Background: Recent efforts in the field of mesoscale effects on the structure and properties of thin polymer films call to revival interest in conformational structure and defects of a polymer backbone which has a crucial influence on electronic properties of the material. Oligo[methyl(phenyl)silylene]s (OMPSi) as exemplary molecules were studied theoretically by DFT in the form of optimal decamers and conformationally disrupted decamers (with a kink).
Results: We proved that transoid backbone conformation is true energy minimum and that a kink in the backbone causes significant hypsochromic shift of the absorption maximum (λ max ), while backbone conformation altering from all-eclipsed to all-anti affects λ max in the opposite way. π-π stacking was investigated qualitatively through optimal geometry of OMPSi and mutual position of their phenyls along the backbone and also quantitatively by an evaluation of molecular energies obtained from single point calculations with functionals, which treat the dispersion effect in the varying range of interaction.
Conclusions: The kink was identified as a realistic element of the conformational structure that could be able to create a bend in a real aryl substituted polysilylene chain because it is stabilized by attractive π-π interactions between phenyl side groups.Graphical abstract.
Keywords: Density functional calculations; Kink; Methyl(phenyl)silylene; Stacking interaction; UV/Vis spectroscopy.