ABSTRACT
By harnessing a highly efficient metal-catalyzed tandem cycloaddition reaction as the key benzannulation step, a series of cyclopolyarene nanorings of varied sizes are obtained from poly(arylene-butadiynylene) macrocyclic precursors, which can be synthesized relatively conveniently. Interestingly, due to the nonparallel bond connectivity of the repeat unit, unique Möbius topology is manifested by the cyclopolyarene nanorings composed of an odd number of repeat units, whereas cylindrical tubular structures with radial conjugation are formed with those consisting of an even number of repeat units.
ABSTRACT
The nanostructures of a series of conjugated oligo(p-phenylene-ethynylene)s (OPE) adsorbed on a surface were thoroughly studied using scanning tunneling microscopy (STM). These oligomers have different backbone lengths and side chains. As a result, various nanostructures displaying periodic linear patterns at a single molecule level were obtained. Based on careful measurements on the STM images in combination with density functional theory (DFT) calculations, it could be found that the vertical and parallel distances between neighboring oligomers were responsible for the specific arrangement of the backbone and side chains. The results showed that these molecular designs strongly affect their self-assembled structure, which is important to clarify the structure-property relationship in the nanoscience field.
ABSTRACT
The folding and aggregation behavior of a pair of oligo(phenylene ethynylene) (OPE) foldamers are investigated by means of UV/Vis absorption and circular dichroism spectroscopy. With identical OPE backbones, two foldamers, 1 with alkyl side groups and 2 with triethylene glycol side chains, manifest similar helical conformations in solutions in n-hexane and methanol, respectively. However, disparate and competing folding and aggregation processes are observed in alternative solvents. In cyclohexane, oligomer 1 initially adopts the helical conformation, but the self-aggregation of unfolded chains, as a minor component, gradually drives the folding-unfolding transition eventually to the unfolded aggregate state completely. In contrast, in aqueous solution (CH3 OH/H2 O) both folded and unfolded oligomer 2 appear to undergo self-association; aggregates of the folded chains are thermodynamically more stable. In solutions with a high H2 O content, self-aggregation among unfolded oligomers is kinetically favored; these oligomers very slowly transform into aggregates of helical structures with greater thermodynamic stability. The folded-unfolded conformational switch thus takes place with the free (nonaggregated) molecules, and the very slow folding transition is due to the low concentration of molecularly dispersed oligomers.
ABSTRACT
In the present investigation, we reported the fabrication of host networks formed by two newly prepared phenanthrene-butadiynylene macrocycles (PBMs) at the liquid-solid interface. Size, shape and concentration controlled experiments have been performed to investigate the PBMs/coronene (COR) host-guest system with the structural polymorphism phenomenon. Initially, PBM1 could form a regular linear network structure and PBM2 form a well-ordered nanoporous network structure. When the COR molecules were introduced, the self-assembled structure of PBM1 remained unchanged, while COR could be entrapped into the cavities of the PBM2 nanoporous network, and the co-assembly of the PBM2/COR host-guest systems underwent a structural transformation with the increase of concentration of COR. Scanning tunneling microscopy (STM) measurements and density functional theory (DFT) calculations are utilized to reveal the formation mechanism of the molecular nanoarrays controlled by the solution concentration.
ABSTRACT
Molecular assemblies with well-defined structures capable of photo-induced electron transfer and charge transport or photochemical reactions are reviewed. Hierarchical supramolecular architectures, which assemble the modular units into specific spatial arrangements and facilitate them to work cooperatively, are vital for the achievement of photo-functions in these systems. The chemical design of molecular building blocks and noncovalent interactions exploited to realize supramolecular organizations are particularly discussed. Reviewing and recapitulating the chemical evolution traces of these accomplished systems will hopefully delineate certain fundamental design principles and guidelines useful for developing more advanced functions in the future.
ABSTRACT
As a representative folding system that features a conjugated backbone, a series of monodispersed (o-phenyleneethynylene)-alt-(p-phenyleneethynylene) (PE) oligomers of varied chain length and different side chains were studied. Molecules with the same backbone but different side-chain structures were shown to exhibit similar helical conformations in respectively suitable solvents. Specifically, oligomers with dodecyloxy side chains folded into the helical structure in apolar aliphatic solvents, whereas an analogous oligomer with tri(ethylene glycol) (Tg) side chains adopted the same conformation in polar solvents. The fact that the oligomers with the same backbone manifested a similar folded conformation independent of side chains and the nature of the solvent confirmed the concept that the driving force for folding was the intramolecular aromatic stacking and solvophobic interactions. Although all were capable of inducing folding, different solvents were shown to bestow slightly varied folding stability. The chain-length dependence study revealed a nonlinear correlation between the folding stability with backbone chain length. A critical size of approximately 10â PE units was identified for the system, beyond which folding occurred. This observation corroborated the helical nature of the folded structure. Remarkably, based on the absorption and emission spectra, the effective conjugation length of the system extended more effectively under the folded state than under random conformations. Moreover, as evidenced by the optical spectra and dynamic light-scattering studies, intermolecular association took place among the helical oligomers with Tg side chains in aqueous solution. The demonstrated ability of such a conjugated foldamer in self-assembling into hierarchical supramolecular structures promises application potential for the system.