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Updated: May 24, 2026

Conventional BODIPY Conjugates for Live-Cell Super-Resolution Microscopy and Single-Molecule Tracking
Published on: June 8, 2020
S2 emission from chemically modified BODIPYs.
Dae Won Cho1, Mamoru Fujitsuka, Jung Ho Ryu
1Konkuk University-Fraunhofer ISE Next Generation Solar Cell Research Center, Konkuk University, Seoul 143-701, Korea. dwcho@konkuk.ac.kr
Novel boron dipyrromethene (BODIPY) derivatives were synthesized for longer wavelength applications. These BODIPY compounds exhibit unusual S(2) emission, influenced by internal conversion and intersystem crossing.
Area of Science:
- Organic Chemistry
- Photophysics
- Spectroscopy
Background:
- Boron dipyrromethene (BODIPY) dyes are widely used in various applications due to their photophysical properties.
- Extending the absorption and emission of BODIPY dyes to longer wavelengths is crucial for advanced applications.
- Understanding the excited-state dynamics of BODIPY is essential for designing new functional dyes.
Purpose of the Study:
- To synthesize novel BODIPY derivatives with enhanced absorption and emission in the longer wavelength region.
- To investigate the anomalous S(2) emission from the second excited state observed in these new BODIPY compounds.
- To elucidate the photophysical processes governing the S(2) state dynamics.
Main Methods:
- Synthesis of novel boron dipyrromethene (BODIPY) derivatives.
- Spectroscopic measurements including fluorescence up-conversion and transient absorption.
- Theoretical calculations using time-dependent density functional theory (TD-DFT).
Main Results:
- Successful synthesis of BODIPY derivatives with significant absorption and emission in the longer wavelength region.
- Observation of anomalous S(2) emission at shorter wavelengths from the second excited state.
- Determination that the S(2) emission decay time is influenced by internal conversion and intersystem crossing.
Conclusions:
- The synthesized BODIPY derivatives offer promising photophysical properties for longer wavelength applications.
- The photodynamics of the S(2) state in these BODIPY compounds are complex, involving competing relaxation pathways.
- Theoretical calculations support the assignments of electronic transitions and provide insights into the observed photobehavior.
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