Abstract

The ability of supramolecular transition metal coordination complexes to form stabilized, long-living, radiative charge-separated states has drawn interest to employ these triplet-state emitters for the design of photonic devices. Their applicability as photosensitizers of electron transfer in molecular photonic systems is directly coupled to fundamental studies of their rich and highly versatile photochemical and photophysical properties. Here, we demonstrate that the properties of individual dual-luminescent Ru2+-bis-terpyridine complexes can be addressed with excellent sensitivity in single-complex antenna-enhanced phosphorescence investigations. This sensitivity enables studying environmentally imposed alterations of their photophysical properties, e.g., in thin film applications. In contrast to ensemble averaging investigations in solution, single-complex antenna-enhanced phosphorescence investigations corroborate the existence of Ru2+-bis-terpyridine complexes with spectrally shifted emission peaks ...

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.