Synthesis and characterization of heteroleptic rare earth double-decker complexes involving tetradiazepinoporphyrazine and phthalocyanine macrocycles

Autor: Dmitry V. Konev, Nagao Kobayashi, Ekaterina N. Tarakanova, Taniyuki Furuyama, I. V. Sulimenkov, Larisa G. Tomilova, Stanislav Trashin, Victor E. Pushkarev, Pavel A. Tarakanov, Viatcheslav I. Kozlovskiy, Vasily V. Filatov, O.A. Goncharova, Karolien De Wael, Anton O. Simakov, Pavel A. Stuzhin
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Zdroj: Journal of the Chemical Society: Dalton transactions
ISSN: 0300-9246
Popis: Reaction of (2,3,9,10,16,17,23,24-octabutylphthalocyaninato)lanthanide(iii) acetylacetonates ((Bu)PcLn(acac), 1a-c, Ln = Lu (a), Eu (b), La (c)) with a tetrakis(5,7-bis(4-tert-butylphenyl)-6H-1,4-diazepino)[2,3-b,g,l,q]porphyrazine ligand ((tBuPh)DzPzH(2), 2) produced sandwich compounds ((tBuPh)DzPz)Ln(Pc-Bu) (3a-c), which represent the first heteroleptic double-deckers incorporating both Pc and DzPz decks. A combination of high-resolution mass spectrometry, UV-Vis/NIR, MCD, and H-1 NMR spectroscopy, and square-wave voltammetry provided unambiguous characterization of target complexes 3 indicating that their spectral and electrochemical properties are generally intermediate with respect to their homoleptic relatives. Based on the data of solution-state H-1-H-1 NMR (COSY, NOESY) correlation spectroscopy supported by DFT calculations, a dimerization tendency of compounds 3 proportional to the Ln(iii) ion size was found. The spectroelectrochemical study of 3 and the corresponding homoleptic double-deckers revealed a pronounced tendency to aggregation of the one-electron oxidized forms of DzPz-containing double-decker complexes compared to homoleptic Pc(2)Ln compounds.
Databáze: OpenAIRE