Search results for "Side chain"

showing 10 items of 345 documents

Fluidizing efficiency of comb-like superplasticizers: The effect of the anionic function, the side chain length and the grafting degree

2015

Superplasticizers and especially polycarboxylate grafted polyethylene oxide (PCE) demonstrated their efficiency to fluidify concrete. The aim of this work is to investigate the evolution of the fluidity as a function of adsorption in a sulfated solution with a wide variety of comb-like superplasticizers and at incomplete adsorption rate. Polymers with various side chain lengths, grafting ratios and also with modified anionic functions (carboxylate, dicarboxylate and phosphate) were synthesized. Inert calcite suspensions were used to mimic early age cementitious materials avoiding the cement hydration. Models of polymer conformation and yield stress prediction have been tested. But the most …

chemistry.chemical_classificationMaterials scienceSuperplasticizerBuilding and ConstructionPolymerGraftingchemistry.chemical_compoundAdsorptionchemistryRheologyChemical engineeringSide chainOrganic chemistryGeneral Materials ScienceCementitiousCarboxylateCement and Concrete Research
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Dielectric Relaxation Measurements and X-Ray Investigations of Liquid Crystalline Side-Chain Polymers

1985

In the last few years several liquid crystalline side-chain polymers have been synthesized,1 – 4 which combine the properties of low molecular weight liquid crystals with those of polymers.5 – 9

chemistry.chemical_classificationMaterials sciencechemistryLiquid crystalLiquid crystallineX-raySide chainRelaxation (physics)Physical chemistryDielectricPolymer
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Main-Chain and Side-Chain C60-Polymers

2009

chemistry.chemical_classificationMaterials sciencechemistryPolymer scienceChain (algebraic topology)Fullerene Polymers SynthesisSide chainPolymerSettore CHIM/06 - Chimica Organica
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Crystal structure of the bifunctional soybean Bowman-Birk inhibitor at 0.28-nm resolution. Structural peculiarities in a folded protein conformation.

1996

The Bowman-Birk inhibitor from soybean is a small protein that contains a binary arrangement of trypsin-reactive and chymotrypsin-reactive subdomains. In this report, the crystal structure of this anticarcinogenic protein has been determined to 0.28-nm resolution by molecular replacement from crystals grown at neutral pH. The crystal structure differs from a previously determined NMR structure [Werner, M. H. & Wemmer, D. E. (1992) Biochemistry 31, 999-1010] in the relative orientation of the two enzyme-insertion loops, in some details of the main chain trace, in the presence of favourable contacts in the trypsin-insertion loop, and in the orientation of several amino acid side chains. The p…

chemistry.chemical_classificationModels MolecularMagnetic Resonance SpectroscopyStereochemistryProtein ConformationMolecular Sequence DataWaterCrystal structureCrystallography X-RayBiochemistryProtein tertiary structureProtein Structure SecondaryAmino acidCrystallographychemistry.chemical_compoundKineticsProtein structurechemistrySide chainChymotrypsinProtein foldingMolecular replacementAmino Acid SequenceBifunctionalTrypsin Inhibitor Bowman-Birk SoybeanEuropean journal of biochemistry
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Synthesis and solid state structures of macromolecular cylindrical brushes with varying side chain length

2004

Abstract Cylindrical brushes with a macromolecular backbone and well-defined side chains of different length (4≤ P n sc ≤38) were synthesized by polymerization of macromonomers. The effect of side chain length on the intermolecular order has been investigated by means of X-ray scattering on the melt-extruded samples. The increase of the side chain molar mass results in an increase of the intermolecular distance d according to d ∼( M n sc ) 0.476 . The contour length of the cylindrical brush polymers per main chain monomer unit, l m , was determined to slightly vary with side chain molar mass M n sc according to l m ∼( M n sc ) 0.059 . The resulting values are much less than the maximum exte…

chemistry.chemical_classificationMolar massMaterials sciencePolymers and PlasticsOrganic ChemistryIntermolecular forcePolymerchemistry.chemical_compoundCrystallographyMonomerchemistryPolymerizationIntramolecular forcePolymer chemistryMaterials ChemistrySide chainCopolymerPolymer
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Polymers with Side-chain Mesogenic Units

