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The Oxidation Catalyst Por Ru CO L

A very prominent class of metalloporphyrins are the tetra(aryl)porphyrin ruthenium carbonyl complexes [(Aryl)4Por)Ru(CO)(L)] (L = solvent) that, in [Pg.104]

Thorough spectroscopic investigation of the first oxidised states using UV-Vis absorption and EPR spectroscopy lead to the assignment of mainly porphyrin-centred oxidations. 87a,b,88a,b,c,s9 typical UV- [Pg.107]

The species generated during the second oxidation were not studied so far, [Pg.107]

However, the interpretation of Ru(I) species being the products of the transformation is not very plausible, since the CO-stretching frequency of the resulting species is closer to the parent complex than the primary radical anions. Another study revealed that the radical anionic [(TPP)Ru(CO)(THF)] readily undergoes formation of the corresponding chlorine complex in the presence of MeL Such electrophilic attack might also be the reason for the above-described transformations in protic or highly polar media. [Pg.108]


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