl) and ethylenebis(N-methylimidazolium) chloride have been used in the preparation of several new Ru(II)-p-cymene complexes where the ligand behaves as mono- and bidentate. The molecular structures of the two biscarbene-complexes are reported. From the data reported, we can conclude that steric reasons (mainly the bisimidazolium linkers, methylene/ethylene) are the main factors determining both reactivity and synthetic difficulties of the products reported.

chemistry.chemical_classificationSteric effectsDenticityLigandStereochemistryIodidechemistry.chemical_elementMedicinal chemistryRutheniumInorganic Chemistrychemistry.chemical_compoundchemistryReactivity (chemistry)Physical and Theoretical ChemistryMethyleneAlkylInorganic Chemistry
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Surfactant Assisted Polymerization of Tetrafluoroethylene in Supercritical Carbon Dioxide with a Pilot Scale Batch Reactor.

2008

Chain-free radical polymerization of tetrafluoroethylene (TFE) was carried out in supercritical carbon dioxide (scCO2), at 50 °C and 121–133 bar, with tertiary-amyl-per-pivalate as a free radical initiator, using a 5-L pilot scale batch reactor. Experiments were carried out both in the absence and in the presence of perfluoropolyether (PFPE) carboxylate surfactants. Stabilizers were employed under the free acid form and as sodium and calcium salts. An expanded fibrillated poly(TFE) was obtained in all experiments. In the case of surfactant-free polymerizations, the product was mainly constituted by irregular shape macroparticles having size in the range 200–500 μm. Quite interestingly, when…

chemistry.chemical_classificationSupercritical carbon dioxidePolymers and Plasticsperfluoropolyether surfactantOrganic ChemistryRadical polymerizationBatch reactorSolution polymerizationPolymerSettore ING-IND/27 - Chimica Industriale E Tecnologicaradical polymerizationsurfactantschemistry.chemical_compoundpoly(tetrafluoroethylene)chemistryChemical engineeringPolymerizationsupercritical carbon dioxidePolymer chemistryMaterials ChemistryRadical initiatorTetrafluoroethylenemembrane
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Impact of surface state on polyethylene glycol conformation confined inside a nanopore.

2021

Solid-state nanopores are a promising platform for characterizing proteins. In order to improve their lifetime and prevent fouling, Polyethylene Glycol (PEG) grafting is one of the most efficient and low-cost solutions. Different models to calculate the PEG thickness do not consider their interaction with the nanopore inner surface nor the effect of confinement. Here, we investigate by molecular dynamic simulation the PEG conformation inside a nanopore in the case of hydrophobic and hydrophilic nanopores. Our results reveal that the nanopore inner surface plays a role in the PEG organization and, thus, in the speed of the salt constituent. The resulting pair interaction between PEG and its …

chemistry.chemical_classificationSurface (mathematics)Materials science010304 chemical physicsFoulingtechnology industry and agricultureGeneral Physics and AstronomySalt (chemistry)Polyethylene glycol010402 general chemistryGrafting01 natural sciences0104 chemical sciencesMolecular dynamicsNanoporechemistry.chemical_compoundChemical engineeringchemistry0103 physical sciencesPEG ratioPhysical and Theoretical ChemistryThe Journal of chemical physics
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Sustainable nanocomposites based on halloysite nanotubes and pectin/polyethylene glycol blend

2013

Abstract This study was focused on the preparation and characterization of biofilms based on pectin/polyethylene glycol 20000 (PEG) blend and halloysite nanotubes (HNTs). The obtained blends loaded with a natural nanoclay are proposed as sustainable alternative to the polymers produced from non-renewable resources such as fossil fuels. Properties of technological interest have been monitored and they were correlated to the structural features of the nanocomposites. It turned out that the wettability of the films can be tuned by changing the composition and the distribution of HNTs into the material as well as the surface roughness. The tensile properties of the blend are enhanced by the pre…

chemistry.chemical_classificationTGAMaterials scienceNanocompositeNanocompositePolymers and PlasticsPlasticizerNanoparticleHalloysitePolymerPolyethylene glycolThermal stabilityengineering.materialCondensed Matter PhysicsHalloysiteThermal stability; TGA; Halloysite; Nanocompositechemistry.chemical_compoundCrystallinitychemistryMechanics of MaterialsUltimate tensile strengthMaterials ChemistryengineeringComposite materialSettore CHIM/02 - Chimica Fisica
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Analysis of odour and taste problems in high-density polyethene

