RAS Chemistry & Material ScienceЖурнал неорганической химии Russian Journal of Inorganic Chemistry

  • ISSN (Print) 0044-457X
  • ISSN (Online) 3034-560X

STEPWISE OPENING OF CYCLIC SUBSTITUENTS OF (OXONIUM) DERIVATIVES OF IRON(II) (DICARBOLLIDE) BY PYRIDINE

PII
S3034560X25100105-1
DOI
10.7868/S3034560X25100105
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 70 / Issue number 10
Pages
1324-1332
Abstract
The reaction of bis(dioxane) and bis(tetrahydropyran) derivatives of iron(II) bis(dicarbollide) [8,8'-{О(СНСН)X}-3,3'-Fe(1,2-CBH)] (X = О, СН) with pyridine in an inert atmosphere has been studied. It was found that the ring-opening of oxonium cycles proceeds stepwise, with the formation of the corresponding mono- and dipyridinium iron(II) complexes. Using the bis(dioxane) dipyridinium derivative as an example, it was found that, when in solution, oxidation of the resulting products to the corresponding paramagnetic complexes of iron(III) is possible. This approach opens the way to obtain bifunctional iron bis(dicarbolide) derivatives with different substituents. The obtained compounds were characterized by multinuclear NMR and IR spectroscopy, as well as high-resolution mass spectrometry. The structure of the symmetrical dipyridinium iron(II) complex [8,8'-{СHNCHCHOCHCHO}2-3,3'-Fe(1,2-CBH)] was determined by single crystal X-ray diffraction.
Keywords
металлокарбораны бис(дикарболлид) железа циклические оксониевые производные синтез свойства нуклеофильное раскрытие пиридин
Date of publication
01.10.2025
Year of publication
2025
Number of purchasers
0
Views
71

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