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Stereocontrolled Self-Assembly of Ln(III)–Pt(II) Heterometallic Cages with Temperature-Dependent Luminescence

Qiang‐Yu Zhu, Li‐Peng Zhou, Li‐Xuan Cai, Shao‐Jun Hu, Xiaozhen Li, Qing‐Fu Sun

2022Inorganic Chemistry20 citationsDOI

Abstract

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.

Topics & Concepts

LuminescenceLanthanideChemistryEnantiopure drugExcited stateSupramolecular chemistryLigand (biochemistry)MetalCrystallographyIonOptoelectronicsMaterials scienceAtomic physicsCrystal structureCatalysisPhysicsEnantioselective synthesisOrganic chemistryBiochemistryReceptorSupramolecular Chemistry and ComplexesMagnetism in coordination complexesLanthanide and Transition Metal Complexes
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