Conclusions
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1.
Triferrocenylchloromethane hydrochloride reacts with diazomethane to give triferrocenylethylene.
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2.
Triferrocenylethylene was reduced to 1,1,2 -triferrocenylethane and oxidized with potassium permanganate in alkaline medium.
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3.
Diferrocenyl (phenyl) chloromethane hydrochloride reacts with diazomethane to give a mixture of 1,2-diferrocenyl-1-phenylethylene and 1,1-diferrocenyl-2-phenylethylene.
Literature cited
H. W. Whitlock, Jr., J. Am. Chem. Soc.,84, 2807 (1962).
A. N. Nesmeyanov, É. G. Perevalova, L. I. Leont'eva, and Yu. A. Ustynyuk, Izv. AN SSSR, Ser. Khim.,1966, 556.
A. N. Nesmeyanov, É. G. Perevalova, L. I. Leont'eva, and O. F. Filippov, Izv. AN SSSR, Ser. Khim.,1967, 464.
A. N. Nesmeyanov, É. G. Perevalova, R. V. Golovnya, and O. A. Nesmeyanova, Dokl. AN SSSR,97, 459 (1954).
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 3, pp. 681–682, March, 1967.
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Nesmeyanov, A.N., Perevalova, É.G., Leont'eva, L.I. et al. Reaction of diazomethane with triferrocenyl- and diferrocenyl(phenyl)carbonium salts. Russ Chem Bull 16, 657–658 (1967). https://doi.org/10.1007/BF00906016
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DOI: https://doi.org/10.1007/BF00906016