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Double J-Coupling Strategy for Near Infrared Emitters

Chia‐An Shen, Matthias Stolte, Jin Hong Kim, Anja Rausch, Frank Würthner

2021Journal of the American Chemical Society53 citationsDOI

Abstract

Fluorophores emitting in the near-infrared (NIR) are highly desired for various applications, but increasing nonradiative rates cause severe fluorescence quenching for wavelengths beyond 800 nm. Here, a bis(squaraine) dye is reported that bears two NIR dyes in a head-to-tail chromophore arrangement. This arrangement leads to intramolecular J-type exciton coupling, resulting in an absorption maximum at 961 nm and a fluorescence peak at 971 nm with a quantum yield of 0.33% in chloroform. In less polar toluene, the bis(squaraine) self-assembles into nanofibers, affording another bathochromic shift with an absorption maximum at 1095 nm and a fluorescence peak at 1116 nm originating from intermolecular J-type coupling.

Topics & Concepts

Bathochromic shiftChemistryChromophorePhotochemistryQuantum yieldIntramolecular forceIntermolecular forceFluorescenceAbsorption (acoustics)ExcitonTolueneQuenching (fluorescence)OpticsMoleculeStereochemistryOrganic chemistryPhysicsQuantum mechanicsLuminescence and Fluorescent MaterialsPerovskite Materials and ApplicationsOrganic Light-Emitting Diodes Research
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