Search results for "polymer chemistry"

showing 10 items of 3410 documents

Selective Extraction and Efficient Binding in a Protic Solvent of Contact Ion Triplets by Using a Thiourea-Based Bis-Calix[6]arene Receptor

2013

We report a D3h-symmetric tail-to-tail bis-calix[6]thiourea 5 that displays two divergent cavities triply connected by thiourea linkages. This calix[6]tube was efficiently synthesized through a [1+1] macrocyclization reaction and characterized by X-ray diffraction analysis. The binding properties of this heterotritopic receptor were evaluated in a protic environment (i.e., CD3OD/CDCl3) through NMR studies. Thus, bis-calix[6]thiourea 5 exhibits a remarkable ability in the cooperative complexation of an anion sandwiched between two ammonium ions, a high selectivity for ammonium sulfate salts being observed. The anion is bound through multiple hydrogen-bonding interactions at the thiourea bind…

Ammonium sulfate010405 organic chemistryOrganic ChemistryInorganic chemistrySupramolecular chemistry010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryThioureaPolymer chemistryCalixareneAmmoniumPhysical and Theoretical ChemistrySelectivityChirality (chemistry)Protic solventEuropean Journal of Organic Chemistry
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Immobilization of functionalized lipids in a random poly(methacrylate) copolymer monolayer

1995

It is shown that a monolayer of random poly(methacrylate) copolymer with a hydrophobic and a hydrophilic substituent exhibits a transition from the fluid to amorphous state. Above this transition any amphiphilic molecules mixed with the monolayer are immobile. Furthermore, such functionalized lipids are immobilized in the monolayer during the Langmuir-Blodgett transfer. The hydrophilic head-groups of the biotin-lipids remain on the formerly water-adjacent side of the monolayer, even if this side is exposed to air

Amphiphilic moleculeMaterials scienceMethacrylate copolymerMechanical EngineeringSubstituentMethacrylatePoly methacrylateAmorphous solidchemistry.chemical_compoundchemistryMechanics of MaterialsPolymer chemistryMonolayerCopolymerlipids (amino acids peptides and proteins)General Materials ScienceAdvanced Materials
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Über die verzweigung von polydodecylmethacrylat

1970

Zur Untersuchung der Losungseigenschaften und des Ausmases der Verzweigung von radikalisch gewonnenem Polydodecylmethacrylat wurden Fraktionen von niedrig- und hochumgesetzten Praparaten im Molekulargewichtsbereich von 1,5·105 bis 8·106 auf ihr Molekulargewicht und ihre Knaueldimension hin vermessen. Die Methoden der Lichtstreuung, der Viskosimetrie, der Sedimentation in der Ultrazentrifuge, der Osmometrie und der Gelchromatographie wurden benutzt. Fur die Streulichtmessungen diente ein Eigenbaulichtstreuungsgerat, das wegen seines grosen Winkelmesbereiches eine recht genaue Festlegung der Anfangssteigung der Streukurve und damit des Tragheitsradius ermoglicht. Das Quadrat des Tragheitsradi…

Angular rangeChemistryIntrinsic viscosityPolymer chemistryRadius of gyrationBranching pointsBranching (polymer chemistry)Die Makromolekulare Chemie
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Polymerization with heterogeneous metalorganic catalysts. VI. Differences in polymerization activity of α-olefins and some kinetic results on butene-…

1967

Relative changes in polymerization activity of ethylene, propylene, and butene-1 in Ziegler-Natta polymerization were compared by use of TiCl3 samples contaminated with O2 and H2O to various extents. Catalyst depletion varied for the three monomers which supported the existence of different active centers. In butene-1 polymerizations with the system Al(C2H5)2Cl–TiCl3, the formation of active centers involves an irreversible and a reversible (adsorption) reaction, the former pertaining to the formation of Al(C2H5)Cl2 and dependent upon the purity of the TiCl3. The kinetic treatment of the rate curves suggests a mixed order of catalyst deactivation and again points to the importance of Al(C2H…

Anionic addition polymerizationChain-growth polymerizationBulk polymerizationPolymerizationChemistryPolymer chemistryGeneral EngineeringCationic polymerizationPrecipitation polymerizationCoordination polymerizationPhotochemistryIonic polymerizationJournal of Polymer Science Part A-1: Polymer Chemistry
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Some New Copolymers by Ionic Polymerization

1980

In the first part the cationic polymerization of a homologous series of cyclic ether–acetals with ring sizes of 11, 14, and 17 atoms is described. During the polymerization of triethylene glycol formal (TGF) an equilibrium is reached and besides high polymers cyclic oligomers are formed. The oligomers and the polymers are built up of a regular sequence of one oxymethylene unit and three oxyethylene units –[–(OCH2) (OC2H4)3–]–x. They are therefore be labelled a “sequenced copolymer.” The equilibrium concentrations of the cyclic oligomers with a polymerization degree from 2 to 15 follow the Jacobson–Stockmayer equation. The 14- and 17-membered monomers POC and HOC forms cyclic oligomers and h…

Anionic addition polymerizationChain-growth polymerizationPolymers and PlasticsPolymerizationChemistryPolymer chemistryMaterials ChemistryCationic polymerizationCopolymerLiving polymerizationIonic polymerizationRing-opening polymerizationPolymer Journal
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Über zwei formen des initiators Na-naphthalin und die bestimmung der „lebenden” kettenenden bei der anionischen polymerisation

