Mono-, di-, tri- and tetra-silacyclobutenes: Strain energy, hyperconjugation and ring-opening reaction

The ring strain, pi-sigma hyperconjugation and ring-opening reaction of silicon-substituted cyclobutenes (monosilacyclobutenes, disilacyclobutadienes, trisilacyclobutenes and tetrasilacyclobutene) are systemically studied at the level of B3LYP/6-311 + G(d,p). The strengths of the ring strains are characterized by the bond angle deviation from the normal angle of hybrid orbitals of the silicon and carbon atoms. A reasonable correlation is found between the strain energy and the departure of the bond path length from a linear geometrical bond. The positions of strongly-bent sigma bonds are regarded as an important factor that causes different strains in silacyclobutenes. The pi-sigma hyperconjugation is directly estimated using the second order perturbation energy from the NBO analysis and we found that hyperconjugation is responsible for relaxing the ring strain in silacyclobutenes. The thermal ring opening reactions of silacyclobutenes are predicted to possess a symmetry-allowed conrotatory mechanism. The contribution of the bond energy is the main factor that dictates the ring-opening process to be either endothermic or exothermic.

Automated summary

The ring strain, pi-sigma hyperconjugation, and ring-opening reactions of silicon-substituted cyclobutenes were studied systematically. The strength of the ring strain was characterized by the deviation of bond angles and bond lengths, while pi-sigma hyperconjugation was found to relax the ring strain. The thermal ring opening reactions were predicted to follow a symmetry-allowed mechanism, with the contribution of bond energy determining whether the process is endothermic or exothermic.