A direct dynamics study of protonated alcohol dehydration and the Diels-Alder reaction

• Autor(a) principal: Santos,Marcus V. P. dos
• Data de Publicação: 2009
• Outros Autores: Teixeira,Erico S., Longo,Ricardo L.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Journal of the Brazilian Chemical Society (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000400009
• topic: protonated pinacolyl; ethene + 1,3-butadiene; cycloaddition; non-IRC

The dynamics of dehydration of the protonated (R)-3,3-dimethylbutan-2-ol (pinacolyl alcohol), [(CH3)3C-CH(OH2)CH3]+, and of ethene + 1,3-butadiene cycloaddition were studied with the Born-Oppenheimer molecular dynamics (BOMD) technique for direct dynamics using the AM1 method. More than 10,000 trajectories were generated, most of them related to the unexplored simulated annealing/fragmentation approach. The AM1 potential energy surface (PES) for the protonated pinacolyl alcohol presents two transition states related to the [(CH3)3C-CHCH3]+hhhOH2 intermediate complex and to CH3 migration leading to the [(CH3)2C-CH(CH)3]2+hhhOH2 product complex. Direct dynamics yielded negligible trajectories involving these complexes, since the momentum acquired by the H2O fragment led to a complete dissociation. Thus, rearrangement of the secondary carbocation [(CH3)3C-CHCH3]+ was practically inexistent during the dynamics. Despite the concerted path (H2O dissociation and CH3 migration) not being an IRC (intrinsic reaction coordinate) path in AM1-PES, a statistically significant number of trajectories involved this path. As for the Diels-Alder reaction, even when started from a symmetric transition state using the spin restricted AM1 wavefunction, the dynamics yielded a significant number of trajectories that followed asymmetric, i.e.non-IRC, paths toward cyclohexene, independent of the initialization approach. It is noteworthy that all these asymmetric path trajectories led to a concerted reaction mechanism.