Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis-clathrochelate iron(II) and cobalt(II, III) dioximates with ribbed perfluoroarylsulfide substituents Научная публикация
Журнал |
Dalton Transactions
ISSN: 1477-9226 , E-ISSN: 1477-9234 |
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Вых. Данные | Год: 2012, Том: 41, Номер: 3, Страницы: 737-746 Страниц : DOI: 10.1039/c1dt10500k | ||||
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Реферат:
The nucleophilic substitution of six chlorine atoms of the n-butylboron-capped clathrochelate iron and cobalt(II) precursors with perfluoroarylthiolate anions afforded the hexaperfluoroarylsulfide macrobicyclic iron and cobalt(II) tris-dioximates. The complexes obtained are soluble in aromatic and aliphatic hydrocarbons as well as in polar aprotonic solvents due to the presence of the superhydrophobic fluorine-containing molecular periphery. As it follows from the X-ray data for five iron and cobalt mono- and bis-clathrochelates, the geometry of their macrobicyclic frameworks is affected by both the nature of an encapsulated metal ion and that of the ribbed substituents. Bis-capping fragment (CoO6)-O-II of the (CoCoCoIII)-Co-III-Co-II bis-clathrochelate possesses a trigonal antiprismatic geometry, all the (CoN6)-N-II coordination polyhedra are trigonal-prismatic, and those of the encapsulated iron(II) and cobalt(III) ions are intermediate between them. The wide range of Co-N distances as well as the significant shifts of the encapsulated cobalt(II) ions from the centres of their N-6-coordination polyhedra were explained by the Jahn-Teller distortion. The EPR and magnetometry data are also characteristic of the low-spin cobalt(II) complexes with this distortion. The parameters of the Fe-57 Mossbauer spectra of the iron macrobicycles are characteristic of the low-spin iron(II) complexes. The cyclic voltammograms (CVs) for the complexes studied contain the one-electron oxidation and reduction waves assigned to metal-centered redox-processes. The Fe2+/3+ and Co2+/3+ oxidations are quasi-reversible or irreversible. The anionic clathrochelate species resulting from the reversible Co2+/+ reductions are stable on the CV time scale, whereas their iron(I)-containing analogs are unstable.
Библиографическая ссылка:
Voloshin Y.Z.
, Belaya (Makarenko) I.G.
, Belov A.S.
, Platonov V.E.
, Maksimov A.M.
, Vologzhanina A.V.
, Starikova Z.A.
, Dolganov A.V.
, Novikov V.V.
, Bubnov Y.N.
Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis-clathrochelate iron(II) and cobalt(II, III) dioximates with ribbed perfluoroarylsulfide substituents
Dalton Transactions. 2012. V.41. N3. P.737-746. DOI: 10.1039/c1dt10500k WOS Scopus РИНЦ
Formation of the second superhydrophobic shell around an encapsulated metal ion: synthesis, X-ray structure and electrochemical study of the clathrochelate and bis-clathrochelate iron(II) and cobalt(II, III) dioximates with ribbed perfluoroarylsulfide substituents
Dalton Transactions. 2012. V.41. N3. P.737-746. DOI: 10.1039/c1dt10500k WOS Scopus РИНЦ
Идентификаторы:
Web of science | WOS:000298753800007 |
Scopus | 2-s2.0-84555196190 |
РИНЦ | 17970777 |
OpenAlex | W2040623099 |