Related Experiment Video
Updated: Feb 26, 2026

A Bright NIR-II Fluorescence Probe for Vascular and Tumor Imaging
Published on: March 17, 2023
Indolizine-Squaraines: NIR Fluorescent Materials with Molecularly Engineered Stokes Shifts
Louis E McNamara1, Tana A Rill1, Aron J Huckaba1
1Department of Chemistry and Biochemistry, University of Mississippi, 322 Coulter Hall, University, MS, 38677, USA.
Abstract:
The development of deep red and near infrared emissive materials with high quantum yields is an important challenge. Several classes of squaraine dyes have demonstrated high quantum yields, but require significantly red-shifted absorptions to access the NIR window. Additionally, squaraine dyes have typically shown narrow Stokes shifts, which limits their use in living biological imaging applications due to dye emission interference with the light source. Through the incorporation of indolizine heterocycles we have synthesized novel indolizine squaraine dyes with increased Stokes shifts (up to >0.119 eV, >50 nm increase) and absorptions substantially further into the NIR region than an indoline squaraine benchmark (726 nm versus 659 nm absorption maxima). These materials have shown significantly enhanced water solubility, which is unique for squaraine dyes without water-solubilizing substituents. Absorption, electrochemical, computational, and fluorescence studies were undertaken and exceptional fluorescence quantum yields of up 12 % were observed with emission curves extending beyond 850 nm.
More Related Videos
Related Concept Videos
Photoluminescence: Applications
Fluorescence and Phosphorescence: Instrumentation
Super-resolution Fluorescence Microscopy
Total Internal Reflection Fluorescence Microscopy
Labeling DNA Probes
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...

