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Stereoselective hydrogenation of acetylene on copper catalysts: A quantum-chemical study

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Abstract

The structure of the alkyne adsorption complex on the copper surface is favorable for the stereoselective formation of cis isomers in the hydrogenation reaction. The pathway of dissociative hydrogen adsorption on copper is reported. It is assumed that the electron-donating promoter acts to reduce the electron work function of the copper catalyst by partially covering or “decorating” the surface of the copper particles.

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References

  1. Bond, G.C. and Wells, P.B., Adv. Catal., 1964, vol. 15, p. 91.

    Article  CAS  Google Scholar 

  2. Webb, G., Stud. Surf. Sci. Catal., 1978, vol. 20, p. 1.

    CAS  Google Scholar 

  3. Boitiaux, J.P., Cosyns, J., Derrien, M., and Leger, G., Hydrocarbon Process., 1985, p. 51.

  4. Sarkany, A., Appl. Catal., A, 1997, vol. 149, p. 207.

    Article  CAS  Google Scholar 

  5. Wells, P.B., J. Catal., 1978, vol. 52, p. 498.

    Article  CAS  Google Scholar 

  6. Renouprez, A., Lebas, K., and Bergeret, G., J. Mol. Catal. A: Chem., 1997, vol. 120, p. 217.

    Article  CAS  Google Scholar 

  7. Bando, K.K., Sayama, K., Kusama, H., Okabe, K., and Arakawa, H., Appl. Catal., A, 1997, vol. 165, p. 391.

    Article  CAS  Google Scholar 

  8. Marino, F., Baronetti, G., Jobbagy, M., and Laborde, M., Appl. Catal., A., 2003, vol. 238, p. 41.

    Article  CAS  Google Scholar 

  9. Xu, M. and Iglesia, E., Catal. Lett., 1998, vol. 51, p. 47.

    Article  CAS  Google Scholar 

  10. Imamura, H., Miura, Y., Fujita, K., Sakata, Y., and Tsuchiya, S., J. Mol. Catal. A: Chem., 1999, vol. 140, p. 81.

    Article  CAS  Google Scholar 

  11. Zhang, X. and Shi, P., J. Mol. Catal. A: Chem., 2003, vol. 194, p. 99.

    Article  CAS  Google Scholar 

  12. Wang, J.B., Tsai De-Hao, and Huang Ta-Jen, J. Catal., 2002, vol. 208, p. 370.

    Article  CAS  Google Scholar 

  13. Yefremenko, I.G., Zilberberg, I.L., Zhidomirov, G.M., and Pak, A.M., React. Kinet. Catal. Lett., 1995, vol. 56, p. 77.

    Article  CAS  Google Scholar 

  14. Gallaher, G.R., Goodwin, J.G., Huang, C., and Houalla, M., J. Catal., 1991, vol. 127, p. 719.

    Article  CAS  Google Scholar 

  15. Gallaher, G.R., Goodwin, J.G., and Guczi, L., Appl. Catal., 1991, vol. 73, p. 1.

    Article  CAS  Google Scholar 

  16. Underwood, R.P. and Bell, A.T., Appl. Catal., 1987, vol. 34, p. 289.

    Article  CAS  Google Scholar 

  17. Guvelioglu, G.H., Pingping Ma, and Xiaoyi He, Phys. Rev. Lett., 2005, vol. 94, p. 026103.

  18. Zhaksibaev, M.Zh., Kartonozhkina, O.I., Abylkasova, G.E., Izdebskaya, G.T., Mambetkazieva, R.A., and Pak, A.M., Rus. J. Appl. Chem., 2002, vol. 75, p. 1101.

    Article  CAS  Google Scholar 

  19. Bronsted, J.N., Chem. Rev., 1928, vol. 5, p. 231.

    Article  CAS  Google Scholar 

  20. Evans, M.G. and Polanyi, N.P., Trans. Faraday Soc., 1938, vol. 34, p. 11.

    Article  CAS  Google Scholar 

  21. Batista, J., Pintar, A., Mandrino, D., Jenko, M., and Martin, V., Appl. Catal., A, 2001, vol. 206, p. 113.

    Article  CAS  Google Scholar 

  22. Pestryakov, A.N. and Lunin, V.V., J. Mol. Catal. A: Chem., 2000, vol. 158, p. 325.

    Article  CAS  Google Scholar 

  23. Komova, O.V., Simakov, A.V., Rogov, V.A., Kochubei, D.I., Odegova, G.V., Kriventsov, V.V., Paukshtis, E.A., Ushakov, V.A., Sazonova, N.N., and Nikoro, T.A., J. Mol. Catal. A: Chem., 2000, vol. 161, p. 191.

    Article  CAS  Google Scholar 

  24. Chaturvedi, S. and Rodriguez, J.A., Surf. Sci., 1998, vol. 401, p. 282.

    Article  CAS  Google Scholar 

  25. Lamberti, C., Bordiga, S., Bonino, F., Prestipino, C., Berlier, G., Capello, L., D’Acapito, F., Llabres i Xamena, F.X., and Zecchina, A., Phys. Chem. Chem. Phys., 2003, vol. 5, p. 4502.

    Article  CAS  Google Scholar 

  26. De Asha, A.M., Critchley, J.T.S., Siokou, A.E., and Nix, R.M., Phys. Chem. Chem. Phys., 2000, vol. 2, p. 4758.

    Article  Google Scholar 

  27. Larichev, Y.V., Moroz, B.L., Zaikovskii, V.I., Yunusov, S.M., Kalyuzhnaya, E.S., Shur, V.B., and Bukhtiyarov, V.I., J. Phys. Chem., 2007, vol. 111, p. 9427.

    CAS  Google Scholar 

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Correspondence to S. E. Malykhin.

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Original Russian Text © M.Zh. Zhaksibaev, S.E. Malykhin, Yu.V. Larichev, A.M. Pak, 2008, published in Kinetika i Kataliz, 2008, Vol. 49, No. 4, pp. 552–555.

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Zhaksibaev, M.Z., Malykhin, S.E., Larichev, Y.V. et al. Stereoselective hydrogenation of acetylene on copper catalysts: A quantum-chemical study. Kinet Catal 49, 527–530 (2008). https://doi.org/10.1134/S0023158408040113

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  • DOI: https://doi.org/10.1134/S0023158408040113

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