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 in | New journal of chemistry Vol. 47; no. 26; pp. 12287 - 12295 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
CAMBRIDGE
Royal Soc Chemistry
03.07.2023
Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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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). |
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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 |