A chromium-incorporated microporous aluminophosphate, CrAPO-5, was tested as a catalyst for the oxidation of tetralin using either a combination of aldehyde and O2 (1 atm) or tert-butyl hydroperoxide as an oxidant system. The former resulted in significantly improved catalytic performance (69.6% yield to 1-tetralone) over the latter (38.5% yield to 1-tetralone) at 80 °C in 8 h, and conversion increased in the sequence of acetaldehyde<

Keywords: CrAPO-5; Tetralin Oxidation; Pivalaldehyde; Acylperoxy Radicals; Tert-butyl Hydroperoxide

[References]

1. Muzart J, Bull. Soc. Chim., 65, 1986
2. Franck HG, Stadelhofer JW, Industrial Aromatic Chemistry, Springer-Verlag, Berlin, 313 (1988).
3. Wachter GA, Hartman RW, Sergejew T, Grun GL, Ledergerber D, J. Med. Chem., 39, 834, 1996
4. Tailleur RG, Salva GA, Garcia G, Fuel, 88(4), 744, 2009
5. Muzart J, Tetrahedron Lett., 28, 2131, 1987
6. Muzart J, J. Chem. Rev., 92, 113, 1992
7. J. Mol. Catal. A-Chem., 92, 277, 1994
8. Rebelo SLH, Simoes MMQ, Neves MGPMS, Silva AMS, Tagliatesta P, Cavaleiro JAS, J. Mol. Catal. A-Chem., 232(1-2), 135, 2005
9. Csanyi LJ, Jaky K, Kota Z, Pali T, J. Mol. Catal. A-Chem., 209(1-2), 59, 2004
10. Chung YM, Ahn WS, Lim PK, J. Catal., 173(1), 210, 1998
11. Cho SH, Cheong MS, Jung KD, Kim CS, Han SH, Appl. Catal. A: Gen., 267(1-2), 241, 2004
12. Sithambaram S, Nyutu EK, Suib SL, Appl. Catal. A: Gen., 348(2), 214, 2008
13. Xamena FXLI, Casanova O, Tailleur RG, Garcia H, Corma A, J. Catal., 255(2), 220, 2008
14. Kim J, Bhattacharjee S, Jeong KE, Jeong SY, Ahn WS, Chem. Commun., 3904, 2009
15. Bhattacharjee S, Jeong KE, Jeong SY, Ahn WS, New J. Chem., 34, 156, 2010
16. Chen JD, Sheldon RA, J. Catal., 153(1), 1, 1995
17. Lempers HE, Sheldon RA, Appl. Catal. A: Gen., 143(1), 137, 1996
18. Tian P, Liu Z, Wu Z, Xu L, He Y, Catal. Today, 93, 735, 2004
19. Shaikh RA, Chandrasekar G, Biswas K, Choi JS, Son WJ, Jeong SY, Ahn WS, Catal. Today, 132(1-4), 52, 2008
20. Ryan OB, Akporiaya DE, Holm RH, Stocker M, Stud. Surf. Sci. Catal., 108, 369, 1997
21. Dapurkar SE, Kawanami H, Yokoyama T, Ikushima Y, New J. Chem., 33, 538, 2009
22. Dapurkar SE, Kawanami H, Yokoyama T, Ikushima Y, Catal. Commun., 10, 1025, 2009
23. Mohapatra SK, Hussain F, Selvam P, Catal. Lett., 85, 217, 2009
24. Sakthivel A, Badamali SK, Selvam P, J. Catal., 80, 73, 2002
25. Lounis Z, Riahi A, Djafri F, Muzart J, Appl. Catal. A: Gen., 309(2), 270, 2006
26. Choudary BM, Prasad AD, Bhuma V, Swapna V, J. Org. Chem., 57, 5841, 1992
27. Mohapatra SK, Selvam P, J. Catal., 249(2), 394, 2007
28. Mahendiran C, Sangeetha P, Vijayan P, Basha SJ, Shanthi K, J. Mol. Catal. A-Chem., 275(1-2), 84, 2007
29. Sheldon RA, J. Mol. Catal. A-Chem., 107, 75, 1996
30. Sharpless KB, Verhoeven TR, Aldrichim. Acta., 12, 63, 1979
31. Kim J, Bhattacharjee S, Jeong KE, Jeong SY, Choi M, Ryoo R, Ahn WS, New J. Chem., 34, 2971, 2010
32. Sakthivel A, Dapurkar SE, Selvam P, Catal. Lett., 77(1-3), 155, 2001
33. Karandikar P, Agashe M, Vijayamohanan K, Chandwadkar AJ, Appl. Catal. A: Gen., 257(2), 133, 2004
34. Aguirre P, Zolezzi S, Parada J, Bunel E, Moya SA, Sariego R, Appl. Organometal. Chem., 20, 260, 2006
35. Murahashi SI, Naota T, Komiya N, Tetrahedron Lett., 36, 8059, 1995
36. Dell’Anna MM, Mastrorilli P, Nobile CF, J. Mol. Catal. A-Chem., 130, 65, 1998
37. Yamauchi T, Nabu H, US Patent, 4,283,352 (1981).
38. Martan M, Manassen J, Vofsi D, Tetrahedron, 26, 3815, 1970
39. Moro-oka Y, Catal. Today, 45(1-4), 3, 1998

[Cited By]

1. Yang C, Jiang L, Wang H, Zheng Y, Wang Y, Korean Journal of Chemical Engineering, 35(2), 409, 2018
2. Yao F, Xu L, Luo J, Li X, An Y, Wan C, Korean Journal of Chemical Engineering, 35(4), 853, 2018

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