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Abstract Bottom‐up self‐organization of unordered molecules into ordered, spatiotemporal patterns of complex structures through non‐equilibrium reaction–diffusion (RD) processes is ubiquitous in nature across all scales. Unlike many RD processes that typically lead to transient patterns, periodic precipitation reactions governed by the Liesegang phenomenon are distinguished by the formation of stable, permanent structures. This unique characteristic makes them valuable tools in the development of hierarchical multifunctional materials, an area that has seen significant progress in recent decades. This review summarizes the fundamental aspects of the Liesegang phenomenon, focusing on the key characteristics, compositional features, inherent properties, and formation mechanisms of Liesegang patterns in chemical systems, while also highlighting their occurrence in biological and geological settings. We discuss recent advancements in applying periodic precipitation to address global challenges in microelectronics and environmental monitoring, concluding with a forward‐looking perspective on the promising future applications of the Liesegang periodic precipitation in materials science, nanotechnology, medicine, and environmental engineering. 

Abstract This paper describes the use of a highly crystalline conductive 2D copper₃(hexaiminobenzene)₂(Cu₃(HIB)₂) as an ultrasensitive (limit of detection of 1.8 part‐per‐billion), highly selective, reversible, and low power chemiresistive sensor for nitric oxide (NO) at room temperature. The Cu₃(HIB)₂‐based sensors retain their sensing performance in the presence of humidity, and exhibit strong signal enhancement towards NO over other highly toxic reactive gases, such as NO₂, H₂S, SO₂, NH₃, CO, as well as CO₂. Mechanistic investigations of the Cu₃(HIB)₂‐NO interaction through spectroscopic analyses and density functional theory revealed that the Cu‐bis(iminobenzosemiquinoid) moieties serve as the binding sites for NO sensing, while the Ni‐bis(iminobenzosemiquinoid) MOF analog shows no noticeable response to NO. Overall, these findings provide a significant advance in the development of crystalline metal‐bis(iminobenzosemiquinoid)‐based conductive 2D MOFs as highly sensitive, selective, and reversible sensing materials for the low‐power detection of toxic gases. 

Abstract Controlled modulation of electronic and magnetic properties in stimuli‐responsive materials provides valuable insights for the design of magnetoelectric or multiferroic devices. This paper demonstrates the modulation of electrical and magnetic properties of a semiconductive, paramagnetic metal−organic framework (MOF) Cu₃(C₆O₆)₂with small gaseous molecules, NH₃, H₂S, and NO. This study merges chemiresistive and magnetic tests to reveal that the MOF undergoes simultaneous changes in electrical conductance and magnetization that are uniquely modulated by each gas. The features of response, including direction, magnitude, and kinetics, are modulated by the physicochemical properties of the gaseous molecules. This study advances the design of multifunctional materials capable of undergoing simultaneous changes in electrical and magnetic properties in response to chemical stimuli. 

Abstract Owing to high modularity and synthetic tunability, metal–organic frameworks (MOFs) on textiles are poised to contribute to the development of state‐of‐the‐art wearable systems with multifunctional performance. While these composite materials have demonstrated promising functions in sensing, filtration, detoxification, and biomedicine, their applicability in multifunctional systems is only beginning to materialize. This review highlights the multifunctionality and versatility of MOF‐integrated textile systems. It summarizes the operational goals of MOF@textile composites, encompassing sensing, filtration, detoxification, drug delivery, UV protection, and photocatalysis. Building upon these recent advances, this review concludes with an outlook on emerging opportunities for the diverse applications of MOF@textile systems in the realm of smart wearables. 

Abstract The use of engineered cells, tissues, and organs has the opportunity to change the way injuries and diseases are treated. Commercialization of these groundbreaking technologies has been limited in part by the complex and costly nature of their manufacture. Process-related variability and even small changes in the manufacturing process of a living product will impact its quality. Without real-time integrated detection, the magnitude and mechanism of that impact are largely unknown. Real-time and non-destructive sensor technologies are key for in-process insight and ensuring a consistent product throughout commercial scale-up and/or scale-out. The application of a measurement technology into a manufacturing process requires cell and tissue developers to understand the best way to apply a sensor to their process, and for sensor manufacturers to understand the design requirements and end-user needs. Furthermore, sensors to monitor component cells’ health and phenotype need to be compatible with novel integrated and automated manufacturing equipment. This review summarizes commercially relevant sensor technologies that can detect meaningful quality attributes during the manufacturing of regenerative medicine products, the gaps within each technology, and sensor considerations for manufacturing. 

