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|Title:||A tandem cyclization and hydrogenation of (±)-citronellal to menthol over bifunctional Ni/Zr-beta and mixed Zr-beta and Ni/MCM-41|
|Authors:||Nie, Y. |
|Citation:||Nie, Y., Niah, W., Jaenicke, S., Chuah, G.-K. (2007-05-15). A tandem cyclization and hydrogenation of (±)-citronellal to menthol over bifunctional Ni/Zr-beta and mixed Zr-beta and Ni/MCM-41. Journal of Catalysis 248 (1) : 1-10. ScholarBank@NUS Repository.|
|Abstract:||The addition of nickel to Zr-beta gave a useful bifunctional catalyst that combines a high rate of cyclization of (±)-citronellal to isopulegols over zirconium sites and subsequent hydrogenation to menthols. The diastereoselectivity to the desired (±)-menthol was 90%. A loading of 4 wt% is optimal; lower loadings led to a low rate of hydrogenation, whereas a higher nickel loading appears to block the zirconium Lewis acid sites essential for the cyclization of citronellal. A mixture of Zr-beta and Ni/MCM-41 also formed an effective bifunctional catalyst system where the selectivity toward menthols remained high even with nickel loadings up to 15 wt%. The yield of (±)-menthol over the dual-catalyst system was 86-89% with < 5 % of byproducts, citronellol and 3,7-dimethyloctanol. Besides nickel, bifunctional Rh/Zr-beta catalysts also formed menthols with selectivity > 93 %, although the diastereoselectivity to (±)-menthol was lower (85%). In comparison, a 2% Pd/Zr-beta catalyst exhibited lower activity and selectivity to menthols, forming substantial amounts of 3,7-dimethyloctanal. © 2007 Elsevier Inc. All rights reserved.|
|Source Title:||Journal of Catalysis|
|Appears in Collections:||Staff Publications|
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