首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Near IR luminescent rare earth 3,4,5,6-tetrafluoro-2-nitrophenoxide complexes: Synthesis, X-ray crystallography and spectroscopy
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Near IR luminescent rare earth 3,4,5,6-tetrafluoro-2-nitrophenoxide complexes: Synthesis, X-ray crystallography and spectroscopy

机译:近红外发光稀土3,4,5,6-四氟-2-硝基苯酚配合物:合成,X射线晶体学和光谱学

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摘要

3,4,5,6-Tetrafluoro-2-nitrophenoxide (L-) forms complexes with rare earth M3+ ions. X-ray crystal structures of substances with the stoichiometry Cs2ML5 - mEt(2)O (M = Er, m = 0; M = Er, m = 1; M = Y, m = 1.5; M = Yb, m = 1) have been determined. Each M3+ ion is coordinated to two bidentate and three monodentate L- ions; Et2O does not coordinate to M3+. The complexes absorb both visible and ultraviolet light. The solid Er3+ and Yb3+ complexes have unusually long lifetimes (tau = 20.2 mu s and 142 mu s, respectively) for the decay of their luminescence in the near-infrared region following photoexcitation; this is attributed to the lack of C-H bonds and other high frequency oscillators that could cause vibrational quenching. (C) 2008 Elsevier Ltd. All rights reserved.
机译:3,4,5,6-四氟-2-硝基苯氧基(L-)与稀土M3 +离子形成络合物。化学计量为Cs2ML5-mEt(2)O的物质的X射线晶体结构(M = Er,m = 0; M = Er,m = 1; M = Y,m = 1.5; M = Yb,m = 1)已经确定。每个M3 +离子与两个二齿和三个单齿L-离子配位; Et2O与M3 +不协调。络合物吸收可见光和紫外线。固态Er3 +和Yb3 +配合物在光激发后在近红外区域的发光衰减具有异常长的寿命(分别为tau = 20.2μs和142μs)。这归因于缺少C-H键和其他可能引起振动猝灭的高频振荡器。 (C)2008 Elsevier Ltd.保留所有权利。

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