Abstract
This paper reported a diamine ligand 2-(4-fluorophenyl)-5-(pyridin-2-yl)-1,3,4-oxadiazole (referred to as FPOZ) owing two typical electron-withdrawing moieties of an oxidiazole group and a fluorine atom, as well as its corresponding Re(I) complex Re(CO)3(FPOZ)Br. Geometric structure and electronic nature of Re(CO)3(FPOZ)Br were explored and discussed by single crystal analysis and theoretical calculation, which suggested that Re(CO)3(FPOZ)Br took a distorted octahedral coordination field. The onset electronic transitions owned a mixed character of metal-to-ligand-charge-transfer (MLCT) and ligand-to-ligand-charge-transfer (LLCT). Re(CO)3(FPOZ)Br was then doped into a polymer host. Photophysical difference between resulting composite fibers and bulk Re(CO)3(FPOZ)Br was carefully performed, so that the correlation between emissive performance and electron-withdrawing group/geometric relaxation could be investigated. It was found that the immobilization in polymer matrix could repress MLCT excited state geometric relaxation, leading to improved PL parameters such as emission blue shift, longer excited state lifetime and higher photostability.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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.