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Poly polymer synthesis

Kozlov, G. V Beeva, D. A. Zaikov, G. E. Mikitaev, A. K. The fractal physics of branched polymers synthesis poly hydroxy ether. J. Characterization and Development of Novel Materials, 2012, 4(4), 357-386. [Pg.307]

These pioneer studies laid dormant until 1977 and, influenced by Kondo and colleagues [59] reports on the synthesis of po]y(vinylsulfonium yiide) with a trivaient sulfur attached directly to the polymer chain, poly[ethyl-vinylsulfonium bis-(methoxycarbonyl) methylide] (Scheme 25) was prepared by irradiation of a benzene... [Pg.378]

PLA degradation, 43 Planar polymer, synthesis of, 505 PLLA. See Poly(L-lactic acid) (PLLA) PMDA. See Pyromellitic dianhydride (PMDA)... [Pg.593]

Poly(phenyleneethynylene)s, 482 optically active, 516-517 synthesis of, 496-500, 502 Poly(m-phenylene isophthalamide), 136 synthesis of, 185-186 Poly(l,4-phenylene terephthalate) liquid crystalline polymers, 51 Poly(para-phenylene)s, 472. See also Poly (p -pheny lene)... [Pg.597]

The requirements outlined above represent a considerable challenge for polymer synthesis. This article describes an appealing development, based on two central substance-classes of conjugated polymers, poly(para-phenylene)s and poly(para-phenylenevinylene)s. [Pg.165]

Polymer Synthesis and Characterization of Poly(N-Pheny1-3,4-Dimethy-lenepyrroline) (VI)... [Pg.131]

Although the amount of poly(3HB-co-3HV) produced in transgenic plants is at present lower than poly(3HB), the demonstration of co-polymer synthesis in seeds of transgenic B. napus represent an important step in the development of crop plants for the production of PHA. [Pg.217]

The knockout of PARP-1 or PARP-2 significantly reduces the cells ability to repair damaged DNA following their exposure to radiation or cytotoxic insult [6,7]. Poly (ADP-ribose) polymer synthesis consumes substantial amounts of NAD+, and hyperactivation of PARP results in depletion of cellular NAD+ pools and energy stores, leading to cell death by necrosis. [Pg.230]

Figure 1. Polymer synthesis scheme for crosslinked poly anhydrides. Figure 1. Polymer synthesis scheme for crosslinked poly anhydrides.
D.A.M. Egbe, S. Sell, C. Ulbricht, E. Birckner, and U.-W. Grummt, Mixed alkyl- and alkoxy-substituted poly[(phenylene ethynylene)-a/t-(phenylene vinylene)] hybrid polymers synthesis and photophysical properties, Macromol. Chem. Phys., 205 2105-2115, 2004. [Pg.269]

H. Liang, J. Yan, and J. Lu, Synthesis and optical characterization of a novel blue luminescent polymer regioregular poly(l-alkoxy-2,4 -m-phenylene vinylene), Synth. Met., 142 143-145, 2004. [Pg.269]

Commercially available hyperbranched polymer, a poly(ester-amide) is currently being marketed by DSM under the product name Hybrane [13] (Figure 8.2). It is also a hydroxyl-functionalized product, but contains both amide and ester linkages. The synthesis is accomplished in two steps cyclic anhydrides are reacted with diisopropanolamine to give an amide-intermediate, possessing two hydroxyl groups and one carboxylic acid. The subsequent polymerization takes places via an oxazolinium intermediate which results in the formation of a... [Pg.200]

Tomalia et al. reported that the surface amines of PAM AM dendrimer can successfully react with methyl esters of other PAMAM dendrimers to afford core-shell tecto-(dendrimer) molecules [65]. Furthermore, they also reported the synthesis of rod-shaped cylindrical dendronized polymers from poly(ethyleneimine) cores without any crosslinking, albeit with the use of excess reagents [58]. These reports lead us to propose a new approach toward hybridized dendrimers and polymers (path C, Figure 15.3). As shown in Scheme 12,... [Pg.378]

We have shown that polymeric micelles constmcted of block copolymers of poly(ethylene oxide) (PEG) and poly(L-asparate) containing the anticancer dmg (adriamycin, ADR) selectively accumulate at solid tumor sites by a passive targeting mechanism. This is likely due to the hydrophilicity of the outer PEG chains and micellar size (<100 nm) that allow selective tissue interactions [17,18]. Polymeric micelle size ranges are tailored during polymer synthesis steps. Carefully selection of block polymer chemistry and block lengths can produce micelles that inhibit nonselective scavenging by the reticuloendothelial system (RES) and can be utilized as targetable dmg... [Pg.28]

The Pd-catalyzed C-C coupling (Sonogashira coupling) was applied to polymer synthesis about 20 years ago [23-25], and has especially been developed for the synthesis of n-conjugated poly(aryleneethynylene)s (PAEs) (for reviews, see refs. [16,26-33]). Recently other synthetic routes for PAEs were also developed, e.g., the alkyne metathesis method [28, 34] and the coupling reaction of =C-MR3 with R X (M=Si [35, 36] or Sn [37, 38]). In this review, we are concerned with the synthesis and chemical properties of PAEs with heteroaromatic rings. [Pg.183]

Polymer Synthesis and Modification. The condensation reaction between either BTDA or BDSDA and ODA was performed in DMAc at room temperature under a nitrogen atmosphere. ODA (0.004 mole) was added to a nitrogen-purged glass septum bottle with 7 ml DMAc. One of the dianhydrides (0.004 mole) was then added to the diamine solution with an additional milliliter of DMAc resulting in 15-25 wt% solids depending upon the monomer combination. The resulting solution was stirred for 20-24 hours to form the poly(amide acid), a polyimide precursor. For the modified polyimides, anhydrous cobalt(II) chloride (0.001 mole) was added as a solid within one-half hour after the dianhydride. [Pg.396]

Lohmeijer BGG, Schubert US (2003) Water-soluble building blocks for metallo-supramo-lecular polymers synthesis, complexation and decomplexation studies of poly(ethylene-oxide) moities. Macromol Chem Phys 204 1072-1078... [Pg.61]

K. Nagai, T. Masuda, T. Nakagawa, B.D. Freeman, and I. Pinnau, Poly[l-(trimethylsilyl)-l-propyne] and related polymers Synthesis, properties and functions, Prog. Polym. Sci., 26(5) 721-798, June 2001. [Pg.38]

Exercise 29-28 Devise a synthesis of a block polymer with poly-1,2-ethanediol and nylon 66 segments. What kind of physical properties would you expect such a polymer to have ... [Pg.1455]


See other pages where Poly polymer synthesis is mentioned: [Pg.745]    [Pg.111]    [Pg.745]    [Pg.111]    [Pg.190]    [Pg.127]    [Pg.332]    [Pg.96]    [Pg.1215]    [Pg.38]    [Pg.595]    [Pg.259]    [Pg.120]    [Pg.565]    [Pg.338]    [Pg.214]    [Pg.9]    [Pg.283]    [Pg.577]    [Pg.663]    [Pg.65]    [Pg.528]    [Pg.71]    [Pg.238]    [Pg.332]    [Pg.431]    [Pg.70]    [Pg.32]   
See also in sourсe #XX -- [ Pg.240 ]




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