Search results for "Mono"

showing 10 items of 6843 documents

Rheological Consequences of Hydrogen Bonding: Linear Viscoelastic Response of Linear Polyglycerol and Its Permethylated Analogues as a General Model …

2014

Viscoelastic properties of linear, hydroxyl-functional polymers are only little understood with respect to the effect of functional group interactions. Melt rheology and thermal phase transitions of linear polyethers (polyglycerol, linPG-OH) and their methylated analogues (linPG-OMe) in a broad molecular weight range (Mn = 1–100 kg/mol) with low polydispersities (PDI) have been investigated as a general model for hydroxyl-functional polymers with respect to their functionality and hydrogen bond interactions. We provide detailed insight into the rheodynamics of nonentangled and well-entangled polyethers bearing one functional group per monomer unit. Booij–Palmen plots (BBP) revealed failure …

chemistry.chemical_classificationPhase transitionMaterials sciencePolymers and PlasticsHydrogen bondOrganic ChemistryThermodynamicsPolymerViscoelasticityInorganic Chemistrychemistry.chemical_compoundMonomerchemistryRheologyPolymer chemistryMaterials ChemistryRelaxation (physics)Functional polymersMacromolecules
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Two-Dimensional Assembly Formation of Hydrophobic Helical Peptides at the Air/Water Interface: Fluorescence Microscopic Study

1995

Monolayer formation of hydrophobic α-helical peptides, X-(Ala-Aib) 8 -Y (X=Boc-, HOOCCH 2 CH 2 CO-, biotinyl, biotinyl-(Sar) 3 -; Y=OMe, OBzl, OH), at the air/water interface was studied by the fluorescence microscopic method. Some peptides showed a mound in the π-A isotherm. When the monolayer containing a small amount of FITC-labeled peptide was held at the surface pressure corresponding to the top of the mound, bright and dark domains were observed by fluorescence microscopy. Domain formation was also observed by the addition of a cationic dye (DiIC 1 ) into the subphase underneath the peptide monolayer. The mound in the π-A isotherm is, therefore, ascribed to the phase transition from a…

chemistry.chemical_classificationPhase transitionStereochemistryfungiCationic polymerizationPeptideSurfaces and InterfacesCondensed Matter PhysicsSurface pressureFluorescencelaw.inventionCrystallographychemistrylawMonolayerElectrochemistryFluorescence microscopeGeneral Materials ScienceCrystallizationSpectroscopyLangmuir
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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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Hunting the plant surrender signal activating apoplexy in grapevines after Neofusicoccum parvum infection

2021

SummaryApoplectic breakdown from Grapevines Trunk Diseases (GTDs) has become a serious challenge to viticulture in consequence to drought stress. We hypothesise that fungal aggressiveness is controlled by a chemical communication between host and colonising fungus.We introduce the new concept of a “plant surrender signal” accumulating in host plants under stress and triggering aggressive behaviour of the strain Neofusicoccum parvum (Bt-67) causing Botryosphaeriaceae-related dieback in grapevines.Using a cell-based experimental system (Vitis cells) and bioactivity-guided fractionation, we identify trans-ferulic acid, a monolignol precursor, as “surrender signal”. We show that this signal spe…

chemistry.chemical_classificationPhenylpropanoidHost (biology)PhytoalexinFungusPhytotoxinBiologybiology.organism_classificationMicrobiologychemistry.chemical_compoundchemistryFusicoccinSecretionMonolignol
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Reaction kinetics in dense two-dimensional polymer solutions : an excimer probe study

1994

We report measurements of the time dependent reaction rate of excimer formation in two-dimensional solutions of a polymerized amphiphile with partially pyrene-labelled chains in monolayers at the air-water-interface. We find a time dependent reaction rate for excimer formation obeying a power law r(t) ∞ t -β . The exponent β has a value of 0.22±0.12. This value is consistent with β=1/4, as has been predicted for bimolecular diffusion-controlled reactions in two-dimensional polymer melts by de Gennes. The measurements demonstrate the usefulness of the excimer technique to explore polymer dynamics

chemistry.chemical_classificationPhysics and Astronomy (miscellaneous)ChemistryKineticsGeneral EngineeringThermodynamicsTwo-dimensional polymerPolymerExcimerAtomic and Molecular Physics and OpticsReaction rateChemical kineticsPolymerizationMonolayerPolymer chemistryJournal de Physique II
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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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High-energy radiation processing, a smart approach to obtain PVP-graft-AA nanogels

