Two-dimensional (2D) covalent organic frameworks (COFs) are composed of structurally precise, permanently porous, layered macromolecular sheets, which are traditionally synthesized as polycrystalline solids with crystalline domain lengths smaller than 100 nm. Here, we polymerize imine-linked 2D COFs as suspensions of faceted single crystals in as little as 5 min at moderate temperature and ambient pressure. Single crystals of two imine-linked 2D COFs were prepared, consisting of a rhombic 2D COF (TAPPy-PDA) and a hexagonal 2D COF (TAPB-DMPDA). The sizes of TAPPy-PDA and TAPB-DMPDA crystals were tuned from 720 nm to 4 μm and 450 nm to 20 μm in width, respectively. High-resolution transmission electron microscopy revealed that the COF crystals consist of layered, 2D polymers comprising single-crystalline domains. Continuous rotation electron diffraction resolved the unit cell and crystal structure of both COFs, which are single-crystalline in the a–b plane but disordered in the stacking c dimension. Single crystals of both COFs were incorporated into gas chromatography separation columns and exhibited unusual selective retention of cyclohexane over benzene, with single-crystalline TAPPy-PDA significantly outperforming single-crystalline TAPB-DMPDA. Polycrystalline TAPPy-PDA exhibited no separation, while polycrystalline TAPB-DMPDA exhibited poor separation and the opposite order of elution, retaining benzene more than cyclohexane, indicating the importance of improved material quality for COFs to exhibit properties that derive from their precise, crystalline structures. This work represents the first example of synthesizing imine-linked 2D COF single crystals at ambient pressure and short reaction times and demonstrates the promise of high-quality COFs for molecular separations.

Interest in the design and development of artificial molecular muscles has inspired scientists to pursue new stimuli-responsive systems capable of exhibiting a physical and mechanical change in a material in response to one or more external environmental cues. Over the past few decades, many different types of stimuli have been investigated as a means to actuate materials. In particular, materials that respond to reduction and oxidation of their constituent molecular components have shown great promise on account of their ability to be activated either chemically or electrochemically. Here, we introduce a novel redox-responsive mechanism of actuation in hydrogels by describing a systematic investigation into the radical-based self-assembly of a series of unimolecular viologen-based oligomeric links, present at only 5 mol % of the polymer linkers in a three-dimensional network. The actuation process results in an overall reversible contraction of a family of hydrogels, down to 35% of their original volume in the first 25 min and ultimately to 9% after a few hours, even while remaining submerged in water. The mechanism of contraction starts with a decrease in electrostatic repulsion upon chemical reduction, leading to a loss of counterions and intramolecular self-assembly of the main-chain viologen subunits. The overall mode of actuation takes place relatively quickly in comparison to hydrogels of similar size, and the rate of contraction is accelerated as higher molecular weight oligoviologen links are implemented. The contraction process ultimately leads to a 2-fold increase in elasticity of the material, and upon exposure to oxygen and water, the hydrogels quickly oxidize and regain their original size and mechanical properties, thus resulting in a reversible actuation process that is capable of lifting objects which are 5–6 times heavier than the contracted hydrogel itself.

Two-dimensional polymers (2DPs), in the form of layered 2D covalent organic frameworks (COFs), are promising candidates for adsorbent-based separations because their pore sizes, shapes, functionalities, and interlayer stacking arrangements can be tuned by modifying their building blocks. Recently, high-quality single crystals of two 2D COFs exhibited distinct and improved separation characteristics in the gas chromatography (GC) separation of benzene and cyclohexane relative to polycrystalline samples of the same materials. These surprising findings motivate the present study, in which inverse pulse gas chromatography (IGC) was used to characterize the dispersive and specific adsorption properties of the surfaces of single-crystalline and polycrystalline TAPPy-PDA COFs for the separation of linear n-alkanes as well as a series of standard polar probes. Major differences in separation behavior were again observed that provide insight into how analytes interact with the single-crystalline and polycrystalline 2D COFs. A polarity study based on McReynolds constants revealed the nonpolar nature of the single-crystalline TAPPy-PDA COF, whereas the polycrystalline TAPPy-PDA COF surface was found to have a slightly polar character. Three common approaches to calculating the specific interaction parameter, I sp, were tested to examine their validity in the context of 2D COFs, revealing that the single-crystalline TAPPy-PDA COF possessed an electron donor character that we attribute to the imine nitrogen atoms inside the well-defined pore channels. In contrast, the polycrystalline TAPPy-PDA COF showed a relative electron acceptor character, which may be more heavily influenced by interactions between the analytes and dangling bonds or functionalities at grain boundaries. These findings provide a quantitative comparison of 2D COF materials quality by determining the acid–base interactions (represented by the electron donor–acceptor properties), polarity, and other physiochemical parameters. Furthermore, these results indicate the importance of establishing high materials quality for 2D COF samples prior to establishing rigorous structure–property relationships for separation performance.

