Ochs Nellie A K, Lewandowska Urszula, Zajaczkowski Wojciech, Corra Stefano, Reger Stephan, Herdlitschka Andreas, Schmid Sylvia, Pisula Wojciech, Müllen Klaus, Bäuerle Peter, Wennemers Helma
Laboratory of Organic Chemistry , ETH Zürich , Vladimir-Prelog-Weg 3 , 8093 Zürich , Switzerland . Email:
Max Planck Institute for Polymer Research , Ackermannweg 10 , 55128 Mainz , Germany . Email:
Chem Sci. 2019 May 2;10(20):5391-5396. doi: 10.1039/c8sc05742g. eCollection 2019 May 28.
Control over the molecular organization of π-conjugated oligothiophenes into different types of supramolecular assemblies is key to their use in organic electronics but difficult to achieve as these chromophores have a pronounced tendency to aggregate. Herein we show that oligoprolines, which do not self-assemble on their own, control the self-assembly of quaterthiophenes. Spectroscopic, microscopic, and diffraction studies with quaterthiophene-oligoproline conjugates revealed the formation of mono- or double-layered sheets or, alternatively, helically twisted ribbons - depending on the length of the oligoproline. The dimensions of the nanoscopic objects, which extend into the micrometer regime, correlate with the molecular dimensions of the quaterthiophene-oligoproline building blocks.
将π共轭低聚噻吩分子组织成不同类型的超分子组装体是其在有机电子学中应用的关键,但由于这些发色团有明显的聚集倾向,所以很难实现。在此我们表明,自身不会自组装的寡聚脯氨酸能控制四噻吩的自组装。对四噻吩-寡聚脯氨酸共轭物进行的光谱、显微镜和衍射研究表明,根据寡聚脯氨酸的长度,会形成单层或双层薄片,或者是螺旋扭曲的条带。延伸至微米级的纳米物体尺寸与四噻吩-寡聚脯氨酸结构单元的分子尺寸相关。