Aims: Experimental and computational studies of a series of multi-halogenated
boron subphthalocyanine (Cl-BsubPcXn) derivatives are reported. This family of compounds
with various degrees of chlorine or fluorine peripheral substitution (n = 4, 8, or 12) was
studied by density functional theory (B3LYP model) in order to characterize the optimized
geometries and electronic structures.
Method: The boron subphthalocyanines with one, two and three fully fluorinated rings (Cl-
BsubPcF4, Cl-BsubPc F8, and Cl-BsubPcF12 respectively) were prepared in a single pot
synthesis, purified, and characterized.
Observation: While the yields (0.6%, 5.2%, 1.9% respectively) are low, this is the first report
of isolated separation and characterization of these subphthalocyanine structures.
Result: Absorption spectroscopy and electrochemical studies confirmed that the ring
substitution has a strong effect on the electronic properties of Cl-BsubPcXn. Cyclic
voltammetry and UV-Vis support theoretical results where bandgaps decreased as the degree
of fluorine substitution increased.