Excited-State Photolytic Mechanism of Cyclopentene Containing a Group 14 Element: An MP2-CAS//CASSCF Study

The potential energy surfaces corresponding to the photolytic reactions of 1,2-dimethyl-cyclopentene, 3,4-dimethyl-silacyclopent-3-ene, and 3,4-dimethyl-germacyclopent-3-ene were investigated by employing the CAS(6,6)/6-311G(d) and MP2-CAS-(6,6)/6-311++G(3df,3pd)//CAS(6,6)/6-311G(d) methods. Also, six kinds of substituted germacyclopent-3-ene were used as model reactants by way of the CASSCF and MP2-CAS methods to study their photolytic mechanisms. The theoretical findings indicate that the photolysis of the above reactants all adopt the same reaction path as follows: reactant → Franck-Condon region → conical intersection → germylene and 1,3-butadiene. However, the theoretical results demonstrate that no photolysis ((1)(π →π*)) can be observed in the 1,2-dimethyl-cyclopentene system. Above all, the theoretical investigations strongly suggest that both steric effects, originating from the bulky substituents, and the atomic radius of the group 14 element (C, Si, and Ge) play a crucial role in determining the cis/trans selectivity of the conformation of 1,3-butadiene during their photolytic reactions.