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机构地区:[1]兰州大学化学化工学院,兰州730000 [2]茂名学院应用化学系,茂名520000
出 处:《无机化学学报》2006年第12期2235-2238,共4页Chinese Journal of Inorganic Chemistry
基 金:国家自然科学基金资助项目(No.20401008)
摘 要:Eu(Ⅲ) complexes with bipyO2 ligand were intercalated into the interlayer spacing of montmorillonite (MMT) by solid-solid ion exchanging and coordination reaction of bipyO2 with the Eu3+ ion existing in the interlayer spacing of Eu-MMT at room temperature, respectively. The obtained luminescent supramolecular composite materials, Eu(bipyO2)4Cl2+-MMT and Eu(bipyO2)43+-MMT were characterized by elemental analysis, XRD and FTIR spectroscopy. At the same time, the luminescent properties of the materials were also studied. The results show that the intercalation assembly materials have regular layered structures and good luminescent properties. They emit characteristic red emissions of Eu3+ strongly under ultraviolet light excitation. The relative luminescence intensities of the unit mass of Eu3+ of intercalation assemblies are much better than that of the corresponding pure Eu3+ complex possibly due to the rigid layered structures of the materials and the supramolecular interaction between the host layers and the guest complex ions.Eu(Ⅲ) complexes with bipyO2 ligand were intercalated into the interlayer spacing of montmorillonite (MMT) by solid-solid ion exchanging and coordination reaction of bipyO2 with the Eu^3 + ion existing in the interlayer spacing of Eu-MMT at room temperature, respectively. The obtained luminescent supramolecular composite materials, [Eu(bipyO2)4Cl2]^+ -MMT and [Eu(bipyO2)4]^3+ -MMT were characterized by elemental analysis, XRD and FFIR spectroscopy. At the same time, the luminescent properties of the materials were also studied. The results show that the intercalation assembly materials have regular layered structures and good luminescent properties. They emit characteristic red emissions of Eu^3+ strongly under ultraviolet light excitation. The relative luminescence intensities of the unit mass of Eu^3+ of intercalation assemblies are much better than that of the corresponding pure Eu^3 + complex possibly due to the rigid layered structures of the materials and the supramolecular interaction between the host layers and the guest complex ions.
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