1998

Abstract The compounds that cause off-flavours in plastics, have been recognized mainly as carbonyl compounds (aldehydes, ketones and esters). They occur in low concentrations, and due to their low-threshold odour concentrations, their typical odours were identified. Most of these off-flavour compounds are volatile. Chemical analysis of smelling compounds requires a very sensitive method with a high-resolution capability. The analysis of volatile organic compounds (VOCs) in high density polyethene (HD-PE) granules and waters in which the granules have been shaken for 4 h, were carried out by gas chromatography–mass spectrometry–sniffing system (GC–MS–SNIFF) and by gas chromatography–fourier…

chemistry.chemical_classificationTasteChromatography GasChromatographyOrganic ChemistryOrganolepticReproducibility of ResultsGeneral MedicineSensitivity and SpecificityBiochemistrySensory analysisMass SpectrometryAnalytical Chemistrylaw.inventionchemistryOdorLeaching (chemistry)Water SupplylawTasteOdorantsFlame ionization detectorVolatile organic compoundGas chromatographyPolyethylenesJournal of Chromatography A
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Hetero-Multifunctional Poly(ethylene glycol) Copolymers with Multiple Hydroxyl Groups and a Single Terminal Functionality

2009

Hetero-multifunctional poly(ethylene glycol-co-glycerol) random copolymers with multiple hydroxyl functionalities and a single terminal functionality have been prepared by copolymerization of ethylene oxide (EO) and ethoxy ethyl glycidyl ether (EEGE) with the use of a suitable initiator, introducing a protected amino group or a double bond, respectively. Acidic deprotection was used for removal of the acetal protecting groups in the chain, and the terminal amino group was regenerated by catalytic hydrogenation. A series of copolymers with narrow polydispersity was obtained, varying comonomer fractions from 3 to 67% and molecular weights in the range of 5 000-32 000 g · mol(-1) (1.05 < $\ove…

chemistry.chemical_classificationTelechelic polymerEthyleneMaterials sciencePolymers and PlasticsDouble bondEthylene oxideComonomerOrganic ChemistryAcetalchemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistryAlkoxy groupMacromolecular Rapid Communications
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Review: Solution equilibria of ternary complexes formed from copper(II), aliphatic amines, and bioligands

2014

This review provides a summary of the coordination chemistry of ligands in the ternary system: copper(II)–aliphatic amine–bioligand, where amine = ethylenediamine – En, diethylenetriamine – Dien, or N, N, N′, N″, N″-pentamethyldiethylenetriamine – Me5dien, and bioligand = selected amino acid, aminohydroxamic acid, or aminophosphonic acid, in aqueous solution. We would like to show the specific interactions of copper(II) in ternary systems in the context of complex equilibria chemistry.

chemistry.chemical_classificationTernary numeral systemAqueous solutionamineschemistry.chemical_elementContext (language use)equilibriaCopperheteroligand complexesAmino acidCoordination complexstability constantschemistry.chemical_compoundchemistrybioligandsDiethylenetriamineMaterials ChemistryCopper(II) complexesOrganic chemistryPhysical and Theoretical ChemistryTernary operationJournal of Coordination Chemistry
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1975

The formation and the behaviour of radiation induced free radicals in poly[1-(tert-butoxy carbonylthio)ethylene] (2) and in a statistical copolymer 4 from O-tert-butyl S-vinyl thiocarbonate (1) with N-vinylpyrrolidone (1:1) was studied, using ESR spectroscopy. After γ-irradiation at 77 K, tert-butyl radicals and other species were detected in the polymers. The yield for the homopolymer was evaluated to be Gtert-butyl = 0.18. Investigations on the behaviour of radicals with an annealing procedure revealed, that at first the tert-butyl radicals disappear with increasing temperature and that a further warming up leads to a concentration rise of this radical species. A radical cation localized …

chemistry.chemical_classificationTert butylchemistry.chemical_compoundEthyleneRadical ionChemistryRadicalPolymer chemistryRadiation inducedThiocarbonateIrradiationPolymerDie Makromolekulare Chemie
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