Experimental synthesis reveals alkali metal-dependent iron silsesquioxane cages with high activity in alkane oxidation and carbon dioxide fixation, indicating efficient sustainable catalysts.
Unprecedented iron-based silsesquioxane/acetylacetonate complexes were synthesized. The intriguing cage-like structure of compounds is alkaline metal-dependent: the Fe 2 Li 2 complex includes condensed Si 6 -silsesquioxane and four acetylacetonate ligands; the Fe 4 Na 4 complex exhibits two cyclic Si 4 -silsesquioxane and eight acetylacetonate ligands, while the Fe 3 K 3 complex features two cyclic Si 3 -silsesquioxane and six acetylacetonate ligands. The latter case is the very first observation of small trimeric silsesquioxane ligands in the composition of cage-like metallasilsesquioxanes. The Fe 4 Na 4 -based complex exhibits a record high activity in the oxidation of inert alkanes with peroxides (55% yield of oxygenates in cyclohexane oxidation). It also acts as a catalyst in the cycloaddition of CO 2 with epoxides, leading to cyclic carbonates in good yields (58–96%).
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Bilyachenko et al. (2024) studied this question.
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