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
Department of Chemistry, University of Florence, via della Lastruccia 3, 50019 Sesto Fiorentino, Florence, Italy.
Dalton Trans. 2004 Jul 21(14):2180-7. doi: 10.1039/B403743J. Epub 2004 Jun 8.
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.
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。