Kahl Robert T, Erhardt Andreas, Krauss Gert, Seibold Ferdinand, Dolynchuk Oleksandr, Thelakkat Mukundan, Thurn-Albrecht Thomas
Experimental Polymer Physics, Martin Luther University Halle-Wittenberg, Von-Danckelmann-Platz 3, 06120 Halle, Germany.
Applied Functional Polymers, University of Bayreuth, Universitätsstr. 30, 95440 Bayreuth, Germany.
Macromolecules. 2024 May 29;57(11):5243-5252. doi: 10.1021/acs.macromol.4c00264. eCollection 2024 Jun 11.
The chemical architecture of conjugated polymers is often designed by contemplating and understanding the consequences of structural changes on electronic properties at the molecular level. However, even minor changes to the chemical structure of a polymer can significantly influence the packing arrangement, which also influences the electronic properties of the bulk material. Here, we investigate the molecular arrangement in the ordered state at room temperature of a series of three different polydiketopyrrolopyrroles (PDPPs) in bulk and oriented thin films in detail by wide-angle X-ray scattering and by atomic force microscopy. The changes in the chemical structure of the investigated PDPPs, namely, an additional side chain or a different flanking unit, lead to an increase in long-range order and thereby to a change in the phase state from sanidic ordered via sanidic rectangular or oblique to crystalline.
共轭聚合物的化学结构通常是通过在分子水平上思考和理解结构变化对电子性质的影响来设计的。然而,即使聚合物的化学结构发生微小变化,也会显著影响堆积排列,而堆积排列也会影响块状材料的电子性质。在这里,我们通过广角X射线散射和原子力显微镜详细研究了一系列三种不同的聚二酮吡咯并吡咯(PDPPs)在本体和取向薄膜中室温下有序态的分子排列。所研究的PDPPs化学结构的变化,即额外的侧链或不同的侧翼单元,导致长程有序增加,从而使相态从板状有序经由板状矩形或斜方转变为结晶态。