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Mechanism of the hydrogenation of pentynes and hexynes over raney nickel

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    The mechanism of the hydrogenation of n-pentynes and n-hexynes in presence of Raney nickel was studied by a method based on the poisoning of the catalyst with pyridine.

  2. 2.

    β- and γ-Acetylenic hydrocarbons are hydrogenated mainly with desorption of the olefin formed from the catalyst surface into the general reaction space.

  3. 3.

    α-Acetylenic hydrocarbons are hydrogenated by two mechanisms simultaneously: with and without desorption of the intermediately formed olefin into the general reaction space.

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Literature cited

  1. G. C. Bond, D. A. Dowden, and N. Mackenzie, Trans. Faraday Soc.54, 1537 (1958).

    Google Scholar 

  2. L. Kh. Freidlin and B. D. Polkovnikov, Izv. AN SSSR. Otd. khim. n. 1956, 1052.

  3. L. Kh. Freidlin, A. A. Balandin, and I. F. Zhukova, Kinetika i kataliz1, 447 (1960).

    Google Scholar 

  4. L. Kh. Freidlin, Yu. Yu. Kaup, E. F. Litvin, and T. I. Ilomet-s, Dokl. AN SSSR143, 883 (1962).

    Google Scholar 

  5. L. Kh. Freidlin and Yu. Yu. Kaup, Neftekhimiya2, 154 (1962).

    Google Scholar 

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Freidlin, L.K., Kaup, Y.Y. Mechanism of the hydrogenation of pentynes and hexynes over raney nickel. Russ Chem Bull 11, 1570–1572 (1962). https://doi.org/10.1007/BF00907238

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  • DOI: https://doi.org/10.1007/BF00907238

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