Yuhara Kazuhiro, Tanaka Kazuo
Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto, 615-8510, Japan.
Angew Chem Int Ed Engl. 2024 Apr 8;63(15):e202319712. doi: 10.1002/anie.202319712. Epub 2024 Feb 27.
Herein, we report the unique multiple-stimuli responsiveness of anthracene-tethered o-carborane derivatives. We designed and synthesized anthracene derivatives with different substitution positions and numbers of the o-carborane units. Two compounds had characteristic crystal structures involving the columnar π-stacking structures of the anthracene units. From the analysis of crystalline-state structure-property relationships, it was revealed that the crystals exhibited the photosalient effect accompanied by photochemical [4+4] cycloaddition reactions and temperature-dependent photophysical dual-emission properties including excimer emission of anthracene. Those properties were considered as non-radiative and radiative deactivation pathways through the excimer formation in the excited state and the formation of excimer species was facilitated by the π-stacking structure of anthracene units. Moreover, we found unusual temperature dependency on the occurrence of the photosalient effect. According to the data from variable temperature X-ray crystallography, a strong correlation between lattice shrinkage and strain accumulation is suggested.
在此,我们报道了蒽连接的邻碳硼烷衍生物独特的多重刺激响应性。我们设计并合成了具有不同邻碳硼烷单元取代位置和数量的蒽衍生物。两种化合物具有涉及蒽单元柱状π堆积结构的特征晶体结构。通过对晶态结构-性质关系的分析表明,这些晶体表现出光致突出效应,伴随着光化学[4+4]环加成反应以及包括蒽的激基缔合物发射在内的温度依赖性光物理双发射性质。这些性质被认为是通过激发态激基缔合物形成的非辐射和辐射失活途径,并且蒽单元的π堆积结构促进了激基缔合物物种的形成。此外,我们发现光致突出效应的发生存在不寻常的温度依赖性。根据可变温度X射线晶体学的数据,表明晶格收缩与应变积累之间存在很强的相关性。