کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1332753 | 979052 | 2008 | 6 صفحه PDF | دانلود رایگان |
Six new lanthanide complexes, (H3O)[Ln3(H2O)17(α2–As2W17O61)]·nH2O ((1) Ln=CeIII and n≈13; (2) Ln=PrIII and n≈9; (3) Ln=NdIII and n≈14; (4) Ln=SmIII and n≈8; (5) Ln=EuIII and n≈4; (6) Ln=GdIII and n≈7), have been isolated by conventional solution method and characterized by elemental analysis, IR spectroscopy and single crystal X-ray diffraction. All the complexes are isomorphic and crystallize in the triclinic space group P-1. These complexes are 1D chain-like structures constructed by lanthanide cations and monovacant Dawson-type [α2-As2W17O61]10− polyoxoanions. The striking feature of the structures is that there are three kinds of coordination environments for lanthanide cations, which are responsible for the formation of polymeric structures. Photoluminescence measurements reveal that 4 and 5 exhibit orange and red fluorescent emission at room temperature, respectively.
Six new lanthanide complexes based on monovacant Dawson-type tungstoarsenates have been synthesized. These complexes are one-dimensional chain-like structures constructed by lanthanide cations and [α2-As2W17O61]10− anions. There are three kinds of coordination environment for lanthanide cations. Photoluminescence measurement reveals that 4 and 5 exhibit orange and red fluorescent emission at room temperature, respectively.Figure optionsDownload as PowerPoint slide
Journal: Journal of Solid State Chemistry - Volume 181, Issue 9, September 2008, Pages 2488–2493