A series of π-expanded coplanar BODIPY dyes with deep-red emission: Synthesis, optical properties, and application in amplified spontaneous emission

Boron dipyrromethene (BODIPY)-derived dyes are a class of superior emitters, and a classic BODIPY structure has absorption and emission at ∼500 nm. To meet the practical application requirements, this work was dedicated to the design and synthesis of BODIPY emitters covering the deep-red region with...

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Published inNew journal of chemistry Vol. 47; no. 26; pp. 12287 - 12295
Main Authors Wang, Yang, Xie, Lei, Sun, Qinning, Liu, Liang
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 03.07.2023
Royal Society of Chemistry
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Summary:Boron dipyrromethene (BODIPY)-derived dyes are a class of superior emitters, and a classic BODIPY structure has absorption and emission at ∼500 nm. To meet the practical application requirements, this work was dedicated to the design and synthesis of BODIPY emitters covering the deep-red region with a high emission quantum yield. Aromatic rings and a well-known electron-withdrawing group, -CF 3 , were introduced into a π-expanded BODIPY structure. These BODIPY emitters were discussed in detail, including their thermal stability and optical parameters, as well as their photodynamic therapy performance. The correlation between the BODIPY photophysical performance and their substituents was discussed. It was found that the formation of a π-expanded coplanar conjugation chain successfully shifted BODIPY emission to the deep-red region (626 nm) with a high quantum yield (0.99). The -CF 3 modification on the BODIPY meso -C, however, quenched its emission. A threshold energy for the ASE (amplified spontaneous emission) effect of 980 μJ was exhibited with an efficiency of 5.5%. The cell viability was decreased to 9.0 ± 4.6% using these BODIPY dyes as a photosensitizer. Aromatic rings and a -CF 3 group were introduced into a π-expanded BODIPY structure. The formation of a π-expanded coplanar conjugation chain successfully shifted BODIPY emission to the deep-red region (626 nm) with a high quantum yield (0.99).
Bibliography:in various solvents. Page S7: Table S2. OPA and TPA values of
calculated at the RB3LYP/6-31G(d) level. See DOI
B1-B5
Pages S8-S11: Emission decay results of
,
in various solvents. Pages S3-S6: Absorption and emission spectra of
Pages S17-S43: One photon absorption (OPA) and two photon absorption (OPA) TD-DFT calculation results of
B1
B2
B4
B5
Electronic supplementary information (ESI) available: Page S2: Table S1. Photophysical parameters of
and
B3-B5
Pages S12−S16: NMR spectra of
https://doi.org/10.1039/d3nj01667f
ISSN:1144-0546
1369-9261
DOI:10.1039/d3nj01667f