Abstract
Time-resolved spectroscopy was exploited to gain new insights into the nature and dynamics of charge transfer excited states of bis-cyclometalated Ir(iii) complexes. We showed that its dynamics is strongly influenced by the nature of the diimine ligand due to the existence of a ligand-ligand charge transfer process in the picosecond timescale. All the results are supported by DFT/TD-DFT calculations and spectroelectrochemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 27256-27260 |
| Number of pages | 5 |
| Journal | Physical Chemistry Chemical Physics |
| Volume | 20 |
| Issue number | 43 |
| DOIs | |
| Publication status | Published - 1 Jan 2018 |
| Externally published | Yes |