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The energetics of N2 reduction by vanadium containing nitrogenase.

Authors :
Siegbahn, Per E. M.
Wei, Wen-Jie
Source :
Physical Chemistry Chemical Physics (PCCP); 1/21/2024, Vol. 26 Issue 3, p1684-1695, 12p
Publication Year :
2024

Abstract

The main class of nitrogenases has a molybdenum in its cofactor. A mechanism for Mo-nitrogenase has recently been described. In the present study, another class of nitrogenases has been studied, the one with a vanadium instead of a molybdenum in its cofactor. It is generally believed that these classes use the same general mechanism to activate nitrogen. The same methodology has been used here as the one used for Mo-nitrogenase. N<subscript>2</subscript> activation is known to occur after four reductions in the catalytic cycle, in the E<subscript>4</subscript> state. The main features of the mechanism for Mo-nitrogenase found in the previous study are an activation process in four steps prior to catalysis, the release of a sulfide during the activation steps and the formation of H<subscript>2</subscript> from two hydrides in E<subscript>4</subscript>, just before N<subscript>2</subscript> is activated. The same features have been found here for V-nitrogenase. A difference is that five steps are needed in the activation process, which explains why the ground state of V-nitrogenase is a triplet (even number) and the one for Mo-nitrogenase is a quartet (odd number). The reason an additional step is needed for V-nitrogenase is that V<superscript>3+</superscript> can be reduced to V<superscript>2+</superscript>, in contrast to the case for Mo<superscript>3+</superscript> in Mo-nitrogenase. The fact that V<superscript>3+</superscript> is Jahn–Teller active has important consequences. N<subscript>2</subscript>H<subscript>2</subscript> is formed in E<subscript>4</subscript> with reasonably small barriers. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14639076
Volume :
26
Issue :
3
Database :
Complementary Index
Journal :
Physical Chemistry Chemical Physics (PCCP)
Publication Type :
Academic Journal
Accession number :
174836940
Full Text :
https://doi.org/10.1039/d3cp04698b