Percorrer por autor "Buvaylo, Elena A."
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- Application of the hirshfeld atom refinement to determine the spin state of the novel Fe(III) schiff base complexPublication . Buvaylo, Elena A.; Goreshnik , Evgeny; Nesterova, Oksana V.; Nesterov, DmytroThe novel complex [FeIII(HL)(L)]·2dmf (1) was successfully synthesized by reacting iron chloride with dimethylformamide solution of the Schiff base ligand (H2L). The ligand was prepared in situ through the condensation of 5-bromo-salicylaldehyde and benzhydrazide. The compound 1 was investigated by single crystal X-ray diffraction, IR spectroscopy, CASSCF/NEVPT2 and DFT theoretical calculations, revealing the high-spin (S = 5/2) state of Fe(III). The Hirshfeld Atom Refinement (HAR) of the crystal structure confirmed the sextet ground spin state of 1 through the comparison of R-factors and Hirshfeld deformation maps of the structures refined assuming high, indeterminate (S = 3/2) and low (S = 1/2) ground spin states. A series of basis sets and DFT functionals was screened, indicating that in most cases the combinations allow the correct determination of the ground state of 1. The def2-SVP double-zeta basis set combined with the GGA (Generalized Gradient Approximation) functional such as PBE or BP86 was found to be a sufficiently precise low-cost computational level. While further investigation is necessary, the results of the work tentatively suggest that the HAR could be successfully used for determination of the ground spin state of Fe(III) complexes even in the case of regular quality X-ray structures.
- Heterometallic CuCd and Cu2Zn complexes with o-vanillin and its Schiff-base derivative: slow magnetic relaxation and catalytic activity associated with Cu(II) centresPublication . Vassilyeva, Olga Yu; Nesterova, Oksana V.; Bienko, Alina; Komarnicka, Urszula K.; Buvaylo, Elena A.; Vasylieva, Svitlana M.; Skelton, Brian W.; Nesterov, Dmytro S.Abstract In this work, two novel heterometallic mixed-ligand mixed-anion complexes [CuIICdIIClL(o-Van) (OAc)]·3H2O (1) and [CuII2ZnIICl2L2(o-Van)(OAc)] (2) were prepared by reacting fine copper powder and Cd(II) or Zn(II) acetate with an ethanol solution of the Schiff-base ligand HL formed in situ in the condensation reaction of 2-hydroxy-3-methoxy-benzaldehyde (o-VanH) and CH3NH2·HCl. The compounds were thoroughly characterized by elemental analysis, FT-IR, UV/Vis and EPR spectroscopy, cyclic voltammetry, and single-crystal X-ray diffraction, revealing the neutral molecular nature of both the compounds. Catalytic properties of 1 and 2 were studied in the oxidation of hydrocarbons with H2O2 under mild conditions, showing the maximum reaction rate of 4 × 10−5 M s−1 and TOF up to 640 h−1. Both compounds undergo complex transformations in solution as evidenced by kinetic analysis and time-dependent UV/Vis spectroscopy, indicating that the reduced Cu(I) form of 1 is unexpectedly unfavorable. Complex 1 demonstrates slow magnetic relaxation dominated by the direct relaxation process between T = 1.8 and 7 K under an external DC field of 0.2 and 0.4 T, a very rarely observable effect in the coordination compounds of Cu(II). Complex 2 possesses weak ferromagnetism (J = 4.50 cm−1, zJ’ = −0.201 cm−1 for H = −JS1S2 formalism) occurring through the Cu–O–Cu pathways. Theoretical CASSCF, DFT and TDDFT calculations were applied to investigate the electronic structures of 1 and 2 and rationalize their behavior in solution.