A series of novel BODIPY dyes has been prepared through the introduction of an N-bridged annulated meso-phenyl ring at one of the β-positions of the BODIPY core. An unusual blueshift of the main spectral bands is observed, since the fusion of a meso-substituent results in a marked relative destabilization of the LUMO. The greater rigidity of the ring-fused structure leads to very high fluorescence quantum yields. The position of the main spectral bands can be fine-tuned by introducing electron withdrawing and donating groups onto the meso-phenyl ring.
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http://dx.doi.org/10.1002/asia.201700584 | DOI Listing |
Org Lett
December 2024
DFG Cluster of Excellence livMatS @FIT, Institute of Organic Chemistry, Albertstraße 21, 79104 Freiburg (Breisgau), Germany.
facile access to -heteroaryl-fused bis-BODIPY scaffolds has been developed. A BODIPY dimer with an α,α-amine linker serves as a starting material to obtain pyrrole- and pyridine-fused BODIPYs, either by direct oxidation or by oxidative condensation with an aldehyde building block. Both species mark antipodal conjugative coupling conditions that result in distinct spectral outcomes.
View Article and Find Full Text PDFChem Asian J
September 2017
Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou, 311121, China.
A series of novel BODIPY dyes has been prepared through the introduction of an N-bridged annulated meso-phenyl ring at one of the β-positions of the BODIPY core. An unusual blueshift of the main spectral bands is observed, since the fusion of a meso-substituent results in a marked relative destabilization of the LUMO. The greater rigidity of the ring-fused structure leads to very high fluorescence quantum yields.
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