Publications by authors named "Stavros A Diamantis"

Trivalent lanthanide ions (Ln) hold an exceptional position in the field of optoelectronic materials due to their atomic-like emission spectra and long luminescence lifetimes. Metal-organic frameworks (MOFs) and coordination polymers are particularly suited as luminescent materials due to their structural diversity and ease of functionalization both at bridging ligands and/or metal centers. In this contribution, we present a series of mixed-metal Ln/Eu (Ln = La, Gd) and mixed-ligand (2,6-naphthalenedicarboxylate (ndc) and 4-aminonaphthalene-2,6-dicarboxylate (andc)) MOFs belonging to three different structural types, with emissions spanning most of the visible region, thereby constituting favorable materials for color tuning and white-light emission.

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Increasing global environmental pollution due to heavy metal ions raises the importance of research on new multifunctional materials for simultaneous detection and removal of these contaminants from water resources. In this study, we report a microporous 8-connected Zr metal-organic framework (MOF) based on a terephthalate ligand decorated with a chelating 2-picolylamine side group (), which shows highly efficient fluorescence sensing and sorption of heavy metal cations. We demonstrate by detailed fluorescence studies the ability of a water-dispersible composite of with polyvinylpyrrolidone for real-time detection of Cu, Pb, and Hg in aqueous media.

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Alkaline earth metal ion organic frameworks (AEMOFs) represent a relatively underexplored subcategory of metal-organic frameworks (MOFs). In this contribution, we present the synthesis and structural study of the new MOFs 1-8 based on the alkaline earth ions Mg2+, Ca2+, Sr2+ and Ba2+ and the amino substituted bridging ligands 4-aminonaphthalene-2,6-dicarboxylate (ANDC2-) and 4,8-diaminonaphthalene-2,6-dicarboxylate (DANDC2-). Compounds 1, 5, 6, 7 and 8 constitute rare examples of three-dimensional MOFs which feature square planar M4 secondary building units (SBUs) surrounded by eight bridging ditopic ligands.

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In this study, we report the luminescence color tuning in the lanthanide metal-organic framework (LnMOF) ([La(bpdc)Cl(DMF)] (); bpdc = [1,1'-biphenyl]-4,4'-dicarboxylate, DMF = ,-dimethylformamide) by introducing dual emission properties in a La MOF scaffold through doping with the blue fluorescent 2,2'-diamino-[1,1'-biphenyl]-4,4'-dicarboxylate (dabpdc) and the red emissive Eu. With a careful adjustment of the relative doping levels of the lanthanide ions and bridging ligands, the color of the luminescence was modulated, while at the same time the photophysical characteristics of the two chromophores were retained. In addition, the photophysical properties of the parent MOF () and its doped counterparts with various dabpdc/bpdc and Eu/La ratios and the photoinduced energy transfer pathways that are possible within these materials are discussed.

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