Abstract
The reaction of [(Dpp-Bian)Mg(THF)3] (I) (Dpp-Bian is 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene) with tosyl azide (TosN3) affords the binuclear amide complex [(Dpp-Bian)Mg(THF)(NTos)(THF)Mg(Dpp-Bian)] (II) in which the magnesium atoms are linked with the nitrogen atom by the bridging p-tolylsulfamide group. In the presence of pyridine, the reaction leads to the compound [(Dpp-Bian)Mg(Py)(NTos)(Py)Mg(Dpp-Bian)] (III) in which NTos has different coordination modes with the metal atoms. The diimine ligand is in the radical anion state in both compounds. New paramagnetic compounds II and III are characterized by IR spectroscopy, EPR spectroscopy, elemental analysis, and X-ray diffraction analysis (СFА files CCDC no. 1878433 (II · 1.5C5H12) and 1878432 (III · 2C7H8 · 0.5OC4H8)).
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ACKNOWLEDGMENTS
The work on the synthesis and X-ray diffraction studies of the compounds obtained was carried out with the financial support of the Russian Science Foundation (project 14-13-01063), the EPR spectroscopic characterization of metal complexes was supported by the Russian Fund for Basic Research (project 18-33-01057).
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Dedicated to the 90th birthday of Academician I.I. Moiseev
Translated by E. Yablonskaya
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Dodonov, V.A., Skatova, A.A. & Fedushkin, I.L. Synthesis and Crystal Structures of the Reaction Products of the Magnesium Acenaphthenediimine Complex with Tosyl Azide. Russ J Coord Chem 45, 301–307 (2019). https://doi.org/10.1134/S1070328419040031
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DOI: https://doi.org/10.1134/S1070328419040031