This study investigates mixed-carboxylate benzoate (bz)-pentafluorobenzoate (pfb) {EuZn} and {TbZn} compounds with 1,10-phenanthroline (phen) molecules. It is demonstrated that variation of the synthesis conditions yields mixed-carboxylate compounds with different compositions: [LnZn(phen)(bz)(pfb)] (Ln = Eu (1Eu), Tb (1Tb)) and [EuZn(phen)(bz)(pfb)]·4MeCN (2Eu). In these structures, bz and pfb anions occupy specific positions in various ratios. Benzoate compounds [LnZn(phen)(bz)] (Ln = Eu (3Eu), Tb (3Tb)) were synthesized in order to compare the structures and photoluminescence properties of complexes 1 and 2 with their homoanionic analogues, and comparison was also made with previously reported pentafluorobenzoate complexes [LnZn(pfb)(phen)] (Ln = Eu (4Eu), Tb (4Tb)). It was found that the introduction of a second type of anion into the studied compounds improves the photoluminescence properties and alters the geometry of the metal core, the polyhedra of rare-earth elements (REEs), and the system of non-covalent interactions compared to benzoate and pentafluorobenzoate complexes.
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http://dx.doi.org/10.1039/d4dt03414g | DOI Listing |
Chem Commun (Camb)
March 2015
Department of Chemistry, Key Laboratory of Advanced Energy Material Chemistry, MOE, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071, P. R. China.
Two cationic heterometal-organic frameworks (Eu-Zn (1·NO₃⁻) and Tb-Zn (2·NO₃⁻)) with NO3(-) counter-anions in the channels are structurally and luminously characterized. Both of them can serve as highly sensitive and highly selective luminescent probes for detecting I(-) ions in aqueous solutions. In particular, 2·NO₃⁻ can selectively and reversibly detect I(-) with a fast response time of just 10 s and an extremely low detection limit of 0.
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