1989

Liquid crystalline (LC) polymers are usually prepared by combining formanisotropic structural units (so-called mesogenic groups) and polymer chains (Figure 1). The mesogenic groups used for this purpose are rigid rod-like or disc-like units, which are known to favour LC phases in the case of low molar mass substances. There are two main ways of combining the mesogenic groups and polymer chains. The mesogenic groups can either be incorporated actually into the polymer chains (LC main-chain polymers, see Volume 5, Chapter 38) or they can be attached to flexible polymer chains as side groups (LC side-chain polymers).

chemistry.chemical_classificationMolar massMaterials sciencechemistryLiquid crystallineMesogenPolymer chemistrySide chainPolymer
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Molecular aggregation in selected crystalline 1:1 complexes of hydrophobicD- andL-amino acids. IV. TheL-phenylalanine series

2009

The amino acid L-phenylalanine has been cocrystallized with D-2-aminobutyric acid, C(9)H(11)NO(2).C(4)H(9)NO(2), D-norvaline, C(9)H(11)NO(2).C(5)H(11)NO(2), and D-methionine, C(9)H(11)NO(2).C(5)H(11)NO(2)S, with linear side chains, as well as with D-leucine, C(9)H(11)NO(2).C(6)H(13)NO(2), D-isoleucine, C(9)H(11)NO(2).C(6)H(13)NO(2), and D-allo-isoleucine, C(9)H(11)NO(2).C(6)H(13)NO(2), with branched side chains. The structures of these 1:1 complexes fall into two classes based on the observed hydrogen-bonding pattern. From a comparison with other L:D complexes involving hydrophobic amino acids and regular racemates, it is shown that the structure-directing properties of phenylalanine closel…

chemistry.chemical_classificationMolecular StructureChemistryStereochemistryAminobutyratesPhenylalanineHydrogen BondingStereoisomerismStereoisomerismPhenylalanineGeneral MedicineCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyAmino acidValineSide chainIsoleucineLeucineAminobutyratesHydrophobic and Hydrophilic InteractionsActa Crystallographica Section C Crystal Structure Communications
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1990

New monomers are described for the synthesis of rod-like poly(1,4-phenyleneethynylene)s with long flexible aliphatic side chains. By palladium catalyzed polycondensation soluble polymers with melting points around 100°C could be obtained. The molecular weight was estimated by GPC, VPO and elemental analysis: GPC showed a multimodale distribution with Pn = 9–15. NMR spectra were found to be in agreement with the assumed polymer structure, but signals of the acetylenic carbons could not be detected. A broad, structureless absorption with a maximum at λ = 410 nm is seen in the UV-VIS-spectra. The thermal decomposition of the substituted PPE's starts at about 400°C and is comparable to that of …

chemistry.chemical_classificationNMR spectra databasechemistry.chemical_compoundMonomerCondensation polymerchemistryPolymer chemistryThermal decompositionSide chainchemistry.chemical_elementThermal stabilityPolymerPalladiumDie Makromolekulare Chemie
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Study by FT-IR spectroscopy of ageing of adhesives used in restoration of archaeological glass objects

1999

Abstract A study by FT-IR spectroscopy which aims to compare the stability of five polymers, Araldit XW396/XW 397, Vitralit 7256, Loctite 350, Desmodur N 75/Viacryl SM 564/65 and Krafft silicone commonly used in the restoration of archaeological glass objects when subjected to thermal ageing, UV light ageing and cyclic ageing in SO 2 pollutant chamber has been carried out. Two series of test specimens were prepared in order to reproduce the two methods of application of polymers commonly used in restoration treatments as adhesive and consolidant or coating of glass fragments. Modifications in the chain or side chain structure of polymers, alterations of carbonyl groups in Araldit and isocya…

chemistry.chemical_classificationOrganic ChemistryPolymerengineering.materialArchaeologyIsocyanateAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundSiliconechemistryCoatingAgeingSide chainengineeringAdhesiveSpectroscopySpectroscopyJournal of Molecular Structure
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Combinatorial synthesis of amino acid- and peptide-carbohydrate conjugates on solid phase

2004

Carbohydrates are useful polyfunctional scaffold molecules which allow the selective attachment of a number of different side chains. The combinatorial solid phase synthesis of diverse amino acid or peptide conjugates of a polyfunctional glucose scaffold based on a set of selectively removable and orthogonally stable protecting groups is described. The resulting carbohydrate-peptide hybrids constitute potential turn mimetics.

chemistry.chemical_classificationPeptidomimeticOrganic ChemistryPeptideCarbohydrateBiochemistryCombinatorial chemistryAmino acidTurn (biochemistry)Solid-phase synthesischemistryDrug DiscoverySide chainConjugateTetrahedron
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