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, pp. 830-838
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Dijkstra, H.P.1
Slagt, M.Q.2
McDonald, A.R.3
Kruithof, C.A.4
Krcitcr, R.5
Mills, A.M.6
Lutz, M.7
Spek, A.L.8
Klopper, W.9
van Klink, G.P.M.10
van Koten, G.11
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a of free triazole, and its attraction for a proton, which we believe does not give a strong argument for this particular study. Ripin, D. H.; Evans, D. H. Chem 206. http://www2.lsdiv.harvard.edu/labs/evans/pdf/evans-pKa-table.pdf.
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a of free triazole, and its attraction for a proton, which we believe does not give a strong argument for this particular study. Ripin, D. H.; Evans, D. H. Chem 206. http://www2.lsdiv.harvard.edu/labs/evans/pdf/evans-pKa-table.pdf.
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75
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Suijkerbuijk, B. M. J. M.; Aerts, B. N. H.; Dijkstra, H. P.; Lutz, M.; Spck, A. L.; van Koten, G.; Klein Gcbbink, R. J. M. Dalton Trans. 2007, 13, 1273-1276.
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(2007)
Dalton Trans
, vol.13
, pp. 1273-1276
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Suijkerbuijk, B.M.J.M.1
Aerts, B.N.H.2
Dijkstra, H.P.3
Lutz, M.4
Spck, A.L.5
van Koten, G.6
Klein Gcbbink, R.J.M.7
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An alternative explanation for the high catalytic activity of materials 3, 4, and 7 could be that capped silanol groups have become deprotected. Recent work has demonstrated that functionalized amines have been tethered to a silica/zeolite support and the resulting materials were applied in the double Michael addition reaction. However, that work requires that remnant acid sites (uncapped silanol groups) play a role in the catalysis. We have capped all silanol groups to the best of our knowledge, with the hope of avoiding effects from the inorganic support, and therefore we believe this option to be unlikely. Furthermore, postcatalysis DRIFT-IR of the supported catalytic material shows minimal changes in the SiOH region of the spectrum, suggesting the silanol group capping has not been affected. See: Motokura, K, Tada, M, Iwasawa, Y. J. Am. Chem. Soc. 2007, 129, 9540-9541
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An alternative explanation for the high catalytic activity of materials 3, 4, and 7 could be that capped silanol groups have become deprotected. Recent work has demonstrated that functionalized amines have been tethered to a silica/zeolite support and the resulting materials were applied in the double Michael addition reaction. However, that work requires that remnant acid sites (uncapped silanol groups) play a role in the catalysis. We have capped all silanol groups to the best of our knowledge, with the hope of avoiding effects from the inorganic support, and therefore we believe this option to be unlikely. Furthermore, postcatalysis DRIFT-IR of the supported catalytic material shows minimal changes in the SiOH region of the spectrum, suggesting the silanol group capping has not been affected. See: Motokura, K.; Tada, M.; Iwasawa, Y. J. Am. Chem. Soc. 2007, 129, 9540-9541.
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