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Oxidants, soluble polymer-bound

Modification of the Swem oxidation has also been achieved by the use of a soluble, polymer-bound, recyclable, and odorless sulfoxide 1873a [1394]. Sulfoxides bound... [Pg.477]

Ford, W. T. (ed.), Polymeric Reagents and Catalysts , ACS, Washington, DC, 1986. Reviews, of special materials—soluble, polymer bound reagents, ion exchange resins, transition metal catalysts, photosensitizers and polymer bound oxidizing agents. [Pg.1412]

The qualitative thermodynamic explanation of the shielding effect produced by the bound neutral water-soluble polymers was summarized by Andrade et al. [2] who studied the interaction of blood with polyethylene oxide (PEO) attached to the surfaces of solids. According to their concept, one possible component of the passivity may be the low interfacial free energy (ysl) of water-soluble polymers and their gels. As estimated by Matsunaga and Ikada [3], it is 3.7 and 3.1 mJ/m2 for cellulose and polyvinylalcohol whereas 52.6 and 41.9 mJ/m2 for polyethylene and Nylon 11, respectively. Ikada et al. [4] also found that adsorption of serum albumin increases dramatically with the increase of interfacial free energy of the polymer contacting the protein solution. [Pg.137]

It has been outlined by several authors that the single macromolecule may be irreversibly bound because of the large number of weakly interacting segments. The first papers on the construction of polymer-coated silica adsorbents involved the physical adsorption of water-soluble polymers. Polyethylene oxides [28, 29] and poly-/V-vinylpyrrolidone [30] are examples of the stationary phases of this type. [Pg.142]

For example, the cobalt(II) complex for phthalocyanine tetrasodium sulfonate (PcTs) catalyzes the autoxidation of thiols, such as 2-mercaptoethanol (Eq. 1) [4] and 2,6-di(t-butyl)phenol (Eq. 2) [5]. In the first example the substrate and product were water-soluble whereas the second reaction involved an aqueous suspension. In both cases the activity of the Co(PcTs) was enhanced by binding it to an insoluble polymer, e.g., polyvinylamine [4] or a styrene - divinylbenzene copolymer substituted with quaternary ammonium ions [5]. This enhancement of activity was attributed to inhibition of aggregation of the Co(PcTs) which is known to occur in water, by the polymer network. Hence, in the polymeric form more of the Co(PcTs) will exist in an active monomeric form. In Eq. (2) the polymer-bound Co(PcTs) gave the diphenoquinone (1) with 100% selectivity whereas with soluble Co(PcTs) small amounts of the benzoquinone (2) were also formed. Both reactions involve one-electron oxidations by Co(III) followed by dimerization of the intermediate radical (RS or ArO ). [Pg.474]

The reactivity of functionalised crosslinked polymers may significantly differ from that of analogous soluble reagents. Polymer-bound benzyne, generated by Pb(OAc)4-oxidation of resin-bound 1-aminobenzotriazole 3, for example was converted into aryl acetates 4. This reaction was not observed if an analogous 1-aminobenzotriazole derivative 6 was oxidised in solution, where the formation of dimers (7 and 8) was predominant (Scheme 1.6.3). [Pg.46]


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Polymer oxide))

Polymer-bound

Polymers solubility

Soluble polymers

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