Article,

Double J-Coupling Strategy for Near Infrared Emitters

, , , , and .
J. Am. Chem. Soc., 143 (31): 11946--11950 (July 2021)
DOI: 10.1021/jacs.1c05934

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.

Tags

Users

  • @wuerthner_group

Comments and Reviews