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Copper 8-hydroxyquinoline General

Discussion. Various metals (e.g. aluminium, iron, copper, zinc, cadmium, nickel, cobalt, manganese, and magnesium) under specified conditions of pH yield well-defined crystalline precipitates with 8-hydroxyquinoline. These precipitates have the general formula M(C9H6ON) , where n is the charge on the metal M ion [see, however, Section 11.11(c)]. Upon treatment of the oxinates with dilute hydrochloric acid, the oxine is liberated. One molecule of oxine reacts with two molecules of bromine to give 5,7-dibromo-8-hydroxyquinoline ... [Pg.407]

H. 8-Hydroxyquinaldine (XI). The reactions of 8-hydroxyquinaldine are, in general, similar to 8-hydroxyquinoline described under (C) above, but unlike the latter it does not produce an insoluble complex with aluminium. In acetic acid-acetate solution precipitates are formed with bismuth, cadmium, copper, iron(II) and iron(III), chromium, manganese, nickel, silver, zinc, titanium (Ti02 + ), molybdate, tungstate, and vanadate. The same ions are precipitated in ammoniacal solution with the exception of molybdate, tungstate, and vanadate, but with the addition of lead, calcium, strontium, and magnesium aluminium is not precipitated, but tartrate must be added to prevent the separation of aluminium hydroxide. [Pg.444]

General Order of Rate Constants. The rate constants of electrophilic reactions of aromatic ligands and their metal complexes fall in the order fo, > kML > kffL. The difference between these rate constants becomes greater as the activity of the attacking reagent decreases. When L is a phenolate, HL is the phenol when L is an amine, HL is the corresponding ammonium derivative. The possible synthetic applications of this sequence can be appreciated from the fact that 8-hydroxyquinoline is usually sulfonated with 15 to 30% oleum, while its copper (II) complex can be readily sulfonated in 70% sulfuric add (5). [Pg.157]

Once the fungicides penetrate to the cell membrane or into the cytoplasm they may operate by devious means to disrupt vital functions. There is substantial evidence that the quinones immobilize the sultliydryl and imino prosthetic group of enzymes. The 8-hydroxyquinoline and dithiocarbamate compounds are active against copper and other metallic members of an enzyme system, presumably hy their ability to chelate metals. Heavy metals such as mercury alTect certain enzymes such as amylases and may serve as general protein precipitants. [Pg.693]


See other pages where Copper 8-hydroxyquinoline General is mentioned: [Pg.195]    [Pg.124]    [Pg.683]    [Pg.464]    [Pg.464]    [Pg.361]    [Pg.5556]    [Pg.6609]    [Pg.248]    [Pg.473]    [Pg.39]    [Pg.826]    [Pg.14]    [Pg.473]   


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