Poly sodium salt

Two inorganic water-soluble polymers, both polyelectrolytes in their sodium salt forms, have been known for some time poly(phosphoric acid) (12) and poly(siHcic acid) (13). A more exciting inorganic water-soluble polymer with nonionic... 

Trilialophenols can be converted to poly(dihaloph.enylene oxide)s by a reaction that resembles radical-initiated displacement polymerization. In one procedure, either a copper or silver complex of the phenol is heated to produce a branched product (50). In another procedure, a catalytic quantity of an oxidizing agent and the dry sodium salt in dimethyl sulfoxide produces linear poly(2,6-dichloro-l,4-polyphenylene oxide) (51). The polymer can also be prepared by direct oxidation with a copper—amine catalyst, although branching in the ortho positions is indicated by chlorine analyses (52). 

Halophenols without 2,6-disubstitution do not polymerize under oxidative displacement conditions. Oxidative side reactions at the ortho position may consume the initiator or intermpt the propagation step of the chain process. To prepare poly(phenylene oxide)s from unsubstituted 4-halophenols, it is necessary to employ the more drastic conditions of the Ullmaim ether synthesis. A cuprous chloride—pyridine complex in 1,4-dimethoxybenzene at 200°C converts the sodium salt of 4-bromophenol to poly(phenylene oxide) (1) ... 

Low molecular weight poly(l,3-phenylene oxide) [25190-64-1] has been prepared from the sodium salt of y -chlorophenol with copper as a catalyst... 

Poly(L-malate) decomposes spontaneously to L-ma-late by ester hydrolysis [2,4,5]. Hydrolytic degradation of the polymer sodium salt at pH 7.0 and 37°C results in a random cleavage of the polymer, the molecular mass decreasing by 50% after a period of 10 h [2]. The rate of hydrolysis is accelerated in acidic and alkaline solutions. This was first noted by changes in the activity of the polymer to inhibit DNA polymerase a of P. polycephalum [4]. The explanation of this phenomenon was that the degradation was slowest between pH 5-9 (Fig. 2) as would be expected if it were acid/base-catalyzed. In choosing a buffer, one should be aware of specific buffer catalysis. We found that the polymer was more stable in phosphate buffer than in Tris/HCl-buffer. 

Figure 2 Stability of /3-poly(L-malate) measured by its activity to inhibit purified DNA polymerase a of P. polyceph-alum. The relative degree of inhibition is shown (100 rel. units refer to complete inhibition). The DNA polymerase assay was carried out in the presence of 5 /tg/ml /S-poly(L-malate) as described [4]. The polymer was preincubated for 7 days at 4°C in the following buffer solutions (50 mM) KCl/HCl (—A—). Citrate (—V—). 2-(A/-Morpholino)-ethanesulfonic acid, sodium salt (—O—). Sodium phosphate (— —). N-(2-Hydroxyethyl)piperazine-N -(2-ethanesul-fonic acid), sodium salt (— — ). N,N-b s (2-Hydroxyethyl)-glycine, sodium salt (—T—). Tris/HCl (— —). 3-(Cyclo-hexylamino)-l-propanesulfonic acid, sodium salt (— —).

There are several other interesting polymers forming SAH with swellings up to 1500 ml g 1 under irradiation in aqueous solutions, such as sodium salts of PAAc [83], copolymers of AAm with AAc [22], poly-N-vinylpyrrolidone [84], PVA... 

Polyphosphazenes sulfonates XIX with the anion covalently attached to the polymer are a new class of cation conductors that have been synthesized by Shriver [625]. They were obtained by reaction of Na0C2H4S03Na with an excess of polydichlorophosphazene in the presence of 15-crown-5, followed by the reaction of the partially substituted product with the sodium salt of poly(ethylene glycol methyl ether). The conductivity at 80 °C of the polymer with x=1.8, m=7.22 is 1.7x10 S cm This low conductivity can be attributed to an extensive ion pair formation between the sodium and sulfonate ions. 

Compared to polycarbonates, little work has so far been published on the synthesis of poly(iminocarbonates). The first attempted synthesis of a poly (iminocarbonate) was reported by Hedayatullah (44), who reacted aqueous solutions of various chlorinated dipheno-late sodium salts with cyanogen bromide dissolved in methylene chloride. Unfortunately, Hedayatullah only reported the melting points and elemental analyses of the obtained products which, according to Schminke (40), were oligomers with molecular weights below 5000. 

