Formation of spatially periodic patterns is a ubiquitous process in nature and man-made systems. Periodic precipitation is the oldest type of pattern formation, in which the formed colloid particles are self-assembled into a sequence of spatially separated precipitation zones in solid hydrogels. Chemical systems exhibiting periodic precipitation mostly comprise oppositely charged inorganic ions. Here, we present a new sub-group of this phenomenon driven by the diffusion and reaction of several transition metal cations (Zn 2+ , Co 2+ , Cd 2+ , Cu 2+ , Fe 2+ , Mn 2+ , and Ni 2+ ) with an organic linker (2-methylimidazole) producing periodic precipitation of zeolitic imidazolate frameworks. In some cases, the formed crystals reached the size of ∼50 μm showing that a gel matrix can provide optimal conditions for nucleation and crystal growth. We investigated the effect of the gel concentration and solvent composition on the morphology of the pattern. To support the experimental observations, we developed a reaction−diffusion model, which qualitatively describes the spatially periodic pattern formation.
Here we show a time-programmed and autonomous synthesis of zeolitic imidazole framework-8 (ZIF-8) using a methylene glycol−sulfite clock reaction. The induction period of the driving clock reaction, thus, the appearance...
The beat in physical systems is a transparent and well-understood phenomenon. It may occur in forced oscillatory systems and as a result of the interference of two waves of slightly different frequencies. However, in chemical systems, the realization of the latter type of the beat phenomenon has been lacking. Here we show that a periodic titration of acid and alkaline solutions with each other using programmable syringe pumps in a continuous stirred-tank reactor exhibits the beat phenomenon in the temporal pH oscillation pattern if the time periods of sinusoidal inflow rates of the reagents are slightly different. Interestingly, the frequency of the chemical beat pattern follows the well-known relationship from physics, namely the frequency of the beat is equal to the absolute value of the difference of the two wave frequencies. Based on our strategy, we can design and engineer non-autonomous pH oscillatory systems, in which the characteristics of the temporal oscillations (amplitude, time period) can easily and precisely be controlled by the experimental conditions such as the inflow rates and feed concentrations. The demonstrated phenomena can be exploited in practical applications, we use the non-autonomous pH oscillators to drive the reversible assembly and disassembly of pH-sensitive building blocks (oleic acid and gold nanoparticles), both highly relevant in nanotechnology and biomedical applications.
In the past decade, much effort has been devoted to using chemical clock-type reactions in material design and driving the self-assembly of various building blocks. Urea-urease enzymatic reaction has chemical pH clock behavior in an unbuffered medium, in which the induction time and the final pH can be programmed by the concentrations of the reagents. The urea-urease reaction can offer a new alternative in material synthesis, where the pH and its course in time are crucial factors in the synthesis. However, before using it in any synthesis method, it is important to investigate the possible effects of the reagents on the enzymatic reaction. Here we investigate the effect of the reagents of the zeolite imidazole framework-8 (zinc ions and 2-methylimidazole) on the urea-urease reaction. We have chosen the zeolite imidazole framework-8 because its formation serves as a model reaction for the formation of other metal–organic frameworks. We found that, besides the inhibition effect of the zinc ions which is well-known in the literature, 2-methylimidazole inhibits the enzymatic reaction as well. In addition to the observed inhibition effect, we report the formation of a hybrid urease-zinc-2-methylimidazole hybrid material. To support the inhibition effect, we developed a kinetic model which reproduced qualitatively the experimentally observed kinetic curves.
Strategies for designing autonomous oscillatory systems have gained much attention in the past few decades. A broadly accepted and used strategy for the generation of forced oscillations in the originally non-oscillatory subsystems is to couple a pH (driving) oscillator to a pH-sensitive substance (forced oscillatory subsystem) in a one-compartment system. The forced oscillatory subsystem comprises pH-sensitive components, which inevitably generate negative feedback and affect the characteristics of the driving oscillatory system. Here, we present a different approach by separating the driving and forced oscillatory systems into a two-compartment system using a silicone membrane, and the forced oscillations of the absorbance of a pH-sensitive chemical species (methyl red dye) were realized by the transport of carbon dioxide through the membrane generated periodically by the driving pH oscillator. The transported carbon dioxide produced the pH change in the separated compartment by carbon dioxide−hydrogen carbonate−carbonate equilibria and created forced oscillations of a pHsensitive chemical species manifested in the oscillation of its absorbance at a fixed wavelength. This approach avoids any feedback from the forced oscillatory system to the driving system via the cross-membrane transport of the chemical species from the forced to the driving oscillatory system. Additionally, we present that this carbon dioxide coupling to the methyl red dye can be used to estimate the carbon dioxide content in both liquid and gas phases.
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