Search results for "Amide"

showing 10 items of 3119 documents

Thermomechanical degradation of polyethylene/polyamide 6 blend-clay nanocomposites

2014

Abstract Polymer nanocomposites are gaining a growing interest both in the academia and in the industrial field, because of some specific properties they can assure. However, the rise in the attention from the industry is also leading to concerns about their processing, which can involve issues which are not present in traditional polymers processing; furthermore, additional issues can arise when nanocomposites are based on a polymer blend rather than a single polymer. In this work, a systematic study on thermomechanical degradation and reprocessing behaviour of LDPE/PA6/Cloisite 15A systems has been performed. The characterization was based on rheological, mechanical and morphological anal…

chemistry.chemical_classificationNanocompositeMaterials sciencePolymers and PlasticsPolymer nanocompositePolymerPolyethyleneCondensed Matter PhysicsLow-density polyethylenechemistry.chemical_compoundchemistryRheologyMechanics of MaterialsPolyamideMaterials ChemistryPolymer blendComposite materialPolymer Degradation and Stability
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Selective localization of organoclay and effects on the morphology and mechanical properties of LDPE/PA11 blends with distributed and co-continuous m…

2010

A study was made on the effect of small amounts of organically modified clay on the morphology and mechanical properties of blends of low-density polyethylene and polyamide 11 at different compositions. The influence of the filler on the blend morphology was investigated using wide angle X-ray diffractometry, scanning and transmission electron microscopy and selective extraction experiments. The filler was found to locate predominantly in the more hydrophilic polyamide phase. Although such uneven distribution does not have a significant effect on the onset of phase co-continuity of the polymer components, it brings about a drastic refinement of the microstructure for the blends both with dr…

chemistry.chemical_classificationNanocompositeMaterials sciencePolymers and PlasticsPolymerCondensed Matter PhysicsMicrostructureLow-density polyethylenechemistryPhase (matter)PolyamideMaterials ChemistryOrganoclayPolymer blendPhysical and Theoretical ChemistryComposite materialJournal of Polymer Science Part B: Polymer Physics
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Compatibilization of a polyethylene/polyamide 6 blend nanocomposite

2014

Polymer blends of incompatible components need to be compatibilized to give rise to a blend with good properties. At the same way, polymer/clay nanocomposites show the same problem because of different chemical nature of the polymer matrix and of the clay. Compatibilization is then necessary if an incompatible polymer blend is filled with an organomodified clay. In this work a polyethylene/polyamide 6 blend filled with an organomodified clay has been compatibilized with a maleic anyhidride grafted SEBS (styrene-ethylene-butylene-styrene) copolymer and a glicidylmethacrylate-ethylene copolymer. The results show that compatibilization improves the mechanical properties in terms of elongation …

chemistry.chemical_classificationNanocompositeMaterials sciencenanocompositeCompatibilizationPolymerPolyethylenechemistry.chemical_compoundchemistryPolyamideCopolymerPolymer blendElongationComposite materialAIP Conference Proceedings
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Nanotube Friendly Poly(N-isopropylacrylamide).

2010

Poly(N-ispropylacrylamide) [PNIPAM] is a widely studied polymer for use in biological applications due to its lower critical solution temperature (LCST) being so close to the human body temperature. Unfortunately, attempts to combine carbon nanotubes (CNTs) with PNIPAM have been unsuccessful due to poor interactions between these two materials. In this work, a PNIPAM copolymer with 1 mol-% pyrene side group [p-PNIPAM] was used to produce a thermoresponsive polymer capable of stabilizing both single and multi-walled carbon nanotubes (MWNTs) in water. The presence of pyrene in the polymer chain lowers the LCST less than 4 °C and the interaction with nanotubes does not show any influence on LC…

chemistry.chemical_classificationNanotubeMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerCarbon nanotubeExfoliation jointLower critical solution temperaturelaw.inventionchemistry.chemical_compoundchemistryChemical engineeringlawSelf-healing hydrogelsPolymer chemistryMaterials ChemistryPoly(N-isopropylacrylamide)CopolymerMacromolecular rapid communications
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Photoinduced and Self‐Activated Nuclease Activity of Copper(II) Complexes with N ‐(Quinolin‐8‐yl)quin­olin‐8‐sulfonamide – DNA and Bovine Serum Album…

2016

Two CuII complexes with a new quinoline sulfonamide derivative and phenanthroline (phen), [Cu(QSQ)(phen)]ClO4·0.5H2O (1) and [Cu(QSQ)(phen)(H2O)]ClO4 (2) [HQSQ = N-(quinolin-8-yl)quinolin-8-sulfonamide], have been synthesized and physicochemically characterized. Single-crystal X-ray diffraction studies have revealed a highly distorted trigonal-bipyramidal structure for 1 (τ = 0.68) and an almost perfect trigonal-bipyramidal geometry for 2 (τ = 0.92). DNA binding studies, which were performed by thermal denaturation, viscometry, fluorescence spectroscopy, and cyclic voltammetry, indicated a partial intercalation of 1 with Kapp = 2.45 × 106 M–1. The nuclease activity of 1 was investigated upo…

chemistry.chemical_classificationNucleasebiology010405 organic chemistryStereochemistryPhenanthrolineQuinolineIntercalation (chemistry)Plasma protein binding010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesSulfonamideInorganic Chemistrychemistry.chemical_compoundchemistrybiology.proteinBovine serum albuminDNAEuropean Journal of Inorganic Chemistry
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Influence of the position of two dehydro-amino acids residues in the oligopeptide sequence on the binding ability towards Cu(II) ions

