The synergy of aromatic gain and hydrogen bonding in a supramolecular polymer is
explored. Partially aromatic bis (squaramide) bolaamphiphiles were designed to self …

Despite a growing understanding of factors that drive monomer self-assembly to form
supramolecular polymers, the effects of aromaticity gain have been largely ignored. Herein …

Hydrogen‐bonded squaramide (SQ) supramolecular polymers exhibit uncommon
thermoreversible polymorph transitions between particle‐and fiber‐like nanostructures. SQs …

Supramolecular polymers are linear chains of low molar mass monomers held together by
reversible andhighly directional non-covalent interactions. In suitable experimental …

Supramolecular polymer chemistry has emerged as a major research focus within polymer
science, because of the potential to improve material properties, through the combination of …

Structure and performance are two fundamental characteristics of a polymeric material.
Therefore, controlling the structure to get a desired property remains one of the main goals …

Abstract N‐Centred benzene‐1, 3, 5‐tricarboxamides (N‐BTAs) composed of chiral and
achiral alkyl substituents were synthesised and their solid‐state behaviour and self …

We report the synthesis and self-assembly of a library of squaramide-based
bolaamphiphiles with variable hydrophobic and hydrophilic domain sizes, consisting of …

The amide bond is a versatile functional group and its directional hydrogen‐bonding
capabilities are widely applied in, for example, supramolecular chemistry. The potential of …

With the introduction of supramolecular polymers, which are polymers based on monomeric
units held together with directional and reversible secondary interactions, the playground for …