Conclusions
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1.
The reaction of 1,2,3-trithia[3]ferrocenophane with triphenylphosphinegold tetrafluoroborate leads to tris(triphenylphosphinegold)sulfonium tetrafluoroborate.
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2.
Relative to the auration of ethyl cyanoacetate, the aurating capacity of the tris-(triphenylphosphinegold)sulfonium tetrafluoroborate is significantly lower than that of (Ph3PAu)3O]+BF4 − and [(Ph3PAu)4N]+BF4 −.
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3.
The reaction of ferrocenylene-1,1′-dithiol with tris(triphenylphosphinegold)oxonium tetrafluoroborate gives (Ph3PAuSC5H4FeC5H4S)2.
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Literature cited
V. P. Dyadchenko, The Auration of Organic Compounds, Dissertation, Moscow (1977).
A. N. Nesmeyanov et al., Vestn. Mosk. Univ., No. 4, 387 (1973).
E. G. Perevalova, D. A. Lemenovskii, K. I. Grandberg, and A. N. Nesmeyanov, Dokl. Akad. Nauk SSSR,203, 1320 (1972).
I. I. Bishop, A. Davison, et al., J. Organomet. Chem.,27, 241 (1972).
A. Davison and I. C. Smart, J. Organomet. Chem.,19, 7 (1969).
P. G. Jones, G. M. Sheldrick, and E. Hüdicke, Acta Crystallogr.,B36, 2777 (1980).
A. N. Nesmeyanov, E. G. Perevalova, Yu. T. Struchkov, M. Yu. Antipin, K. I. Grandberg, and V. P. Dyadchenko, J. Organomet. Chem.,201, 343 (1980).
C. Kowala and I. M. Swan, Austr. J. Chem.,19, 547 (1966).
E. G. Perevalova, E. I. Smyslova, V. P. Dyadchenko, K. I. Grandberg, and A. N. Nesmeyanov, Izv. Akad. Nauk SSSR, Ser. Khim., 1455 (1980).
E. I. Smyslova, E. G. Perevalova, V. P. Dyadchenko, K. I. Grandberg, Yu. L. Slovokhotov, and Yu. T. Struchkov, J. Organomet. Chem.,215, 269 (1981).
A. D. Westland, Can. J. Chem.,47, 4135 (1969).
J. Wilkinson, Organic Syntheses [Russian translation], Coll. 8, Inostr, Lit., Moscow (1958), p. 64.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1873–1876, August, 1985.
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Perevalova, É.G., Baukova, T.V., Sazonenko, M.M. et al. Reaction of monovalent gold complex salts with ferrocene thio derivatives. Russ Chem Bull 34, 1722–1726 (1985). https://doi.org/10.1007/BF00948525
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DOI: https://doi.org/10.1007/BF00948525