Abstract
For decades, extensive surfactant libraries have been developed to meet the requirements of downstream applications. However, achieving functional diversity has traditionally demanded a vast array of chemical motifs and synthetic pathways. Herein, a new approach for surfactant design based on structural isomerism is utilised to access a wide spectrum of functionalities. A library of C18-aliphatic maltosides was prepared through Koenigs-Knorr glycosylation, with their properties tuned through anomerism, stereoisomerism, regioisomerism, and the degree of tail unsaturation. Self-assembly of the amphiphiles gave rise to various morphologies, ranging from small micelles to large one-dimensional semiflexible assemblies, which were ultimately defined by the directionality of the supramolecular interactions imposed by the angular restraints of the isomeric centres. Remarkably, the microscopic phase determines the rheological behaviour of the system, which accesses Newtonian solutions, viscoelastic fluids, and gels with customised mechanical properties. The approach outlined in this study serves as a blueprint for the design of novel bioderived surfactants with diverse behaviours without altering the chemical composition of the surfactants, where the understanding of molecular interactions can potentially be used to predict and design the assembly and function of isomerically varied amphiphiles.