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Reactivity of an All-Ferrous Iron-Nitrogen Heterocubane under Reductive and Oxidative Conditions.

Chemistry (Weinheim an der Bergstrasse, Germany) (2015-09-17)
Crispin Lichtenberg, Demyan E Prokopchuk, Mario Adelhardt, Liliana Viciu, Karsten Meyer, Hansjörg Grützmacher
RÉSUMÉ

The reactivity of the all-ferrous FeN heterocubane [Fe4 (Ntrop)4 ] (1) with i) Brønsted acids, ii) σ-donors, iii) σ-donors/π-acceptors, and iv) one-electron oxidants has been investigated (trop = 5H-dibenzo[a,d]cyclo-hepten-5-yl). 1 showed self-re-assembling after reactions with i) and proved surprisingly inert in reactions with ii) and iii), with the exception of CO. Reductive and oxidative cluster degradation was observed in reactions with CO and TEMPO, respectively. These reactions yielded new cluster compounds, namely a trinuclear bis(μ3 -imido) 48 electron complex in the former case and a tetranuclear all ferric μ-oxo-μ-imido species in the latter case. Characterization techniques include NMR and in situ IR spectroscopy, single crystal X-ray analysis, Mössbauer spectroscopy, cyclic voltammetry, magnetic susceptibility measurements, and DFT calculations.

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Description du produit

Sigma-Aldrich
Tetrahydrofurane, contains 250 ppm BHT as inhibitor, ACS reagent, ≥99.0%
Sigma-Aldrich
TEMPO, 98%
Sigma-Aldrich
Tetrahydrofurane, ACS reagent, ≥99.0%, contains 250 ppm BHT as inhibitor
Sigma-Aldrich
Trimethylphosphine, 97%
Sigma-Aldrich
Trimethylphosphine solution, 1.0 M in THF
Sigma-Aldrich
TEMPO, purified by sublimation, 99%
Sigma-Aldrich
Trimethylphosphine solution, 1.0 M in toluene