TY - JOUR
T1 - Variational transition state theory as a tool to determine kinetic selectivity in reactions involving a valley-ridge inflection point
AU - Moreno, Miquel
AU - González-Lafont, Àngels
AU - Lluch, José M.
PY - 2004/10/13
Y1 - 2004/10/13
N2 - Variational transition state theory has been used to calculate the kinetic isotope effects affecting product ratios in the reaction between 1O2 and d6-tetramethylethylene. The minimum energy path on the potential energy surface for this process reaches a valley-ridge inflection point and then bifurcates leading to the two final products. Using canonical Variational transition state theory, two distinct dynamical bottlenecks were located corresponding to the H- and the D-abstraction, respectively. The calculated KIE at 263 K turns out to be 1.126. Analogously, a H/T KIE of 1.17 at the same temperature has been found for the reaction of 1O2 with the tritiated derivative of tetramethylethylene.
AB - Variational transition state theory has been used to calculate the kinetic isotope effects affecting product ratios in the reaction between 1O2 and d6-tetramethylethylene. The minimum energy path on the potential energy surface for this process reaches a valley-ridge inflection point and then bifurcates leading to the two final products. Using canonical Variational transition state theory, two distinct dynamical bottlenecks were located corresponding to the H- and the D-abstraction, respectively. The calculated KIE at 263 K turns out to be 1.126. Analogously, a H/T KIE of 1.17 at the same temperature has been found for the reaction of 1O2 with the tritiated derivative of tetramethylethylene.
UR - https://dialnet.unirioja.es/servlet/articulo?codigo=1009362
UR - https://www.scopus.com/pages/publications/5644273803
U2 - 10.1021/ja039561r
DO - 10.1021/ja039561r
M3 - Article
SN - 0002-7863
VL - 126
SP - 13089
EP - 13094
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 40
ER -