From One-Dimensional Disordered Racemate to Ordered Racemic Conglomerates through Metal-Coordination-Driven Self-Assembly at the Liquid-Solid Interface.

In recent years, there has been significant focus on investigating and controlling chiral self-assembly, specifically in the context of enantiomeric separation. This study explores the self-assembly behavior of 4-dodecyl-3,6-di(2-pyridyl)pyridazine (DPP-C12) at the interface between heptanoic acid (HA) and highly oriented pyrolytic graphite (HOPG) using a combination of scanning tunneling microscopy (STM) and multiscale molecular modeling. The self-assembled monolayer structure formed by DPP-C12 is periodic in one direction, but aperiodic in the direction orthogonal to it. These structures resemble 1D disordered racemic compounds. Upon introducing palladium [Pd(II)] ions, complexing with DPP-C12, these 1D disordered racemic compounds spontaneously transform into 2D racemic conglomerates, which is rationalized with the assistance of force-field simulations. Our findings provide insights into the regulation of two-dimensional chirality.

[2 × 2] metallo-supramolecular grids based on 4,6-bis((1H-1,2,3-triazol-4-yl)-pyridin-2-yl)-2-phenylpyrimidine ligands: from discrete [2 × 2] grid structures to star-shaped supramolecular polymeric architectures.

The self-assembly of bis-tridentate ligands leads to the spontaneous formation of [2 × 2] grid-like metal complexes. However, the synthesis of such ligands is rather cumbersome. In the work, we demonstrate a straightforward synthesis route to prepare bis-tridentate 4,6-bis((1H-1,2,3-triazol-4-yl)-pyridin-2-yl)-2-phenylpyrimidine ligands through double CuAAC click chemistry with 4,6-bis(6-ethynylpyridin-2-yl)-2-phenylpyrimidine as well as their self-assembly into [2 × 2] grid-like metal complexes. In addition, four macromolecular ligands were synthesized starting from azido-end-functionalized poly(2-ethyl-2-oxazoline) (PEtOx) or poly(ethylene glycol) (PEG). These macromolecular ligands were used in the construction of star-shaped supramolecular polymers through complexation with transition metal ions (e.g., Fe2+ or Zn2+). The successful fabrication of complexes and star-shaped polymers was confirmed by UV-vis titration measurements and MALDI-TOF mass spectrometry. However, the chemical structure of the polymer was found to have a strong influence on the [2 × 2] grid formation, which was successful with the PEG-ligands but not with the PEtOx-ligands, while the molecular weight of the PEG did not interfere with grid formation.

Effect of Host-Guest Complexation on the Thermoresponsive Behavior of Poly(oligo ethylene glycol acrylate)s Functionalized with Dialkoxynapththalene Guest Side Chains.

The combination of thermoresponsive polymers with supramolecular host-guest interactions enables accurate tuning of the phase transition temperature, while also providing additional response mechanisms based on host-guest complexation. Most studies focused on a single thermoresponsive polymer to demonstrate the effect of host-guest complexation on the responsive behavior. In this work, the effect of the polymer structure on the host-guest complexation and thermoresponsive behavior is reported. Therefore, different poly(oligoethylene glycol acrylate)s, namely, poly(2-hydroxyethylacrylate) (PHEA), poly(methoxy diethylene glycol acrylate), poly(methoxy triethylene glycol acrylate), and poly(methoxy tetraethylene glycol acrylate), are synthesized functionalized with 1,5-dialkoxynaphthalene guest molecules in the side chain. Their complexation with the cyclobis(paraquat-p-phenylene) tetrachloride host is studied to understand the effect of polymer structure on the supramolecular association and the polymer phase transition, revealing that the oligoethylene glycol side chains lead to weaker host-guest complexation and also have a smaller increase in the cloud point temperature compared to PHEA.

Multiresponsive Behavior of Functional Poly(p-phenylene vinylene)s in Water.

The multiresponsive behavior of functionalized water-soluble conjugated polymers (CPs) is presented with potential applications for sensors. In this study, we investigated the aqueous solubility behavior of water-soluble CPs with high photoluminescence and with a particular focus on their pH and temperature responsiveness. For this purpose, two poly(phenylene vinylene)s (PPVs)-namely 2,5-substituted PPVs bearing both carboxylic acid and methoxyoligoethylene glycol units-were investigated, with different amount of carboxylic acid units. Changes in the pH and temperature of polymer solutions led to a response in the fluorescence intensity in a pH range from 3 to 10 and for temperatures ranging from 10 to 85 °C. Additionally, it is demonstrated that the polymer with the largest number of carboxylic acid groups displays upper critical solution temperature (UCST)-like thermoresponsive behavior in the presence of a divalent ion like Ca2+. The sensing capability of these water-soluble PPVs could be utilized to design smart materials with multiresponsive behavior in biomedicine and soft materials.