Photoinduced Electron Transfer‐based Halogen‐free Photosensitizers: Covalent meso‐Aryl (Phenyl, Naphthyl, Anthryl, and Pyrenyl) as Electron Donors to Effectively Induce the Formation of the Excited Triplet State and Singlet Oxygen for BODIPY Compounds

Pristine BODIPY compounds have negligible efficiency to generate the excited triplet state and singlet oxygen. In this report, we show that attaching a good electron donor to the BODIPY core can lead to singlet oxygen formation with up to 58 % quantum efficiency. For this purpose, BODIPYs with meso‐...

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Veröffentlicht in:Chemistry, an Asian journal an Asian journal, 2017-09, Vol.12 (18), p.2447-2456
Hauptverfasser: Zhang, Xian‐Fu, Feng, Nan
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description Pristine BODIPY compounds have negligible efficiency to generate the excited triplet state and singlet oxygen. In this report, we show that attaching a good electron donor to the BODIPY core can lead to singlet oxygen formation with up to 58 % quantum efficiency. For this purpose, BODIPYs with meso‐aryl groups (phenyl, naphthyl, anthryl, and pyrenyl) were synthesized and characterized. The fluorescence, excited triplet state, and singlet oxygen formation properties for these compounds were measured in various solvents by UV/Vis absorption, steady‐state and time‐resolved fluorescence methods, as well as laser flash photolysis technique. In particular, the presence of anthryl and pyrenyl showed substantial enhancement on the singlet oxygen formation ability of BODIPY with up to 58 % and 34 % quantum efficiency, respectively, owing to their stronger electron‐donating ability. Upon the increase in singlet oxygen formation, the fluorescence quantum yield and lifetime values of the aryl‐BODIPY showed a concomitant decrease. The increase in solvent polarity enhances the singlet oxygen generation but decreases the fluorescence quantum yield. The results are explained by the presence of intramolecular photoinduced electron transfer from the aryl moiety to BODIPY core. This method of promoting T1 formation is very different from the traditional heavy atom effect by I, Br, or transition metal atoms. This type of novel photosensitizers may find important applications in organic oxygenation reactions and photodynamic therapy of tumors. Functional BODIPY: Photosensitizers that efficiently produce singlet oxygen play a key role in photodynamic therapy of cancers. Pristine BODIPYs (boron‐dipyrromethenes) lack the ability to generate the excited triplet state and singlet oxygen. However, attaching a meso‐aryl as a good electron donor to the BODIPY core leads to the formation of the triplet state and singlet oxygen with up to 58 % efficiency.
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In this report, we show that attaching a good electron donor to the BODIPY core can lead to singlet oxygen formation with up to 58 % quantum efficiency. For this purpose, BODIPYs with meso‐aryl groups (phenyl, naphthyl, anthryl, and pyrenyl) were synthesized and characterized. The fluorescence, excited triplet state, and singlet oxygen formation properties for these compounds were measured in various solvents by UV/Vis absorption, steady‐state and time‐resolved fluorescence methods, as well as laser flash photolysis technique. In particular, the presence of anthryl and pyrenyl showed substantial enhancement on the singlet oxygen formation ability of BODIPY with up to 58 % and 34 % quantum efficiency, respectively, owing to their stronger electron‐donating ability. Upon the increase in singlet oxygen formation, the fluorescence quantum yield and lifetime values of the aryl‐BODIPY showed a concomitant decrease. 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In this report, we show that attaching a good electron donor to the BODIPY core can lead to singlet oxygen formation with up to 58 % quantum efficiency. For this purpose, BODIPYs with meso‐aryl groups (phenyl, naphthyl, anthryl, and pyrenyl) were synthesized and characterized. The fluorescence, excited triplet state, and singlet oxygen formation properties for these compounds were measured in various solvents by UV/Vis absorption, steady‐state and time‐resolved fluorescence methods, as well as laser flash photolysis technique. In particular, the presence of anthryl and pyrenyl showed substantial enhancement on the singlet oxygen formation ability of BODIPY with up to 58 % and 34 % quantum efficiency, respectively, owing to their stronger electron‐donating ability. Upon the increase in singlet oxygen formation, the fluorescence quantum yield and lifetime values of the aryl‐BODIPY showed a concomitant decrease. The increase in solvent polarity enhances the singlet oxygen generation but decreases the fluorescence quantum yield. The results are explained by the presence of intramolecular photoinduced electron transfer from the aryl moiety to BODIPY core. This method of promoting T1 formation is very different from the traditional heavy atom effect by I, Br, or transition metal atoms. This type of novel photosensitizers may find important applications in organic oxygenation reactions and photodynamic therapy of tumors. Functional BODIPY: Photosensitizers that efficiently produce singlet oxygen play a key role in photodynamic therapy of cancers. Pristine BODIPYs (boron‐dipyrromethenes) lack the ability to generate the excited triplet state and singlet oxygen. 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subjects Aromatic compounds
aryl-BODIPY
Chemistry
Efficiency
Electron transfer
Flash photolysis
Fluorescence
Oxygenation
Photodynamic therapy
photosensitizers
Polarity
Pollutants
Quantum efficiency
Singlet oxygen
solvent effects
Tumors
title Photoinduced Electron Transfer‐based Halogen‐free Photosensitizers: Covalent meso‐Aryl (Phenyl, Naphthyl, Anthryl, and Pyrenyl) as Electron Donors to Effectively Induce the Formation of the Excited Triplet State and Singlet Oxygen for BODIPY Compounds
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