Universität Würzburg, Center for Nanosystems Chemistry and Institut für Organische Chemie, Am Hubland, 97074 Würzburg (Germany).
Angew Chem Int Ed Engl. 2014 Jan 27;53(5):1270-4. doi: 10.1002/anie.201308963. Epub 2013 Dec 18.
Dye aggregates are becoming increasingly attractive for diverse applications, in particular as organic electronic and sensor materials. However, the growth processes of such aggregates from molecular to small assemblies up to nanostructures is still not properly understood, limiting the design of materials' functional properties. Here we elucidate the supramolecular growth process for an outstanding class of functional dyes, perylene bisimides (PBIs), by transmission electron microscopy (TEM), cryogenic scanning electron microscopy (cryo-SEM), and atomic force microscopy (AFM). Our studies reveal a sequential growth of amphiphilic PBI dyes from nanorods into nanoribbons in water by fusion and fission processes. More intriguingly, the fluorescence observed for higher hierarchical order nanoribbons was enhanced relative to that of nanorods. Our results provide insight into the relationship between molecular, morphological, and functional properties of self-assembled organic materials.
染料聚集体在各种应用中越来越具有吸引力,特别是作为有机电子和传感器材料。然而,从分子到小组装体再到纳米结构的这种聚集体的生长过程仍然没有得到很好的理解,限制了材料功能特性的设计。在这里,我们通过透射电子显微镜(TEM)、低温扫描电子显微镜(cryo-SEM)和原子力显微镜(AFM)阐明了一类出色的功能染料——苝二酰亚胺(PBIs)的超分子生长过程。我们的研究揭示了两亲性 PBI 染料在水中通过融合和裂变过程从纳米棒到纳米带的顺序生长。更有趣的是,观察到较高层次有序纳米带的荧光相对于纳米棒的荧光增强。我们的结果提供了对自组装有机材料的分子、形态和功能特性之间关系的深入了解。