Neocuproine/nitrato complexes of Ni(II). Neutral and cationic species including salts with TCNQ: Preparation, chemical and spectroscopic properties and comparative structural chemistry

0578773 - FZÚ 2025 RIV NL eng J - Článek v odborném periodiku
Šterbinská, S. - Smolko, R. - Černák, J. - Dušek, Michal - Falvello, L.R. - Tomás, M.
Neocuproine/nitrato complexes of Ni(II). Neutral and cationic species including salts with TCNQ: Preparation, chemical and spectroscopic properties and comparative structural chemistry.
Journal of Molecular Structure. Roč. 1295, Jan (2024), č. článku 136746. ISSN 0022-2860. E-ISSN 1872-8014
Grant CEP: GA MŠMT LM2023051
Institucionální podpora: RVO:68378271
Klíčová slova: Nickel(II) * TCNQ * neocuproine * NO₃⁻ * crystal structure * spectral properties
Obor OECD: Condensed matter physics (including formerly solid state physics, supercond.)
Impakt faktor: 3.8, rok: 2022
Způsob publikování: Open access

The cationic complex [Ni(neoc)2(NO3)]+ with NO3- (1), TCNQ- (3), or (TCNQ-TCNQ)2- (4) as counterions, and the neutral complex [Ni(neoc)([NO3]- -κ1O)([NO3]- -κ2O,O´)(H2O)] (2) can be obtained from different reactions involving Ni(II), neoc, NO3- and TCNQ. The molecular and extended crystal structure of compound 2, which displays two different coordination modes for NO3- , are compared to those of the analogous Mn, Fe and Co compounds, revealing a correlation between the coordination geometry of the nominally monodentate nitrato ligand and the covalent radius of the central metal atom. Despite the differences in molecular geometry, the extended structures of the Ni (2) and Mn compounds are similar to each other but different from those of the Fe and Co complexes, which are similar to each other.
Trvalý link: https://hdl.handle.net/11104/0347688