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Updated: Jun 22, 2026

ARL Spectral Fitting as an Application to Augment Spectral Data via Franck-Condon Lineshape Analysis and Color Analysis
Published on: August 19, 2021
Photophysics of heteroleptic iridium(III) complexes of current interest; a closer look on relaxation dynamics
Hsin-Sheng Duan1, Pi-Tai Chou, Cheng-Chih Hsu
1Department of Chemistry, National Taiwan University, No. 1, Section 4, Roosevelt Road, Taipei 10617, Taiwan, ROC.
Abstract:
The excited-state dynamics of heteroleptic iridium(III) complexes have been investigated using femto-nanosecond time-resolved luminescence and transient absorption spectroscopy. Two prototypical examples illustrated here are iridium(III) bis[2-(2,4-difluorophenyl)pyridinato-N,C(2')] quinaldinate (1) and iridium(III) bis[2-(2,4-difluorophenyl)pyridinato-N,C(2')][2-(6-methylbenzoxazol-2-yl)phenolate] (2). Upon photoexcitation at, for example, 400 nm, the emission decay, monitored at the region of phosphorescence, for both 1 and 2 consists of a system response limited rise (<300 ps) and a single exponential decay. Further single wavelength as well as full spectrum of femto-picosecond transient absorption acquired in CH(2)Cl(2) at room temperature reveals an ultrafast S(1) --> T(n) intersystem crossing (<1 ps) and a rapid T(n) --> T(1) internal conversion/vibrational relaxation within a time period of <10 ps. The results lead us to conclude that following Franck-Condon excitation, the time scale required to populate the lowest triplet state should be <10 ps.
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