Tracking the Intramolecular Charge Transfer Process of 2,6-Substituted D-A BODIPY Derivatives.

Three 2,6-electron donor-substituted boron dipyrromethene (BODIPY) exhibiting an intramolecular charge transfer (ICT) character with large Stokes shift and moderate fluorescence quantum yields were designed and synthesized. Broadband femtosecond transient absorption (fs-TA) spectroscopy measurements were performed to directly detect the CT state in nonpolar or less polar solvents and the charge separation (CS) state in more polar solvents. A solid foundation for the fs-TA assignment can be found in electrolysis experiments. In addition, the ICT character of the newly designed compounds was investigated by density functional theory (DFT) calculations. Meanwhile, the reference compounds without the donor groups were synthesized, and their photophysical behaviors and ultrafast time-resolved spectra confirmed that no ICT process occurred regardless of the nature of the solvent. This work emphasizes the importance of decorating the BODIPY core with electron-donating substituents at 2,6-positions to efficiently adjust its photofunctional behaviors demonstrating the ICT character. Importantly, the photophysical processes could be easily regulated by changing the solvent with different polarities.