Yang Bo, Yan Suqiong, Ban Shirong, Ma Hui, Zhang Yuan, Feng Fanda, Huang Wei
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University Nanjing 210023 P. R. China
Shenzhen Research Institute of Nanjing University Shenzhen 518057 P. R. China.
Chem Sci. 2025 Apr 21. doi: 10.1039/d4sc08710k.
Overcoming spin-forbidden radiation in chiral phosphors has attracted enormous attention because of their capacity to exhibit circularly polarized organic ultra-long room temperature phosphorescence (CP-OURTP). However, their development has been hindered by the short lifetimes and low dissymmetry factors, which are attributed to the differing parity selection rules that govern the electric and magnetic dipole moments in chiral molecules and poor triplet populations intersystem crossing (ISC). Considering stepwise chiral amplification at molecular and supramolecular aspects, herein, we first reported donor-decorated BINAPs/BINAPOs with tunable D-A character and triplet incubation, which could enable hybridized local and charge-transfer (HLCT) characteristics, heavy atoms, and p-π* effects. These emitters could serve as guests in the polymer matrix. The doped phosphorescent polymer exhibits unimolecular circularly polarized luminescence (C) with high quantum efficiency, impressive CP-OURTP lifetimes (up to 1.02 s), and decent dissymmetry factors (10 level). Comprehensive studies unveil that the impressive CP-OURTP from monomer emission is ascribed to the HLCT-controlled ISC, long-lived LE-governing triplet radiation, and superior electric-magnetic dipole moment environments. Moreover, given the high RTP activity of rigid polymerization, we demonstrate their potential application in CP-OURTP amplification. Using chiral liquid crystal polymerization, RM257 liquid crystals doped with 0.1-1.0 wt% PO1 guests demonstrate a secondary helical assembly, showing an amplified factor (±0.11) and a long lifetime (0.83 s) after photopolymerization. The current materials' excellent performance in CP-OURTP and structural dependence could lead to their use in afterglow patterns for multiple optical encryption.
由于具有展现圆偏振有机超长室温磷光(CP-OURTP)的能力,克服手性磷光体中的自旋禁阻辐射已引起了极大关注。然而,它们的发展受到了短寿命和低不对称因子的阻碍,这归因于手性分子中控制电偶极矩和磁偶极矩的宇称选择规则不同以及三重态布居数的系间窜越(ISC)较差。考虑到分子和超分子层面的逐步手性放大,在此,我们首次报道了具有可调D-A特性和三重态孕育的供体修饰的联萘二膦/联萘二膦氧化物,其能够实现杂化局域和电荷转移(HLCT)特性、重原子以及p-π*效应。这些发光体可作为聚合物基质中的客体。掺杂的磷光聚合物表现出具有高量子效率、令人印象深刻的CP-OURTP寿命(长达1.02秒)和良好不对称因子(10-6水平)的单分子圆偏振发光(C)。综合研究表明,单体发射产生的令人印象深刻的CP-OURTP归因于HLCT控制的ISC、长寿命的LE主导的三重态辐射以及优异的电-磁偶极矩环境。此外,鉴于刚性聚合的高RTP活性,我们展示了它们在CP-OURTP放大中的潜在应用。使用手性液晶聚合,掺杂0.1-1.0 wt% PO1客体的RM257液晶表现出二次螺旋组装,在光聚合后显示出放大因子(±0.11)和长寿命(0.83秒)。当前材料在CP-OURTP方面的优异性能及其结构依赖性可能使其用于多种光学加密的余辉图案。