Department of Applied Chemistry, Faculty of Science and Engineering, Saga University, Honjo machi 1, Saga-shi, Saga, Japan.
Org Biomol Chem. 2013 Apr 7;11(13):2186-97. doi: 10.1039/c3ob27320b.
The synthesis, crystal structures and photophysical properties of two types of pyrene-cored blue-light emitting [4]helicenes (7 and 9) are reported. The chemical structures of all synthesized compounds were fully confirmed by 1H and 13C NMR spectra, mass spectroscopy as well as elemental analysis. Single-crystal X-ray analysis of these [4]helicenes revealed that there are two types of laterally naphthalene annulated helical architectures, which are clearly influenced by different R substituents. The photophysical properties of the [4]helicenes (7 and 9) were fully investigated in both solutions and films, along with the pre-cyclization products, 4,9- and 4,10-bis(phenylethenyl)pyrenes (6 and 8). Notable optical features were obtained in these compounds, which make them promising candidates for several important applications in modern electronic and optoelectronic devices, such as blue emitters in organic light-emitting devices (OLEDs), or as models for further exploring the development of a new generation of organic materials based on pyrene.
报告了两种以苝为核的蓝光发射[4]螺芳烃(7 和 9)的合成、晶体结构和光物理性质。所有合成化合物的化学结构均通过 1H 和 13C NMR 光谱、质谱和元素分析得到充分证实。这些[4]螺芳烃的单晶 X 射线分析表明,存在两种类型的侧萘并环合的螺旋构象,这明显受到不同 R 取代基的影响。[4]螺芳烃(7 和 9)及其预环化产物 4,9-和 4,10-双(苯乙炔基)苝(6 和 8)在溶液和薄膜中的光物理性质得到了充分研究。这些化合物具有显著的光学特性,使它们成为现代电子和光电设备中几个重要应用的有前途的候选材料,例如有机发光器件(OLED)中的蓝色发射器,或作为进一步探索基于苝的新一代有机材料发展的模型。