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• 554-95-0 benzene-1,3,5-tricarboxylic acid 

Relevant academic research and scientific papers

Green synthesis of a large series of bimetallic MIL-100(Fe,M) MOFs

Here we present a scalable and green methodology to synthesize a large variety of MIL-100(Fe,M), metal-doped iron-based MOFs with high thermal stability and surface areas. Our synthesis is performed at room temperature in aqueous media and can be applied to doping with p-, d- and f-elements in oxidation states from +I to +V, therefore being highly general. The influence of the doping metal nature on the thermal and textural properties is systematically investigated. We show that large differences between the ionic radius of the doping and the templating metals does not lead to phase segregation. The incorporation of Cu(i) drastically lowers the thermal stability of MIL-100(Fe,Cu), while the incorporation of V, Al and Ti induces the formation of mesopores. Finally, we developed a PXRD-based method that can be combined with TGA to easily access the metal ratios in complex mixed-metal MOFs.

Sensing of fluoride ions in aqueous media using a luminescent coordination polymer and liposome composite

The synthesis of a luminescent coordination polymer (Tb-BTC) within the confined environment of a liposome allowed for the anisotropic growth of nanosized Tb-BTC crystals. Consequently, the resulting composite Tb-BTC@Lipo exhibited a higher fluorescence s

The advantage of covalent capture in the combinatorial screening of a dynamic library for the detection of weak interactions

In this paper we address the advantage of screening a dynamic library by covalent capture in comparison with an approach in which the target is not covalently bound to the molecular receptor. The aim is the selection of recognition units for the binding of an anion (or polyanion) by relatively weak binding interactions, a situation typically found in supramolecular chemistry. To compare the two approaches, two model systems have been studied both based on the functionalization of a molecular platform, by reversible imine formation. In the case of the noncovalently bound substrate, the platform P1 is a trisubstituted benzene unit, 2,4,6-trimethylbenzene-1,3,5-tricarbaldehyde, to select: three recognition arms for the binding of the trisodium salt of benzene-1,3,5tricarboxylate. For the covalent-capture-based approach the platforms P2 and P4 are benzene derivatives with a tethered phosphonate target (tetrabutylammonium 2-formylphenyl ethylphosphonate) for the selection of a single recognition unit. The library of recognition elements comprises phenyl and ammonium-functionalized amines. We show that the selection of recognition units for the binding of the substrate with weak to medium, binding constants may encounter, by using a noncovalently bound substrate, serious problems. This is because the best conditions for the amplification of the library, that is, a large excess of variable recognition elements and target, lead also to competitive binding of the elements not bound to the platform, with the target. This may result in negligible amplification of the best-fit members of the library. In contrast, upon tethering the target to the platform and using the covalent-capture strategy for the selection of the recognition elements, significant amplification is observed, even for systems with much lower binding constants. Although competition with excess recognition units may also become an issue in the case of the tethered target, there is a way to overcome the problem by working at low concentrations.