Maeda Chihiro, Nomoto Shuichi, Takaishi Kazuto, Ema Tadashi
Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University, Tsushima, Okayama, 700-8530, Japan.
Chemistry. 2020 Oct 9;26(57):13016-13021. doi: 10.1002/chem.202001463. Epub 2020 Sep 16.
A variety of carbazolyl-appended Schiff bases were readily synthesized from 1-formylcarbazoles and aniline derivatives. Boron complexation of the resulting ligands allowed for facile preparation of new carbazole-based BODIPY analogues showing solid-state fluorescence. Furthermore, some dyes were converted into chiral compounds through the Et AlCl-mediated incorporation of a binaphthyl unit. The chiral dyes showed aggregation-induced fluorescence and circularly polarized luminescence (CPL) with the Φ and g of up to 0.22 and -3.5×10 , respectively, in the solid state. The solid-state fluorescence and CPL were well characterized by the crystal packing analyses and DFT calculations.
通过1-甲酰基咔唑和苯胺衍生物可轻松合成多种咔唑基席夫碱。所得配体与硼络合后,可方便地制备出具有固态荧光的新型咔唑基BODIPY类似物。此外,通过EtAlCl介导引入联萘单元,一些染料被转化为手性化合物。这些手性染料在固态下表现出聚集诱导荧光和圆偏振发光(CPL),其Φ和g值分别高达0.22和-3.5×10 。通过晶体堆积分析和密度泛函理论(DFT)计算对固态荧光和CPL进行了很好的表征。