Anorganische Chemie I-Festkörperchemie und Materialien, Ruhr-Universität Bochum, 44780 Bochum, Germany.
Chemistry. 2010 Mar 15;16(11):3355-65. doi: 10.1002/chem.200802660.
Several ionic liquids (ILs) based on complex manganate(II) anions with chloro, bromo, and bis(trifluoromethanesulfonyl)amido (Tf(2)N) ligands have been synthesized. As counterions, n-alkyl-methylimidazolium (C(n)mim) cations of different chain length (alkyl=ethyl (C(2)), propyl (C(3)), butyl (C(4)), hexyl (C(6))) were chosen. Except for the 1-hexyl-3-methylimidazolium ILs, all of the prepared compounds could be obtained in a crystalline state at room temperature. However, each of the compounds displayed a strong tendency to form a supercooled liquid. Generally, solidification via a glass transition took place below -40 degrees C. Consequently, all of these compounds can be regarded as ionic liquids. Depending on the local coordination environment of Mn(2+), green (tetrahedrally coordinated Mn(2+)) or red (octahedrally coordinated Mn(2+)) luminescence emission from the (4)T(G) level is observed. The local coordination of the luminescent Mn(2+) centre has been unequivocally established by UV/Vis as well as Raman and IR vibrational spectroscopies. Emission decay times measured at room temperature in the solid state (crystalline or powder) were generally a few ms, although, depending on the ligand, values of up to 25 ms were obtained. For the bromo compounds, the luminescence decay times proved to be almost independent of the physical state and the temperature. However, for the chloro- and bis(trifluoromethanesulfonyl)amido ILs, the emission decay times were found to be dependent on the temperature even in the solid state, indicating that the measured values are strongly influenced by nuclear motion and the vibration of the atoms. In the liquid state, the luminescence of tetrahedrally coordinated Mn(2+) could only be observed when the tetrachloromanganate ILs were diluted with the respective halide ILs. However, for [C(3)mim][Mn(Tf(2)N)(3)], in which Mn(2+) is in an octahedral coordination environment, a weak red emission from the pure compound was found even in the liquid state at elevated temperatures.
已经合成了几种基于复杂锰酸盐(II)阴离子的离子液体 (ILs),这些阴离子带有氯、溴和双 (三氟甲烷磺酰基) 酰胺 (Tf(2)N) 配体。作为抗衡离子,选择了不同链长的 n-烷基-甲基咪唑鎓 (C(n)mim) 阳离子 (烷基=乙基 (C(2))、丙基 (C(3))、丁基 (C(4))、己基 (C(6)))。除了 1-己基-3-甲基咪唑鎓 ILs 之外,所有制备的化合物都可以在室温下以结晶状态获得。然而,每个化合物都表现出强烈的形成过冷液体的趋势。通常,通过玻璃化转变在-40 度以下发生固化。因此,所有这些化合物都可以被视为离子液体。根据 Mn(2+)的局部配位环境,观察到来自 (4)T(G) 能级的绿色 (四面体配位 Mn(2+)) 或红色 (八面体配位 Mn(2+)) 发光发射。通过紫外/可见以及拉曼和红外振动光谱,明确确定了发光 Mn(2+)中心的局部配位。在室温下在固态(结晶或粉末)中测量的发射衰减时间通常为数毫秒,尽管取决于配体,也可以获得高达 25 毫秒的值。对于溴化物化合物,发光衰减时间几乎与物理状态和温度无关。然而,对于氯和双 (三氟甲烷磺酰基) 酰胺 ILs,即使在固态下,发射衰减时间也发现与温度有关,表明测量值受核运动和原子振动的强烈影响。在液态下,只有当四氯锰酸盐 ILs 与相应的卤化物 ILs 稀释时,才能观察到四面体配位的 Mn(2+)的发光。然而,对于 [C(3)mim][Mn(Tf(2)N)(3)],其中 Mn(2+)处于八面体配位环境中,即使在高温下的液态中,也发现纯化合物存在微弱的红色发射。