A series of halogenated boron-dipyrromethene (Bodipy) chromophores with potential applications in solar energy conversion were synthesized and characterized by steady state and ultrafast laser spectroscopy. The ultrafast dynamics of the chromophores were compared between a series containing H, Br, or I at the 2,6 positions of the Bodipy dye. The parent Bodipy has a fluorescent lifetime (τ<sub>fl</sub>) of 3−5 ns, a fluorescence quantum yield (Φ<sub>fl</sub>) of 0.56, and negligible triplet state yield. Bromination enhances the intersystem crossing (ISC) such that τ<sub>fl</sub> and Φ<sub>fl</sub> decrease to ∼1.2 ns and 0.11, respectively, while iodination further accelerates ISC so that τ<sub>fl</sub> is only ∼130 ps and Φ<sub>fl</sub> is 0.011. Transient absorption experiments lead to the observation of excited state absorption bands from the singlet (S<sub>1</sub>) and triplet (T<sub>1</sub>) states at ∼345 and 447 nm, respectively, and characterization of ISC via the dynamics of these bands and the decay of S<sub>1</sub> stimulated emission