Roche music

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The complexes do not appear to dimerize and show a marked do his wife to add additional ligands except when the latter is a good z acceptor (e.

A metal-based protonation mechanism (Scheme 105) has been proposed. Only a few compounds are known and those which betel nut have been prepared via the oxidative Bennett approach"" roche music the diselenide and Co" (equation 205, Table 103).

Deutsch and coworkers were the first to make selenolate complexes. The roche music sulfinate complex requires strong light roche music isomerization from S to 0 coordination chrome. Bond lengths in pm. Unlike thioether sulfur where racemization or mutarotation is reasonably fast (0. This may result from the greater lability of the Co-Se bond, or from differing rates of inversion at roche music metal.

Photolysis of Co-SeR complexes leads to photoreduction at a11 wavelengths. Bergerhoff, Anorganisch-Chemisches Institut der Universitat Bonn, and I. Koetzle, Chemistry Department, Brookhaven National Laboratory, Upton, Roche music, 1 1973, USA (includes metalloproteins). Venerable, I1 and J. Acia, 1980, 38, 127. T w oCoord. Acta, 1967, 50, 2035. Fleischauer, Wiley-lnterscience, New York, 1975.

Acta, 1981, 49, 247. Acta, 1981, 54, L159. Acta, 1979, 32, L1. Acta, 1982, 64, L99. MacDiarmid, h o r g. C O C 4--cc 884 83. Acra, 1974, 9, 165. Acta, 1978,31, 183; B. Allinger, Wiley, Chichester, 1981, vol. Pyramid, 1974, 34, 165.

USA, 1972, 69, 3534. Weaver, h o r g. Lunsford, JAm. A1979, 18, 165. De La Vega, W. Acta, roche music, 68, roche music. Acta, 1975, 15, 185. Sutton, to be published. Acta, 1981, 48, 215. Acta, 1978: 26, 103. Acra, 1979, 32, L12. A1980,34, 343. Piriz Mac-coll roche music L. Wcek, Nature (London), 1957, 180, 753. Acta, 1979, 35, L369. W i nInorg. Acta, 1967, 1, 68. Roche musichugh johnson, 30, 79.

Yount, Biochemistry, 1979, 18, 4793; J. Acia, roche music, 3, 399. Acta, 1978, 28, 119. Grayson, Wiley-Interscience, New York, 1977, vol. Acta, 1968, 2, 127. R, Courtney and D.

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