Browsing by Author "Poater, Albert"

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    Decomposition of the electronic activity in competing [5,6] and [6,6] cycloaddition reactions between C-60 and cyclopentadiene
    (2019) Villegas, Nery Andrés; Poater, Albert; Sola, Miquel.; Schaefer III, Henry F.; Toro Labbé, Alejandro
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    Decomposition of the electronic activity in competing [5,6] and [6,6] cycloaddition reactions between C60 and cyclopentadiene
    (2019) Villegas-Escobar, Nery; Poater, Albert; Sola, Miquel; Schaefer, Henry F., III; Toro-Labbe, Alejandro
    Fullerenes, in particular C-60, are important molecular entities in many areas, ranging from material science to medicinal chemistry. However, chemical transformations have to be done in order to transform C-60 in added-value compounds with increased applicability. The most common procedure corresponds to the classical Diels-Alder cycloaddition reaction. In this research, a comprehensive study of the electronic activity that takes place in the cycloaddition between C-60 and cyclopentadiene toward the [5,6] and [6,6] reaction pathways is presented. These are competitive reaction mechanisms dominated by sigma and fluctuating activity. To better understand the electronic activity at each stage of the mechanism, the reaction force (RF) and the symmetry-adapted reaction electronic flux (SA-REF, J(i)()) have been used to elucidate whether or sigma bonding changes drive the reaction. Since the studied cycloaddition reaction proceeds through a C-s symmetry reaction path, two SA-REF emerge: J(A)() and J(A)(). In particular, J(A)() mainly accounts for bond transformations associated with bonds, while J(A)() is sensitive toward sigma bonding changes. It was found that the [6,6] path is highly favored over the [5,6] with respect to activation energies. This difference is primarily due to the less intensive electronic reordering of the sigma electrons in the [6,6] path, as a result of the pyramidalization of carbon atoms in C-60 (sp(2) sp(3) transition). Interestingly, no substantial differences in the electronic activity from the reactant complex to the transition state structure were found when comparing the [5,6] and [6,6] paths. Partition of the kinetic energy into its symmetry contributions indicates that when a bond is being weakened/broken (formed/strengthened) non-spontaneous (spontaneous) changes in the electronic activity occur, thus prompting an increase (decrease) of the kinetic energy. Therefore, contraction (expansion) of the electronic density in the vicinity of the bonding change is expected to take place.