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Thiocyanate complexes electronic spectra

The lowest energy MLCT transition of Ru polypyridyl complexes of the type tris-[Ru(4,4/-dicarboxy-2,2/-bipyridine)3] (1), can be lowered so that it absorbs more in the red region of the visible spectrum by replacing one 4,4/-dicarboxy-2,2/-bipyridine (dcbpy) with two thiocyanate donor ligands [Ru(dcbpy)2(NCS)2] (2). In complex 2, the two 4,4/-dicarboxylic acid 2,2 -bipyridine ligands pull while the two thiocyanate donor ligands push electrons. The oxidation potential of the complex 2 is 0.85 V vs. SCE, which is cathodically shifted significantly (0.65 V vs. SCE) compared to the homoleptic type of complex 1, which shows Ru(III/II) couple at 1.5 V vs. SCE. Thus, the... [Pg.122]


See other pages where Thiocyanate complexes electronic spectra is mentioned: [Pg.57]    [Pg.250]    [Pg.274]    [Pg.246]    [Pg.350]    [Pg.73]    [Pg.516]    [Pg.142]    [Pg.174]    [Pg.156]    [Pg.305]    [Pg.474]   
See also in sourсe #XX -- [ Pg.263 , Pg.264 ]




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Thiocyanate complexes

Thiocyanate electronic spectra

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