کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1329666 | 1500083 | 2016 | 8 صفحه PDF | دانلود رایگان |
• New cerium and praseodymium coordination polymers based on N-O-bifunctional ligands have been synthesized In situ hydrothermal decarboxylation.
• 2,5-pyridinedicarboxylic acid and piperazine were used as ligands.
• In situ hydrothermal decarboxylation and formation of ligands were observed.
Two novel 3D lanthanide metal-organic frameworks [Ln(pydc)(pip)1/2(H2O] (Ln=Ce (1) and Pr (2), H2pydc=2,5-pyridinedicarboxylic acid, H2pip=2,5-piperazinedicarboxylic acid have been synthesized under hydrothermal conditions and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA), powder X-ray diffractions (PXRD), and single-crystal X-ray diffractions. Field emission scanning electron microscopy (FESEM) was used for morphological analysis. Complexes are isostructural and feature interesting 3D frameworks. Both compounds crystallize in the monoclinic system, space group P21/c. Structural analyses of 1 and 2 show that Ln3+ ions connect with each other through H2pydc and H2pip. To the best of our knowledge, they are the first heteroleptic lanthanide polymers obtained through in situ 2,5-piperazinedicarboxylic acid syntheses. Moreover, thermal and luminescent properties of the compounds have been investigated.
Two novel 3D lanthanide metal-organic frameworks have been synthesized under hydrothermal conditions. Luminescent properties of the compounds in different temperatures have been also investigated.Figure optionsDownload as PowerPoint slide
Journal: Journal of Solid State Chemistry - Volume 233, January 2016, Pages 44–51