1H-Benzo[f]indole (Bd)
is a significant
phosphorescence unit in the field of room-temperature ultralong organic
phosphorescence (RTUOP). However, the synthesis of Bd is rather hard
and has a low yield, which greatly limits the wide applications of
RTUOP. Therefore, exploring readily obtained alternatives to Bd is
of great significance and demands to be addressed although it is full
of challenges. Herein, we report a new phosphorescence unit named
5H-benzo[b]carbazole (BCz), which
can function similarly as Bd in RTUOP. BCz can be obtained facilely
via two steps of reactions, while the synthesis of Bd requires seven
steps of tedious reactions. Excitingly, readily obtained BCz is an
excellent alternative to Bd in RTUOP in the following aspects and
shows some advantages in comparison with Bd: First, BCz and its derivatives
can exhibit distinctive redshifted red ultralong phosphorescence in
the self-aggregated state at 77 K while Bd and its derivatives cannot.
Second, BCz demonstrates remarkable photo-activated yellow ultralong
phosphorescence at room temperature while the intrinsic phosphorescence
of Bd is difficult to be activated at room temperature. Third, BCz
derivatives (CNPyBCz and CNBrBCz) display similar photo-activated
yellow ultralong phosphorescence as Bd derivatives at room temperature
but their phosphorescent lifetimes are longer. Fourth, it is shown
that BCz and its derivatives emit yellow RTUOP in powder matrixes
as their carbazole counterparts do. It is revealed that BCz and Bd
share the same cation-radical-involved phosphorescence mechanism featuring
charge separation and charge recombination and the redshift of ultralong
phosphorescence in the self-aggregated state arises from enhanced
π–π interactions among BCz units. To the best of
our knowledge, this study paves a simple way for future applications
of RTUOP. Moreover, this work indicates that the cation-radical-involved
mechanism may be universal in the field of RTUOP.