Apically linked iron(ii) α-dioximate and α-oximehydrazonate bis-clathrochelates: synthesis, structure and electrocatalytic propertiesElectronic supplementary information (ESI) available: The UV-vis spectral data. CCDC 932044. For crystallographic data in CIF or other electronic format see DOI: 10.1039/c3dt50881a

• Main Authors: Belaya, Irina G, Svidlov, Semen V, Dolganov, Alexander V, Zelinskii, Genrikh E, Potapova, Tamara V, Vologzhanina, Anna V, Varzatskii, Oleg A, Bubnov, Yurii N, Voloshin, Yan Z
• Format: Article
• Language: English
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/c3dt50881a

Iron( ii ) α-oximehydrazonate and α-dioximate bis-clathrochelates with apical hydrocarbon linkers were obtained by template condensation on an iron( ii ) ion followed by H + -catalyzed macrobicyclization of the bis-semiclathrochelate precursor with formaldehyde and triethyl orthoformate, and by transmetallation of the triethylantimony-containing clathrochelate precursor with diboron-containing bifunctional Lewis acids, respectively. The geometry of the para -phenylenediboron-capped iron( ii ) bis-clathrochelate studied by single-crystal X-ray diffraction is intermediate between a trigonal prism and a trigonal antiprism with a distortion angle of 20.4°; the rigidity of its C 6 H 4 linker results in the presence of the expected three-fold pseudo-rotational B Fe B B Fe B axis and a staggered conformation of the cyclohexane-containing chelate moieties. The cyclic voltammograms (CVs) for the oximehydrazonate bis-clathrochelates contain single one-electron (for each metallocentre, and therefore, two electrons per molecule) quasi-reversible reduction waves assigned to the redox-processes of Fe 2+/+ , and no interaction is observed between the two encapsulated iron( i )-containing metallocenters; six strong electron-withdrawing ethoxy substituents in the 1,3,5-triazacyclohexane capping fragments substantially affect the potential of this reduction. The corresponding waves for the dioximate complexes are irreversible: due to the structural rigidity of the caging tris-dioximate ligands, their reduced dianionic forms are unstable on the CV time scale. The CV for the hexaethoxy bis-clathrochelate complex contains one two-electron reversible oxidation wave assigned to the metal-centered oxidation of Fe 2+/3+ , whereas those for its dioximate analogs are quasi-reversible. The relative lability of the ligand cavity in binuclear oximehydrazonates causes a stabilization of both the oxidized and the reduced forms; the reduced iron( i )-containing species are highly electrocatalytically active in the hydrogen-producing 2H + /H 2 reaction. Their higher activity as compared with that for dioximate bis-clathrochelates was explained by the higher availability of the catalytically active metallocentres for H + ions. New apically linked iron( ii ) bis-clathrochelates with hydrocarbon linkers, which are efficient electrocatalysts of H 2 production, were obtained.