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全氟烷基链长对镧系元素-锂 β-二酮配合物晶体堆积和[LnO]配位几何结构的影响:发光和单离子磁体行为。

Perfluoroalkyl Chain Length Effect on Crystal Packing and [LnO] Coordination Geometry in Lanthanide-Lithium β-Diketonates: Luminescence and Single-Ion Magnet Behavior.

机构信息

International Tomography Center, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russia.

Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 620137 Yekaterinburg, Russia.

出版信息

Int J Mol Sci. 2023 Jun 5;24(11):9778. doi: 10.3390/ijms24119778.

Abstract

Functionalized perfluoroalkyl lithium β-diketonates (LiL) react with lanthanide(III) salts (Ln = Eu, Gd, Tb, Dy) in methanol to give heterobimetallic Ln-Li complexes of general formula [(LnL)(LiL)(MeOH)]. The length of fluoroalkyl substituent in ligand was found to affect the crystal packing of complexes. Photoluminescent and magnetic properties of heterobimetallic β-diketonates in the solid state are reported. The effect of the geometry of the [LnO] coordination environment of heterometallic β-diketonates on the luminescent properties (quantum yields, phosphorescence lifetimes for Eu, Tb, Dy complexes) and single-ion magnet behavior ( for Dy complexes) is revealed.

摘要

功能化全氟烷基锂β-二酮(LiL)与甲醇中的镧系(III)盐(Ln = Eu、Gd、Tb、Dy)反应,生成通式为[(LnL)(LiL)(MeOH)]的异双金属Ln-Li 配合物。配体中氟烷基取代基的长度被发现会影响配合物的晶体堆积。报道了异双金属β-二酮在固态下的光致发光和磁性性质。揭示了异金属β-二酮的[LnO]配位环境的几何形状对发光性质(量子产率、Eu、Tb、Dy 配合物的磷光寿命)和单离子磁行为(Dy 配合物)的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e0c/10253746/13d669943cfd/ijms-24-09778-g001.jpg

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