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dipyrrins

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(A) Boron dipyrrin (BODIPY) structure with the dipyrrin core highlighted in green. (B) BODIPY sample in the solid state (crystals on flask wall) and in solution.
Published: 01 August 2017
Figure 2 ( A ) Boron dipyrrin (BODIPY) structure with the dipyrrin core highlighted in green. ( B ) BODIPY sample in the solid state (crystals on flask wall) and in solution.
Journal Article
Journal: Elements
Published: 01 August 2017
Elements (2017) 13 (4): 255–260.
...Figure 2 ( A ) Boron dipyrrin (BODIPY) structure with the dipyrrin core highlighted in green. ( B ) BODIPY sample in the solid state (crystals on flask wall) and in solution. ...
FIGURES | View All (8)
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Schematic illustrating the boron dipyrrin (BODIPY)–sugar concept. When F-BODIPY links to sugar OH groups, such as glucose, the resulting O-BODIPY complex fluoresces.
Published: 01 August 2017
Figure 5 Schematic illustrating the boron dipyrrin (BODIPY)–sugar concept. When F-BODIPY links to sugar OH groups, such as glucose, the resulting O-BODIPY complex fluoresces.
Image
Photoinduced electron transfer (PET) mechanism for a turn-ON boron dipyrrin (BODIPY) sensor. (A) The free chelator quenches BODIPY fluorescence via photoinduced electron transfer. (B) When the target is bound to the chelator, then PET is inhibited and fluorescence turned ON. Commercially available BODIPY probes have been developed for fluorescence microscopy of lysosomes (subcellular organelles). The green- and red-labelled NMe2 chelator groups target the protons (H+) in acidic compartments in cells. (C) LysoTracker® Green, a green fluorescent dye that stains acidic compartments in live cells. (D) LysoTracker® Red, is very similar to LysoTracker® Green, but the extra small ring attached to the BODIPY (labelled red) changes the fluorescence wavelength from green to red.
Published: 01 August 2017
Figure 3 Photoinduced electron transfer (PET) mechanism for a turn-ON boron dipyrrin (BODIPY) sensor. ( A ) The free chelator quenches BODIPY fluorescence via photoinduced electron transfer. ( B ) When the target is bound to the chelator, then PET is inhibited and fluorescence turned