Supramolecular copolymers formed by the noncovalent synthesis of multiple components expand the complexity of functional molecular systems. However, varying the composition and microstructure of copolymers through tuning the interactions between building blocks remains a challenge. Here, we report a remarkable discovery of the temperature-dependent supramolecular copolymerization of the two chiral monomers 4,4′,4″-(1,3,5triazine-2,4,6-triyl)tribenzamide (S-T) and 4,4′,4″-(benzene-1,3,5-triyl)tribenzamide (S-B). We first demonstrate in the homopolymerization of the two individual monomers that a subtle change from the central triazine to benzene in the chemical structure of the monomers significantly affects the properties of the resulting homopolymers in solution. Homopolymers formed by S-T exhibit enhanced stability in comparison to S-B. More importantly, through a combination of spectroscopic analysis and theoretical simulation, we reveal the complex process of copolymerization: S-T aggregates into homopolymers at elevated temperature, and upon slow cooling S-B gradually intercalates into the copolymers, to finally give copolymers with almost 80% alternating bonds at 10 °C. The formation of the predominantly alternating copolymers is plausibly contributed by preferred heterointeractions between triazine and benzene cores in S-T and S-B, respectively, at lower temperatures. Overall, this work unravels the complexity of a supramolecular copolymerization process where an intermediate heterointeraction (higher than one homointeraction and lower than the other homointeraction) presents and proposes a general method to elucidate the microstructures of copolymers responsive to temperature changes.

Squaraine dyes are well knownf or their strong absorption in the visible regime. Reports on chiral squaraine dyes are, however,s carce. To address this gap, we here report two novel chiral squaraine dyes and their achiral counterparts. The presented dyes are aggregated in solution and in thin films. Ad etailed chiroptical study shows that thin films formed by co-assembling the chiral dye with its achiral counterparte xhibit exceptionalp hotophysical properties. The circulard ichroism (CD) of the co-assembled structures reaches am aximum when just 25 %o ft he chiral dye are present in the mixture. The solid structures with the highestr elative CD effect are achieved when the chiral dye is used solely as ad irector,r ather than the structural component. The chiroptical data are further supported by selected spin-filtering measurements using mc-AFM.T hese findings provideapromisingp latform for investigating the relationship between the dissymmetry of as upramolecular structure and emerging material properties rather than ac omparison between ac hiral molecular structure and an achiral counterpart.

The fabrication of highly ordered nanostructured surfaces is desirable in supramolecular chemistry and envisaged to bolster advances in heterogeneous catalysis and microelectronic applications. Here, we report on a novel set of alkylated double N,N′-bis­(n-alkyl)-naphthalenediimides (NDIs) for the functionalization of highly oriented pyrolytic graphite (HOPG) with precise double lamellar morphologies. A detailed analysis of the two-dimensional (2D) self-assembled monolayers by scanning tunneling microscopy (STM) reveals that the structural repeating unit of the double lamellae is tuned precisely by the length of the alkyl chain that is connecting the NDI units. However, the expected odd–even effect is disturbed within the monolayers of a series of homologues. In contrast, a clear odd–even effect is observed for the melting temperatures of the respective bulk materials. Small-angle X-ray scattering reveals that these bulk materials exhibit nanophase-separated lamellar phases with domain spacings that are slightly larger than the repeating units of the double lamellar structures formed on the HOPG surface. The discrepancy is assigned to a partial desorption of the alkyl spacer from the HOPG surface, which becomes more pronounced when increasing its length. Our findings suggest that this lengthening increases the conformational freedom of the molecules on the surface while retaining a double lamellar morphology.

Recent studies on water‐splitting photoelectrochemical cells (PECs) have demonstrated the intriguing possibility of controlling the spin state in this chemical reaction to form H2 and O2 by exploiting the chirality of organic π‐conjugated supramolecular polymers. Although this fascinating phenomenon has been disclosed, the chiral supramolecular materials reported thus far are not optimized for acting as efficient photosensitizer for dye‐sensitized PECs. In this work we report on the design, synthesis, and characterization of chiral supramolecular aggregates based on C3‐symmetric triphenylamine‐based dyes that are able to both absorb visible light and control the spin state of the process. Variable temperature‐dependent spectroscopic measurements reveal the assembly process of the dyes and confirm the formation of chiral aggregates, both in solution as well as on solid supports. Photoelectrochemical measurements on TiO2‐based anodes validate the advantage of using chiral supramolecular aggregates as photosensitizer displaying higher photocurrent compared to achiral analogues. Moreover, fluorimetric tests for the quantification of the hydrogen peroxide produced, confirm the possibility of controlling the spin of the reaction exerting spin‐selection with chiral supramolecular polymers. These results represent a further step towards the next‐generation of organic‐based water‐splitting solar cells.

The conformational analysis of a 2,4-bis(4-dialkylamino-2-amido)phenyl squaraine dye revealed the presence of two rotational isomers at room temperature. Combination of spectroscopic and computational techniques showed that the rotational barrier is influenced by hydrogen bonds between the amido substituents and the oxygen atoms at the quadratic core. Even small amounts of trifluoroacetic acid interfered with the intramolecular hydrogen bond formation and accelerated the interconversion of the conformers.