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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Multi-channel receptors based on thiopyrylium functionalised with macrocyclic receptors for the recognition of transition metal cations and anions
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Multi-channel receptors based on thiopyrylium functionalised with macrocyclic receptors for the recognition of transition metal cations and anions

机译:基于大环受体官能化的基于硫代吡啶鎓的多通道受体,用于识别过渡金属阳离子和阴离子

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摘要

We report herein the synthesis and characterization of a family of ligands containing different cation binding sites covalently connected to a thiopyrylium signalling reporter. The receptors L-1-L-6 are able to signal the presence of certain metal cations via three different channels; i.e. electrochemically, fluorogenically and chromogenically. An acetonitrile solution of L-1-L-6 shows a bright blue colour due to a charge-transfer band in the 575-585 nm region. The colour variation in acetonitrile of L-1-L-6 in the presence of the metal cations Ag+, Cd2+, Cu2+, Fe3+, Hg2+, Ni2+, Pb2+ and Zn2+ has been studied. A selective hypsochromic shift of the blue band was found for the systems L-4-Pb2+ and L-5-Hg2+. Additionally, L-1-L-6 are poorly fluorescent but coordination with certain metal cations induces an enhancement of the fluorescence at ca 500 nm. For instance, the presence of Cu2+ and Fe3+ induced a remarkable 42-fold and 45-fold enhancement in the emission intensity of L-1 centred at 500 nm, respectively. Also remarkable was the 18-fold enhancement observed for L-4 and L-5 in the presence of Fe3+ and Cu2+, respectively. The electrochemical behaviour of receptors L-1-L-6 was studied in acetonitrile using platinum as a working electrode and [Bu4N][BF4] as a supporting electrolyte. This family of receptors showed a one-electron reversible redox process at ca.-0.46 V versus sce attributed to the reduction of the thiopyrylium group. A moderate anodic shift in the presence of certain metal cations was observed. The effect in the UV-visible spectra of acetonitrile solutions of receptor L-1-L-6 in the presence of anions was also studied. A remarkable bleaching was found in the presence of cyanide.
机译:我们在这里报告了一个合成和表征的配体家族,该配体包含共价连接到硫代吡啶鎓信号传导报告分子的不同阳离子结合位点。受体L-1-L-6能够通过三个不同的通道发出某些金属阳离子的信号。即电化学地,荧光地和发色地。 L-1-L-6的乙腈溶液由于在575-585 nm范围内的电荷转移带而显示出亮蓝色。研究了在金属阳离子Ag +,Cd2 +,Cu2 +,Fe3 +,Hg2 +,Ni2 +,Pb2 +和Zn2 +存在下L-1-L-6乙腈的颜色变化。对于系统L-4-Pb2 +和L-5-Hg2 +,发现了蓝带的选择性七色移。此外,L-1-L-6的荧光较差,但与某些金属阳离子的配位会导致约500 nm处荧光增强。例如,Cu2 +和Fe3 +的存在分别导致以500 nm为中心的L-1的发射强度显着提高42倍和45倍。同样显着的是在Fe3 +和Cu2 +的存在下,L-4和L-5分别观察到18倍的增强。以铂为工作电极,以[Bu4N] [BF4]为支持电解质,在乙腈中研究了受体L-1-L-6的电化学行为。该受体家族在约-0.46 V下显示出单电子可逆氧化还原过程,而相对于sce,归因于硫代吡啶基团的还原。在某些金属阳离子的存在下观察到中等的阳极位移。还研究了在阴离子存在下,受体L-1-L-6的乙腈溶液在紫外可见光谱中的作用。在氰化物的存在下发现了显着的漂白。

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