Wu Yanping, Li Zhenyu, Liu Qingsong, Wang Xiaoqing, Yan Hui, Gong Shuwen, Liu Zhipeng, He Weijiang
Institute of Functional Organic Molecules and Materials, School of Chemistry and Chemical Engineering, Liaocheng University, No. 1 Hunan Road, Liaocheng, 252000, People's Republic of China.
Org Biomol Chem. 2015 May 28;13(20):5775-82. doi: 10.1039/c5ob00607d. Epub 2015 Apr 23.
Two pyridine-ketoiminate-based organoboron complexes (2 and 3) were developed. 2 and 3 showed very weak emission in low-viscosity organic solvents because of the intramolecular rotation induced non-radiative process. Their emission can be dramatically enhanced by the increase in solvent viscosity or by molecular aggregation in the solid state. Moreover, 2 and 3 exhibited intense emission with high quantum yield of 0.53 and 0.46, respectively. X-ray crystallographic analysis showed that the weak intermolecular interactions such as C-H···F and C-H···π by fixing the molecular conformations of 2 and 3 were responsible for intense luminescence in the solid state. The large Stokes shifts and high efficient solid-state emission of 2 and 3 make them valuable AIE luminophores for further potential applications in the fields of fluorescence imaging and materials science.
开发了两种基于吡啶酮亚胺的有机硼配合物(2和3)。由于分子内旋转引起的非辐射过程,2和3在低粘度有机溶剂中显示出非常弱的发射。溶剂粘度的增加或固态下的分子聚集可显著增强它们的发射。此外,2和3分别表现出强烈的发射,量子产率高达0.53和0.46。X射线晶体学分析表明,通过固定2和3的分子构象,诸如C-H···F和C-H···π等弱分子间相互作用是固态中强烈发光的原因。2和3的大斯托克斯位移和高效固态发射使其成为有价值的聚集诱导发光体,可在荧光成像和材料科学领域进一步潜在应用。