Search results for "Polymers"

showing 10 items of 3567 documents

Solvent-Free Synthesis of a Pillared Three-Dimensional Coordination Polymer with Magnetic Ordering

2015

A new magnetic coordination polymer, [Fe(bipy)(im)2] (bipy = 4,4-bipyridine and im = imidazole), has been synthesized in a solvent-free reaction. Structural analysis reveals a pillared 3D coordination polymer composed by neutral layers, formed by iron(II) and imidazolate linkers, interconnected by bipy ligands which serve as pillars. Magnetic measurements show that the material magnetically orders at low temperatures (Tc = 14.5 K) as a weak ferromagnet, likely due to a spin canting.

chemistry.chemical_classificationSolvent freePolymersCoordination polymerInorganic chemistryPolymerCrystallography X-RayInorganic ChemistryThermogravimetryMagneticschemistry.chemical_compoundCrystallographychemistryFerromagnetismThermogravimetryImidazolateSolventsImidazolePhysical and Theoretical ChemistrySpin cantingInorganic Chemistry
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Interrelation between the thermodynamic and viscometric behaviour of aqueous solutions of hydrophobically modified ethyl hydroxyethyl cellulose

2000

Abstract Aqueous solutions of a commercial sample of hydrophobically modified ethyl hydroxyethyl cellulose (HC, Mw=100 kg/mol, nonylphenol substitution ca. 1.7 mol%) were studied with respect to their demixing behaviour and flow characteristics. Phase separation temperatures were measured turbidimetrically and by determining the first discernible macroscopic phase separation. In some cases demixing was also monitored viscometrically. Phase volume ratios yielded a critical polymer concentration of 1.87 wt.% HC (displaced considerably out of the minimum of the demixing curve towards higher polymer concentrations) and a lower critical solution temperature of 47°C. Model calculations of the spi…

chemistry.chemical_classificationSpinodalAqueous solutionChromatographyShear thinningPolymers and PlasticsOrganic ChemistryThermodynamicsPolymerEntropy of mixingLower critical solution temperatureDilutionViscositychemistryMaterials ChemistryPolymer
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Recognition-Directed Supramolecular Assemblies of Metal Complexes of Terpyridine Derived Ligands with Self-Complementary Hydrogen Bonding Sites

2000

The synthesis and X-ray structures of three metal complexes with terpyridine-derived ligands that contain amino-pyrimidine and amino-pyrazine moieties are presented. They have been designed in view of directing their self-assembly into specific supramolecular arrays through molecular recognition interactions. The solid-state structures indeed reveal extensive hydrogen-bonded networks. The Co complex 4a with PF6- counterions builds a two-dimensional infinite interwoven grid through strong double hydrogen bonds (d(N-H-N) =2.918-3.018 A) between the amino groups and the N atoms of the rings, with all H-bonding sites saturated. Changing the anions to BF4- in 4b leads to a similar infinite but p…

chemistry.chemical_classificationStereochemistryHydrogen bondOrganic ChemistrySupramolecular chemistryGeneral ChemistryCrystal engineeringCatalysisCoordination complexSupramolecular assemblySupramolecular polymerschemistry.chemical_compoundCrystallographyMolecular recognitionchemistryTerpyridineChemistry
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Impact of Molecular Size and Shape on the Supramolecular Co‐Assembly of Chiral Tricarboxamides: A Comparative Study

2020

We report herein a comparative investigation of the chiral amplification features of a series of three families of C 3 -symmetric tricarboxamides: 1,3,5-triphenylbenzenetricarboxamides (TPBAs), benzenetricarboxamides (BTAs) and oligo(phenylene ethynylene) tricarboxamides (OPE-TAs). As previously observed for BTAs and OPE-TAs, a similar dichroic response is obtained for TPBAs decorated with three, two or only one chiral side chain bearing stereogenic centers, thus confirming the efficient transfer of point chirality to the supramolecular helical aggregates. Unlike BTAs and OPE-TAs, the chiral amplification ability of TPBAs in majority rules experiments shows a negligible dependence on the nu…

chemistry.chemical_classificationSteric effects010405 organic chemistryChemistryOrganic ChemistrySupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesStereocenterSupramolecular polymersCrystallographyPhenyleneSide chainMoleculeChirality (chemistry)Chemistry – A European Journal
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Synthetic approaches towards new polymer systems by the combination of living carbocationic and anionic polymerizations