Conditions for which imine-linked 2D COF polymerizations are temperature-sensitive are identified that enable a dissolution/repolymerization process akin to molecular recrystallization.

Supramolecular polymers are compelling platforms for the design of stimuli-responsive materials with emergent functions. Here, we report the assembly of an amphiphilic nanotube for Li-ion conduction that exhibits high ionic conductivity, mechanical integrity, electrochemical stability, and solution processability. Imine condensation of a pyridine-containing diamine with a triethylene glycol functionalized isophthalaldehyde yields pore-functionalized macrocycles. Atomic force microscopy, scanning electron microscopy, and in solvo X-ray diffraction reveal that macrocycle protonation during their mild synthesis drives assembly into high-aspect ratio (>103) nanotubes with three interior triethylene glycol groups. Electrochemical impedance spectroscopy demonstrates that lithiated nanotubes are efficient Li+ conductors, with an activation energy of 0.42 eV and a peak room temperature conductivity of 3.91 ± 0.38 × 10–5 S cm–1. 7Li NMR and Raman spectroscopy show that lithiation occurs exclusively within the nanotube interior and implicates the glycol groups in facilitating efficient Li+ transduction. Linear sweep voltammetry and galvanostatic lithium plating-stripping tests reveal that this nanotube-based electrolyte is stable over a wide potential range and supports long-term cyclability. These findings demonstrate how the coupling of synthetic design and supramolecular structural control can yield high-performance ionic transporters that are amenable to device-relevant fabrication, as well as the technological potential of chemically designed self-assembled nanotubes.

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<p>Supramolecular polymers are compelling platforms for the design of stimuli-responsive materials with emergent functions. Here, we report the assembly of an amphiphilic nanotube for Li-ion conduction that exhibits high ionic conductivity, mechanical integrity, electrochemical stability, and solution processability. Imine condensation of a pyridine-containing diamine with a triethylene glycol functionalized isophthalaldehyde yields pore-functionalized macrocycles. Atomic force microscopy, scanning electron microscopy, and <i>in solvo</i> X-ray diffraction reveal that macrocycle protonation under their mild synthetic conditions drives assembly into high-aspect ratio (>10³) nanotubes with three interior triethylene glycol groups. Electrochemical impedance spectroscopy demonstrates that lithiated nanotubes are efficient Li⁺ conductors, with an activation energy of 0.42 eV and a peak room temperature conductivity of 3.91 × 10^-5 S cm^-1. ⁷Li NMR and Raman spectroscopy demonstrate that lithiation occurs exclusively within the nanotube interior and implicates the glycol groups in facilitating efficient Li⁺ transduction. Linear sweep voltammetry and galvanostatic lithium plating-stripping tests reveal that this nanotube-based electrolyte is stable over a wide potential range and supports long-term cyclability. These findings demonstrate how coupling synthetic design and supramolecular structural control can yield high-performance ionic transporters that are amenable to device relevant fabrication. More broadly, these results demonstrate the technological potential of chemically designed self-assembled nanotubes. </p>

<p>Supramolecular polymers are compelling platforms for the design of stimuli-responsive materials with emergent functions. Here, we report the assembly of an amphiphilic nanotube for Li-ion conduction that exhibits high ionic conductivity, mechanical integrity, electrochemical stability, and solution processability. Imine condensation of a pyridine-containing diamine with a triethylene glycol functionalized isophthalaldehyde yields pore-functionalized macrocycles. Atomic force microscopy, scanning electron microscopy, and <i>in solvo</i> X-ray diffraction reveal that macrocycle protonation under their mild synthetic conditions drives assembly into high-aspect ratio (>10³) nanotubes with three interior triethylene glycol groups. Electrochemical impedance spectroscopy demonstrates that lithiated nanotubes are efficient Li⁺ conductors, with an activation energy of 0.42 eV and a peak room temperature conductivity of 3.91 × 10^-5 S cm^-1. ⁷Li NMR and Raman spectroscopy demonstrate that lithiation occurs exclusively within the nanotube interior and implicates the glycol groups in facilitating efficient Li⁺ transduction. Linear sweep voltammetry and galvanostatic lithium plating-stripping tests reveal that this nanotube-based electrolyte is stable over a wide potential range and supports long-term cyclability. These findings demonstrate how coupling synthetic design and supramolecular structural control can yield high-performance ionic transporters that are amenable to device relevant fabrication. More broadly, these results demonstrate the technological potential of chemically designed self-assembled nanotubes. </p>