Fluorescent magnesium(II) coordination polymeric hydrogel

TL;DR: A pH and mechano-responsive coordination polymeric gel was developed without the use of long chain hydrophobic groups and may find utility as a novel soft material in biomedical applications and viscoelastic properties and biocompatibility.

Abstract: A pH and mechano-responsive coordination polymeric gel was developed without the use of long chain hydrophobic groups. The hydrogel was synthesised by reacting the aqueous solution of Mg2+ with the basic aqueous solution of N-(7-hydroxyl-4-methyl-8-coumarinyl)-alanine. The gelation is attributed to the self-aggregation of ID coordination polymers to form 3D nanostructures through non-covalent interactions to entrap water molecules. The freeze-dried hydrogel exhibits a fibrillar network structure with a uniform ribbon shape. UV/vis absorption studies illustrate that the hydrogel displays a typical pi-pi* transition. The fluorescence intensity of the hydrogel is enhanced drastically with a longer lifetime upon gel formation. Mechanical analysis including dynamic oscillation on shear, steady shear and creep (retardation-relaxation) testing have been performed to elucidate the supramolecular nature of the 3D assembly. Together with the viscoelastic properties and biocompatibility, the Mg2+ hydrogel may find utility as a novel soft material in biomedical applications. A pH and mechano-responsive coordination polymeric gel was developed without the use of long chain hydrophobic groups. The hydrogel was synthesised by reacting the aqueous solution of Mg2+ with the basic aqueous solution of N-(7-hydroxyl-4-methyl-8-coumarinyl)-alanine. The gelation is attributed to the self-aggregation of ID coordination polymers to form 3D nanostructures through non-covalent interactions to entrap water molecules. The freeze-dried hydrogel exhibits a fibrillar network structure with a uniform ribbon shape. UV/vis absorption studies illustrate that the hydrogel displays a typical I?-I?* transition. The fluorescence intensity of the hydrogel is enhanced drastically with a longer lifetime upon gel formation. Mechanical analysis including dynamic oscillation on shear, steady shear and creep (retardation-relaxation) testing have been performed to elucidate the supramolecular nature of the 3D assembly. Together with the viscoelastic properties and biocompatibility, the Mg2+ hydrogel may find utility as a novel soft material in biomedical applications.