2020ACS CatalysisRequires access

Electrocatalytic Multielectron Nitrite Reduction in Water by an Iron Complex

Jesse R. Stroka, Banu Kandemir, Ellen M. Matson, Kara L. Bren

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Abstract

Catalytic reduction of nitrite by an iron complex in water near neutral pH to form hydroxylamine and ammonium is reported. The catalyst is an iron center coordinated by the pentadentate macrocycle 2,13-dimethyl-3,6,9,12,18-pentaazabicyclo[12.3.1]octadeca-1(18),2,12,14,16-pentaene (FeN 5 H 2 ). Catalysis is observed by cyclic voltammetry at a half-wave potential of E p/2 = −0.98 V vs Ag/AgCl (1 M KCl) when FeN 5 H 2, nitrite, and a buffer (pH 7.2) are present. Controlled potential electrolysis of FeN 5 H 2 and nitrite in pH 7.2 buffer at −0.98 V produces hydroxylamine (faradaic efficiency > 90%). FeN 5 H 2 catalyzes ammonium production by disproportionation of hydroxylamine with concomitant formation of nitrous oxide and dinitrogen. These results are a rare example of multielectron electrocatalytic nitrite reduction by an iron complex near neutral pH.

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What this paper is about

Catalytic reduction of nitrite by an iron complex in water near neutral pH to form hydroxylamine and ammonium is reported. The catalyst is an iron center coordinated by the pentadentate macrocycle 2,13-dimethyl-3,6,9,12,18-pentaazabicyclo[12.3.1]octadeca-1(18),2,12,14,16-pentaene (FeN 5 H 2 ). Catalysis is observed by cyclic voltammetry at a half-wave potential of E p/2 = −0.98 V vs Ag/AgCl (1 M KCl) when FeN 5 H 2, nitrite, and a buffer (pH 7.2) are present. Controlled potential electrolysis of FeN 5 H 2 and nitrite in pH 7.2 buffer at −0.98 V produces hydroxylamine (faradaic efficiency > 90%). FeN 5 H 2 catalyzes ammonium production by disproportionation of hydroxylamine with concomitant formation of nitrous oxide and dinitrogen. These results are a rare example of multielectron electrocatalytic nitrite reduction by an iron complex near neutral pH.

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Available abstract

Catalytic reduction of nitrite by an iron complex in water near neutral pH to form hydroxylamine and ammonium is reported. The catalyst is an iron center coordinated by the pentadentate macrocycle 2,13-dimethyl-3,6,9,12,18-pentaazabicyclo[12.3.1]octadeca-1(18),2,12,14,16-pentaene (FeN 5 H 2 ). Catalysis is observed by cyclic voltammetry at a half-wave potential of E p/2 = −0.98 V vs Ag/AgCl (1 M KCl) when FeN 5 H 2, nitrite, and a buffer (pH 7.2) are present. Controlled potential electrolysis of FeN 5 H 2 and nitrite in pH 7.2 buffer at −0.98 V produces hydroxylamine (faradaic efficiency > 90%). FeN 5 H 2 catalyzes ammonium production by disproportionation of hydroxylamine with concomitant formation of nitrous oxide and dinitrogen. These results are a rare example of multielectron electrocatalytic nitrite reduction by an iron complex near neutral pH.

Key concepts: Hydroxylamine, Chemistry, Nitrite, Inorganic chemistry, Catalysis, Disproportionation, Electrolysis, Ammonium

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