发光
对映体药物
化学
镧系元素
激发态
超分子化学
配体(生物化学)
金属
结晶学
离子
光电子学
材料科学
原子物理学
晶体结构
物理
催化作用
对映选择合成
受体
有机化学
生物化学
作者
Qiang‐Yu Zhu,Li‐Peng Zhou,Li‐Xuan Cai,Shao‐Jun Hu,Xiaozhen Li,Qing‐Fu Sun
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-10-07
卷期号:61 (42): 16814-16821
被引量:11
标识
DOI:10.1021/acs.inorgchem.2c02718
摘要
Structurally well-defined discrete d/f heterometallic complexes show diverse application potential in electrooptic and magnetic materials. However, precise control of the component and topology of such heterometallic compounds with fine-tuned photophysical properties is still challenging. Herein, we report the stereocontrolled syntheses of a series of LnIII-PtII heterometallic cages through coordination-driven self-assembly of enantiopure alkynylplatinum-based metalloligands (L1R/S, L2R/S) with lanthanide ions (Ln = EuIII, YbIII, NdIII, LuIII). Taking advantage of the metal-to-ligand charge transfer (MLCT) excited state on the designed alkynylplatinum ligands, the excitation window for the sensitized near-infrared (NIR) luminescence on the YbIII- and NdIII-containing cages can be extended to the visible region (up to 500 nm). Linear temperature-dependent red and NIR emissions observed on the Ln4(L2R/S)6 (LnIII = EuIII and YbIII, respectively) complexes suggest their potential applications as luminescent temperature sensors, with sensitivities of -0.54% (LnIII = EuIII, 77-250 K) and -0.17% (LnIII = YbIII, 77-300 K) per K achieved. This work not only offers a good strategy to prepare new d/f heterometallic supramolecular cages but also paves the way for the design of stimuli-responsive luminescent materials.
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