The ultrafast relaxation pathways
in a hexaiodide bismuth(III)
complex, BiI6
3–, excited at 530 nm in
acetonitrile solution are studied by means of femtosecond transient
absorption spectroscopy supported by steady-state absorption/emission
measurements and DFT computations. Radiationless relaxation out of
the Franck–Condon, largely metal-centered (MC) triply degenerate 3T1u state (46 ± 19 fs), is driven by vibronic
coupling due to the Jahn–Teller effect in the excited state.
The relaxation populates two lower-energy states: a ligand-to-metal
charge transfer (LMCT) excited state of 3π I(5pπ) → Bi(6p) nature and a luminescent “trap” 3A1u(3P0) MC state. Coherent
population transfer from the initial 3T1u into
the 3π LMCT state occurs in an oscillatory, stepwise
manner at ∼190 and ∼550 fs with a population ratio of
∼4:1. The 3π LMCT state decays with a 2.9
ps lifetime, yielding two short-lived reaction intermediates of which
the first one reforms the parent ground state with a 15 ps time constant,
and the second one decays on a ∼5 ps timescale generating the
triplet product species, which persists to the longest 2 ns delay
times investigated. This product is identified as the η2 metal-ligated diiodide-bismuth adduct with the intramolecularly
formed I–I bond, [(η2-I2)Bi(II)I4]3–, which is the species
of interest for solar energy conversion and storage applications.
The lifetime of the “trap” 3A1u state is estimated to be 13 ns from the photoluminescence quenching
of BiI6
3–. The findings give insight
into the excited-state relaxation dynamics and the photochemical reaction
mechanisms in halide complexes of heavy ns2 metal ions.