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Self base polymer

Polyimides (PI) are polycondensation products (1) prepared from derivatives of tetracarboxylic acids and primary diamines (1—5). Descriptions of self-polycondensation polymers (2) based on aminodicarboxylic acid derivatives are also found in the literature (6—9). [Pg.396]

To be successful in these applications, it is important that materials can self-assemble into precisely defined structures. Peptide-based polymers have many advantages over conventional synthetic polymers since they are able to hierarchically assemble into stable, ordered conformations [4]. Depending on the substituents of the amino acid side chain, polypeptides are able to adopt a multitude of... [Pg.2]

M. Granstrom, M. Berggren, D. Pede, O. Inganas, M.R. Andersson, T. Hjertberg, and O. Wennerstrom, Self-organizing polymer films — a route to novel electronic devices based on conjugated polymers, Supramol. Sci., 4 27-34, 1997. [Pg.284]

Other self-reinforced polymers are being developed. For example, PURE is based on highly oriented co-extruded tapes of polypropylene and a consolidation binder. Properties vary according to the form (see Table 6.27) - sheets, tapes or fabrics. [Pg.817]

Water self-diffusion coefficients (Dh o) have been determined by pulse field gradient NMR for Nation (Nil/) , BPSH, and SPEEKK and have been shown to increase with increasing acid and water content. At high water contents, the values for PEMs approach the corresponding value for pure water. This is due to the increase in volume fraction of free water. At low water content, however. Nation exhibits greater Dnp values than either BPSH or SPEEKK. In corranon with the observations for EOD, this has been attributed to the smaller channels in aromatic-based polymers, leading to a considerably lower dielectric constant for the water in the channels. [Pg.128]

The recognition that self-limited arylamine-based polymers could be electrochemically activated in aqueous acids has led to a new class of 3-D hybrid... [Pg.248]

Self-Associative Polymer Network. In self-associative polymer networks (often called one component systems), the hydrogen bonding recognition units that are covalently attached to the polymer backbone have an appreciable tendency for self-association, that is, self-dimerize, which leads to interchain cross-linking of the polymers. As a result, the system is inherently cross-linked and does not require any external cross-linking agents for network formation (Fig. 5.11a). Because the cross-linking is based on dimerization phenomena, to achieve effective... [Pg.121]

Syntheses of Self-Sensitized Polymers by Cationic Copolymerizations. The cationic polymerizations of several vinyl ethers containing pendant ester groups such as cinnamic ester 12), methacrylic ester 16), acrylic ester (77), and crotonic ester 18) have been reported. Based on these reports, cationic copolymerizations of CEVE with photosensitizer monomers such as NPVE, NNVE, VNP and NPEVE were carried out using TFB as a catalyst in toluene at — 65 °C. Each copolymer was obtained with high yield except in the case of copolymerization of CEVE with VNP as summarized in Table I. [Pg.228]

As early as 1968, self-assembled Schiff base polymers were developed by O Connell and co-workers, by the reactions between divalent metal ions with monomers consisting of two Schiff base type cheating units separated by a... [Pg.376]

As in the case of terpyridine-based polymers, we first reported the application of Zn(II) Schiff base polymers in PLEDs.33 We prepared a family of soluble self-assembled Zn(II) Schiff base polymers, which are thermally stable, structurally diverse and easily modified (Fig. 17). The number-average molecular weight (Mn) of the polymers range from 13580 to 20440, as determined using gel permeation chromatography (GPC) with polystyrene as a standard in THF (tetrahydrofuran) at 35°C. The decomposition temperature (Td) of the polymers range from 389° (2g) to 461°C (2h). No phase transition was observed in DSC up to 300°C for these polymers (Table 4). [Pg.378]

One assembly example is polyethylenamine (PEI)-mediated self-assembly of FePt nanoparticles [56]. PEI is an all -NH-based polymer that can replace oleate/oleylamine molecules around FePt nanoparticles and attach to hydrophilic glass or silicon oxide surface through ionic interactions [52], A PEI/FePt assembly is readily fabricated by dipping the substrate alternately into PEI solution and FePt nanoparticle dispersion. Figure 10 shows the assembly process and TEM images of the 4 nm Fes8Pt42 nanoparticle self-assemblies on silicon oxide surfaces. Characterizations of the layered structures with X-ray reflectivity and AFM indicate that PEI-mediated FePt assemblies have controlled thickness and the surfaces of the assemblies are smooth with root mean square roughness less than 2 nm. [Pg.249]

First, given the wide range of prebiotic nucleic acids, ribose-based polymers may be the most eminently suited for catalysis. Eschenmoser has pointed out, for example, that nucleic acids constructed from hexose nucleotides form inflexible ribbon structures,61 poorly suited for convoluting into the complex shapes that are required for catalysis (e.g., the backbone of the projected tertiary structure of the Tetrahymena self-splicing intron folds back on itself a number of times).62 Conversely, backbones composed of acyclic nucleotides may be too flexible to adopt stable secondary structures (since a great deal of entropy would necessarily be lost on freezing into a given conformer). Ribose, on the other hand, has a limited flexibility because of its pseudorotation cycle, and RNA can adopt a variety of helical conformations. [Pg.657]

With conventional chips, it is well known that thiolated-DNA can be easily immobilized on gold but does not interact by ordered self-assembly, due to nonspecific interactions between the DNA bases and the gold. Different alkanethiols have been used to improve the hybridization efficiency and the selectivity, followed by immobilization of thiolated-DNA on the substrate [59,61,69]. Hence, this method requires two steps and needs consideration concerning the experimental conditions. However, DNA-conjugated polymer does not only prevent desorption of probe DNA from the surface, because the DNA is covalently bound to the self-assembly polymer, but it also... [Pg.102]

Fig. 7 Illustration depicting molecular recognition based polymer-mediated nanoparticle self-assembly. Interparticle distance and corresponding blocking temperature (Tb) of hexanes induced precipitations and polymer mediated aggregates... Fig. 7 Illustration depicting molecular recognition based polymer-mediated nanoparticle self-assembly. Interparticle distance and corresponding blocking temperature (Tb) of hexanes induced precipitations and polymer mediated aggregates...
Figure 4. PFGSE H self diffusion in PolyPOMSOs Based Polymers and Monomers. Figure 4. PFGSE H self diffusion in PolyPOMSOs Based Polymers and Monomers.
Besides the self-assembled polymer vesicles there are other types of membranes or capsules, which will not be mentioned here. Commercial membranes based on cellulose include dialysis bags or filter paper, to mention just the most common and widely spread examples [14], Capsules made with sophistication through layer-by-layer assembly on sacrificial templates [15,16] or using viruses as building blocks [17,18] have recently been reviewed elsewhere. [Pg.169]

Over the past 10 years, research into water-soluble ferrocene-based polymers and polyelectrolytes has increased.168-175 Vancso and co-workers have reported the preparation and self-assembly of anionic and cationic polyelectrolytes.171,172 Polyanionic, 89, and polycationic, 90, ferrocene-based electrolytes are two examples of such polyelectrolytes.170... [Pg.65]


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See also in sourсe #XX -- [ Pg.229 , Pg.230 ]




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