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一种用于锌(II)的荧光化学传感器。溶液和固态中的激基复合物形成。

A fluorescent chemosensor for Zn(II). Exciplex formation in solution and the solid state.

作者信息

Bencini Andrea, Berni Emanuela, Bianchi Antonio, Fornasari Patrizia, Giorgi Claudia, Lima Joao C, Lodeiro Carlos, Melo Maria J, de Melo J Seixas, Parola Antonio Jorge, Pina Fernando, Pina Joao, Valtancoli Barbara

机构信息

Department of Chemistry, University of Florence, via della Lastruccia 3, 50019 Sesto Fiorentino, Florence, Italy.

出版信息

Dalton Trans. 2004 Jul 21(14):2180-7. doi: 10.1039/B403743J. Epub 2004 Jun 8.

Abstract

The macrocyclic phenanthrolinophane 2,9-[2,5,8-triaza-5-(N-anthracene-9-methylamino)ethyl]-[9]-1,10-phenanthrolinophane (L) bearing a pendant arm containing a coordinating amine and an anthracene group forms stable complexes with Zn(II), Cd(II) and Hg(II) in solution. Stability constants of these complexes were determined in 0.10 mol dm(-3) NMe(4)Cl H(2)O-MeCN (1:1, v/v) solution at 298.1 +/- 0.1 K by means of potentiometric (pH metric) titration. The fluorescence emission properties of these complexes were studied in this solvent. For the Zn(II) complex, steady-state and time-resolved fluorescence studies were performed in ethanol solution and in the solid state. In solution, intramolecular pi-stacking interaction between phenanthroline and anthracene in the ground state and exciplex emission in the excited state were observed. From the temperature dependence of the photostationary ratio (I(Exc)/I(M)), the activation energy for the exciplex formation (E(a)) and the binding energy of the exciplex (-DeltaH) were determined. The crystal structure of the ZnLBr.H(2)O compound was resolved, showing that in the solid state both intra- and inter-molecular pi-stacking interactions are present. Such interactions were also evidenced by UV-vis absorption and emission spectra in the solid state. The absorption spectrum of a thin film of the solid complex is red-shifted compared with the solution spectra, whereas its emission spectrum reveals the unique featureless exciplex band, blue shifted compared with the solution. In conjunction with X-ray data the solid-state data was interpreted as being due to a new exciplex where no pi-stacking (full overlap of the pi-electron cloud of the two chromophores - anthracene and phenanthroline) is observed. L is a fluorescent chemosensor able to signal Zn(II) in presence of Cd(II) and Hg(II), since the last two metal ions do not give rise either to the formation of pi-stacking complexes or to exciplex emission in solution.

摘要

带有含配位胺和蒽基侧链的大环菲咯啉环番2,9-[2,5,8-三氮杂-5-(N-蒽-9-甲基氨基)乙基]-[9]-1,10-菲咯啉环番(L)在溶液中与Zn(II)、Cd(II)和Hg(II)形成稳定的配合物。通过电位滴定法(pH滴定法)在298.1±0.1K下于0.10 mol dm⁻³四甲基氯化铵H₂O-乙腈(1:1,v/v)溶液中测定了这些配合物的稳定常数。在该溶剂中研究了这些配合物的荧光发射性质。对于Zn(II)配合物,在乙醇溶液和固态下进行了稳态和时间分辨荧光研究。在溶液中,观察到基态下菲咯啉与蒽之间的分子内π堆积相互作用以及激发态下的激基复合物发射。根据光稳定比(I(Exc)/I(M))的温度依赖性,确定了激基复合物形成的活化能(E(a))和激基复合物的结合能(-ΔH)。解析了ZnLBr.H₂O化合物的晶体结构,表明在固态下存在分子内和分子间的π堆积相互作用。这种相互作用在固态的紫外可见吸收和发射光谱中也得到了证实。与溶液光谱相比,固体配合物薄膜的吸收光谱发生红移,而其发射光谱显示出独特的无特征激基复合物带,与溶液相比发生蓝移。结合X射线数据,固态数据被解释为归因于一种新的激基复合物,其中未观察到π堆积(两个发色团 - 蒽和菲咯啉的π电子云完全重叠)。L是一种荧光化学传感器,能够在Cd(II)和Hg(II)存在时检测Zn(II),因为后两种金属离子在溶液中既不会形成π堆积配合物也不会产生激基复合物发射。

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