Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1329492 | Journal of Solid State Chemistry | 2009 | 6 Pages |
A new metal-organic framework, [Zn5(trencba)2(OH)2Cl2·4H2O] (1) [H3trencba=N,N,N′,N′,N′′,N′′-tris[(4-carboxylate-2-yl)methyl]-tris(2-aminoethyl)amine], constructed from a flexible tripodal ligand based on C3 symmetric tris(2-aminoethyl)amine, has been synthesized hydrothermally and characterized by elemental analysis, IR, TG, XRD and single-crystal X-ray diffraction analysis. Compound 1 contains an unprecedented linear penta-nuclear zinc cluster fragment. Each ligand links four penta-nuclear fragments, and every fragment links eight ligands to generate a three-dimensional non-interpenetrated porous framework. The uncoordinated water molecules were observed trapped in the void pores. Compound 1 represents the first example of (6,8)-connected 3D bi-nodal framework based on a single kind of organic ligand. The photoluminescence measurements showed that complex 1 exhibits relatively stronger blue emissions at room temperature than that of the ligand.
Graphical abstractThe MOF [Zn5(trencba)2(OH)2Cl2·4H2O] (H3trencba=N,N,N′,N′,N′,N′-tris[(4-carboxylate-2-yl)methyl]-tris(2-aminoethyl)amine) reveals a (6,8)-connected bi-nodal three-dimensional porous framework with unprecedented penta-nuclear fragment, which appears to be a good candidate of hybrid inorganic-organic photoactive materials.Figure optionsDownload full-size imageDownload as PowerPoint slide