| Literature DB >> 30048568 |
Benjamin Hupp1, Jörn Nitsch1, Tanja Schmitt1, Rüdiger Bertermann1, Katharina Edkins1, Florian Hirsch2, Ingo Fischer2, Michael Auth3, Andreas Sperlich3, Andreas Steffen1.
Abstract
The investigation of the mechanisms of mechanochromic luminescence is of fundamental importance for the development of materials for photonic sensors, data storage, and luminescence switches. The structural origin of this phenomenon in phosphorescent molecular systems is rarely known and thus the formulation of structure-property relationships remains challenging. Changes in the M-M interactions have been proposed as the main mechanism with d10 coinage metal compounds. Herein, we describe a new mechanism-a mechanically induced reversible formation of a cation-anion exciplex based on Cu-F interactions-that leads to highly efficient mechanochromic phosphorescence and unusual large emission shifts from UV-blue to yellow for CuI complexes. The low-energy luminescence is thermo- and vaporesponsive, thus allowing the generation of white light as well as for recovering the original UV-blue emission.Entities:
Keywords: N-heterocyclic carbenes; copper; exciplex formation; mechanochromic luminescence; phosphorescence
Year: 2018 PMID: 30048568 DOI: 10.1002/anie.201807768
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336