Electronic excited state-specific IR spectra for phenylene ethynylene dendrimer building blocks

• Autores: Galindo Cruz, Johan Fabian; Fernández Alberti, Sebastián; Roitberg, Adrián
• Año de publicación: 2013
• Idioma: inglés
• Tipo de recurso: artículo
• Materia: Excited States; Vibrations; Infrared Spectrum
• Institución: Consejo Nacional de Investigaciones Científicas y Técnicas

Dendrimers are excellent candidates for applications in molecular devices and light harvesting where creating an energy gradient is crucial. Poly(phenylene ethynylene) (PPE) molecules are building blocks for dendrimers that also display the necessary characteristics for efficient energy transfer, including differential spatial localization associated with different excited states. In this work we calculated the ground state (S0) as well as the excited IR spectra for the S1 and S2 states of ortho- and meta- substituted PPE (o-PPE and m-PPE). To compute IR spectra, a conformational space exploration was performed using ground-state classical molecular dynamics followed by direct adiabatic and non-adiabatic excited state molecular dynamics. IR spectra were computed from the autocorrelation function of the dipole moment in each state. We identified a band at 2150 cm–1 that is characteristic of S1 in m-PPE. We show that in m-PPE, S1 and S2 have transition densities localized over different regions of the molecule, while in o-PPE the states are spread over the entire molecule. We find that the coupling between vibrations associated to the C≡C triple bonds plays an important role in the non-adiabatic electronic energy transfer. These results are a guide to the experimental characterization of the specific electronic excited states vibrations of these molecules.
Fil: Galindo Cruz, Johan Fabian. University of Florida; Estados Unidos
Fil: Fernández Alberti, Sebastián. Universidad Nacional de Quilmes. Departamento de Ciencia y Tecnología. Area Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Roitberg, Adrián. University of Florida; Estados Unidos