Abstract
The ability to tune optical
features of BODIPY materials is essential
for their photo-related application. However, it is challenging to
efficiently tune the crystal packing of BODIPY derivatives because of their
complex nature. In this study, such control of BODIPY supramolecular assemblies
was achieved by designing a BODIPY containing a halogen bond (XB) acceptor (–NO2) and donor (I, Br) to mediate halogen bonding interactions. The
mono halogenated 2 and 4 was unable to form XB, whereas 3 and 5 formed
isostructural mono-coordinate motif 3, 5-I (1D tubular structure) and symmetric
bifurcated motif 5-II (1D zig-zag chains structure) via N-O···I,Br XB
interactions. The results show that the dispersion and electrostatic component
are the major source of 3, 5-I and 5-II XB formations. The XB interaction between –NO2 and X (I, Br)
promote singlet-to-triplet intersystem crossing and triplet-to-singlet reverse
intersystem crossing due to delocalization of oxygen electrons partially onto
the Br and I. Then this interaction leads to unexpected fluorescence
enhancement of 5-II. Finally, the indirect optical band gaps of the 3, 5-I and
5-II were able to be tuned in the range of 1.9–2.50 eV via XB driven crystal
packings.