Abstract
The helical self-assembly of MOPV4 oligomers dissolved in dodecane solution has a large effect on the experimental fluorescence spectra. To describe the change in fluorescence upon aggregation, we combine a statistical mechanical theory describing the helical self-assembly with a tight-binding model to account for the delocalization of the exciton. We find our combined model to describe the red-shift of the main fluorescence peak upon aggregation qualitatively. © 2009 Elsevier B.V. All rights reserved.
Original language | English |
---|---|
Pages (from-to) | 2384-2386 |
Journal | Synthetic Metals |
Volume | 159 |
Issue number | 21-22 |
DOIs | |
Publication status | Published - 2009 |