乙腈溶液中 Eu(FOD)3 与二氟化氙相互作用过程中 Eu(III) 的配体辅助激发

IF 1.7 4区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR Journal of Fluorine Chemistry Pub Date : 2024-03-05 DOI:10.1016/j.jfluchem.2024.110270
Gulshat A. Masyagutova, Alexander V. Mamykin, Sergey L. Khursan
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引用次数: 0

摘要

研究发现,三(1,1,1,2,2,3,3-七氟-7,7-二甲基-4,6-辛二酮酸)铕(III)(Eu(FOD)3)与二氟化氙在乙腈溶液中的相互作用伴随着化学发光(CL)。在试剂 Eu3+/XeF2 的比例为 1:2 时,化学发光的动力学曲线具有复杂的形式;化学发光强度由最初的快速下降转为上升,在反应开始后约 10 分钟达到最大值。接下来,CL 强度在几十分钟内呈指数衰减。CL 光谱的波长范围为 400-750 纳米,对应于与 FOD 和氟离子配位的电子激发铕(III)离子的发射。利用光谱方法确定了反应产物--沉积物中的氟化铕(III)和气相中的二氟化氧。提出了铕(III)的化学激发机制,包括1) 铕离子接受 XeF2 分子中的氟阴离子,形成活性中间体 XeF+;2) FOD 配体的氧原子与 XeF+ 阳离子相互作用,引发配体氧化氟化,最后形成二氟化氧和电子激发产物 P*,推测为氟化酮;3)激发能量从 P* 向其配位圈内的铕离子的非辐射转移,然后铕离子辐射失活。
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Ligand-assisted excitation of Eu(III) during interaction of Eu(FOD)3 with xenon difluoride in acetonitrile solution

The interaction of tris(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)europium(III), (Eu(FOD)3), with xenon difluoride in acetonitrile solution was found to be accompanied by chemiluminescence (CL). The kinetic curve of CL at a ratio of reagents Eu3+/XeF2 of 1:2 has a complex form; an initial rapid decrease is replaced by an increase in CL intensity, the maximum of which is reached approximately 10 min after the start of the reaction. Next, an exponential decay of the CL intensity is observed over several tens of minutes. The CL spectrum is located in the wavelength range 400–750 nm and corresponds to the emission of an electronically excited europium (III) ion coordinated with FOD and fluoride ion. Spectral methods were used to identify the reaction products – europium (III) fluoride in the sediment and oxygen difluoride in the gas phase. A mechanism for chemiexcitation of europium(III) has been proposed, including: 1) acceptance of fluorine anion from the XeF2 molecule by europium ion with the formation of active intermediate XeF+; 2) oxidative fluorination of the ligand, which is initiated by the interaction of oxygen atom of the FOD ligand with XeF+ cation and ends with the formation of oxygen difluoride and the electronically excited product P*, presumably a fluorinated ketone; 3) non-radiative transfer of excitation energy from P* to the europium ion within its coordination sphere, followed by its radiative deactivation.

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来源期刊
Journal of Fluorine Chemistry
Journal of Fluorine Chemistry 化学-无机化学与核化学
CiteScore
3.80
自引率
10.50%
发文量
99
审稿时长
33 days
期刊介绍: The Journal of Fluorine Chemistry contains reviews, original papers and short communications. The journal covers all aspects of pure and applied research on the chemistry as well as on the applications of fluorine, and of compounds or materials where fluorine exercises significant effects. This can include all chemistry research areas (inorganic, organic, organometallic, macromolecular and physical chemistry) but also includes papers on biological/biochemical related aspects of Fluorine chemistry as well as medicinal, agrochemical and pharmacological research. The Journal of Fluorine Chemistry also publishes environmental and industrial papers dealing with aspects of Fluorine chemistry on energy and material sciences. Preparative and physico-chemical investigations as well as theoretical, structural and mechanistic aspects are covered. The Journal, however, does not accept work of purely routine nature. For reviews and special issues on particular topics of fluorine chemistry or from selected symposia, please contact the Regional Editors for further details.
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