Title: |
The confined space inside carbon nanotubes can dictate the stereo- and regioselectivity of Diels–Alder reactions. |
Authors: |
Smith, Nicole M., Swaminathan Iyer, K., Corry, Ben |
Source: |
Physical Chemistry Chemical Physics (PCCP); 2014, Vol. 16 Issue 15, p6986-6989, 4p |
Abstract: |
Chemical reactions inside carbon nanotubes can yield unusual outcomes. Molecular dynamics simulations show that within the confined space of carbon nanotubes, the 1,4-exo adduct of a Diels–Alder cycloaddition may be produced instead of the 9,10-adduct, which is favoured in bulk. The likely product is highly dependent on the nanotube radius and reactant size. [ABSTRACT FROM AUTHOR] |
|
Copyright of Physical Chemistry Chemical Physics (PCCP) is the property of Royal Society of Chemistry and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
Database: |
Complementary Index |