Melamine-Barbiturate Supramolecular Assembly as a pH-Dependent Organic Radical Trap Material

Chemistry. 2020 Dec 15;26(70):16603-16610. doi: 10.1002/chem.202002947. Epub 2020 Nov 19.

Abstract

In the last two decades, a large number of self-assembled materials were synthesized and they have already found their way into large-scale industry and science. Hydrogen-bond-based supramolecular adducts are found to have unique properties and to be perfect host structures for trapping target molecules or ions. Such chemical systems are believed to resemble living matter and can substitute a living cell in a number of cases. Herein, a report on an organic material based on supramolecular assembly of barbituric acid and melamine is presented. Surprisingly, the structure is found to host and stabilize radicals under mild conditions allowing its use for biological applications. The number of free radicals is found to be easily tuned by changing the pH of the environment and it increases when exposed to light up to a saturation level. We describe a preparation method as well as stability properties of melamine-barbiturate self-assembly, potentiometric titration, and hydrogen ions adsorption data and EPR spectra concerning the composite.

Keywords: electron paramagnetic resonance; hydrogen bonds; radical trap; self-assembly; supramolecular chemistry.

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