2014

Abstract Poly(N-vinylpyrrolidone)-grafted-acrylic acid biocompatible nanogels (NGs) were prepared using an exiting industrial-type electron accelerator and setups, starting from semi-dilute aqueous solutions of a commercial PVP and the acrylic acid monomer. As a result, NGs with tunable size and structure can be obtained quantitatively. Sterility was also imparted at the integrated dose absorbed. The chemical structure of the NGs produced was confirmed through Fourier Transformer Infrared Spectroscopy (FT-IR). The molecular and physico-chemical properties of NGs, such as the hydrodynamic dimensions and surface charge densities, for various polymer and monomer concentrations in the irradiate…

chemistry.chemical_classificationPoly(N-vinylpyrrolidone) Acrylic acid grafting Nanogels E-beam irradiationRadiationMaterials scienceAqueous solutionAbsorption spectroscopyInfrared spectroscopyPolymerchemistry.chemical_compoundMonomerchemistryChemical engineeringPolymer chemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologieSurface chargeSpectroscopyPoly(N-vinylpyrrolidone); acrylic acid grafting; nanogels; e-beam irradiation.Acrylic acidRadiation Physics and Chemistry
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One-pot synthesis of poly(l-lactide) multi-arm star copolymers based on a polyester polyol macroinitiator

2013

Abstract Using a hyperbranched poly(glycolide) ( hb PGA) macroinitiator the synthesis of poly( l -lactide) (PLLA) multi-arm star polyesters has been achieved via a core-first approach. The star-shaped copolymers were prepared in a one-pot two-step process via Sn(Oct) 2 -catalyzed ring-opening polymerization (ROP) conducted in the melt. Complete conversion of the end groups of the hb polyglycolide polyester polyols is ensured by the reactive primary hydroxyl termini. By adjusting the monomer/initiator ratio a series of star copolymers with varying PLLA arm length has been obtained with molecular weights in the range of 1500 to 10,000 g/mol (SEC). The successful coupling of the PLLA arms to t…

chemistry.chemical_classificationPoly(lactide)Materials scienceLactidePolymers and PlasticsPolyglycolideOrganic ChemistryPoly(glycolide)Polyesterchemistry.chemical_compoundMonomerchemistryPolymerizationPolyolPolymer chemistryMaterials ChemistryCopolymerStatic light scatteringpolyester
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Hyperbranched Poly(propylene oxide): A Multifunctional Backbone-Thermoresponsive Polyether Polyol Copolymer

2012

Backbone-thermoresponsive hyperbranched poly(propylene oxide)-based polyether polyols have been synthesized by anionic ring-opening copolymerization of glycidol and propylene oxide. The number of functional hydroxyl end groups and the lower critical solution temperature (LCST) can be readily adjusted by varying the comonomer ratio. Molecular weights in the range of 1200-2000 g/mol were achieved. Hyperbranched polyether polyols with LCST values between 24 and 83 °C can be obtained in a convenient one-step reaction.

chemistry.chemical_classificationPoly(propylene oxide)Materials sciencePolymers and PlasticsComonomerOrganic ChemistryGlycidolLower critical solution temperatureInorganic Chemistrychemistry.chemical_compoundchemistryPolyolPolymer chemistryMaterials ChemistryCopolymerPropylene oxideACS Macro Letters
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Ferrocene-Containing Multifunctional Polyethers: Monomer Sequence Monitoring via Quantitative 13C NMR Spectroscopy in Bulk

2014

Ferrocenyl glycidyl ether (fcGE) and allyl glycidyl ether (AGE) are copolymerized via living anionic ring-opening polymerization to generate polyfunctional copolymers with molecular weights up to 40 300 g/mol and low molecular weight dispersities (Mw/Mn < 1.18). Copolymerizations were carried out in bulk at 100 °C and unexpectedly found to proceed without any isomerization of the allyl double bonds. The copolymerization behavior of fcGE and AGE was monitored by in situ quantitative 13C NMR kinetic measurements in bulk, evidencing the formation of random copolymers under these conditions, showing no gradient of comonomer incorporation. The redox-active behavior of the copolymers and homopoly…

chemistry.chemical_classificationPolymers and PlasticsAllyl glycidyl etherComonomerOrganic ChemistryPolymerCarbon-13 NMRInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationFerrocenePolymer chemistryMaterials ChemistryCopolymerMacromolecules
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