Search results for "Macromolecule"
showing 10 items of 235 documents
Hierarchy of Asymmetry at Work: Chain-Dependent Helix-to-Helix Interactions in Supramolecular Polymers.
2018
A detailed investigation of the hierarchy of asymmetry operating in the self-assembly of achiral (1) and chiral ((S)-2 and (R)-3) 1,3,5-triphenylbenzenetricarboxamides (TPBAs) is reported. The aggregation of these TPBAs is conditioned by the point chirality at the peripheral side chains for (S)-2 and (R)-3. An efficient helix-to-helix interaction that goes further in the organization of fibrillar bundles is experimentally detected and theoretically supported only for the achiral TPBA 1. The effective interdigitation of the achiral aliphatic side chains produces a social self-sorting to form preferentially heterochiral macromolecular aggregates.
1H-nmr studies of polyoxyethylene-bound homo-oligo-L-methionines
1982
The use of 1H-nmr spectroscopy is demonstrated to be a useful analytical method to characterize the structure of synthetic peptides attached to soluble, macromolecular polyoxyethylene (POE) supports in the liquid-phase method (LPM) of peptide synthesis. We report an extensive 360-MHz 1H-nmr study of POE-bound homo-oligo-L-methionine peptides. A combination of high field and selective saturation or Redfield pulse methods allows resolution of individual backbone NH and α-CH resonances of dilute peptides in the presence of strong resonances from macromolecular POE and/or protonated solvents. The nmr spectra for the POE-bound peptides in CDCl3 are qualitatively similar to those of the low-molec…
Progress in Understanding of the Interactions between Functionalized Polyolefins and Organo-Layered Double Hydroxides
2013
The dispersion of organo-layered double hydroxides (O-LDH) in functionalized polyolefins (POs) is investigated. Two different polyethylene matrices (maleic anhydride (MAH) and diethyl maleate functionalized) are tested and a hydrogenated fatty acid modified LDH is used. The attention is focused on evidencing the interaction between the functional groups of the polymer and the O-LDH through FT-IR. Moreover, a combination of solvent fractionation, morphological, and rheological characterizations enables to gain a deeper insight into the structure of these composites. In particular, the formation of bridging bonds between the particles and MAH functionalized macromolecules is assumed, possibly…
Macromolecules in ordered media. II. A fluorescence study of the polymer-liposome association
1995
The interactions of poly (4-vinyl pyridine) with dimyristoylphosphatidic acid-based liposomes were studied in heterogeneous solution systems. The polymer was dispersed in aqueous buffer solutions of small unilamellar vesicles and after a suitable period of incubation to raise the equilibrium, the experiments has been conducted as a function of polymer concentration and temperature. According to the measurements of the steady-state fluorescence spectra, changes in the intensities as well as shifts in the emission peak wavelength, has served as raw data to accounting for the polymer-vesicle interactions. Quantitative evaluation of the interaction has been done using a simple associating model…
Photosensitive polyurethanes for optical record
2011
The method of synthesis of photosensitive polyurethanes polymers on glycerine, toluenediisocyanate and Disperse Red 1 base has been described. Two types of polymers with different amount of Disperse Red 1 fragments in macromolecules were compared. Films of the polymers were obtained from solutions in organic solvents on glass substrate. The dry film thickness was in the range of 3,5 - 4.5 μm. The transmission spectrums of the films were studied. Possibility of formation of side product in the process of synthesis was observed. The photobirefringence measurements of polymers films were performed. Surface relief grating (SRG) formation was observed during polarization holographic recording pr…
Synthesis, properties and processability of a new class of semirigid liquid crystalline copolyesteramides
1995
Abstract A new family of semirigid main chain liquid crystalline polymers (LCPs), referred to as SBAN, characterized by fairly good processability and mechanical properties, and improved thermal resistance, have been synthesized by the melt polycondensation of sebacic acid (S), 4,4′-dihyhxybiphenyl (B), 4-aminobenzoic acid (A), and 2-hydroxy-6-naphthoic acid (N), in a wide range of compositions. The molar concentration of the A ahd N units, in these LCPs must be kept lower than ca 40 and 60%, respectively, in order to avoid the formation of homopolymeric blocks, which impair spinnability. The presence of A units grants the formation of hydrogen bonds between neighboring macromolecules, and …
Microphase separation in linear multiblock copolymers under poor solvent conditions
2010
Molecular dynamics simulations are used to study the phase behavior of linear multiblock copolymers with two types of monomers, A and B, where the length of the polymer blocks $N_{A}$ and $N_{B}$ ($N_{A}=N_{B}=N$), the number of the blocks $n_{A}$ and $n_{B}$ ($n_{A}=n_{B}=n$), and the solvent quality varies. The fraction $f$ of A-type monomers is kept constant and equal to 0.5. Whereas at high enough temperatures these macromolecules form coil structures, where each block A or B forms rather individual clusters, at low enough temperatures A and B monomers from different blocks can join together forming clusters of A or B monomers. The dependence of the formation of these clusters on the va…
Critical adsorption of a single macromolecule in polymer brushes.
2014
The adsorption of long flexible macromolecules by polymer brush-coated surfaces is studied by molecular dynamics simulations and by calculations using density functional and self-consistent field theories. The case of repulsive interactions between the substrate surface and the monomers of both the brush polymers and the extra chains that can get absorbed into the brush is considered. Under good solvent conditions, critical absorption can occur, if the interaction between the monomers of the brush polymers and the extra chain is (weakly) attractive. It is shown that it is possible to map out the details of the critical absorption transition, if the chain length and/or the grafting density o…
Structure Formation of Polymeric Building Blocks: Complex Polymer Architectures
2013
This chapter describes macromolecules with a complex structure, their defined aggregation in solution, their adsorption to surfaces, and their possible aggregation on surfaces. The term “complex structure” implies that the macromolecules show different, distinct structural elements or building blocks on a supra-atomic length scale. Key to understanding the complex structure of macromolecules, their aggregation, and adsorption to surfaces are intra- and intermolecular interactions such as van der Waals, electrostatic, π–π interactions, and hydrogen bonds.
Laponite clay in homopolymer and tri-block copolymer matrices
2007
Macromolecule/laponite nanomaterials were studied by DSC and X-ray diffraction techniques. The matrices are poly(ethylene) glycols at various molecular masses and poly(ethylene oxides)-poly(propylene oxides)-poly(ethylene oxides) tri-block copolymers. The latter were tuned by modulating the molecular masses, at constant hydrophilic/hydrophobic ratio, and the hydrophilicity. For all the investigated systems, the enthalpy of melting (ΔH m) is nearly constant up to a given composition thereafter it increases monotonically reaching the value of the pure macromolecule. We proposed a model to interpret the DSC data. Briefly, it was invoked a mechanism of interaction following which some segments …