Poncet Maxime, Cuevas-Contreras Laura, Ye Yating, Guénée Laure, Cruz Carlos M, Piguet Claude, Jiménez Juan-Ramón
Department of Inorganic and Analytical Chemistry, University of Geneva, Quai E. Ansermet 30, CH-1211 Geneva 4, Switzerland.
Departamento de Química Inorgánica, Facultad de Ciencias, Unidad de Excelencia de Química Aplicada a Biomedicina y Medioambiente, Avda. Fuente Nueva s/n, 18071 Granada, Spain.
J Am Chem Soc. 2025 Jul 9;147(27):23827-23833. doi: 10.1021/jacs.5c06196. Epub 2025 Jun 28.
A novel chiral chromium(III) molecular ruby [Cr(qpp)] (qpp = -methyl--(pyridin-2-yl)-6-(quinolin-8-yl)pyridin-2-amine) has been synthesized, enantiomerically resolved, and fully characterized. The circularly polarized luminescence (CPL) spectra revealed two emission bands of opposite polarization in the near-infrared region (700-800 nm), corresponding to the metal-centered transitions Cr(T(1) → A) and Cr(E(1) → A). Notably, the dissymmetry factor reached 0.11 for the former transition, which is among the highest reported for chromium(III) systems. Comparison with structurally related homo- and heteroleptic chromium(III) complexes underscores the important role of the nephelauxetic effect in tuning CPL properties. Increased metal-ligand covalency, indicative of a stronger nephelauxetic effect, enhances orbital mixing and modifies the electronic character of the emissive states. These changes influence both electric and magnetic transition dipole moments, leading to noticeable variations in dissymmetry factor . Altogether, these observations highlight the potential of fine-tuning metal-ligand covalency as a rational strategy for optimizing the chiroptical properties of chromium(III) complexes, with promising implications for bioimaging, molecular probes, and circularly polarized optoelectronic devices.
一种新型手性铬(III)分子红宝石[Cr(qpp)](qpp = -甲基--(吡啶-2-基)-6-(喹啉-8-基)吡啶-2-胺)已被合成、对映体拆分并完全表征。圆偏振发光(CPL)光谱显示在近红外区域(700 - 800 nm)有两个偏振相反的发射带,分别对应于以金属为中心的跃迁Cr(T(1) → A)和Cr(E(1) → A)。值得注意的是,前一个跃迁的不对称因子达到了0.11,这是铬(III)体系中报道的最高值之一。与结构相关的同配和异配铬(III)配合物的比较强调了电子云扩张效应在调节CPL性质中的重要作用。金属 - 配体共价性的增加,表明更强的电子云扩张效应,增强了轨道混合并改变了发射态的电子特性。这些变化影响了电和磁跃迁偶极矩,导致不对称因子出现显著变化。总之,这些观察结果突出了微调金属 - 配体共价性作为优化铬(III)配合物手性光学性质的合理策略的潜力,对生物成像、分子探针和圆偏振光电器件具有潜在的应用前景。