EPR and Mössbauer Characteristics of Aqueous Solutions of 57Fe-Dinitrosyl Iron Complexes with Glutathione and Hydroxyl Ligands
- Авторлар: Prusakov V.1, Maksimov Y.1, Burbaev D.1, Serezhenkov V.1, Borodulin R.1, Tkachev N.1, Mikoyan V.1, Vanin A.1,2
-
Мекемелер:
- N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
- Institute for Regenerative Medicine, I. M. Sechenov First Moscow State Medical University
- Шығарылым: Том 50, № 7 (2019)
- Беттер: 861-881
- Бөлім: Original Paper
- URL: https://journals.rcsi.science/0937-9347/article/view/248585
- DOI: https://doi.org/10.1007/s00723-019-1112-8
- ID: 248585
Дәйексөз келтіру
Аннотация
Our electron paramagnetic resonance (EPR) studies have demonstrated that at 293 K and 77 K, the spin–lattice relaxation time, T1, of paramagnetic mononuclear dinitrosyl iron complexes (M-DNICs) with glutathione and hydroxyl ligands containing isotopes 57Fe and 56Fe notably exceeds the halflife of the Mössbauer transition, i.e., the lifetime of the 57Fe nucleus in the first excited state (10−7 s). The Mössbauer spectra of M-DNIC with hydroxyl ligands, binuclear DNIC with glutathione (B-DNIC) and sodium dithionite-treated solution of B-DNIC with glutathione did not display the presence of the magnetic hyperfine structure (MHFS) characteristic of M-DNIC with glutathione. The Mössbauer spectra of all these DNICs were characterized by quadrupole splitting. The results of a comprehensive comparative analysis of MHFS of M-DNIC with glutathione and that in DMF reduced sodium nitroprusside suggest that M-DNIC with glutathione have a low-spin (S = ½) d7 electronic configuration with the predominant localization of the unpaired electron on the dz2 orbital of iron. This conclusion is fully consistent with the results of our previous studies of M-DNIC using the EPR method.
Авторлар туралы
Valery Prusakov
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
Email: vanin.dnic@gmail.com
Ресей, Moscow
Yury Maksimov
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
Email: vanin.dnic@gmail.com
Ресей, Moscow
Dosymzhan Burbaev
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
Email: vanin.dnic@gmail.com
Ресей, Moscow
Vladimir Serezhenkov
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
Email: vanin.dnic@gmail.com
Ресей, Moscow
Rostislav Borodulin
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
Email: vanin.dnic@gmail.com
Ресей, Moscow
Nikolay Tkachev
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
Email: vanin.dnic@gmail.com
Ресей, Moscow
Vasak Mikoyan
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences
Email: vanin.dnic@gmail.com
Ресей, Moscow
Anatoly Vanin
N. N. Semenov Institute of Chemical Physics, Russian Academy of Sciences; Institute for Regenerative Medicine, I. M. Sechenov First Moscow State Medical University
Хат алмасуға жауапты Автор.
Email: vanin.dnic@gmail.com
Ресей, Moscow; Moscow