Vadivel Marichandran, Singh Shikha, Singh Dharmendra Pratap, Raghunathan V A, Kumar Sandeep
Soft Condensed Matter Group, Raman Research Institute, C.V.Raman Avenue, Bengaluru 560080, India.
Université du Littoral Côte d'Opale, UR 4476, UDSMM, Unité de Dynamique et Structure des Matériaux Moléculaires, Calais F-62228, France.
J Phys Chem B. 2021 Sep 16;125(36):10364-10372. doi: 10.1021/acs.jpcb.1c06009. Epub 2021 Sep 6.
A series of novel naphthophenanthridine derivatives are synthesized via N-annulation of hexabutoxytriphenylene-1-amine with various aliphatic aldehydes through the Pictet-Spengler reaction. The synthesized derivatives have been found to self-assemble into a columnar hexagonal mesophase over a wide temperature range, as validated through polarized optical microscopy, differential scanning calorimetry and X-ray diffraction experiments. The photophysical properties of these compounds were studied using UV-visible and emission spectroscopy. The synthesized compounds exhibit ambipolar charge transport, showing temperature-independent electron and hole mobility on the order of 3 × 10 cm/V s, as evaluated by the time-of-flight technique. These novel N-annulated derivatives can be of immense potential toward semiconducting applications of self-assembling supramolecular systems.
通过六丁氧基三亚苯-1-胺与各种脂肪醛经皮克特-施彭格勒反应进行N-环化反应,合成了一系列新型萘并菲啶衍生物。通过偏光显微镜、差示扫描量热法和X射线衍射实验验证,所合成的衍生物在很宽的温度范围内自组装成柱状六方中间相。利用紫外可见光谱和发射光谱研究了这些化合物的光物理性质。通过飞行时间技术评估,所合成的化合物表现出双极性电荷传输,显示出与温度无关的电子和空穴迁移率,约为3×10 cm/V s。这些新型N-环化衍生物对于自组装超分子体系的半导体应用可能具有巨大潜力。