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Hydrothermal synthesis of 3D porous architectures
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作者 肖婉艳 谷晓俊 薛冬峰 《Journal of Rare Earths》 SCIE EI CAS CSCD 2009年第2期341-344,共4页
A novel porous lanthanide-organic coordination polymer, [Nd(H2O)(HnicO)(TP)]·2H2O (1) (H2nicO=2-hydroxynicotinic acid, TP= terephthalate), was prepared under hydrothermal condition and characterized by ... A novel porous lanthanide-organic coordination polymer, [Nd(H2O)(HnicO)(TP)]·2H2O (1) (H2nicO=2-hydroxynicotinic acid, TP= terephthalate), was prepared under hydrothermal condition and characterized by single-crystal X-ray diffraction, thermogravimetric analysis and infrared spectroscopy. Compound 1 exhibited a flexible coordination geometry of lanthanide ions, which possessed a three-dimensional (3D) open framework with one-dimensional (1D) channels containing lattice water molecules. This framework structure exhibited a high stability up to 330℃ after removing free water molecules. A homometallic supramolecular framework (Zn(HnicO)2(H2O)2 (2)) was obtained due to the competitive reaction between organic ligands, Nd3+ and Zn2+ ions. The results showed that on the basis of the soft-hard/acid-base principle the coordination selection between metal ions and organic ligands played an essential role in the smart construction of lanthanide architectures. 展开更多
关键词 porous architecture coordination selection supramolecule framework rare earths
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