| Literature DB >> 33030274 |
Jessica Wade1,2, Jochen R Brandt1,2, David Reger3, Francesco Zinna4, Konstantin Y Amsharov5, Norbert Jux3, David L Andrews6, Matthew J Fuchter1,2.
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.Entities:
Keywords: FRET; chirality; circular dichroism; helical structures; polymers
Year: 2020 PMID: 33030274 DOI: 10.1002/anie.202011745
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336