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Carboxylates metal complexes

In contrast to metal complexes of OjoTydroxyazo types, these terminally metallized dyes derived from the o-hydroxy carboxyl stmctures undergo httie color change on metallization and exhibit Httie improvement ia lightfastness (49). [Pg.437]

Entries where the oxidation state of a metal has been specified occur after all the entries for the unspecified oxidation state, and the same or similar entries may occur under both types of heading. Thus cyanide appears under Chromium complexes, Chromium(O) complexes, Chromium(I) complexes, etc. More specific entries, such as Chromium, hexacyano-, may also occur. Similar ligands may also occur in different entries. Thus a carboxylic acid-metal complex may occur under Carboxylic acid complexes, under entries for specific carboxylic acids, and under the specific metal. Coordination complexes may also be listed in the Cumulative Formula Index. [Pg.73]

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]

Oxidative addition of the O-H bond to transition metal complexes gives hydrido(hy-droxo), hydrido(alkoxo) or hydrido(carboxylato) complexes (Eq. 6.1), but web-characterized complexes obtained as primary products from the reaction of the compound, XO-H (XO-H = water, alcohol, and carboxylic acid) with late transition metals are quite rare [1]. Furthermore, the crystal stractures of very few complexes of this type have been reported. In this section we will survey late transition metal complexes resulting from activation of water, alcohol, and carboxylic acid. [Pg.172]

Multinuclear mixed-metal complexes can be formed with carboxylate ligands. [Pg.1177]

The electroreductive carbonylation and carboxylation of organic halides catalyzed by different metal complexes is summarized in Section 9.10.5. Electrogenerated Ni° complexes containing bpy193-196 or pentamethyldiethylenetriamine196-199 ligands are effective catalysts for the electrosynthesis of... [Pg.484]

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]


See other pages where Carboxylates metal complexes is mentioned: [Pg.98]    [Pg.1719]    [Pg.7184]    [Pg.260]    [Pg.98]    [Pg.1719]    [Pg.7184]    [Pg.260]    [Pg.276]    [Pg.348]    [Pg.291]    [Pg.83]    [Pg.90]    [Pg.145]    [Pg.205]    [Pg.207]    [Pg.369]    [Pg.380]    [Pg.228]    [Pg.76]    [Pg.7]    [Pg.238]    [Pg.369]    [Pg.383]    [Pg.50]    [Pg.76]    [Pg.456]    [Pg.18]    [Pg.352]    [Pg.354]    [Pg.611]    [Pg.1181]    [Pg.42]    [Pg.353]    [Pg.373]    [Pg.73]    [Pg.95]    [Pg.91]    [Pg.111]    [Pg.114]    [Pg.826]   


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Carboxylate complexes

Carboxylic acids metal complexes

Carboxylic acids reaction with metal complexes

Carboxylic metalation

Hydrazinium metal complexes carboxylates

Metal carboxylates

Metal carboxylates complex salts

Metal carboxylates manganese complex

Metal carboxylates nickel complex compounds

Metal carboxylates rhodium complex

Metal complexes with carboxylic acids

Pyridine-2-carboxylic acid, formation metal complexes

Rare earth metal carboxylate complexes

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