Exploring supramolecular aggregation behaviour of bioactive thiazolidine-4-carboxylic acid derivatives

A target synthesis of selected biocompatible chiral Thiazolidine-4-carboxylic acid derivatives was attempted to investigate the influence of number, type and position of hydrogen bonding functionalities and solvent molecules in the crystal lattice on the supramolecular aggregation behaviour leading to formation of molecular assemblies. The single crystal X-ray diffraction studies of (R)-thiazolidine-4-carboxylic acid (T4CA, zwitter ion form), 2-propionyl T4CA and (2S,4R)-3-(tert-butoxycarbonyl)-2-(4-methoxyphenyl)T4CA and other reported thiozolidine 4-carboxylic acid derivatives were used to establish the solid state aggregation behaviour. The 1D, 2D and 3D agregrational behaviour of synthesized thiozolidine-4-carboxylic acid derivatives was explored from their crystal packing diagrams and was further extended in light of some appropriate literature reported thiozolidine-4-carboxylic acid derivatives. The explored 1D, 2D and 3D supramolecular aggregrational behaviour in case of the thiazolidine-4-carboxylic acid derivatives can be explored for their further applications as biocompatible supramolecular assemblies towards gas storage, biosensing and template catalysis.

Automated summary

An attempt was made to synthesize biocompatible chiral Thiazolidine-4-carboxylic acid derivatives to investigate the influence of hydrogen bonding functionalities and solvent molecules on supramolecular aggregation behavior, with potential applications in gas storage, biosensing, and template catalysis. Single crystal X-ray diffraction studies were used to establish solid state aggregation behavior of the synthesized derivatives, which were further explored in accordance with literature reports. The findings suggest potential for further applications in biocompatible supramolecular assemblies.