Lanthanide-Dependent Photochemical and Photophysical Properties of Lanthanide–Anthracene Complexes: Experimental and Theoretical Approaches

作者：Liangliang Wu, Xin‐Da Huang, Weijia Li, Xiaoyan Cao, Wei‐Hai Fang, Li‐Min Zheng, Michael Dolg, Xuebo Chen · 发表于：JACS Au · 年份：2024 · DOI：10.1021/jacsau.4c00540 · 被引用次数：17 · 研究领域：Lanthanide and Transition Metal Complexes、Magnetism in coordination complexes、Organometallic Complex Synthesis and Catalysis

High Resolution Image Download MS PowerPoint Slide The structural, photophysical, and photochemical properties of Ln(depma)(hmpa) 2 (NO 3 ) 3 (Ln = La, Ce, Nd, Sm, Eu, Tb, Ho, Er, and Yb) complexes 1-Ln were investigated with a multidisciplinary approach involving synthesis, photocycloaddition-based crystal engineering, spectroscopic analytical techniques and quantum chemical ab initio calculations. Depending on the Ln 3+ ion the isostructural 1-Ln complexes exhibit quite different behavior upon excitation at 350–400 nm. Some 1-Ln complexes (Ln = La, Ce, Sm, Tb, Yb) emit a broad and strong band near 533 nm arising from paired anthracene moieties, whereas others (Ln = Nd, Eu, Ho, Er) do not. 1-Eu is not emissive at all, whereas 1-Nd, 1-Ho, and 1-Er exhibit a Ln 3+ based luminescence. Upon irradiation with 365 nm ultraviolet (UV) light 1-Ln (Ln = La, Ce, Sm, Tb, Yb) dimerize by means of a photochemically induced [4 + 4] cycloaddition of the anthracene moieties, whereas 1-Ln (Ln = Nd, Eu, Ho, Er) remain monomers. We propose three models, based on the matching of the energy levels between the Ln 3+ ion and the paired or dimerized anthracene units in the energy-resonance crossing region, as well as on internal conversion-driven and intersystem crossing-driven energy transfer, which explain the Ln 3+ ion regulated photophysics and photochemistry of the 1-Ln complexes.