Electrochemical Formation of Metal Based Redox Agents Using Water

Session Number

1

Advisor(s)

Aaron H. Shoemaker, Bryan M. Hunter, Northwestern University

Location

A149

Discipline

Chemistry

Start Date

15-4-2026 10:15 AM

End Date

15-4-2026 11:00 AM

Abstract

As an abundant and inert input, water remains a north star of green chemistry. Our research leverages water and green energy inputs (electricity), via cyclic voltammetry, to renewably and sustainably form metal-based reduction and oxidation agents. The reduction agent formed is the cobalt hydride (Co1+–H1- ) species of Cobalt(dppv)2(BF4)2 (dppv = diphenylphosphinovinyl). This species is markedly different from the Co3+–H1 that currently dominates the literature. The oxidation agent being formed is the osmium hydroxide (Os5+–O2-H 1+ ) species of Os(O)2(CN)2( tBu-bpy) (bpy = bipyridine). This cobalt hydride species is anticipated to catalyze olefin hydrogenation, which is the saturation of carbon-carbon double bonds with hydrogen, whereas the osmium hydroxide species is expected to catalyze carbon-hydrogen bond functionalization reactions, or the replacement of a hydrogen with a different functional group. Both of these reactions are extremely important in industrial applications. The difference in behavior between the hydrogens in these two species comes from the charges: negatively charged drives hydride reduction and the positively charged hydrogen in the hydroxide drives oxidation

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Apr 15th, 10:15 AM Apr 15th, 11:00 AM

Electrochemical Formation of Metal Based Redox Agents Using Water

A149

As an abundant and inert input, water remains a north star of green chemistry. Our research leverages water and green energy inputs (electricity), via cyclic voltammetry, to renewably and sustainably form metal-based reduction and oxidation agents. The reduction agent formed is the cobalt hydride (Co1+–H1- ) species of Cobalt(dppv)2(BF4)2 (dppv = diphenylphosphinovinyl). This species is markedly different from the Co3+–H1 that currently dominates the literature. The oxidation agent being formed is the osmium hydroxide (Os5+–O2-H 1+ ) species of Os(O)2(CN)2( tBu-bpy) (bpy = bipyridine). This cobalt hydride species is anticipated to catalyze olefin hydrogenation, which is the saturation of carbon-carbon double bonds with hydrogen, whereas the osmium hydroxide species is expected to catalyze carbon-hydrogen bond functionalization reactions, or the replacement of a hydrogen with a different functional group. Both of these reactions are extremely important in industrial applications. The difference in behavior between the hydrogens in these two species comes from the charges: negatively charged drives hydride reduction and the positively charged hydrogen in the hydroxide drives oxidation