Reactivity of some “ladder” type complexes under conditions of metallation |
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Authors: | T. Yu. Orlova Yu. S. Nekrasov P. V. Petrovskii M. G. Ezernitskaya T. V. Magdesieva S. V. Milovanov K. P. Butin |
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Affiliation: | (1) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation;(2) Department of Chemistry, M. V. Lomonosov Moscow State University, Leninskie Gory, 119899 Moscow, Russian Federation |
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Abstract: | The behavior of binuclear “ladder” type complexes FpL, where Fp=Cp(CO)2Fe, L=p-MeC6H4Cr(CO)3 (4), CH2C6H5Cr(CO)3 (5), andp-FpC6H4Cr(CO)3 (6), under conditions of metallation was studied. Unlike compounds5 and6, the σ-bound ligand L in compound4 migrates from the iron atom to the cyclopentadienyl ring to give complexes Me(CO)2FeC5H4−C6H4(p-Me)Cr(CO)3. The electrochemical reduction potentials of the complexes4–6 and the rearrangement products were measured. The migration activity of L is determined by the ease of reductive cleavage of the Fe−L bond and the susceptibility of the system to undergo intramolecular electron transfer from the Cp ligand to the aromatic ring. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1832–1835, September, 1998. |
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Keywords: | “ ladder” type complex metallation rearrangement electrochemistry |
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