Synthesis of Novel Hyperbranched Polybenzo-Bisthiazole Amide with Donor⁻Acceptor (D-A) Architecture, High Fluorescent...

Two novel highly fluorescent hyperbranched polybenzobisthiazole amides with a donor⁻acceptor architecture and large Stokes shift were rationally designed and synthesized. The chemical structures of the prepared hyperbranched polymers were characterized using Fourier Transform Infrared Spectroscopy (FTIR) analysis, Hydrogen Nuclear Magnetic Resonance (¹H-NMR) analysis, and Gel Permeation Chromatography (GPC) analysis. These two polymers were soluble in dimethyl sulfoxide (DMSO) and N,N-dimethylformamide (DMF), and their DMSO and DMF solutions emitted strong green light (517⁻537 nm) with high quantum yields (QYs) and large Stokes shifts. Their relative fluorescence QYs in the DMSO solution were calculated as 77.75% and 81.14% with the Stokes shifts of 137 nm (0.86 eV) and 149 nm (0.92 eV) for HP⁻COOH and HP⁻NH₂, respectively, using quinine sulfate as the standard. In the DMF solution, the QYs of HP⁻COOH and HP⁻NH₂ were calculated as 104.65% and 118.72%, with the Stokes shifts of 128 nm (0.79 eV) and 147 nm (0.87 eV), respectively. Their films mainly emitted strong blue light with the maximum emission wavelengths of 436 nm and 480 nm for HP⁻COOH and HP⁻NH₂, respectively. The Stokes shifts for HP⁻COOH and HP⁻NH₂ films were 131 nm (0.42 eV) and 179 nm (0.86 eV), respectively. They are promising candidates for luminescent solar concentrators and blue light emitting materials.