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Poly carboxylic group

A linear molecule has a carboxyl group at one end and an amino group at the other, such as poly(e-caprolactam) ... [Pg.31]

The available free carboxyl groups of the DAS—HMS can be linked via a peptide bond to available primary amine groups onto highly antigenic carriers using a carbodiimide (19). The carriers used in this case were bovine semm albumin (BSA) and poly-L-lysine (molecular weight 150,000 to 300,000). The... [Pg.24]

When equal amounts of solutions of poly(ethylene oxide) and poly(acryhc acid) ate mixed, a precipitate, which appears to be an association product of the two polymers, forms immediately. This association reaction is influenced by hydrogen-ion concentration. Below ca pH 4, the complex precipitates from solution. Above ca pH 12, precipitation also occurs, but probably only poly(ethylene oxide) precipitates. If solution viscosity is used as an indication of the degree of association, it appears that association becomes mote pronounced as the pH is reduced toward a lower limit of about four. The highest yield of insoluble complex usually occurs at an equimolar ratio of ether and carboxyl groups. Studies of the poly(ethylene oxide)—poly(methacryhc acid) complexes indicate a stoichiometric ratio of three monomeric units of ethylene oxide for each methacrylic acid unit. [Pg.342]

These association reactions can be controlled. Acetone or acetonylacetone added to the solution of the polymeric electron acceptor prevents insolubilization, which takes place immediately upon the removal of the ketone. A second method of insolubiUzation control consists of blocking the carboxyl groups with inorganic cations, ie, the formation of the sodium or ammonium salt of poly(acryhc acid). Mixtures of poly(ethylene oxide) solutions with solutions of such salts can be precipitated by acidification. [Pg.342]

The reverse reaction is an intramolecular acidolysis of amide group by the o-carboxyhc acid to reform anhydride and amine. This unique feature is the result of an ortho neighboring effect. In contrast, the acylation of an amine with ben2oic anhydride is an irreversible reaction under the same reaction conditions. The poly(amic acid) stmcture (8) can be considered as a class of polyamides. Aromatic polyamides that lack ortho carboxylic groups are very... [Pg.398]

Alpert has shown [47] that poly(succinimide)-silica can be further hydrolyzed to poly (aspartic acid)-silica or condensed with [3-alanine in aqueous solution to form a covalently bonded copolymer of 2-carboxyethyl aspartamide and aspartic acid. The content of carboxyl groups generated by this way has not been quantified directly, but the cation-exchange hemoglobin capacity has been measured for a series of the packings. Thus, the optimal concentration of poly(succinimide) used in the synthesis was found to be 2 5%. [Pg.151]

This reaction was also applied to reduce the nitrile groups in the maeromolecules of cellulose ethyl cyanates and poly(vinyl alcohol)51. In this case it has been found that along with aldehyde groups a considerable amount of carboxylic groups is also formed. [Pg.116]

Hayama et al.132 discussed the catalytic effects of silver ion-polyacrylic add systems toward the hydrolyses of 2,4-dinitrophenylvinylacetate 84 (DNPVA) by using the weak nudeophilicity of carboxylic groups and the change-transfer interactions between olefinie esters and silver ions133Metal complexes of basic polyelectrolytes are also stimulating as esterase models. Hatano etal. 34, 13S) reported that some copper(II)-poly-L-lysine complexes were active for the hydrolyses of amino acid esters, such as D- and L-phenylalanine methyl ester 85 (PAM). They... [Pg.167]

Fig. 18.—Antiparallel packing arrangement of 2-fold poly(ManA) (15) helices, (a) Stereo view of two unit cells roughly normal to the hoplane. The helix at the center (filled bonds) is antiparallel to the two in the back (open bonds). Intrachain hydrogen bonds stabilize each helix. Association of helices through direct hydrogen bonds involve the carboxylate groups for parallel chains, but involve the axial hydroxyl groups for antiparallel chains, (b) A view of the unit-cell contents down the t-axis highlights the interactions between the helices. Fig. 18.—Antiparallel packing arrangement of 2-fold poly(ManA) (15) helices, (a) Stereo view of two unit cells roughly normal to the hoplane. The helix at the center (filled bonds) is antiparallel to the two in the back (open bonds). Intrachain hydrogen bonds stabilize each helix. Association of helices through direct hydrogen bonds involve the carboxylate groups for parallel chains, but involve the axial hydroxyl groups for antiparallel chains, (b) A view of the unit-cell contents down the t-axis highlights the interactions between the helices.
Fig. 2. Poly(amidoamine) (PAMAM) dendrimers with carboxylate groups at the external surface... Fig. 2. Poly(amidoamine) (PAMAM) dendrimers with carboxylate groups at the external surface...
The FTIR spectra of citrus pectin and wheat straw XRPP (Figure 1) appeared to be similar. Both of the spectra have absorptions at 1740, 1608, 1430, 1360, 1244, 1080, 1060, 1035, 890 and 524 cm. The pectic substances belong to a class of carboxy poly saccharides which differ from neutral polysaccharides, with an intense band in the region 1740 cm l (for salts 1608 cm ) related to vibrations of the carboxyl group... [Pg.641]

The progress of polyester-forming reactions between glycols and dibasic acids is easily followed by titrating the unreacted carboxyl groups in samples removed from the reaction mixture. Simple esterification reactions are known to be acid-catalyzed. In the absence of an added strong acid, a second molecule of the acid undergoing esterification functions as catalyst. The rate of the poly esterification process should therefore be written... [Pg.79]

Broadly speaking, in the study of AB cements derived from poly-carboxylic acids, the band of interest falls in the region 1550-1620 cm (Mehrota Bohra, 1983 Bellamy, 1975). This band is the asymmetric stretch of the carboxylate group and its exact position depends on both the nature of the bonding involved (i.e. whether purely ionic or partially covalent), and the nature of any chelation by the carboxylate group (Bellamy, 1975). [Pg.363]

Many acrylic acid copolymers are water-soluble but unlike poly(vinyl alcohol) they are not degraded by alkali. In fact they need alkali for effective desizing as they are more soluble at alkaline pH than in neutral solutions. They are sensitive to acidic media, which should not be used. Solubilisation occurs by the formation of sodium carboxylate groups from the anionic polyacid. The polyelectrolyte formed in this way is readily soluble and shows a rapid rate of dissolution. However, the presence of electrolytes such as magnesium or calcium salts from hard water can inhibit removal [191]. [Pg.107]


See other pages where Poly carboxylic group is mentioned: [Pg.433]    [Pg.488]    [Pg.494]    [Pg.453]    [Pg.98]    [Pg.13]    [Pg.29]    [Pg.24]    [Pg.91]    [Pg.894]    [Pg.94]    [Pg.96]    [Pg.141]    [Pg.144]    [Pg.146]    [Pg.176]    [Pg.584]    [Pg.71]    [Pg.74]    [Pg.75]    [Pg.362]    [Pg.40]    [Pg.42]    [Pg.175]    [Pg.579]    [Pg.385]    [Pg.408]    [Pg.93]    [Pg.77]    [Pg.158]    [Pg.301]    [Pg.160]    [Pg.9]    [Pg.195]   


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Structure, carboxyl group Poly

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