Excited state dynamics of a Bodipy derivative with a twisted molecular structure: Combined experimental and theoretical studies

The photophysical properties of a boron dipyrromethene (Bodipy, BDP) derivative (BDP-SA) in which one F atom at the BDP core was replaced by an O atom and condensed with salicylaldehyde were investigated. This compound has a twisted molecular structure and unusually low fluorescence quantum yield (1% in toluene). No intersystem crossing was observed with a nanosecond transient absorption study. The triplet state lifetime of BDP-SA was determined to be 115 μs by photosensitizing. Femtosecond transient absorption shows a structure relaxation of ∼1.5 ps for the S1 excited state. Theoretical studies show conical intersections, which are responsible for the efficient non-radiative decay of the S1 state, which has extremely weak fluorescence.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-02-04
DOI
https://doi.org/10.1063/5.0245843
Citations
5
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
2.59

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article

Excited state dynamics of a Bodipy derivative with a twisted molecular structure: Combined experimental and theoretical studies

Gloria Mazzone, Gagik G. Gurzadyan, Bernhard Dick, Jianzhang Zhao et al.
5 citations
The Journal of Chemical Physics
Luminescence and Fluorescent Materials
2.59
article

Excited state dynamics of a Bodipy derivative with a twisted molecular structure: Combined experimental and theoretical studies

Gloria Mazzone, Gagik G. Gurzadyan, Bernhard Dick, Jianzhang Zhao, Sheng Liao, Ming‐De Li, Xi Chen, Bei Li, Xue Zhang, Jiayu Li
article en
5 citations

Abstract

The photophysical properties of a boron dipyrromethene (Bodipy, BDP) derivative (BDP-SA) in which one F atom at the BDP core was replaced by an O atom and condensed with salicylaldehyde were investigated. This compound has a twisted molecular structure and unusually low fluorescence quantum yield (1% in toluene). No intersystem crossing was observed with a nanosecond transient absorption study. The triplet state lifetime of BDP-SA was determined to be 115 μs by photosensitizing. Femtosecond transient absorption shows a structure relaxation of ∼1.5 ps for the S1 excited state. Theoretical studies show conical intersections, which are responsible for the efficient non-radiative decay of the S1 state, which has extremely weak fluorescence.

The Journal of Chemical PhysicsVol. 162(5)
Dalian University of Technology (CN), Shantou University (CN), Dalian University (CN), Institute of Art (PL), Smart Material (Germany) (DE), University of Calabria (IT), University of Regensburg (DE)
Shantou University, National Natural Science Foundation of China, China Postdoctoral Science Foundation, Dalian University of Technology, Università della Calabria, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Clean water and sanitation
Openalex Percentile: Top 12%
Luminescence and Fluorescent Materials
2.59
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