The
cobalt complex, [Co(CR)Br2]+, where CR
is the redox-active macrocycle 2,12-dimethyl-3,7,11,17-tetraazabicyclo-[11.3.1]-heptadeca-1(17),2,11,13,15-pentaene,
has been investigated for the electrocatalytic reduction of aqueous
NO2
– and NO3
–. At neutral pH, the bromide ligands are hydrolyzed, providing [Co(CR)(OH2)(OH)]2+ as the major species in aqueous solution.
In the presence of nitrite, [Co(CR)(NO2)2]+ is formed as the major species in solution and is a precursor
to the electrocatalytic reduction of NO2
–, which is selectively converted to ammonium with high Faradaic efficiency.
There is evidence for both homogeneous and heterogeneous electrocatalysis.
Although similar NO3
– binding is not
observed, electrocatalytic reduction to ammonium also occurs, albeit
with a lower Faradaic efficiency. In this case, NO2
– is generated as an intermediate product of NO3
– reduction.
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