Dutta Camelia, Mandal Anannya, Shukla Abhishek, Hemaprabha Elangovan, Nakashima Takuya, Kumar Jatish
Department of Chemistry, Indian Institute of Science Education and Research (IISER) Tirupati, Tirupati, Andhra Pradesh, 517619, India.
Department of Metallurgical and Materials Engineering, Indian Institute of Technology (IIT) Madras, Chennai, Tamil Nadu, 600 036, India.
Angew Chem Int Ed Engl. 2025 Sep 8;64(37):e202511554. doi: 10.1002/anie.202511554. Epub 2025 Jul 24.
Chiral metal clusters have garnered significant research interest in recent years due to their unique photophysical and chiroptical properties. Increased attention is directed toward bimetallic systems, as the synergistic effect of two different metal centers often yields enhanced properties. Despite this progress, obtaining optically active bimetallic clusters with pronounced chirality, both in their ground and excited states, has remained a challenge. Herein, an efficient strategy is formulated for the controlled aggregation of gold(I)-silver(I) coordination clusters leading to enhanced and tunable optical activity. Interactions with chiral and achiral additives resulted in cluster-assembled materials (CAMs) exhibiting morphology-dependent chiroptical responses. The assembly process, in addition to facilitating aggregation-induced enhanced emission (AIEE), generated inverted and amplified chiroptical responses. Interestingly, the resultant Au(I)Ag(I) composite materials exhibited prolonged excited state lifetimes, indicating the possibility of near room temperature thermally activated delayed fluorescence (TADF) and lower temperature phosphorescence. Circularly polarized luminescence with a dissymmetry factor as high as (±)0.05 could be achieved, the highest reported for any metal cluster to date. The enhanced anisotropy highlights the effectiveness of this strategy in modulating excited-state chirality through hierarchical assembly, opening potential for the nanocomposites as chiral light-emitting materials.
近年来,手性金属簇因其独特的光物理和手性光学性质而引起了广泛的研究兴趣。人们越来越关注双金属体系,因为两种不同金属中心的协同效应通常会产生增强的性质。尽管取得了这一进展,但获得在基态和激发态都具有明显手性的光学活性双金属簇仍然是一个挑战。在此,我们制定了一种有效的策略,用于控制金(I)-银(I)配位簇的聚集,从而增强和调节光学活性。与手性和非手性添加剂的相互作用导致簇组装材料(CAMs)表现出形态依赖性的手性光学响应。组装过程除了促进聚集诱导增强发射(AIEE)外,还产生了反转和放大的手性光学响应。有趣的是,所得的Au(I)Ag(I)复合材料表现出延长的激发态寿命,表明在接近室温下存在热激活延迟荧光(TADF)和低温磷光的可能性。可以实现不对称因子高达(±)0.05的圆偏振发光,这是迄今为止报道的任何金属簇中最高的。增强的各向异性突出了该策略通过分级组装调节激发态手性的有效性,为纳米复合材料作为手性发光材料开辟了潜力。