Тип публикации: статья из журнала
Год издания: 2015
Идентификатор DOI: 10.1021/jp510522z
Ключевые слова: DENSITY-FUNCTIONAL THEORY, NICKEL-IRON HYDROGENASE, DEGENERATE PERTURBATION-THEORY, MOLECULAR-ORBITAL METHODS, NIFE HYDROGENASE, CATALYTIC CYCLE, ELECTRONIC-STRUCTURE, WAVE-FUNCTIONS, BASIS-SETS, HIGH-SPIN, Density functional theory, Electronic states, Perturbation techniques, Potential energy, Probability, Torsional stress, Active-site modeling, Inter-system crossings, Landau-Zener theory, Non-adiabatic transitions, Nonadiabatic transition probabilities, Potential energy curves, Singlet and triplet state, Triplet electronic state, Binding energy, hydrogen, hydrogenase, chemistry, enzyme active site, metabolism, quantum theory, Catalytic Domain
Аннотация: We investigate the effect of H-2 binding on the spin-forbidden nonadiabatic transition probability between the lowest energy singlet and triplet electronic states of%NiFe]-hydrogenase active site model, using a velocity averaged Landau-Zener theory. Density functional and multireference perturbation theories were used to provide paПоказать полностьюrameters for the LandauZener calculations. It was found that variation of the torsion angle between the terminal thiolate ligands around the Ni center induces an intersystem crossing between the lowest energy singlet and triplet electronic states in the bare active site and in the active site with bound H-2. Potential energy curves between the singlet and triplet minima along the torsion angle and H-2 binding energies to the two spin states were calculated. Upon H-2 binding to the active site, there is a decrease in the torsion angle at the minimum energy crossing point between the singlet and triplet states. The probability of nonadiabatic transitions at temperatures between 270 and 370 K ranges from 35% to 32% for the active site with bound H-2 and from 42% to 38% for the bare active site, thus indicating the importance of spin-forbidden nonadiabatic pathways for H-2 binding on the%NiFe]-hydrogenase active site.
Журнал: JOURNAL OF PHYSICAL CHEMISTRY A
Выпуск журнала: Vol. 119, Is. 6
Номера страниц: 1066-1073
ISSN журнала: 10895639
Место издания: WASHINGTON
Издатель: AMER CHEMICAL SOC