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Nickel complexes, lability coordinated water

The Variation of the Lability of Coordinated Water in Nickel(II) Complexes... [Pg.36]

It is clear from Table I that there is no evidence that a 1- or 2- complex loses its coordinated water at a faster rate than a 1+ or 2+ complex. In fact, the [Nidien] complex is much more labile to NH substitution than are the negatively charged complexes of nickel. It is also not true that the binding strength of a ligand in the inner coordination sphere of a metal ion depends necessarily on its overall charge (cf. SO as compared to H O (1)). [Pg.291]


See other pages where Nickel complexes, lability coordinated water is mentioned: [Pg.408]    [Pg.452]    [Pg.452]    [Pg.6597]    [Pg.289]    [Pg.292]    [Pg.36]    [Pg.56]    [Pg.272]    [Pg.233]    [Pg.87]    [Pg.291]   
See also in sourсe #XX -- [ Pg.32 ]




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