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Mercury, tris complexes

Metallotropic rearrangement, in mercury tri-azenide complexes, 30 41 Metals, see also Heterobimetallics specific element Transition metal complex alkoxides, 15 159-297 of actinides, 15 290-293 of alkali metals, 15 260-263 of alkaline earths, 15 264-266 of aluminium, 15 266-272 of beryllium, 15 264-266 double type, 15 293-294 of gallium, 15 266-272 of lanthanides, 15 290-293 of magnesium, 15 264-266 properties of, 15 260 of transition metals, 15 272-290 trialkylsilyloxides, 15 295-297 of zinc, 15 264-266... [Pg.177]

The helical disposition of the aromatic ligands in the tris complexes confers optical rotatory strength on the ligand transitions [372, 495). This fact may be used to arrive at the absolute configuration of the complex, e.g., (-l-)Ru(phen) + has been shown to exist as a left-handed helix [495). The optical rotatory dispersion of phenanthroline complexes of zinc, cadmium, and mercury has also been studied [419). [Pg.163]

Mercury, tris(l,10-phenanthroline)-structure, 64 Mercury(II) complexes masking agent, 536 Mercury electrodes potential range aqueous solution, 480 Metal carbonyls structure, 16 Metallocenes nomenclature, 126,127 Metallochromic indicators, 554 Metallofluorescent indicators, 558 Metallothionein proteins, 142 Mettd-metal bonding, 137,169 gravimetry, 525 history, 21,23 nomenclature, 122, 123 Metal nitrosyls structure, 16 Metal-phthalein metallochromic indicator, 557 Metal template reactions, 416,433 equilibrium kinetic, 434 thermodynamic, 434 Methane, dichloro-... [Pg.593]

Zinc dithiocarbamates have been used for many years as antioxidants/antiabrasives in motor oils and as vulcanization accelerators in rubber. The crystal structure of bis[A, A-di- -propyldithio-carbamato]zinc shows identical coordination of the two zinc atoms by five sulfur donors in a trigonal-bipyramidal environment with a zinc-zinc distance of 3.786 A.5 5 The electrochemistry of a range of dialkylthiocarbamate zinc complexes was studied at platinum and mercury electrodes. An exchange reaction was observed with mercury of the electrode.556 Different structural types have been identified by variation of the nitrogen donor in the pyridine and N,N,N, N -tetra-methylenediamine adducts of bis[7V,7V-di- .vo-propyldithiocarbamato]zinc. The pyridine shows a 1 1 complex and the TMEDA gives an unusual bridging coordination mode.557 The anionic complexes of zinc tris( V, V-dialkyldithiocarbamates) can be synthesized and have been spectroscopically characterized.558... [Pg.1196]

With simple Hg thiolates the structures of bis(ethanethiolato)mercury Hg(SEt)2321 and of the cysteamine complex [Hg S(CH2)2NH3 2]Cl2322 have reference character, as only weak or no secondary bonds are present, and therefore the central S—Hg—S entities can be considered to be unperturbed. In mercury bis(tri-t-butoxysilanethiolate) Hg[SSi(o-t-Bu)3], with a strictly linear S—Hg—S unit, two weak intramolecular O II g interactions obviously do not affect the bonding in this unit.323... [Pg.1283]

Phenylmercury(II) fluoride-hydrogen fluoride complex fluorinates phenyl(tribromo-methyl)mereury in 60-65% yield when the reaction is carried out in the presence of 48% hydrogen fluoride. Phenyl(trichloromethyl)mercury can be fluorinated to the trifluoromethyl derivative in this manner, but a reaction temperature of 90 C is required. Partial fluorination of (bromodichloromethyl)phcnylmcrcury to (dichlorofluoromethyl)phenylmercury in 60% yield can be achieved at room temperature, but attempted partial fluorination of phenyl(tri-bromomethyl)mercury, (dibromochloromethyl)phenylmercury, and (dibromofluoromethyl)-phenylmereury was unsuccessful phenyl(trifluoromethyl)mercury is the major product obtained.61... [Pg.652]

Tri(f-butyl)phosphine and tri(o-tolyl)phosphine form 1 1 complexes with mercury(II) halides and with Hg(SCN)2. Physicochemical measurements, Le. conductance, molecular weight determinations, IR and Raman spectra, indicate a dimeric structure (26) of Cy, skeletal symmetry.493... [Pg.1081]

Tri(o-tolyl)stibine reacts with mercury(II) halides in cold benzene solution to form 1 1 complexes. Under reflux the stibine is chlorinated to R3SbCl2 by HgCl2, which is reduced to Hg2Cl2. In refluxing THF the products are RHgCl and R2SbCl.529 Triarylbismuthines... [Pg.1084]

As mentioned earlier, the carbene ligand in our complexes shows nucleophilic character with respect to the metal fragment. Therefore, we decided to combine it with an electrophilic carbene. For this purpose we treated pentacarbonyl[methoxy(phenyl)carbene]chromium(0) with phenyl(tri-chloromethyl) mercury (85). Compounds of this kind have been studied intensively by Seyferth et al. (86) and are known as a source of dihalogeno-carbenes. The carbene complex reacted with the carbenoid compound at... [Pg.20]

Garbometallation of carbon-carbon unsaturated bonds is an important synthetic method for the construction of complex molecules.277-281 An example of carboindation is described with tri(5-hexenyl)indium, prepared from di(5-hexenyl)mercury and indium metal, which is cyclized to a cyclopentylindium compound.282... [Pg.693]


See other pages where Mercury, tris complexes is mentioned: [Pg.713]    [Pg.1075]    [Pg.1245]    [Pg.392]    [Pg.1245]    [Pg.2552]    [Pg.4699]    [Pg.195]    [Pg.161]    [Pg.1278]    [Pg.458]    [Pg.115]    [Pg.92]    [Pg.1053]    [Pg.1060]    [Pg.288]    [Pg.17]    [Pg.324]    [Pg.629]    [Pg.937]    [Pg.1084]    [Pg.1086]    [Pg.657]    [Pg.1016]    [Pg.1606]    [Pg.1060]    [Pg.454]    [Pg.459]    [Pg.11]    [Pg.1293]    [Pg.256]   


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Mercury complexes

Mercury complexing

Tri complexes

Tris complexes

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