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M. Dugal, G. Sankar, R. Raja, J. M. Thomas, Angew. Chem. 2000, 112, 2399-2401; Angew. Chem. Int. Ed. 2000, 39, 2310-2313.
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M. Dugal, G. Sankar, R. Raja, J. M. Thomas, Angew. Chem. 2000, 112, 2399-2401; Angew. Chem. Int. Ed. 2000, 39, 2310-2313.
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85069092625
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note
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Such catalysts are effective for a variety of other reactions, such as epoxidation, the Baeyer-Villiger conversion of ketones to lactones, and the selective oxidation of cyclohexane.
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22
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31444455764
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P. A. Barrett, G. Sankar, C. R. A. Catlow, J. M. Thomas, J. Phys. Chem. 1996, 100, 8977-8985.
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Barrett, P.A.1
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24
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0000884581
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J. M. Thomas, Angew. Chem. 1999, 111, 3800-3843; Angew. Chem. Int. Ed. 1999, 38, 3588-3628.
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Thomas, J.M.1
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0033576565
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J. M. Thomas, Angew. Chem. 1999, 111, 3800-3843; Angew. Chem. Int. Ed. 1999, 38, 3588-3628.
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27
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0011479576
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J. K. Wyles, G. Sankar, D. W. Lewis, C. R. A. Catlow, J. M. Thomas, Proc. 12th Int. Zeolite. Conf. 1999, 1723-1730.
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Wyles, J.K.1
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0033165830
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D. Ozkaya, W. Zhou, J. M. Thomas, P. A. Midgley, V. J. Keast, S. Hermans, Catal. Lett. 1999, 60, 113-120.
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85069098013
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CERIUS, Biosym Inc., San Diego, USA, 1994
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CERIUS, Biosym Inc., San Diego, USA, 1994.
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30
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85069101982
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note
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In order to verify that the above reaction is not affected by the n-hexane:cobalt molar ratio, we carried out two experiments: The first used 0.20 g of CoAlPO-34 (ratio 0.10), so that the number of moles of cobalt corresponds to that used in the CoAlPO-18 (ratio 0.04) experiment; the second used 0.87 g of CoAlPO-18 (ratio 0.04), so thai the cobalt concentration corresponds to that used in the present study with CoAlPO-34 (ratio 0.10). Interestingly, in the case of the former, we still observed 1,6-hexanediol, 1,6-hexanedial, and adipic acid in the reaction mixture (although the conversion was only 5.2% after 24 h), whereas for the latter, we did not observe any of the above-mentioned products.
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31
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85069103067
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note
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[1] framework sites in the AlPO-18 structure, while the conversion of n-hexane remained unaffected. If hexanoic acid or adipic acid leached cobalt from the framework, the cyclohexane molecule would have also been oxidized to cyclohexanol and cyclohexanone. See ref. [12] for further details.
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32
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0012623858
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J. M. Thomas, G. N. Greaves, G. Sankar, P. A. Wright, J. S. Chen, A. J. Dent, L. Marchese, Angew. Chem. 1994, 106, 1922-1925; Angew. Chem. Int. Ed. Engl. 1994, 33, 1871-1873.
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Thomas, J.M.1
Greaves, G.N.2
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Dent, A.J.6
Marchese, L.7
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33
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33748226644
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J. M. Thomas, G. N. Greaves, G. Sankar, P. A. Wright, J. S. Chen, A. J. Dent, L. Marchese, Angew. Chem. 1994, 106, 1922-1925; Angew. Chem. Int. Ed. Engl. 1994, 33, 1871-1873.
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