Hebei Key Laboratory of Applied Chemistry, School of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, China.
Nanoscale. 2019 Apr 11;11(15):7111-7116. doi: 10.1039/c8nr08066f.
The controlled construction of organic heterostructured architectures derived from molecules with similar nucleation thresholds and concentrations has been rare and remains a great challenge. Herein, we report a sequential epitaxial growth to synthesize dual-color-emitting organic heterostructures with 9,10-bis(phenylethynyl)anthracene (BPEA) microwire trunks and tris-(8-hydroxyquinoline)aluminium (Alq3) microstructure branches by an anti-solvent induced sequential crystallization strategy. During the epitaxial growth process, the hydrogen-bonding interactions of the anti-solvent and solvent cause a large change in the solubility and crystallization rate of BPEA and Alq3 molecules in the mixed system, which facilitates sequential crystallization of organic molecule pairs with similar nucleation thresholds and concentrations into desired heterostructures by manipulating the synergism of anti-solvents and solvents. The Förster resonant energy transfer process in heterostructures could be modulated by varying the structure of heterostructures, such as the shape, amount and angles of the branches. The present synthesis strategy provides a unique insight into the detailed formation mechanism of complex organic heterostructures, further guiding the construction of more functional heterostructure materials.
受限于类似成核势垒和浓度的分子,控制构建有机杂化结构非常困难,鲜有报道。在此,我们报道了一种通过反溶剂诱导的顺序结晶策略,以合成具有 9,10-双(苯乙炔基)蒽(BPEA)微米线主干和三(8-羟基喹啉)铝(Alq3)微结构支的双色发射有机杂化结构。在晶化过程中,反溶剂和溶剂的氢键作用使混合体系中 BPEA 和 Alq3 分子的溶解度和结晶速率发生很大变化,通过控制反溶剂和溶剂的协同作用,有利于具有类似成核势垒和浓度的有机分子对顺序结晶形成所需的杂化结构。通过改变杂化结构的形状、数量和分支角度等,可以调节杂化结构中的Förster 共振能量转移过程。本研究为复杂有机杂化结构的详细形成机制提供了独特的见解,进一步指导了更多功能杂化结构材料的构建。