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Blue-emitting acridine-tagged silver(i)-bis-N-heterocyclic carbene

机译:发射蓝色a啶标记的银(i)-双-N-杂环卡宾

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Herein, the photophysical properties of an acridine derivative of a bis-N-heterocyclic carbene silver complex were investigated. The HOMO and LUMO energy differences between 9-[( N -methyl imidazol-2-ylidene)]acridine and 4,5-bis[( N -methyl-imidazol-2-ylidene)methyl]acridine were theoretically compared. Based on the calculation, the 4,5-bis N-heterocyclic carbene-tethered acridine type of ligand was found to be a potential source for tuning the fluorescent nature of the resultant metal derivatives. Thus, a 4,5-bis N-heterocyclic carbene (NHC)-tethered acridine silver( I ) salt was synthesized, and its photophysical properties were investigated. The 4,5-bis[( N -isopropylimidazol-2-ylidene)methyl]acridine silver( I ) hexafluorophosphate complex was obtained from the reaction between [4,5-bis{( N -isopropylimidazolium)methyl}acridine] hexafluorophosphate and Ag _(2) O in very good yield; this molecule was characterized by elemental analysis and FTIR, multinuclear ( ~(1) H and ~(13) C) NMR, UV-Vis, and fluorescence spectroscopic techniques. The molecular structure has been confirmed by single-crystal X-ray diffraction analysis, which has revealed that the complex is a homoleptic mononuclear silver( I ) cationic solid. The charge of the Ag( I )–NHC cation is balanced by the hexafluorophosphate anion. The cationic moieties are closely packed in the chair and inverted chair forms where silver( I ) possesses a quasi-linear geometry. Moreover, the silver complex provided blue emission from all the three excitations with good fluorescence quantum yield. The fluorescence lifetime of the silver( I ) complex has been determined using the time-correlated single photon counting technique. Interestingly, the fluorescence decay pattern and the fluorescence lifetimes of the silver complex are largely different from those of the parent ligand acridine imidazolium salt. Moreover, the theoretical predictions have been found to be in good agreement with the experimental results.
机译:在此,研究了双-N-杂环卡宾银配合物的a啶衍生物的光物理性质。从理论上比较了9-[(N-甲基咪唑-2-亚甲基)]啶和4,5-双[(N-甲基咪唑-2-亚甲基)甲基] methyl啶的HOMO和LUMO能量差。基于该计算,发现4,5-双N-杂环卡宾连接的a啶类型的配体是调节所得金属衍生物的荧光性质的潜在来源。因此,合成了4,5-双N-杂环卡宾(NHC)系链的a啶银(I)盐,并对其光物理性质进行了研究。从[4,5-双{(N-异丙基咪唑鎓)甲基} ac啶]六氟磷酸酯与Ag的反应中获得4,5-双[(N-异丙基咪唑-2-亚甲基)甲基] ac啶银(I)六氟磷酸盐配合物_(2)O的收率很高;该分子的特征在于元素分析和FTIR,多核(〜(1)H和〜(13)C)NMR,UV-Vis和荧光光谱技术。通过单晶X射线衍射分析已经证实了分子结构,这揭示了该络合物是均均的单核银(I)阳离子固体。 Ag(I)–NHC阳离子的电荷由六氟磷酸根阴离子平衡。阳离子部分紧密地堆积在椅子和倒椅子形式中,其中银(I)具有准线性几何形状。此外,银配合物提供了来自所有三个激发的蓝色发射,并具有良好的荧光量子产率。已经使用时间相关的单光子计数技术确定了银(I)配合物的荧光寿命。有趣的是,银配合物的荧光衰减模式和荧光寿命与母体配体a啶咪唑鎓盐的荧光衰减模式和荧光寿命有很大不同。此外,已经发现理论预测与实验结果非常吻合。

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