Directed molecular self-assembly (DMSA) has emerged as a promising approach to achieve spatial organization of materials from molecular to macroscopic length scale, showing enticing applications in, e.g., molecular robots, [1] microelectronics, [2] and energy materials. [3] In recent years, some strategies toward DMSA have been developed. For instance, the employment of self-assembly systems that are sensitive to external stimuli such as light, [4] enzymatic action, [5] pH, [6] and nucleation seeds, [7] has led to DMSA by controlling the spatial distribution of these stimuli. Another example of DMSA is achieved by reaction-diffusion, [8] i.e., molecular reactants are separately distributed in space and allowed to react after meeting by diffusion, leading to local self-assembly at a certain preprogrammed location. Despite the recent progress, a major challenge for Herein, the micropatterning of supramolecular gels with oriented growth direction and controllable spatial dimensions by directing the self-assembly of small molecular gelators is reported. This process is associated with an acid-catalyzed formation of gelators from two soluble precursor molecules. To control the localized formation and self-assembly of gelators, micropatterned poly(acrylic acid) (PAA) brushes are employed to create a local and controllable acidic environment. The results show that the gel formation can be well confined in the catalytic surface plane with dimensions ranging from micro-to centimeter. Furthermore, the gels show a preferential growth along the normal direction of the catalytic surface, and the thickness of the resultant gel patterns can be easily controlled by tuning the grafting density of PAA brushes. This work shows an effective "bottom-up" strategy toward control over the spatial organization of materials and is expected to find promising applications in, e.g., microelectronics, tissue engineering, and biomedicine.
Micropatterned Supramolecular Gelsfurther advance lies in control of the spatial parameters of the self-assembled structures. [9] We have recently proposed a catalysisresponsive supramolecular self-assembly system that involves an in situ formation of hydrazone-based gelator (HA 3 ) from water-soluble tris-hydrazide (H) and aldehyde (A) (Figure 1). The rate of HA 3 formation can be remarkably increased by acid catalysis, thereby providing a handle to control subsequent gelation. [10] Using this gelator system, we previously achieved surface confined formation of gels using surfaces modified with a monolayer of sulfonic acid that act as a catalyst for gelator formation. [11] That system has, however, several limitations which hamper further progress. First, the spatial resolution of gel formation along the surface plane is limited, presumably by the low interfacial catalytic activity. And second, the continuous growth of the gels along the surface normal to form 3D objects is hampered by adhesion of gel fibers to the surface, which blocks the influx of reagents to the catalytic surface. With these problem...