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Other Low-Valent Transition Metal Complexes as Redox Catalysts

4 Other Low-Valent Transition Metal Complexes as Redox Catalysts [Pg.42]

The electrochemical allylation of carbonyl compounds by electroreductivc regeneration of a diallyltin reagent from allyl bromide and a Sn species leads to formation of homoallylic alcohols in yields of 70-90 % even in methanol or methanol/water (Table 7, No. 12) Bisaryl formation is possible also from aryl iodides or bromides in the presence of electro-generated Pd phosphane complexes (Table 7, No. 13) In the presence of styrenes, 1,3-butadienes, or phenyl acetylene the products of ArH addition are formed in this way (Table 7, No. 14) . The electroreductivc cleavage of allylic acetates is also possible by catalysis of an Pd°-complex (Table K No. 15) [Pg.42]

A copper(O) complex, electro-generated from Cu(acac)2, is able to undergo an oxidative addition with benzyl and allyl bromides. Further reduction leads to the coupling products bibenzyl and 1,5-hexadienes Methyl-3-hexene-l,6-dicarb-oxylate can be prepared from butadiene and CO by electroreduction if di-Fe dicyclopentadienyl tetracarbonyl is used as redox catalyst Electro-generated low-valent tungsten species are able to reductively dimerize benzaldehyde to stilbene according to Eq. 83. The reduction potential was controlled at the third wave of the WClg catalyst (V = -1900 mV/SCE) [Pg.42]

Electro-generated and regenerated bis(bipyridine)rhodium(I) complexes were able to catalyze the selective non-enzymatically coupled electrochemical generation of NADH from NAD . The direct cathodic reduction even at very negative working potentials leads to the formation of large amounts of enzymatically inactive NAD dimers, while the indirect electrochemical reduction via the rhodium complex acting as [Pg.42]

In addition, the reduction potential of —720 mV vj, Ag/AgCl-reference for the complex with the bipyridine sulfonic acid ligand is about 200 mV more positive as compared with the unsubstituted 2,2 -bipyridine ligand. As a consequence, NAD dimer formation is totally suppressed [Pg.43]




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