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基于复杂镧系元素糖精盐的高发光离子液体。

Highly Luminescent Ionic Liquids Based on Complex Lanthanide Saccharinates.

作者信息

Tang Si-Fu, Mudring Anja-Verena

机构信息

College of Chemistry and Pharmaceutical Sciences , Qingdao Agricultural University , Changcheng Road 700, Chengyang District , Qingdao 266109 , China.

Department of Materials and Environmental Chemistry , Stockholm University , Svante Arrhenius väg 16 C , 106 91 Stockholm , Sweden.

出版信息

Inorg Chem. 2019 Sep 3;58(17):11569-11578. doi: 10.1021/acs.inorgchem.9b01411. Epub 2019 Aug 22.

Abstract

Four strongly luminescent ionic liquids with complex lanthanide saccharinate anions, [Cmim][Eu(Sac)(HO)] (), {Cmpy}{[Ln(Sac)(HO)][Ln(Sac)(HO)]}{(HO)(CHCN)} (Ln = Sm for ; Ln = Eu for ), and [Cmpy][Eu(Sac)][CHCN] () (Cmim = 1-butyl-3-methylimidazolium; Cmpy = -butyl-4-methylpyridinium; Sac = saccharinate), have been obtained by reacting the ionic liquids 1-butyl-3-methylimidazolium saccharinate, [Cmim][Sac], and -butyl-4-methylpyridinium saccharinate, [Cmpy][Sac], with the respective lanthanide saccharinates. Single-crystal X-ray diffraction analyses reveal the respective lanthanide center to be six- or eight-coordinated by five or six saccharinate anions and two or three aqua ligands in the cases of and when lanthanide saccharinated hydrate was employed as the starting material. Coordination of water to the lanthanide can be avoided when using the anhydrous lanthanide saccharinate as shown by the structure of . Using a co-solvent, acetonitrile, to facilitate the reaction led to incorporation of solvent molecules into the crystal structure of the final materials ( and ). Differential scanning calorimetry analyses reveal that is an ionic liquid whereas and are low-temperature molten salts. The three europium(III)-containing compounds (, , and ) all show characteristic intense red emissions of Eu(III) upon excitation into levels of the saccharinate ligands (321 nm) or Eu(III) (393 nm). At room temperature, the decay times of and are all ∼0.5 ms, whereas the decay time of amounts to 3.85 ms due to removal of aqua ligands in the first coordination sphere; accordingly, the quantum efficiencies of , , and were determined to be 15.9%, 22.95%, and 57.75%, respectively. The CIE chromaticity coordinates for all Eu compounds are in the red region and approach the NTSC standard CIE values when the temperature is increased. Sm(III)-containing compound shows characteristic Sm(III) emission peaks. As expected, the CIE coordinates of samarium compound fall in the orange-red region.

摘要

通过将离子液体1-丁基-3-甲基咪唑鎓糖精盐([Cmim][Sac])和4-丁基-4-甲基吡啶鎓糖精盐([Cmpy][Sac])与相应的镧系糖精盐反应,得到了四种具有强发光性且带有复杂镧系糖精酸根阴离子的离子液体,即[Cmim][Eu(Sac)(H₂O)₃]()、{Cmpy}{[Ln(Sac)(H₂O)₃][Ln(Sac)(H₂O)₃]}{(H₂O)(CH₃CN)}(Ln = Sm时为;Ln = Eu时为)和[Cmpy][Eu(Sac)₃][CH₃CN]()(Cmim = 1-丁基-3-甲基咪唑鎓;Cmpy = 4-丁基-4-甲基吡啶鎓;Sac = 糖精酸根)。单晶X射线衍射分析表明,当以镧系糖精水合物为起始原料时,在和的情况下,相应的镧系中心分别由五个或六个糖精酸根阴离子以及两个或三个水配体进行六配位或八配位。如的结构所示,当使用无水镧系糖精时,可以避免水与镧系的配位。使用共溶剂乙腈促进反应导致溶剂分子掺入最终材料的晶体结构中(和)。差示扫描量热法分析表明是离子液体,而和是低温熔盐。三种含铕(III)的化合物(、和)在激发到糖精酸根配体的能级(321 nm)或铕(III)(393 nm)时均显示出铕(III)特征性的强红色发射。在室温下,和的衰减时间均约为0.5 ms,而由于第一配位层中水配体的去除,的衰减时间为3.85 ms;因此,、和的量子效率分别测定为15.9%、22.95%和57.75%。所有铕化合物的CIE色度坐标均在红色区域,并且当温度升高时接近NTSC标准CIE值。含钐(III)的化合物显示出钐(III)特征发射峰。正如预期的那样,钐化合物的CIE坐标落在橙红色区域。

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