Loading...
|
Please use this identifier to cite or link to this item:
http://ir.ncue.edu.tw/ir/handle/987654321/10068
|
| Title: | Reactions of 2-Propanol with Cu+ in the Gas Phase: A Density Functional Theory Study |
| Authors: | Cheng, M. J.;Hu, Ching-Han;Yeh, C. S. |
| Contributors: | 化學系 |
| Date: | 2002-11
|
| Issue Date: | 2012-05-03T06:17:18Z
|
| Publisher: | American Chemical Society |
| Abstract: | The gas phase reactions between Cu+ and 2-propanol have been investigated using density functional theory at the B3LYP/6-311+G(d) and B3LYP/6-311++G(d,p) levels of theories. Seven reaction pathways have been studied. Of all reaction paths, the mechanism involving an electrophile-induced one step syn elimination of H2O has the lowest energy barrier. Dehydration also occurs via the intermediate corresponding to C−O insertion of Cu+. On the H2 elimination channel, reaction begins with C−H insertion of Cu+, followed by hydrogen migrations to form H2−Cu+−acetone or the H2−Cu+−2-propenol intermediates. Our results show that the reaction with copper cation insertion into the H−OCH(CH3)2 bond is unlikely, for its activation energy is 24.5 kcal/mol higher than those of the reactants (Cu+ and 2-propanol). The mechanism involving C−C insertion of Cu+ is also energetically unfavorable. The predicted potential energy surface of reaction and relative energies of the fragmentation products are consistent with available gas phase experiments. |
| Relation: | J. Phys. Chem. A, 106(47): 11570-11580 |
| Appears in Collections: | [化學系] 期刊論文
|
Files in This Item:
| File |
Size | Format | |
|---|
| index.html | 0Kb | HTML | 716 | View/Open |
|
All items in NCUEIR are protected by copyright, with all rights reserved.
|
