An intersystem crossing (ISC), the non-radiative transition
between
two electronic states with different spin multiplicities, is ubiquitous
and imperative in molecular photochemistry. The manifestation of a
triplet manifold in π-conjugated chromophoric materials has
a crucial role in enhancing the efficiency of photofunctional devices.
Herein, we explore the triplet-state population in a series of chalcogen-annulated
perylene bisimides (O-PBI, S-PBI, and Se-PBI), where the selenium-annulated
PBI (Se-PBI) exhibits a near-quantitative triplet quantum yield (
= 94 ± 1%). Annulation of Se in the
PBI core results in a drastic decrease in the fluorescence quantum
yield (
= 1.5 ± 0.2%) compared to the bare
PBI (
= 97.0 ± 1%), indicating the possibility
of an efficient non-radiative decay pathway in the Se-PBI motif. Femtosecond
and nanosecond transient absorption measurements unambiguously confirmed
the ultrafast triplet population in Se-PBI with an ISC rate constant
of
= 2.39 × 1010 s–1 and the triplet-state decay to the ground state with a time constant
of 3.78 μs. A theoretically calculated spin–orbit coupling
constant (V
SOC) of 122.4 cm–1 employing the SA-CASSCF/NEVPT2 method has rationalized the excited-state
dynamics of Se-PBI. By virtue of the poor SOC between the singlet
and triplet states, we observed a partial triplet population in S-PBI,
whereas ISC is negligible in O-PBI. We demonstrate an increase in
the spin–orbit coupling constant (
≪
<
) and rate constant of ISC (
≪
<
) across the series of chalcogen-annulated
PBIs (O-PBI, S-PBI, and Se-PBI). The heavier chalcogenide PBI (Se-PBI)
thus adds to the array of potential organic photoactive materials
for the design of efficient solar energy conversion devices.