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Gold complex vanadium

SNC, Thiocyanate, gold complex, 26 90 SNOjCjH, 1,2-Benzisothiazol-3(2//)-one 1,1-dioxide, chromium and vanadium complex, 27 307, 309 SOOsPCvH45. Osmium, carbonyl(thiocar-bonyl)tris(triphenylphosphine)-,... [Pg.426]

Many metals are used as chromophores. These can include, but are not limited to, cobalt, nickel, iron, chromium, tungsten, ruthenium, gold, copper, vanadium, titanium, manganese, zinc, aluminum, zirconium, palladium, and tin. Organometallic complexes with these metals are often used as coloring agents for a variety of materials. Coupled with the appropriate ligands, they can be made soluble in a slew of solvents and so can be distributed to wherever they are needed. [Pg.158]

The preparation of two cyclo-octatetraene-gold complexes, (ct)AuCl and (cot)-AU2CI4, has been reported. The structures of biscyclo-octatetraenyl complexes of titanium, vanadium, thallium, and uranium, were deduced from their i.r. spectra. Protonation of (p-cyclo-octatetraene) (p-cyclopentadienyl) complexes has been studied. For the ruthenium and osmium complexes protonation occurs on the eight-membered ring to give CgH moiety co-ordinated to the metal atom via both an T -alkyl and an olefin-metal bond. For the cobalt and rhodium complexes a bicyclic cation (287) is produced which undergoes isomerization to the monocyclic (288). ... [Pg.329]

There are several reasons for performing speciation. Of course there are the academic studies of various types of trace metals and their conversion and equilibria of various forms. Industrial speciation is important. The effectiveness of chromium plating baths depends on the amounts of Cr(III) and Cr(VI) that are present. Gold plating processes involve the use of Au(I) and Au(III) cyanide complexes. Vanadium speciation is important in the recovery of sulfur from geothermal water. [Pg.213]

There are scattered reports on isocyanide complexes of other metals including copper and gold, vanadium, and several lanthanides and actinides. [Pg.80]

Additional examples of the reactions of transition metal complexes with PhICl2 include the oxidation of heterobimetaUic Pt(II)-Au(I) complexes to Pt(III)-Au(II) complexes [75] and the chlorinations or oxidations of palladium [76-78], cobalt [79], vanadium [80], iridium [81] and gold [82] complexes. [Pg.158]

The parent oxacalix[3] arenas show little ability to bind alkali metals,however, a range of quaternary ammonium cations are attracted to the symmetric cavity. Deprotonation of the phenol moieties allows them to bind to transition metals (scandium, titanium, vanadium, rhodium, molybdenum, gold, etc.), lanthanides (lutetium. yttrium, and lanthanum), and actinides (uranium as uranyl). Oxacalix[3]arenes derivatized on the lower rim can complex gallium, mercury, and alkali metals, including sodium, in a manner reminiscent of natural transmembrane cation filters. One major use was to purify crude samples of fullerenes. The pseudo-Cs symmetry of the macrocyclic cavity is complementary to threefold symmetry elements of Cgo. which binds preferentially in... [Pg.651]

Other metal complexes of titanium, zirconium, vanadium, chromium, molybdenum, tungsten, manganese, rhenium, iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium, platinum, copper, silver and gold to synthesize a wide variety of interesting new compounds. It utilizes Hoffmann s [51] isolobal relationship between the C=C bond and the metal-carbon triple bond. [Pg.237]


See other pages where Gold complex vanadium is mentioned: [Pg.72]    [Pg.225]    [Pg.132]    [Pg.134]    [Pg.353]    [Pg.164]    [Pg.179]    [Pg.182]    [Pg.969]    [Pg.1088]    [Pg.12]    [Pg.268]    [Pg.14]    [Pg.317]    [Pg.28]    [Pg.1666]    [Pg.223]    [Pg.5]    [Pg.245]    [Pg.138]    [Pg.1674]    [Pg.4695]    [Pg.618]    [Pg.475]    [Pg.62]    [Pg.39]    [Pg.43]    [Pg.189]    [Pg.179]    [Pg.2762]    [Pg.5]    [Pg.106]    [Pg.112]    [Pg.278]    [Pg.154]   
See also in sourсe #XX -- [ Pg.24 , Pg.25 ]




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