0467828 - ÚFCH JH 2017 RIV GB eng J - Článek v odborném periodiku
Hazari, A. S. - Paretzki, A. - Fiedler, Jan - Záliš, Stanislav - Kaim, W. - Lahiri, G. K.
Different manifestations of enhanced π-acceptor ligation at every redox level of [Os(9-OP)L2]n, n = 2+, +, 0, − (9-OP− = 9-oxidophenalenone and L = bpy or pap).
Dalton Transactions. Roč. 45, č. 45 (2016), s. 18241-18251. ISSN 1477-9226. E-ISSN 1477-9234
Grant CEP: GA MŠMT LD14129
Institucionální podpora: RVO:61388955
Klíčová slova: Spectroelectrochemistry * Redox reactions * Ruthenium
Kód oboru RIV: CG - Elektrochemie
Impakt faktor: 4.029, rok: 2016 ; AIS: 0.766, rok: 2016
Způsob publikování: Open access
DOI: https://doi.org/10.1039/c6dt03764j

The title complexes were isolated as structurally characterised compounds [Os-II(9-OP)L-2]ClO4, L = 2,2'-bipyridine (bpy) or 2-phenylazopyridine (pap), and were compared with ruthenium analogues. A reversible one-electron oxidation and up to three reduction processes were observed by voltammetry (CV, DPV) and spectroelectrochemistry (UV-vis-NIR, partially EPR). Supporting calculations (DFT, TD-DFT) were used to assess the oxidation state combinations of the different redox active ligands and of the metal, revealing the effects of Os versus Ru exchange and of bpy versus pap acceptor ligation. Several unexpected consequences of these variations were observed for members of the new osmium-containing redox series. Remarkably, the EPR results exhibit a clear dichotomy between the complex ion [Os-III(9-OP-)( bpy)(2)](2+) and the radical species [Os-II(9-OP-)(pap)(2)](2+), which has not been similarly observed for the analogous [Ru-III(9-OP-)(L2)](2+) systems. This difference, unprecedented for 5d(n) systems, is attributed to the superior stabilisation of the Os-II state by the strongly pi-accepting pap ligands. The reduced forms [Os-II(9-OP-)(pap(-))(pap)] and [OsII(9-OP-)(pap(-))(2)](-) exhibit strong inter-ligand interactions, leading to spin isomers and electron hopping.
Trvalý link: http://hdl.handle.net/11104/0265848