Dual Emission in a Ligand and Metal Co-Doped Lanthanide-Organic Framework: Color Tuning and Temperature Dependent Luminescence.

In this study, we report the luminescence color tuning in the lanthanide metal-organic framework (LnMOF) ([La(bpdc)Cl(DMF)] (1); bpdc2- = [1,1'-biphenyl]-4,4'-dicarboxylate, DMF = N,N-dimethylformamide) by introducing dual emission properties in a La3+ MOF scaffold through doping with the blue fluorescent 2,2'-diamino-[1,1'-biphenyl]-4,4'-dicarboxylate (dabpdc2-) and the red emissive Eu3+. 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 (1) and its doped counterparts with various dabpdc2-/bpdc2- and Eu3+/La3+ ratios and the photoinduced energy transfer pathways that are possible within these materials are discussed. Finally, the temperature dependence study on the emission profile of a doped analogue containing 10% dabpdc2- and 2.5% Eu3+ (7) is presented, highlighting the potential of this family of materials to behave as temperature sensors.

Temperature-dependent interchromophoric interaction in a fluorescent pyrene-based metal-organic framework.

Compounds exhibiting tuneable fluorescence emission upon heating or cooling are considered smart materials as their optical properties can be exquisitely controlled by adjusting the external temperature. Herein, we report such a material, which is a porous pyrene-based metal-organic framework with a chemical formula of [Mg1.5(HTBAPy)(H2O)2]·3DMF (H4TBAPy = 1,3,6,8-tetrakis(p-benzoic acid)pyrene), named SION-7. The bulk solid material of SION-7 can display either monomer or excimer fluorescence emission due to the temperature-dependent extent of interchromophoric interactions between the HTBAPy3- ligands within the framework. Consequently, the fluorescence emission colours gradually change from blue at low temperature (80 K) to yellow-green at high temperature (450 K). Interestingly, while kept in a relatively wide temperature range of 80-200 K, SION-7 displays a structured monomer-like spectrum and its colour changes reversibly from deep to light blue. Ex situ variable-temperature (100-350 K) single-crystal X-ray diffractometry studies revealed the impact of solvent content on the optical properties of SION-7, and illustrated the correlation between the position of the phenylene groups of the HTBAPy3- ligands at different temperatures and the interchromophoric interaction. Our study demonstrates a step forward towards the design of tuneable thermofluorochromic materials sought by optoelectronics.

Selective, Fast-Response, and Regenerable Metal-Organic Framework for Sampling Excess Fluoride Levels in Drinking Water.

Prolonged consumption of water contaminated with fluoride ions (F-) at concentrations exceeding 1.5 ppm can lead to considerable health implications, particularly in children and developing embryos. With irreversible and potentially severe forms of fluoride (F-) toxicity such as skeletal fluorosis being endemic in at least 25 countries, constructing affordable, remote-access, reliable water-sampling methods for F- contamination is an important goal. In this work, we present a novel lanthanide-based luminescent metal-organic framework, named SION-105, with a boron (B) receptor site whose interactions with F- in aqueous solutions are simultaneously electrostatic and specific in nature because of its carefully designed structural environment. This allows the material to be easily regenerated and used over 10 cycles, setting it apart from most existing molecular and polymeric F- sensors. SION-105 has been combined with a portable prototype sampling device that was designed and built in-house to measure F- concentrations in natural groundwater samples taken from three different countries, with the results showing excellent agreement with ion chromatography analysis.