Citation:
ZHAO Shun-Sheng, ZHANG Zhao, SHI Guo-Xiang, FENG Wei-Xu, LÜ Xing-Qiang, LIU Xiang-Rong. Heterobinuclear Zn-Eu or Zn-Tb Complexes Formed from Benzimidazole Derivatives and Metal Salts: Synthesis, Structures and Photophysical Properties[J]. Acta Physico-Chimica Sinica,
;2013, 29(07): 1408-1414.
doi:
10.3866/PKU.WHXB201305081
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Four isostructural heterobinuclear Zn-Ln (Ln=Eu or Tb) complexes are prepared through the self-assembly of benzimidazole derivatives 2-(2-hydroxy-3-methoxyphenyl)benzimidazole (HL1) or 2-(5-bromo-2-hydroxy-3-methoxyphenyl)benzimidazole (HL2) with Zn(CH3COO)2·2H2O and Eu(NO3)3·6H2O or Tb(NO3)3·6H2O). The complexes are characterized by single-crystal X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy, elementary analysis, and electrospray ionization mass spectrometry (ESIMS). Three of the complexes form single crystals, while the fourth is polycrystalline. UV-Vis absorption, excitation and emission spectra of the Tb3+-based complexes reveal strong, characteristic luminescence from Tb3+ with emissive lifetimes in the microsecond range. Therefore, Tb3+ has been sensitized from the excited state of the ligands because of effective intramolecular energy transfer. The Eu3+ complexes do not show characteristic emission because of deactivation by a different pathway.
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