Commercially available poly(a-D)galacturonic acid PGA) was purchased from Fluka Chemie. To obtain an aqueous solution of the polyacid, insoluble PGA was converted to its soluble sodium salt and then percolated through a cation-exchange resin in the H-form [3]. 

Figure 1. Scheme showing the polymerization of the trimeric phosphonitrilic chloride to poly(dichlorophosphazene) and its subsequent substitution with the sodium salts of alcohols or phenols... 

Poly(dG-dC) poly(dG-dC) and its methylated analogue structures assume left-handed conformation (Z-DNA) in high molar sodium salt (Na", K" ), in low molar divalent cations (Ca", Mg", Ni ), micromolar concentrations of hexaamine cobalt chloride (Co(NH3)6)Cl3 and in millimolar concentrations of polyamines. In order to analyse the binding of berberine to Z-form DNA, Kumar et al. [186] reported that the Z-DNA structure of poly(dG-dC) poly(dG-dC) prepared in either a high salt concentration (4.0 M) or in 40 mM (Co(NH3)6)Cl3 remained invariant in the presence of berberine up to a nucleotide phosphate/alkaloid molar ratio of 0.8 and suggested that berberine neither bormd to Z-form DNA nor converted the Z-DNA to the... 

Nakano, A. and Minoura, Y., Degradation of aqueous poly(acrylic acid) and its sodium salt solutions by high-speed stirring, /. Appl. Polym. Sci., 22, 2207, 1978. 

Polystyrene-g-poly(ethylene oxide) was synthesized by the copolymerization of styrene and styrenic PEO with CpTiCb/MAO catalyst [190]. In this case the macromonomer was prepared by first reacting the sodium salt of PEO-OH with NaH and then with a 5-fold amount of p-chloromethyl styrene. 

As indicated later (see Section VI,8), on addition of the chloride of praseodymium, europium, or other lanthanides to mono- or poly-sac-charide phosphates in D20, the signals of carbon atoms substituted with phosphate groups are recognizable, as they are displaced, relative to the rest of the 13C-n.m.r. spectrum.155 However, this diagnostic method is not applicable to sulfated polysaccharides, as signal displacements were not observed on addition of praseodymium or europium chloride to a solution of a,/3-D-galactose 6-sulfate or its sodium salt.156... 

PVA/Poly(ethylene glycol) (PEG) membranes crosslinked by aldehydes and sodium salts were used in water desalination by pervaporation. The desalination of 8 % NaCl solution by... 

Scheme II The lysozyme detection mechanism (left) and the chemical structure (right) of poly [9,9-bis(4 -sulfonatobutyl)fluorene-C0-alt-l,4-phenylene] sodium salt (5)...

Sodium ionomers are commercially recognized as the most effective nucleating agents for PET compounds. The typical use rate of sodium ionomer-based nucleating agents is 3-4 wt%. The sodium salt of poly(ethylene-co-methacrylic acid) is a particularly effective nucleating agent for PET. 

Direct copolymerization of sulfonated monomers has been used to synthesize sulfonated poly (benzimidazoles), poly(benzoxazole)s, and poly(benzothia-zole)s. As an example, Kim et al. synthesized poly-(benzthiazole)s from 2,5-diamino-1,4-benzenedithiol dihydrochloride and either 2-sulfoterethphthalic acid sodium salt, 5-sulfoisophthalic acid sodium salt, or 2,4-disulfoisophthalic acid potassium salt in poly-phosphoric acid (PPA), as shown in Figure 34. Similar sulfonated poly(benzimidazole) and sulfonated poly(benzoxazole) ° structures have also been synthesized. A general synthetic scheme for each is shown in Figure 35. The stability of these polymers in aqueous acidic environments appears... 

Water-soluble derivatives of polythiophene have been made allowing counterions bound to the polymer backbone to self-dope with the protons (e.g., lithium and sodium ions) injecting electrons into the pi-system. Thus, combinations of sodium salts and proton salts (e.g., prepared from poly-3-(2-ethanesulfonate)thiophene) have been prepared that are both water-soluble and conducting. 

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