1996

This study summarizes recent efforts to obtain by combination of living carbocationic and anionic polymerizations block copolymers which are potential precursors for building new well-defined polymeric architectures with microphase separated morphology. Living carbocationic polymerization (LCCP) yields telechelic polyisobutylene (PIB) chains with a variety of useful endgroups, such as tert-chlorine, isopropenyl, primary hydroxyl, tolyl etc. When tolyl-ended PIB was used as precursor for macroinitiator of living anionic polymerization of 2-(tert-butyldimethylsilyloxy)ethyl methacrylate (tBuMe2SiOEMA), mixtures of homopolymers and block copolymers were formed due to incomplete lithiation of t…

chemistry.chemical_classificationSteric effectsMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerCondensed Matter PhysicsMethacrylatechemistryPolymerizationAmphiphilePolymer chemistryMaterials ChemistryCopolymerSurface modificationOrganic chemistryLiving anionic polymerization
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Insight into the synthesis of N-methylated polypeptides

2020

The ring-opening polymerization (ROP) of N-carboxy anhydrides (NCAs) is mostly divided into two classes: NCAs of α-substituted amino acids and N-methylated NCAs of α-unsubstituted glycine derivatives (NNCAs). The use of both monomer types offers different mechanistic features and results in a multitude of functional materials. To combine these properties, the synthesis and ROP of α-substituted and N-methylated NCAs (αNNCAs) of several amino acids were investigated. The current study provides insight into the influence of polymerization conditions and the limitations caused by the enhanced steric demand of the amino acid NCA monomers and their N-methylated derivatives. Namely, the effects of…

chemistry.chemical_classificationSteric effectsPolymers and PlasticsOrganic ChemistryBioengineeringPolymerBiochemistryCombinatorial chemistryAmino acidchemistry.chemical_compoundMonomerchemistryPolymerizationGlycineElectronic effectAmine gas treatingPolymer Chemistry
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Decoding the Consequences of Increasing the Size of Self-Assembling Tricarboxamides on Chiral Amplification

2019

A complete series of experimental and theoretical investigations on the supramolecular polymerization of chiral (1 and 2) and achiral (3) oligo(phenylene ethynylene) tricarboxamides (OPE-TAs) is reported. The performance of seargents-and-soldiers (SaS) and majority rules (MR) experiments has allowed deriving a full set of thermodynamic parameters, including the helix reversal penalty (HRP) and the mismatch penalty (MMP). The results described illustrate the influence exerted by the number of stereogenic centers per monomeric unit and the temperature on the chiral amplification phenomenon. While the HRP decreases upon decreasing the number of chiral side chains, the MMP follows an opposite t…

chemistry.chemical_classificationSteric effectsSupramolecular chemistryGeneral Chemistry010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesStereocenterSupramolecular polymersCrystallographyColloid and Surface ChemistrychemistryPhenyleneHelixSide chainChirality (chemistry)Journal of the American Chemical Society
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A clickable NHC–Au(i)-complex for the preparation of stimulus-responsive metallopeptide amphiphiles

2018

We report the synthesis of an alkyne functionalised NHC-Au(i)-complex which is conjugated with amphiphilic oligopeptides using a copper(i) catalysed cycloaddition. The resulting Au(i)-metalloamphiphiles are shown to self-assemble into charge-regulated stimulus-responsive supramolecular polymers in water via a weakly cooperative polymerisation mechanism.

chemistry.chemical_classificationStimuli responsive010405 organic chemistryChemistryMetals and AlloysAlkyneGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCycloaddition0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSupramolecular polymersPolymerizationAmphiphileMaterials ChemistryCeramics and CompositesClickableChemical Communications
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Stable Expression of Heterologous Sulfotransferase in V79 Cells: Activation of Primary and Secondary Benzylic Alcohols

1994

Abstract A sulfotransferase (ST) capable of activating 1-hydroxymethylpyrene (HMP) and 9-hydroxymethylanthracene (HMA) to mutagens was purified from rat liver. This enzyme appeared to be identical with hydroxysteroid STa, whose cDNA was cloned and stably expressed in Chinese hamster V79 cells. Several primary and secondary benzylic alcohols derived from polycyclic aromatic hydrocarbons induced gene mutations, sister chromatid exchanges (SCE) and/or cytotoxicity in these cells.

chemistry.chemical_classificationSulfotransferasePolymers and PlasticsbiologyOrganic ChemistryHeterologousGene mutationbiology.organism_classificationChinese hamsterchemistry.chemical_compoundEnzymeBiochemistrychemistryComplementary DNAMaterials ChemistryHydroxysteroidCytotoxicityPolycyclic Aromatic Compounds
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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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