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Hydroxy acids metal complexes

Glycolic acid is the simplest of these hydroxy acids. Metal complexes of this ligand with a wide variety of metal ions have been studied14-16,90-96 and their stereochemistry reviewed.86,871... [Pg.472]

Hydroxy ethylated Carpet printing/dyeing acid, metal-complex dyes Cotton African prints with azoics Polyester disperse dyes Nylon acid, metal-complex dyes Acrylic fibres basic dyes... [Pg.189]

In mordant dyes, phenols, naphthols, and enolizable carbonyl compounds, such as pyrazolones, are generally the couplers. As a rule, 2 1 metal complexes are formed ia the afterchroming process. A typical example of a mordant dye is Eriochrome Black T (18b) which is made from the important dyestuff iatermediate nitro-l,2,4-acid, 4-amiQO-3-hydroxy-7-nitro-l-naphthalenesulfonic acid [6259-63-8]. Eriochrome Red B [3618-63-1] (49) (Cl Mordant Red 7 Cl 18760) (1, 2,4-acid — l-phenyl-3-methyl-5-pyrazolone) is another example. The equiUbrium of the two tautomeric forms depends on the nature of the solvent. [Pg.437]

Metal ion complexes. These classic CSPs were developed independently by Davankov and Bernauer in the late 1960s. In a typical implementation, copper (II) is complexed with L-proline moieties bound to the surface of a porous polymer support such as a Merrifield resin [28-30]. They only separate well a limited number of racemates such as amino acids, amino alcohols, and hydroxy acids. [Pg.59]

Metal complexes of hydroxy-acids. I. V. Pyatnitskii, Russ. Chem. Rev. (Engl. Transl.), 1963, 32, 44-58 (278). [Pg.58]

Naphthalene-3,7-disulfonic acid, 1,2-diamino-iron complexes filter dyes, 6,104 Naphthoic acid, hydroxy-metal complexes, 2, 480, 482... [Pg.171]

Naphthoic acid, 3-hydroxy-copper(II) complexes, 2, 483 metal complexes IR spectra, 2, 469... [Pg.171]

Naphthoic acid, 3-hydroxy-7-sulfonato-metal complexes structure, 2, 482... [Pg.171]

Pinacolone, o-(diphenylphosphino)benzoyl-coordination chemistry, 2, 401 Ping-pong reactions copper(II) complexes, 5, 717 Piperidine, /V-hydroxy-metal complexes, 2, 797 P a values azole ligands, 2, 77 Plant roots amino acids, 2, 962 carboxylic adds, 2,962 Plants... [Pg.196]

Quinoline, 8-mercapto-2-methyl-metal complexes, 2, 800 Quinoline, 2-methyl-8-(methylthio)-metal complexes, 2,801 Quinoline, 8-methylthio-metal complexes, 2, 801 Quinoline-2-carboxylic-acid, 8-hydroxy-methyl ester... [Pg.207]

Quinoline-5-sulfonic acid, 8-hydroxy-7-iodo-metal complexes absorptiometry, 1,549 Quinolinium salts in gravimetry, 1, 535 Quinolinol metal complexes color photography, 6,107 8-Quinolinol biological activity, 6, 771 gallium and indium complexes radiopharmacology, 6, 971 radionuclide complexes radiopharmacology, 6,994 8-Quinolyl sulfate hydrolysis metal catalysis, 6,465 Quinones... [Pg.207]

Good non-colored negative charging CCAs have been obtained by making non-colored analogues of the 2 1 chromium complex azo dyes. This is achieved by making the metal complex of an aromatic ortho-hydroxy carboxylic acid. Typical examples are the chromium, aluminum, and zinc complexes of di-tert-butyl salicylic acid, e.g., BONTRON E-8136 41 (53) and BON-acid36,41,42 e.g., BONTRON E-82 (54). [Pg.567]

Metal-deactivating antioxidants. Transition metal compounds decompose hydroperoxides with the formation of free radicals, thereby increasing the rate of oxidation. Such an enhanced oxidation can be slowed down by the addition of a compound that interacts with metal ions to form complexes that are inactive with respect to hydroperoxides. Diamines, hydroxy acids, and other bifunctional compounds exemplify this type of antioxidants. [Pg.490]

Separation is based on the reversible chelate-complex formation between the chiral selector covalently bonded to the chromatographic support, and the chiral solute with transition metal cations. Chelation properties of both the chiral selector and the chiral solute are required. Compounds therefore need to have two polar functional groups in a favorable arrangement to each other, like a )3-amino acids, amino alcohols and a-hydroxy acids, which can form rings membered with central chelating metal ions, like Cu(II), Zn(II), Cyclic... [Pg.468]


See other pages where Hydroxy acids metal complexes is mentioned: [Pg.116]    [Pg.1076]    [Pg.1722]    [Pg.116]    [Pg.1076]    [Pg.1722]    [Pg.151]    [Pg.234]    [Pg.153]    [Pg.522]    [Pg.426]    [Pg.289]    [Pg.85]    [Pg.90]    [Pg.95]    [Pg.126]    [Pg.171]    [Pg.182]    [Pg.204]    [Pg.207]    [Pg.207]    [Pg.327]    [Pg.238]    [Pg.70]    [Pg.234]    [Pg.154]    [Pg.225]    [Pg.9]    [Pg.860]    [Pg.394]    [Pg.206]    [Pg.168]    [Pg.321]    [Pg.406]    [Pg.437]   
See also in sourсe #XX -- [ Pg.2 , Pg.472 , Pg.480 ]




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