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Arylisoquinoline-derived organoboron dyes with a triaryl skeleton show dual fluorescence.


ABSTRACT: Four new dyes that derive from borylated arylisoquinolines were prepared, containing a third aryl residue (naphthyl, 4-methoxynaphthyl, pyrenyl or anthryl) that is linked via an additional stereogenic axis. The triaryl cores were synthesized by Suzuki couplings and then transformed into boronic acid esters by employing an Ir(I)-catalyzed reaction. The chromophores show dual emission behavior, where the long-wavelength emission band can reach maxima close to 600 nm in polar solvents. The fluorescence quantum yields of the dyes are generally in the range of 0.2-0.4, reaching in some cases values as high as 0.5-0.6. Laser-flash photolysis provided evidence for the existence of excited triplet states. The dyes form fluoroboronate complexes with fluoride anions, leading to the observation of the quenching of the long-wavelength emission band and ratiometric response by the build-up of a hypsochromically shifted emission signal.

SUBMITTER: Pais VF 

PROVIDER: S-EPMC6880824 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Arylisoquinoline-derived organoboron dyes with a triaryl skeleton show dual fluorescence.

Pais Vânia F VF   Neumann Tristan T   Vayá Ignacio I   Jiménez M Consuelo MC   Ros Abel A   Pischel Uwe U  

Beilstein journal of organic chemistry 20191104


Four new dyes that derive from borylated arylisoquinolines were prepared, containing a third aryl residue (naphthyl, 4-methoxynaphthyl, pyrenyl or anthryl) that is linked via an additional stereogenic axis. The triaryl cores were synthesized by Suzuki couplings and then transformed into boronic acid esters by employing an Ir(I)-catalyzed reaction. The chromophores show dual emission behavior, where the long-wavelength emission band can reach maxima close to 600 nm in polar solvents. The fluoresc  ...[more]

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