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Received September 19, 2016
Accepted November 1, 2016
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Oxidation of tetralin to 1-tetralone over CrAPO-5
Centre for Advanced Research in Sciences (CARS), University of Dhaka, Dhaka 1000, Bangladesh, Korea 1Department of Chemical Engineering, Inha University, Incheon 22212, Korea
whasahn@inha.ac.kr
Korean Journal of Chemical Engineering, March 2017, 34(3), 701-705(5), 10.1007/s11814-016-0310-4
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Abstract
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<
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Csanyi LJ, Jaky K, Kota Z, Pali T, J. Mol. Catal. A-Chem., 209(1-2), 59 (2004)
Chung YM, Ahn WS, Lim PK, J. Catal., 173(1), 210 (1998)
Cho SH, Cheong MS, Jung KD, Kim CS, Han SH, Appl. Catal. A: Gen., 267(1-2), 241 (2004)
Sithambaram S, Nyutu EK, Suib SL, Appl. Catal. A: Gen., 348(2), 214 (2008)
Xamena FXLI, Casanova O, Tailleur RG, Garcia H, Corma A, J. Catal., 255(2), 220 (2008)
Kim J, Bhattacharjee S, Jeong KE, Jeong SY, Ahn WS, Chem. Commun., 3904 (2009)
Bhattacharjee S, Jeong KE, Jeong SY, Ahn WS, New J. Chem., 34, 156 (2010)
Chen JD, Sheldon RA, J. Catal., 153(1), 1 (1995)
Lempers HE, Sheldon RA, Appl. Catal. A: Gen., 143(1), 137 (1996)
Tian P, Liu Z, Wu Z, Xu L, He Y, Catal. Today, 93, 735 (2004)
Shaikh RA, Chandrasekar G, Biswas K, Choi JS, Son WJ, Jeong SY, Ahn WS, Catal. Today, 132(1-4), 52 (2008)
Ryan OB, Akporiaya DE, Holm RH, Stocker M, Stud. Surf. Sci. Catal., 108, 369 (1997)
Dapurkar SE, Kawanami H, Yokoyama T, Ikushima Y, New J. Chem., 33, 538 (2009)
Dapurkar SE, Kawanami H, Yokoyama T, Ikushima Y, Catal. Commun., 10, 1025 (2009)
Mohapatra SK, Hussain F, Selvam P, Catal. Lett., 85, 217 (2009)
Sakthivel A, Badamali SK, Selvam P, J. Catal., 80, 73 (2002)
Lounis Z, Riahi A, Djafri F, Muzart J, Appl. Catal. A: Gen., 309(2), 270 (2006)
Choudary BM, Prasad AD, Bhuma V, Swapna V, J. Org. Chem., 57, 5841 (1992)
Mohapatra SK, Selvam P, J. Catal., 249(2), 394 (2007)
Mahendiran C, Sangeetha P, Vijayan P, Basha SJ, Shanthi K, J. Mol. Catal. A-Chem., 275(1-2), 84 (2007)
Sheldon RA, J. Mol. Catal. A-Chem., 107, 75 (1996)
Sharpless KB, Verhoeven TR, Aldrichim. Acta., 12, 63 (1979)
Kim J, Bhattacharjee S, Jeong KE, Jeong SY, Choi M, Ryoo R, Ahn WS, New J. Chem., 34, 2971 (2010)
Sakthivel A, Dapurkar SE, Selvam P, Catal. Lett., 77(1-3), 155 (2001)
Karandikar P, Agashe M, Vijayamohanan K, Chandwadkar AJ, Appl. Catal. A: Gen., 257(2), 133 (2004)
Aguirre P, Zolezzi S, Parada J, Bunel E, Moya SA, Sariego R, Appl. Organometal. Chem., 20, 260 (2006)
Murahashi SI, Naota T, Komiya N, Tetrahedron Lett., 36, 8059 (1995)
Dell’Anna MM, Mastrorilli P, Nobile CF, J. Mol. Catal. A-Chem., 130, 65 (1998)
Yamauchi T, Nabu H, US Patent, 4,283,352 (1981).
Martan M, Manassen J, Vofsi D, Tetrahedron, 26, 3815 (1970)
Moro-oka Y, Catal. Today, 45(1-4), 3 (1998)
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