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Keywords = 9,10-anthracenedicarboxylate

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19 pages, 7303 KiB  
Article
Exploring the Slow Magnetic Relaxation of a Family of Photoluminescent 3D Lanthanide–Organic Frameworks Based on Dicarboxylate Ligands
by Itziar Oyarzabal, Sara Rojas, Ana D. Parejo, Alfonso Salinas-Castillo, José Ángel García, José M. Seco, Javier Cepeda and Antonio Rodríguez-Diéguez
Magnetochemistry 2021, 7(3), 41; https://doi.org/10.3390/magnetochemistry7030041 - 16 Mar 2021
Viewed by 3836
Abstract
A family of metal–organic frameworks with general formula {[Nd2(ant)2((NH2)2-bdc)(DMF)4]·2DMF}n (1) and {[Ln2(ant)2((NH2)2-bdc)(DMF)4]·2DMF·2H2O}n (Ln = Tb (2 [...] Read more.
A family of metal–organic frameworks with general formula {[Nd2(ant)2((NH2)2-bdc)(DMF)4]·2DMF}n (1) and {[Ln2(ant)2((NH2)2-bdc)(DMF)4]·2DMF·2H2O}n (Ln = Tb (2), Ho (3), and Er (4)) has been obtained from reactions between 9,10-anthracenedicarboxylic (H2ant) and 2,5-diaminoterephthalic ((NH2)2-H2bdc) acids, and lanthanide ions in dimethylformamide (DMF). These lanthanide–organic frameworks (LnOFs) have been characterized, and their crystal structures have been elucidated by single crystal and powder X-ray diffraction methods (on the basis of a comparative refinement with similar structures), respectively for 1 and 24. All LnOFs present three-dimensional structures composed of dinuclear [Ln2(µ-CO2)4] entities linked through both carboxylate ligands that yield open frameworks in which DMF and water molecules are located in the channels. Magnetic studies of these LnOFs have revealed slow relaxation of the magnetization for the Nd-based counterpart. The compounds also acknowledge relevant photoluminescence (PL) emissions in the visible (for the Tb-based homologue) and near-infrared (for the Nd- and Er-based compounds) regions. The strong green emission yielded by compound 2 at room temperature allows its study for photoluminescence (PL) sensing of various solvent molecules, finding a particular discrimination for acetone. Full article
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15 pages, 3490 KiB  
Article
Anthracene-Based Lanthanide Metal-Organic Frameworks: Synthesis, Structure, Photoluminescence, and Radioluminescence Properties
by Stephan R. Mathis, Saki T. Golafale, Kyril M. Solntsev and Conrad W. Ingram
Crystals 2018, 8(1), 53; https://doi.org/10.3390/cryst8010053 - 22 Jan 2018
Cited by 13 | Viewed by 7437
Abstract
Four anthracene-based lanthanide metal-organic framework structures (MOFs) were synthesized from the combination of the lanthanide ions, Eu3+, Tb3+, Er3+, and Tm3+, with 9,10-anthracenedicarboxylic acid (H2ADC) in dimethylformamide (DMF) under hydrothermal conditions. The 3-D [...] Read more.
Four anthracene-based lanthanide metal-organic framework structures (MOFs) were synthesized from the combination of the lanthanide ions, Eu3+, Tb3+, Er3+, and Tm3+, with 9,10-anthracenedicarboxylic acid (H2ADC) in dimethylformamide (DMF) under hydrothermal conditions. The 3-D networks crystalize in the triclinic system with P-1 space group with the following compositions: (i) {{[Ln2(ADC)3(DMF)4·DMF]}n, Ln = Eu (1) and Tb (2)} and (ii) {{[Ln2(ADC)3(DMF)2(OH2)2·2DMF·H2O]}n, Ln = Er (3) and Tm (4)}. The metal centers exist in various coordination environments; nine coordinate in (i), while seven and eight coordinate in (ii). The deprotonated ligand, ADC, assumes multiple coordination modes, with its carboxylate functional groups severely twisted away from the plane of the anthracene moiety. The structures show ligand-based photoluminescence, which appears to be significantly quenched when compared with that of the parent H2ADC solid powder. Structure 2 is the least quenched and showed an average photoluminescence lifetime from bi-exponential decay of 0.3 ns. On exposure to ionizing radiation, the structures show radioluminescence spectral features that are consistent with the isolation of the ligand units in its 3-D network. The spectral features vary among the 3-D networks and appear to suggest that the latter undergo significant changes in their molecular and/or electronic structure in the presence of the ionizing radiation. Full article
(This article belongs to the Special Issue Structural Design and Properties of Coordination Polymers)
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12 pages, 1250 KiB  
Article
Metal Organic Framework Micro/Nanopillars of Cu(BTC)·3H2O and Zn(ADC)·DMSO
by Arben Kojtari and Hai-Feng Ji
Nanomaterials 2015, 5(2), 565-576; https://doi.org/10.3390/nano5020565 - 9 Apr 2015
Cited by 16 | Viewed by 10791
Abstract
In this work, we report the optical and thermal properties of Cu(BTC)·3H2O (BTC = 1,3,5-benzenetricarboxylic acid) and Zn(ADC)·DMSO (ADC = 9,10- anthracenedicarboxylic acid, DMSO = dimethyl sulfoxide) metal-organic frameworks (MOFs) micro/nanopillars. The morphologies of MOFs on surfaces are most in the [...] Read more.
In this work, we report the optical and thermal properties of Cu(BTC)·3H2O (BTC = 1,3,5-benzenetricarboxylic acid) and Zn(ADC)·DMSO (ADC = 9,10- anthracenedicarboxylic acid, DMSO = dimethyl sulfoxide) metal-organic frameworks (MOFs) micro/nanopillars. The morphologies of MOFs on surfaces are most in the form of micro/nanopillars that were vertically oriented on the surface. The size and morphology of the pillars depend on the evaporation time, concentration, solvent, substrate, and starting volume of solutions. The crystal structures of the nanopillars and micropillars are the same, confirmed by powder XRD. Zn(ADC)·DMSO pillars have a strong blue fluorescence. Most of ADC in the pillars are in the form of monomers, which is different from ADC in the solid powder. Full article
(This article belongs to the Special Issue Nanomaterials for Energy and Sustainability Applications)
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