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Synthesis and characterization of amphiphilic triazole ligand and its complex for potential application in phosphorescent temperature sensor materials

机译:两亲性三唑配体及其配合物的合成与表征,可在磷光温度传感器材料中应用

摘要

Phosphorescent materials have attracted much attention due to their promising applications in sensors, display, and optical imaging. Extensive studies have reported on trinuclear gold (I) complexes such as imidazolate, pyrazolate and carbeniete ; however, triazolate is rarely reported. Although hydrophobic trinuclear gold (I) triazolate complex has been reported in a solid state with luminescence center at near infrared area (750 nm) at room temperature, but no example of phosphorescent amphiphilic trinuclear gold (I) triazolate complex with liquid crystalline properties has been reported for potential application in near infrared phosphorescent temperature sensor materials. Here we report the synthesis of triazole ligand bearing amphiphilic side chain and then use it for complexation with gold salt to form amphiphilic trinuclear gold (I) triazolate complex. Triazole ligand was prepared in six stepwise reactions from triethylene glycol (EG3) to tosilate ethylene glycol (TsEG3,step 1; 180g, 90%), mono substitution triethylene glycol with decanediol (C10EG3OH, step 2; 17g, 43%), bromination (C10EG3Br, step 3; 9g, 45%), Williamson ether substitution reaction (C10EG3BnCOOMe,step 4; 3.5g, 67%), carboxylation (C10EG3COOH,step 5; 2g, 80%) and amidation (C10EG3TzH,step 6; 240mg, 23%). The resulting triazole ligand will be reacted with dimethylsulfide gold (I) chloride ([Au(SMe2]Cl) in methanol in the presence of excess freshly distilled triethylamine (Et3N) to form the gold complex. The phosphorescent properties will be discussed later.
机译:磷光材料因其在传感器,显示器和光学成像中的应用前景而备受关注。关于三核金(I)配合物(如咪唑盐,吡唑酸盐和羧甲酸盐)的广泛研究已有报道。但是,很少报道三唑盐。尽管已经报道了在室温下疏水三核金(I)三唑醇盐配合物处于固态,发光中心位于近红外区(750 nm),但是尚没有具有液晶性质的磷光两亲三核金(I)三唑醇配合物的例子。报告了在近红外磷光温度传感器材料中的潜在应用。在这里,我们报道了带有两亲性侧链的三唑配体的合成,然后将其用于与金盐络合形成两亲性三核金(I)三唑盐配合物。三唑配体是通过三步反应制备的,从三甘醇(EG3)到甲苯磺酸乙二醇酯(TsEG3,步骤1; 180g,90%),用癸二醇的单取代三乙二醇(C10EG3OH,步骤2; 17g,43%),溴化( C10EG3Br,步骤3; 9g,45%),Williamson醚取代反应(C10EG3BnCOOMe,步骤4; 3.5g,67%),羧化反应(C10EG3COOH,步骤5; 2g,80%)和酰胺化(C10EG3TzH,步骤6; 240mg, 23%)。在过量的新鲜蒸馏的三乙胺(Et3N)存在下,将生成的三唑配体与二甲基硫醚氯化金(I)氯化物([Au(SMe2] Cl))在甲醇中反应形成金配合物,磷光性能将在后面讨论。

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