1969

Na-Naphthalin in THF kommt in (mindestens) 2 Formen I und I' vor, die sich beim Start der anionischen Polymerisation von Styrol sehr verschieden verhalten. Ohne Zusatg von NaBPh4 wirken beide Formen als Initiatoren. Bei Zusatz von NzBPh4 wird die From I' desktiviert, wobei auf ein Molekul I' zwei Molekule NaBPh4 entfallen. Die hierbei entstehende inaktive Verbindung hat in der Umgebung der Wellenlange 350 nm fast den gleichen Extinktionskoeffizienten wie die “lebenden” Enden. Bei Nichtberucksichtigung dieses Effektes erhalt man daher fur die Konzentration der “lebenden” enden aus Absorptionsmessungen einen zu hohen Wert und fur die Geschwindigkeitskonstante kw(±) der Polymerisaton uber das …

Anionic addition polymerizationChemistryPolymer chemistryDie Makromolekulare Chemie
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From attraction to repulsion : anion–π interactions between bromide and fluorinated phenyl groups

2011

Anion–π interactions in crystals of fluorobenzyl ammonium salts depend on the degree of fluorination at the aromatics.

AnionsBromidesBenzylaminesHalogenationInorganic chemistryMolecular ConformationChemieElectronsCrystallography X-RayCatalysisPiperazinesDegree (temperature)Ionchemistry.chemical_compoundBromidePolymer chemistryMaterials ChemistryAmmoniumMetals and AlloysHydrogen BondingGeneral ChemistryAttractionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFluorobenzenesQuaternary Ammonium CompoundschemistryCeramics and Composites
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Self-assembly of 3,5-bis(ethoxycarbonyl)pyrazolate anions and ammonium cations of β-phenylethylamine or homoveratrylamine into hetero-double-stranded…

2009

Hydrogen-bonded double-stranded hetero-helices are formed when reacting sodium 3,5-bis(ethoxycarbonyl)pyrazolate with beta-phenethylammonium or homoveratrylammonium chloride, in which one of the strands is defined by the ammonium cations and the other one by the pyrazolate anions.

AnionsCircular DichroismSodiumOrganic Chemistrychemistry.chemical_elementHydrogen BondingCrystallography X-RayBiochemistryChlorideProtein Structure SecondaryQuaternary Ammonium Compoundschemistry.chemical_compoundchemistryPhenethylaminesPolymer chemistrymedicineOrganic chemistryAmmoniumSelf-assemblyBeta-PhenylethylaminePhysical and Theoretical ChemistryDouble strandedmedicine.drugOrganic & Biomolecular Chemistry
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Hyperbranched Polyglycerol-Based Lipids via Oxyanionic Polymerization: Toward Multifunctional Stealth Liposomes

2010

We describe the synthesis of linear-hyperbranched lipids for liposome preparation based on linear poly(ethylene glycol) (PEG) and hyperbranched polyglycerol (PG). Molecular weights were adjusted to values around 3000 g/mol with varying degrees of polymerization of the linear and the branched segments in analogy to PEG-based stealth lipids; polydispersities were generally low and below 1.3. The hydrophobic anchors were introduced into the lipid structures as initiators for the anionic polymerization of ethylene oxide and are either based on cholesterol or on different aliphatic glyceryl ethers. Complete incorporation of the apolar initiators was evidenced by MALDI-ToF analysis at all stages …

AnionsGlycerolLiposomeMagnetic Resonance SpectroscopyPolymers and PlasticsEthylene oxidePolymerstechnology industry and agricultureBioengineeringLipidsSmall-angle neutron scatteringBiomaterialschemistry.chemical_compoundEnd-groupAnionic addition polymerizationchemistryDynamic light scatteringPolymerizationSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationLiposomesSpectroscopy Fourier Transform InfraredPolymer chemistryMaterials Chemistrylipids (amino acids peptides and proteins)Ethylene glycolBiomacromolecules
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Polyfunctional recognition of pyridinedicarboxylate anions with macrocyclic polyamine receptors containing heteroaromatic groups.

2008

The interaction of the biologically relevant anions deriving from the six pyridinedicarboxylic acids (H2PDC) with two macrocyclic receptors containing a pentamine chain and a bipyridine (1) or a phenanthroline (2) moiety, as well as with the aliphatic analogue [21]aneN7 (3), was studied by means of spectroscopic methods (UV-vis, NMR) and potentiometric titrations affording the stability constants of the adducts formed. All three receptors form stable complexes with the substrates thanks to the formation of several salt bridges and hydrogen bond contacts, as observed in the crystal structure of the H8[3(2,6-PDC)4] x H2O x 0.5 EtOH solid compound. Additional pi-stacking interactions between t…

AnionsModels MolecularMacrocyclic CompoundsStereochemistryPyridinesPhenanthrolineStatic ElectricityCarboxylic AcidsHydrocarbons Aromaticchemistry.chemical_compoundBipyridineMolecular recognitionPolymer chemistryPolyaminesMoietychemistry.chemical_classificationBinding SitesHydrogen bondSpectrum AnalysisOrganic ChemistryHydrogen BondingDicarboxylic acidchemistryStability constants of complexesPotentiometryAliphatic compoundThe Journal of organic chemistry
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