2005

Abstract Studies on the binding ability of bis-dehydro-hexa- and pentapeptides have shown that the hexapeptides bind Cu+2 with similar efficacy as pentapeptides. The increase of distance between two dehydro-amino acid residues in the peptide backbone has no impact on the efficacy in metal ion binding. The type of isomeration [(Z) or (E)] has an influence on the coordination of the metal ion only to the first amide nitrogen.

chemistry.chemical_classificationOligopeptideStereochemistrySequence (biology)IonAmino acidInorganic ChemistryMetalchemistry.chemical_compoundBinding abilityCopper(II)Peptide backbonechemistryAmidevisual_artMaterials Chemistryvisual_art.visual_art_mediumdehydro-peptidesOrganic chemistryPhysical and Theoretical ChemistrycomplexPolyhedron
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Carbohydrates as chiral templates: asymmetric ugi-synthesis of alpha-amino acids using galactosylamines as the chiral matrices

1988

Abstract In the presence of Lewis acid catalysts O-acetyl- (1) and O-pivaloyl- (2) protected β-D-galactopyranosylamines react with aldehydes, isocyanides and carboxylic acids in Ugi-four-component-condensations to give the corresponding N-galactosyl-amino acid amide derivatives 3,5 in almost quantitative yields. Zinc chloride is the most effective Lewis acid catalyst. At 0°C or even at room temperature the (2R,β-D)-diastereomers of the amino acid derivatives 3,5 are formed with high diastereoselectivity. If the sterically more demanding O-pivaloyl galactosylamine 2 is used at -78°C to -25°C the stereoselectivity often exeeds 20:1 favouring the (2R,β-D) diastereomers 5. After one recrystalli…

chemistry.chemical_classificationOrganic ChemistryDiastereomerBiochemistryAmino acidCatalysisLewis acid catalysischemistry.chemical_compoundchemistryAmideDrug DiscoveryOrganic chemistryStereoselectivityAcid hydrolysisLewis acids and basesTetrahedron
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Reactions Occurring during the Melt Mixing of Nylon 6 and Oxazoline−Cyclophosphazene Units

2009

Specific reactions of amino and carboxyl end groups of Nylon 6 with the reactive oxazoline groups belonging to a cyclophosphazene compound (referred as CP20XA) were carried out at 240 °C for different times, under inert atmosphere. Ny6 polymers terminated with one specific reactive chain end (-COOH or NH2) were reacted with different amounts of CP20XA to study the kinetic order of the reactions. All Ny6-CP20XA reacted products soluble in trifluoroethanol (TFE) were well characterized by MALDI-TOF MS, FT-IR and ( 1H and 13C) NMR techniques. The MALDI-TOF results show that the oxazoline rings react with the carboxyl chain ends of Ny6 following second-order kinetics. The reactions with amino c…

chemistry.chemical_classificationOxazolineReaction mechanismPolymers and PlasticsOrganic ChemistryKineticsSide reactionPolymerOxazolineReactive BlendingInorganic Chemistrychemistry.chemical_compoundEnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon6Nylon 6chemistrycyclophosphazenes polyamide end-functionalization MALDI-TOFMaterials ChemistryOrganic chemistryInert gasMALDIMacromolecules
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Synthesis, crystallographic and spectroscopic characterization and magnetic properties of dimer and monomer ternary copper(II) complexes with sulfona…

2010

Abstract Three dinuclear and one mononuclear copper(II)-1,10-phenanthroline ternary complexes, [Cu(L1)(phen)(OH)]2 (1), [Cu(L2)(phen)(OH)]2·3H2O (2), [Cu(L3)(phen)(OH)]2 (3) and [Cu(L4)2(phen)(H2O)] (4), with thiadiazole sulfonamide derivative ligands: HL1 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)naphthalene-1-sulfonamide), HL2 (N-(5-ethylthio)-1,3,4-thiadiazol-2-yl)-4-methylbenzenesulfonamide), HL3 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide) and HL4 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)-4-methylbenzenesulfonamide) have been synthesized and characterized. In the four complexes each copper atom is five-coordinated. The structure of complexes 1, 2 and 3 consists of a dimeric unit with a C2 sy…

chemistry.chemical_classificationPhenanthrolineDimerchemistry.chemical_elementCleavage (embryo)Ascorbic acidCopperSulfonamideInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistryMaterials ChemistryHydroxyl radicalPhysical and Theoretical ChemistryPolyhedron
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Use of two-dimensional thin-layer chromatography for the components study of poly(adenosine diphosphate ribose)

1990

Two-dimensional thin-layer chromatography on cellulose plates has been used for separating and quantifying the three adenosine derivatives: AMP, phosphoribosyl AMP (PRAMP), and (PR)2AMP obtained by venom phosphodiesterase digestion of poly(ADP-ribose). In vitro synthesized polymer, up to 300 derivatives in length were studied. Some parameters of the complexity of poly(ADP-ribose) could be deduced from our results: (i) The first branching point appears in fragments of approximately 21 derivatives in length. (ii) The branching points are located at regular distances of approximately 41 derivatives from each other.

chemistry.chemical_classificationPoly Adenosine Diphosphate RiboseChromatographyPolymersChemistryBiophysicsPoly Adenosine Diphosphate RiboseCell BiologyBranching pointsPolymerBiochemistryAdenosineAdenosine MonophosphateIn vitroThin-layer chromatographyVenom phosphodiesterasechemistry.chemical_compoundmedicineElectrophoresis Polyacrylamide GelChromatography Thin LayerCelluloseMolecular Biologymedicine.drugAnalytical Biochemistry
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