Abstract
Strongly dissymmetric circularly polarised (CP) luminescence from small organic molecules could transform a range of technologies, such as display devices. However, highly dissymmetric emission is usually not possible with small organic molecules, which typically give dissymmetric factors of photoluminescence (gPL) less than 10-2. Here we describe an almost 103-fold chiroptical amplification of a π-extended superhelicene when embedded in an achiral conjugated polymer matrix. This combination increases the |gPL| of the superhelicene from approximately 3 × 10-4 in solution to 0.15 in a blend film in the solid-state. We propose that the amplification arises not simply through a chiral environment effect, but instead due to electrodynamic coupling between the electric and magnetic transition dipoles of the polymer donor and superhelicene acceptor, and subsequent CP Förster resonance energy transfer. We show that this amplification effect holds across several achiral polymer hosts and thus represents a simple and versatile approach to enhance the g-factors of small organic molecules.
Original language | English |
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Pages (from-to) | 222-227 |
Number of pages | 6 |
Journal | Angewandte Chemie-International Edition |
Volume | 60 |
Issue number | 1 |
Early online date | 8 Oct 2020 |
DOIs | |
Publication status | Published - 4 Jan 2021 |
Profiles
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David Andrews
- School of Chemistry, Pharmacy and Pharmacology - Emeritus Professor
- Centre for Photonics and Quantum Science - Member
- Chemistry of Light and Energy - Member
Person: Research Group Member, Academic, Teaching & Research