Bipyridyl electrochemical reduction

Electrochemical reduction of pentatluoronitrobenzene produces an intermediate radical anion that couples at position 4 to form the corresponding biphenyl along with hydroxy derivatives from subsequent nucleophilic substitution meta to the nitio groups [44] (equation 34) Similar reduction of halopyridines such as pen-tafluoropyridine leads mainly to 4,4 bipyridyls [45] (equation 35)... 

Systems which fulfil these conditions are tris(2,2 -bipyridyl)rhodium complexes [63] and, more effectively, substituted or unsubstituted (2,2 -bipyridyl) (pentamethylcyclopentadienyl)-rhodium complexes [64], Electrochemical reduction of these complexes at potentials between — 680 mV and — 840 mV vs SCE leads to the formation of rhodium hydride complexes. Strong catalytic effects observed in cyclic voltammetry and preparative electrolyses are... 

Infrared spectral studies have been made for a large number of octahedral metal-carbonyl systems of the types LM(CO)5 (L = pyridine and quinoline), L2M(CO)4 [L2 = ethylene diamine, (pyridine)2, and bipyridyl], [LM(CO)4]2 (L = dimethylarsine or dimethylphosphine M = Cr, Mo, and W), and [LFe(CO)3]2 (L = SMe, PMe2) before and after electrochemical reduction. The force constants for the carbonyl groups... 

The crystal structure of bis(NN-di-isobutyldithiocarbamato)nickel(ii). [Ni(S2-CNBu 2)2], shows that nickel is approximately square planar and co-ordinated by two symmetric bidentate ligands (Ni—S = 2.20 A) the ligand symmetry approximates to 2- The reduction mechanism of a series of nickel(ii) dithiocarbamates has been investigated in DMSO at the mercury electrode it is claimed to involve a dissociation to a nickel species which is more easily reduced than the nickel(ii) dithiocarbamate. An e.p.r. study of the reversible electrochemical reduction of nickel(ii) diethyldithio-carbamates in the presence of 2,2 -bipyridyl show that a bipy radical anion is formed initially. Ligand alkylation occurs when ao -dibromo-o-xylene is added to bis-(NiV-diethyldithiocarbamato)nickel(ii). The electron-transfer properties of 16 nickel(ii) dithiocarbamate complexes have been studied in acetone at a platinum electrode. Their oxidation is difficult and irreversible the overall process is ... 

The rationale behind this design was justified upon electrochemical investigation of the [2]catenane 184+. This catenane - synthesized in 43% yield (Fig. 26) from crown ether BPP34C10, the bipyridinium dibromide derivative 192+ and ( )-l,2-bis(4,4 -bipyridyl)ethylene - was demonstrated to consist, in solution, of mainly co-conformer A, with the more powerful n-electron-accepting bipyridinium unit located inside the cavity of the crown ether. Upon electrochemical reduction of this bipyridinium unit, the cyclophane undergoes a circumrotational movement with respect to the crown ether such that the profoundly more electron-deficient 7t-extended bipyridinium unit resides inside the cavity of the crown ether, affording co-conformer B. When the bipyridinium radical cation is oxidized back down to its dicationic state, the opposite circumrotational process occurs and the system reverts back to co-conformer A, its ground state [49]. 

Electrocatalytic reductive coupling of aryl chlorides to afford biphenyls can be accomplished with dichloro(l,2-bis(di-propylphosphino)benzene)nickel(II) in yields as high as 96% with 2 mol % of the catalyst in polar, coordinating solvents (55). Similar couplings can also be achieved with nickel-2,2 -bipyridyl and Pd(PPh3)2Cl2 as catalysts (56, 57). Indirect electrochemical reduction of vicinal dibromides to alkenes occurs efficiently with iron and cobalt porphyrins as mediators (58). Vitamin B12 is a mediator for the indirect electrochemical reduction of a-halo acids (59). 

Fig. 17. Electroenzymatic reduction of 4-phenyI-2-butanone catalyzed by HLADH with in-situ indirect electrochemical regeneration of NADH using a Cp (2,2 -bipyridyl)aquo rhodium(III) complex as mediator...

While many metal centers can be reversibly cycled between two (or more) oxidation states, few organic moieties can match such reversibility especially in protic media. Nevertheless, the first supramolecular example of an electroswitch-able luminescent device involved the benzoquinone-hydroquinone couple. The luminescence of 55 " is switched off due to PET in the benzoquinone state of the redox couple. Electrochemical or chemical reduction of the benzoquinone under protic conditions to hydroquinone recovers the luminescence of the tris(2,2 -bipyridyl) Ru(II) unit. It is noted that the luminescence of tris(2,2 -bipyridyl) Ru(Il) itself is electroswitchable. Indeed tris(2,2 -bipyridyl) Ru(II) came to fame as a solar energy material from more humble beginnings as a luminescent redox indicator. However 55 achieves the same switching at a lower magnitude of reduction potential. Here lies the advantage of the supramolecular design. Like tris(2,2 -bipyridyl) Ru(II), many lumophores show electroswitchable luminescence. An... 

The ruthenium(II) bipyridyl moiety is also capable of functionally sensing the presence of bound anion. Electrochemical anion recognition experiments showed substantial anion induced cathodic perturbation of the ligand centered amide substituted 2,2 -bipyridine (bpy) reduction redox couple. These perturbations were in agreement with stability constant values, with 134 sensing H2PO4- in the presence of 10-fold excess of HS04 and Cl . Fluorescence emis-... 

Another class of mixed-metal anion receptors has been investigated which possess redox reporter groups based on two different metal complexes. This enables the quahtative comparison of their comparative anion-sensing abih-ties. Macrocycles 35 and 36 combine the Ru (bpy)3 moiety with a bridging ferrocene or cobaltocenium imit [29]. Electrochemical experiments in acetonitrile solution revealed that the Ru VRu redox potential was insensitive to anion binding, whereas the ferrocene/ferrocenium (in 35) and cobal-tocene/cobaltocenium (in 36) redox couples were shifted cathodically (by 60 mV and 110 mV respectively with chloride). However, the first reduction of Ru°(bpy)3, a Hgand-centred process based on the amide substituted bipyridyl, was also found to imdergo an anion induced cathodic shift (40 mV and 90 mV with chloride for 35 and 36, respectively). 

Chemiluminescence can also be produced by electrochemical oxidation or reduction (electrogenerated chemiluminescence). Ruthenium and osmium chelates show the ability to emit light when undergoing an electrochemical process. Based on this phenomenon, an electroluminescence immunoassay has been developed using a ruthenium(II) tris(bipyridyl) chelate as a label. 

---