Multireference Protonation Energetics of a Dimeric Model of Nitrogenase Iron-Sulfur Clusters

Characterizing the electronic structure of the iron-sulfur clusters in nitrogenase is necessary to understand their role in the nitrogen fixation process. One challenging task is to determine the protonation state of the intermediates in the nitrogen fixing cycle. Here, we use a dimeric iron-sulfur model to study relative energies of protonation at C, S, or Fe. Using a composite method based on coupled cluster and density matrix renormalization group energetics, we converge the relative energies of four protonated configurations with respect to basis set and correlation level. We find that accurate relative energies require large basis sets as well as a proper treatment of multireference and relativistic effects. We have also tested ten density functional approximations for these systems. Most of them give large errors in their relative energies. The best performing functional in this system is B3LYP, which gives mean absolute and maximum deviations of only 10 and 13 kJ/mol with respect to our correlated wave function estimates, respectively, comparable to the uncertainty in our correlated estimates. Our work provides benchmark results for the calibration of new approximate electronic structure methods and density functionals for these problems.

Automated summary

Characterizing the electronic structure of iron-sulfur clusters in nitrogenase is crucial for understanding their role in the nitrogen fixation process. This study investigates the protonation state of intermediates in the nitrogen fixing cycle using a dimeric iron-sulfur model. The results reveal the importance of large basis sets and accurate treatment of multireference and relativistic effects for obtaining accurate relative energies. Among the density functional approximations tested, B3LYP performs the best, providing benchmark results for future electronic structure methods and density functionals.