Department of Chemistry and Biochemistry, University of Mississippi, University, MS 38677, USA.
Molecules. 2018 Nov 22;23(12):3051. doi: 10.3390/molecules23123051.
Near-infrared emissive materials with tunable Stokes shifts and solid-state emissions are needed for several active research areas and applications. To aid in addressing this need, a series of indolizine-cyanine compounds varying only the anions based on size, dipole, and hydrophilicity were prepared. The effect of the non-covalently bound anions on the absorption and emission properties of identical π-system indolizine-cyanine compounds were measured in solution and as thin films. Interestingly, the anion choice has a significant influence on the Stokes shift and molar absorptivities of the dyes in solution. In the solid-state, the anion choice was found to have an effect on the formation of aggregate states with higher energy absorptions than the parent monomer compound. The dyes were found to be emissive in the NIR region, with emissions peaking at near 900 nm for specific solvent and anion selections.
需要具有可调 Stoke 位移和固态发射的近红外发射材料,以满足几个活跃的研究领域和应用的需求。为了满足这一需求,我们制备了一系列吲哚嗪-菁染料,这些染料仅基于阴离子的大小、偶极矩和亲水性进行了改变。在溶液中和薄膜中测量了非共价键合阴离子对相同π-系统吲哚嗪-菁化合物的吸收和发射性质的影响。有趣的是,阴离子的选择对染料在溶液中的 Stoke 位移和摩尔吸光率有显著影响。在固态中,阴离子的选择会影响聚集体状态的形成,聚集体状态的吸收能量高于母体单体化合物。这些染料在近红外区域具有发光性,对于特定的溶剂和阴离子选择,发光峰值在近 900nm 附近。