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Oxidation of Methyl Aromatics and Hetero Aromatics to Their Corresponding Aldehydes

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Abstract

The direct partial oxidation of methyl aromatics and hetero aromatics to their corresponding aldehydes strongly depends on nature, strength and concentration of acidic and basic surface sites of the catalysts, the acid-base properties of the reaction mixture and, additionally, on the electronic properties, i.e. nucleophilicity of the reactants. The increase of catalyst basicity by addition of alkali cations as well as the entire reaction mixture basicity by co-feeding of pyridine lead to dramatic improved aldehyde selectivities.

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References

  1. R.K. Grasselli, in: Handbook of Heterogeneous Catalysis, G. Ertl, H. Knözinger and J. Weitkamp(eds)(Wiley-VCH,Weinheim, 1997) p. 2302and references therein.

    Google Scholar 

  2. J. Haber, in: Handbook of Heterogeneous Catalysis, G. Ertl, H. Knözinger and J. Weitkamp(eds)(Wiley-VCH,Weinheim, 1997) p. 2253and references therein.

    Google Scholar 

  3. F. Trifirò, Catal. Today 41 (1998) 21.

    Google Scholar 

  4. F. Cavani and F. Trifirò, Catal. Today 51 (1999) 561.

    Google Scholar 

  5. A. Martin and B. Lücke, Catal. Today 57 (2000) 61.

    Google Scholar 

  6. B. Cornils, W.A. Herrmann, R. Schlögl and C.-H. Wong (eds), Catalysis from A to Z–A Concise Encyclopedia,(Wiley-VCH, Weinheim, 2000) p. 416.

    Google Scholar 

  7. B.M. Choudary, M. Lakshmi Kantam and P. Lakshmi Santhi, Catal. Today 57 (2000) 17.

    Google Scholar 

  8. J.S. Rafelt and J.H. Clark, Catal. Today 57 (2000) 33.

    Google Scholar 

  9. F. Brüh ne and E. Wright, in: Ullmann, 6th edn, (Electronic Release, 1998)(benzaldehyde entry).

  10. R.A. Sheldon, Chem. Tech 24 (1194) 38.

    Google Scholar 

  11. A.K. Suresh, M.M. Sharma and T. Sridhar, Ind. Eng. Chem. Res. 39 (2000) 3958.

    Google Scholar 

  12. B. Müller, A. Martin and B. Lücke, J. Supercrit. Fluids 23 (2002) 243.

    Google Scholar 

  13. G. Centi (ed.), Vanadylpyrophosphate catalysts, Catal. Today,vol. 16 (1993).

  14. A. Martin, H. Berndt, B. Lücke and M. Meisel, Top. Catal. 3 (1996) 377.

    Google Scholar 

  15. A. Martin, U. Bentrup, B. Lücke and A. Brückner, Chem. Commun. (1999) 1169.

  16. A. Brückner, B. Kubias, B. Lücke and R. Stößer, Colloid Surface 115 (1996) 179.

    Google Scholar 

  17. U. Bentrup, A. Brückner, A. Martin and B. Lücke, J. Mol. Catal. A: Chem. 162 (2000) 383.

    Google Scholar 

  18. M. Pontzi, C. Duschatzky, A. Carrascull and E. Ponzi, Appl. Catal. A: Gen. 169 (1998) 373.

    Google Scholar 

  19. A.O. RochaJr., A.L. Chagas, L.S.V.S. Suné, M.F.S. Lopes and J.A.F.R. Pereira, Stud. Surf. Sci. Catal. (1997) 1193.

  20. US Patent 4,054,607(1977), Tanabe Seiyaku Co.

  21. H. Seko, Y. Tokuda and M. Matsuoka, Nip. Kag. Kai. 4 (1979) 558.

    Google Scholar 

  22. B.M. Reddy, M.V. Kumar and K.J. Ratnam, Appl. Catal. A: Gen. 181 (1999) 77.

    Google Scholar 

  23. EP 0723949(1996), Hoechst AG.

  24. F. Wang, J. Xu and S. Liao, Chem. Commun. (2002) 626.

  25. M. Ueshima, N. Saito and N. Shimizu, Stud. Surf. Sci. Catal. 90 (1994) 59.

    Google Scholar 

  26. A. Martin, U. Bentrup, A. Brückner and B. Lücke, Catal. Lett. 59 (1999) 61.

    Google Scholar 

  27. J.E. Gorbunova, S.A. Linde, A.V. Lavrov and I.V. Tananaev, Dokl. Akad. Nauk SSSR 250 (1980) 350.

    Google Scholar 

  28. A. Martin, U. Bentrup and G.-U. Wolf, Appl. Catal. A: Gen. 227 (2002) 131.

    Google Scholar 

  29. R.K. Grasselli in: Handbook of Heterogeneous Catalysis, G. Ertl, H. Knözinger and J. Weitkamp(eds)(Wiley-VCH, (Weinheim, 1997) p. 2318.

    Google Scholar 

  30. W. Mathes, W. Sauermilch and T. Klein, Chem. Ber. 84 (1951) 452.

    Google Scholar 

  31. A. Martin, B. Lücke, H.-J. Niclas and A. Förster, React. Kinet. Catal. Lett. 43 (1991) 583.

    Google Scholar 

  32. A. Martin, B. Lücke, H. Seeboth and G. Ladwig, Appl. Catal. 49 (1989) 205.

    Google Scholar 

  33. S.J. Kulkarni, R. Ramachandra Rao, M. Subrahmanyam, S. Farsinavis, P. Kanta Rao and A.V. Rama Rao, Stud. Surf. Sci. Catal. 98 (1995) 161.

    Google Scholar 

  34. A.R. Prasad and M. Subrahmanyam, J. Mol. Catal. 65 (1991) L25.

    Google Scholar 

  35. E.M. Alkaeva, T.V. Andrushkevich, G.A. Zenkovets, G.N. Kryukova, S.V. Tsybulya and E.B. Burgina, Stud. Surf. Sci. Catal. 110 (1997) 939.

    Google Scholar 

  36. Z. Song, T. Matsushita, T. Shishido and K. Takehira, Chem. Commun. (2002),1306.

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Martin, A. Oxidation of Methyl Aromatics and Hetero Aromatics to Their Corresponding Aldehydes. Topics in Catalysis 29, 201–206 (2004). https://doi.org/10.1023/B:TOCA.0000029804.64785.6d

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