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Polymers chemically synthesized

Because of the interest of this topic, several reviews have been reported previously in the literature, most of them focusing on partial aspects or considered within a broader context of general studies on fullerenes. However, no single volume has so far been compiled on the topic of fullerene polymers chemically synthesized, authored by prominent experts in this hybrid field. Therefore, this book aims to highlight and update the most recent advances in this topic, gathering the huge amount of work reported along the years in a rational and systematic way. [Pg.326]

Uses. Butyrolactone is principally consumed by the manufacturers by reaction with methylamine or ammonia to produce A/-meth5d-2-pyrrohdinone [872-50-4] and 2-pyrrohdinone [616-45-5] C H NO, respectively. Considerable amounts are used as a solvent for agricultural chemicals and polymers, in dyeing and printing, and as an intermediate for various chemical syntheses. [Pg.112]

Olefins are the basic building blocks for many chemical syntheses. These unsaturated materials enter into polymers, rubbers, and plastics, and react to form a wide variety of chemical compounds such as alcohols, amines, chlorides and oxides. [Pg.103]

In the field of soluble conducting polymers new data have been published on poly(3-alkylthiophenes " l They show that the solubility of undoped polymers increases with increasing chain length of the substituent in the order n-butyl > ethyl methyl. But, on the other hand, it has turned out that in the doped state the electro-chemically synthesized polymers cannot be dissolved in reasonable concentrations In a very recent paper Feldhues et al. have reported that some poly(3-alkoxythio-phenes) electropolymerized under special experimental conditions are completely soluble in dipolar aprotic solvents in both the undoped and doped states. The molecular weights were determined in the undoped state by a combination of gel-permeation chromatography (GPC), mass spectroscopy and UV/VIS spectroscopy. It was established that the usual chain length of soluble poly(3-methoxthythiophene) consists of six monomer units. [Pg.36]

Okada M. Chemical syntheses of biodegradable polymers. Prog polym Sci, 2002, 27, 87-133. [Pg.247]

Diamantane-based polymers are synthesized to take advantage of their stiffness, chemical and thermal stability, high glass transition temperature, improved solubility in organic solvents, and retention of their physical properties at high temperatures. All these special properties result from their diamantane-based molecular structure [90]. Polyamides are high-temperature polymers with a broad range of applications in different scientific and industrial fields. However, their process is very difficult because of poor solubility and lack of adequate thermal stability retention [90]. Incorporation of 1,6- or... [Pg.228]

Polymer products synthesized in laboratories and in industry represent a set of individual chemical compounds whose number is practically infinite. Macro-molecules of such products can differ in their degree of polymerization, tactici-ty, number of branchings and the lengths that connect their polymer chains, as well as in other characteristics which describe the configuration of the macromolecule. In the case of copolymers their macromolecules are known to also vary in composition and the character of the alternation of monomeric units of different types. As a rule, it is impossible to provide an exhaustive quantitative description of such a polymer system, i.e. to indicate concentrations of all individual compounds with a particular chemical (primary) structure. However, for many practical purposes it is often enough to define a polymer specimen only in terms of partial distributions of molecules for some of their main characteristics (such as, for instance, molecular weight or composition) avoiding completely a... [Pg.162]

With respect to the polymeric backbone, two approaches exist for the preparation of functional polymers, the polymerization or copolymerization of monomers which carry the desired functionality, and secondly the chemical modification of preformed polymers. The former concept, the polymerization of prefunctionalized monomers, was often tested in the early days of polymer-assisted syntheses, e. g. in the preparation of polymers containing pyridine [12] or quinone [13] residues, and benzaldehyde [14] or phosphine [15] functionalities. Although the latter approach demands that the synthetic organic chemist acquires profound knowledge of polymers and polymerization, this strategy can have advantages because... [Pg.203]

Polymer network synthesized using a reactant or reactants of known molar mass or masses and chemical structure. [Pg.223]

Successful solvent-free chemical syntheses have been reported for a variety of small molecules, both with and without the use of microwave irradiation, and for some polymer preparations (Varma, 2000). Solvent-free coatings formulations have also been developed. [Pg.115]

In the present review, we briefly describe the structures, functions and biosynthesis of teichoic acids. Then the chemical syntheses of TAs and fragments of the polymer chains are described in more detail. [Pg.140]

Fig. 3 Top Photograph of silicon cantilevers used as depositing tool during deposition on a glass slide [53], Bottom Fluorescence microscope images of microdot matrices of the nonimprinted control polymer (left), positive control with the copolymerized template (middle), and imprinted polymer (right) synthesized with DMSO-diglyme-1% PVAc as the porogen (a) directly after deposition, (b) after washing and elution of the template, and (c) after reincubation in a solution of 30 pM fluorescein. Reprinted with permission from [53], Copyright (2007) American Chemical Society... Fig. 3 Top Photograph of silicon cantilevers used as depositing tool during deposition on a glass slide [53], Bottom Fluorescence microscope images of microdot matrices of the nonimprinted control polymer (left), positive control with the copolymerized template (middle), and imprinted polymer (right) synthesized with DMSO-diglyme-1% PVAc as the porogen (a) directly after deposition, (b) after washing and elution of the template, and (c) after reincubation in a solution of 30 pM fluorescein. Reprinted with permission from [53], Copyright (2007) American Chemical Society...
A super-hydrophilic absorbing polymer was synthesized from acrylic monomers and chemically crosslinked during the polymerization reaction to optimize barrierdressing properties ... [Pg.38]

The first reports of using cationic polymers for DNA delivery can be traced back to 1973, before the use of cationic lipids. However, until recently, research in the area of polymer-mediated gene delivery lagged behind that of lipid-based delivery vectors [26]. Recent advances in the development of polymers have regenerated the interest in polymer-mediated gene delivery. Polycationic carriers are either naturally occurring or chemically synthesized compounds. Examples include his-... [Pg.126]


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