A conductive MXene (Ti₃C₂T_x) integrated with 2D Ni₃(HITP)₂-MOFvia in situsynthesis enhances active site exposure, boosting electrocatalytic HER performance for efficient, sustainable hydrogen production. 

This paper describes the scalable fabrication of smart electronic textiles (e-textiles) capable of simultaneous sensing, filtration, and detoxification of sulfur dioxide (SO2). The templated method converts pre-deposited copper metal into copper hydroxide, followed by conversion into a copper-based hexahydroxytriphenylene metal-organic framework (MOF) (Cu3(HHTP)2), to afford a large-area (10 × 10 cm2) conductive coating (sheet resistance = 0.1–0.3 MΩ). The resulting e-textiles achieve sensing (theoretical limit of detection [LOD] of 0.43 ppm), filtration (adsorption uptake of 1.9 and 0.83 mmol g−1 for MOF powder and MOF/textile, respectively, at 1 bar and 298 K), and detoxification (redox conversion of SO2 gas into solid sulfate) due to the selective material-analyte interactions. This scalable method for generating e-textiles is a promising approach for the fabrication of smart membrane materials with multifunctional performance characteristics. 

Metallophthalocyanine (MPc)-linked conductive two-dimensional (2D) metal−organic frameworks (MOFs) hold tremendous promise as modular 2D materials in sensing, catalysis, and energy-related applications due to their combinatory bimetallic system from the MPc core and bridging metal nodes, endowing them with high electrical conductivity and multifunctionality. Despite significant advances, there is a gap in fundamental understanding regarding the periodic effects of metal nodes on the structural properties of MP-linked 2D MOFs. Herein, we report a series of highly crystalline MOFs wherein copper phthalocyanine (CuPc) is linked with Ni, Cu, and Zn nodes (CuPc-O-M, M: Ni, Cu, Zn). The prepared CuPc-O-M MOFs exhibit p-type semiconducting properties with an exceptionally high range of electrical conductivity. Notably, the differences in the 3d orbital configurations of the Ni, Cu, and Zn nodes in CuPc-O-M MOFs lead to perturbations of the interlayer stacking patterns of the 2D framework materials, which ultimately affect material properties, such as semiconducting band gaps and charge transport within the framework. The Cu2+ (3d9) metal node within the eclipsed interlayer stacking of CuPc-O-Cu MOF demonstrates excellent charge transport, which results in the smallest band gap of 1.14 eV and the highest electrical conductivity of 9.3 S m−1, while the Zn2+ (3d10) metal node within CuPc-O-Zn results in a slightly inclined interlayer stacking, leading to the largest band gap of 1.27 eV and the lowest electrical conductivity of 2.9 S m−1. These findings form an important foundation in the strategic molecular design of this class of materials for multifaceted functionality that builds upon the electronic properties of these materials. 

The development of portable electronic chemical sensors is key to solving a number of challenges, including monitoring environmental and industrial hazards, as well as understanding and improving human health. Framework materials possess several desirable characteristics that make them well-suited for electroanalytical applications, including high surface area, atomically precise distribution of active sites, and tunable properties that can be leveraged through modular reticular chemistry. This review highlights the emergence of conductive framework materials as active components in electrically transduced chemical sensors, including the development of new materials for the detection of a wide variety of analytes in both gas and liquid phase. The efforts to gain fundamental understanding of the molecular interactions and sensing mechanisms between framework materials and analytes are described, along with applications of these materials on portable and flexible substrates. The review suggests areas for further study, including the study of material−analyte interactions at the molecular level and the continued development of scalable methods for the integration of framework materials into low-power, portable sensing devices. 

Self-organization under out-of-equilibrium conditions is ubiquitous in natural systems for the generation of hierarchical solid-state patterns of complex structures with intricate properties. Efforts in applying this strategy to synthetic materials that mimic biological function have resulted in remarkable demonstrations of programmable self-healing and adaptive materials. However, the extension of these efforts to multifunctional stimuli-responsive solidstate materials across defined spatial distributions remains an unrealized technological opportunity. This paper describes the use of a nonequilibrium reaction−diffusion process to achieve the synthesis of a multifunctional stimuli-responsive electrically conductive metal−organic framework (cMOF) in a gelled medium with control over particle size and spatial periodicity on a macroscopic scale. Upon integration into chemiresistive devices, the resulting cMOF particles exhibit a size-dependent response toward hydrogen sulfide gas, as determined by their distinct surface-to-volume ratio, porosity, unique synthesis methodology, and unusual microcrystallite morphology compared to their counterparts obtained through bulk solution phase synthesis. Taken altogether, these achievements pave the way toward gaining access to functional nanomaterials with well-defined chemical composition, dimensions, and precisely tailored functions using far-from-equilibrium approaches.