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Seleninates

An elegant application of Se NMR spectroscopy, in conjunction with N NMR spectroscopy, involves the detection of the thermally unstable eight-membered rings (RSeN)4 (3.13) from the reactions of a mixture of seleninic anhydrides (RSeO)20 (R=Ph, Pr) and N-enriched... [Pg.36]

KGS3 K. N. Selenin and V. V. Alekseev, Khim. Geterotsikl. Soedin. 3... [Pg.309]

Gould has reported the following acidity constants (in H20 at 25 °C) for some substituted benzene seleninic acids ArSe 02H. [Pg.244]

Optically active arenetellurinic acid 23 was obtained for the first time by chromatographic resolution of the racemic sample on a chiral column in 2004.37 It is stable toward racemization in solution, whereas the corresponding seleninic acids racemize in solution under similar conditions. Its absolute configuration was assigned by comparing the circular dichroism spectra with that of an optically active seleninic acid (Scheme 10). [Pg.583]

Kinetic studies on racemization, oxygen exchange reaction using H2lsO, and theoretical studies clarified the mechanism for racemization of optically active chalcogenic acids.34,37 The mechanism of racemization of tellurinic acids is different from that of the corresponding seleninic acids. In fact, the mechanism for racemization of optically active tellurinic acids was found to involve an... [Pg.583]

Diorgano diselenides have been used extensively as precursors to seleninic acids in the presence of hydrogen peroxide.The catalytic activity of preformed seleninic acids and seleninic acids generated in situ are identical. Diorgano ditellurides have also been used as catalysts in thiolperoxidase-like reactions for the oxidation of thiols with various peroxides. However, tellurinic acids are not thought to be involved even though RTe(=0)SPh types of structures are proposed as intermediates. [Pg.113]

Oximes, Hydrazones, and Semicarbazones.—Hydrazones and semicarbazones of 3-oxo-A - and -A -steroids may be smoothly converted into the parent ketones by treatment with benzene seleninic anhydride. ... [Pg.244]

Abstract—The results of solving the Schrodinger equation for the simple case of a proton moving in a potential field with two equal minima are given for a series of physically possible parameters. Several examples of infrared spectra containing double voh bands such as potassium hydrogen phosphate, carboxylic acids, and seleninic acid, are discussed wad compared with the results of the calculations. [Pg.147]

Tris(organoseleninate) complexes have been synthesized and, in DMF or nitromethane, are non-conducting.261 The ligands act as bidentate 0,0 -seleninate and the complexes have an octahedral configuration with Z>3 symmetry. [Pg.479]

Iodine in the presence of sodium hydrogen carbonate converts diselenides quantitatively into seleninic acids ... [Pg.14]

Dibenzyl diselenide crystallises from alcohol in yellow needles, which are slightly deeper in colour than those of the p-nitrobenzyl compound, and melt at 92° to 93° C. Exposure to light for an hour or so causes the crystals to turn red. The selenide readily dissolves in hot alcohol, but is only sparingly soluble in ether, insoluble in water. Oxidation with fuming nitric acid converts it into benzyl seleninic acid, and boiling with copper or mercury in suspension precipitates selenium. Boiling with iodine in chloroform solution gives the tetra-iodide, M.pt. 98° C. the tetrabromide melts at 137° C.5... [Pg.27]


See other pages where Seleninates is mentioned: [Pg.333]    [Pg.93]    [Pg.181]    [Pg.110]    [Pg.111]    [Pg.244]    [Pg.254]    [Pg.1204]    [Pg.1569]    [Pg.254]    [Pg.4]    [Pg.577]    [Pg.582]    [Pg.584]    [Pg.584]    [Pg.808]    [Pg.32]    [Pg.154]    [Pg.113]    [Pg.113]    [Pg.336]    [Pg.540]    [Pg.543]    [Pg.333]    [Pg.540]    [Pg.543]    [Pg.154]    [Pg.869]    [Pg.133]    [Pg.62]    [Pg.5]    [Pg.20]    [Pg.40]   
See also in sourсe #XX -- [ Pg.881 ]




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Diselenide/seleninic acid

Diselenides seleninic acids

Esters seleninate, formation

Selenides Seleninic acids

Seleninate ester

Seleninic Acids and their Derivatives

Seleninic acid anhydrides

Seleninic acid anhydrides benzeneseleninic anhydride

Seleninic acid, allyl

Seleninic acid, phenylhydroxylation

Seleninic acid, phenylhydroxylation alkenes

Seleninic acids

Seleninic acids oxidation

Seleninic acids synthesis

Seleninic add

Seleninic anhydride

Seleninic anhydride, 2-pyridine

Seleninic special

Selenins

Selenins

Sulphinic and Seleninic Acids

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