On the unusual Stokes shift in the smallest PPE dendrimer building block: Role of the vibronic symmetry on the band origin?

Abstract

1,3-bis(phenylethynyl)benzene is the primary chromophore of light-harvesting polyphenylene ethynylene (PPE) dendrimers. It is experimentally known to share the same absorption spectrum as its pair of diphenylacetylene (aka. tolane) meta-substituted branches, yet exhibits an unusual Stokes shift of about 2000 cm${}^{-1}$ with respect to its band origin (corresponding to the loss of one vibrational quantum within the antisymmetric acetylenic stretching) in its emission spectrum. We suggest in the present work the unusual but plausible involvement of molecular symmetry selection rules in a situation where the Born-Oppenheimer approximation is far to be valid. Our hypothesis is comforted with quantum dynamics (MCTDH) simulations of absorption and emission UV-visible spectra based on quantum chemistry (TD-DFT) data and a diabatic vibronic coupling Hamiltonian model.

15 pages of manuscript, 15 pages of supplementary information

Cited by in corpus (3)

• Managing Temperature in Open Quantum Systems Strongly Coupled with Structured Environments
• Excitation-Energy Transfer and Vibronic Relaxation through Light-Harvesting Dendrimer Building Blocks: a Nonadiabatic Perspective
• Wavepacket and Reduced-Density Approaches for High-Dimensional Quantum Dynamics: Application to the Nonlinear Spectroscopy of Asymmetrical Light-Harvesting Building Blocks