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Semiconducting Self-Assembled Nanofibers Prepared from Photostable Octafluorinated Bisanthene Derivatives

机译:由光稳定的八氟联苯并蒽衍生物制备的半导体自组装纳米纤维

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摘要

Bisanthene is an important class of small two-dimensional polycyclic aromatic hydrocarbons with a zigzag-edged graphene nanoribbon character. Therefore, the functionalization and deep understanding of the structure-property relationship of bisanthene would provide an effective design for small organic molecular devices. In this study, octa- and tetrafluorinated bisanthene derivatives were synthesized for investigating the effect of electronegative fluorine substitution on the structure and physical property of bisanthene. Firstly, the octafluorinated bisanthene derivative has a twisted structure due to the steric repulsion of fluorine atoms at the bay region. Secondly, the absorption and fluorescence peak maxima are blueshifted with an increase in the degree of fluorine substitution. Notably, a triisopropylsilylethynyl-substituted octafluorinated derivative (F8) exhibited strong fluorescence at 657 nm with high fluorescence quantum yield (84%). Additionally, cyclic voltammograms indicate the positive effect of fluorine substitution on the high highest occupied molecular orbital energy level of the molecules; thus, F8 molecule exhibited a remarkably increased photostability. Finally, the self-assembled behavior of fluorinated compounds was investigated by scanning electron microscopy and X-ray diffraction analysis. Specifically, F8 self-assembled to form bundles of long semicrystalline nanofibers exhibiting hole-transporting properties (3.4×10-3 cm2 V-1 s-1).
机译:联蒽是一类重要的小型二维多环芳烃,具有曲折边缘的石墨烯纳米带特征。因此,对联蒽的功能化和对结构-性质关系的深入理解将为小型有机分子器件提供有效的设计。在这项研究中,八氟和四氟联蒽衍生物被合成用于研究负电氟取代对联蒽的结构和物理性质的影响。首先,由于在海湾区域的氟原子的空间排斥,八氟化联蒽衍生物具有扭曲的结构。其次,随着氟取代度的增加,吸收峰和荧光峰最大值发生蓝移。值得注意的是,三异丙基甲硅烷基乙炔基取代的八氟化衍生物(F8)在657 nm处显示强荧光,并具有较高的荧光量子产率(84%)。此外,循环伏安图表明氟取代对分子的最高最高占据分子轨道能级的积极影响;因此,F8分子表现出显着增加的光稳定性。最后,通过扫描电子显微镜和X射线衍射分析研究了含氟化合物的自组装行为。具体地,F8自组装以形成表现出空穴传输性质(3.4×10-3cm 2 V-1s-1)的长的半结晶纳米纤维束。

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