Structural Building Blocks Research Articles

Programmable Hydrogel-Based Soft Robotics via Encoded Building Block Design

Hydrogels have revolutionized the field of soft robotics with their ability to provide dynamic and programmable responses to different stimuli, enabling the fabrication of highly adaptable and flexible robots. This continual development holds significant promise for applications in biomedical devices, active implants, and sensors due to the biocompatibility of hydrogels. Actuation in hydrogel-based soft robotics relies on variations in material properties, structural design, or a combination of both to generate desired movements and behaviors. While such traditional approaches enable hydrogel actuation, they often rely on complex material design, bringing challenges to hydrogel fabrication and hindering practical use. Therefore, this work seeks to present a simplified and versatile approach for fabricating programmable single-component hydrogel-based soft robotics using an encoded building block design concept and 3D printing. A series of structural building blocks have been designed to achieve various actuation characteristics, including the direction, degree, and kinetics of actuation. By assembling these building blocks into various configurations, a broader range of actuation responses can be encoded, allowing for the fabrication of versatile, programmable soft robotics using a single uniform material through vat photopolymerization 3D printing. This approach enables adaptation to a wide range of applications, providing highly customizable encoding designs.

Mechanism of sucrose improving the mechanical characteristics of foams stabilized by soy protein isolate/gellan gum/guar gum ternary complex

Sucrose shows the potential of stabilizing foam system. This study systematically evaluated the mechanism by which sucrose improved foaming properties and mechanical characteristics of foams stabilized by soy protein isolate/gellan gum/guar gum ternary complex. Results showed that sucrose could bond to the surface of ternary complex or self-aggregate within the continuous phase, resulting in the neutralization of charges (nearly zero) and an increase in particle size (up to 62.54 μm). The addition of 30 % sucrose reinforced foam system with an increased foamability (305.99 %) but a longer foaming time (10 min) during foaming process. Moreover, the mechanical characteristics, including hardness, elastic strength (Power-law constant) and solid characteristic (frequency exponent), were also significantly enhanced to 1.26 N, 354.7956 and 2.5873, respectively, which were 1.65, 1.94 and 1.11 times than those of foams without sucrose. The microscopic mechanism lied in the reduced water freedom degree caused by sucrose, which generated a compact structural network around bubbles for providing a stable and stiff structure to foams. These findings will provide clear theoretical guidance for regulating mechanical characteristics of aerated foods by using sucrose as structural building blocks.

Dual Redox-active Covalent Organic Framework-based Memristors for Highly-efficient Neuromorphic Computing.

Organic memristors based on covalent organic frameworks (COFs) exhibit significant potential for future neuromorphic computing applications. The preparation of high-quality COF nanosheets through appropriate structural design and building block selection is critical for the enhancement of memristor performance. In this study, a novel room-temperature single-phase method was used to synthesize Ta-Cu3 COF, which contains two redox-active units: trinuclear copper and triphenylamine. The resultant COF nanosheets were dispersed through acid-assisted exfoliation and subsequently spin-coated to fabricate a high-quality COF film on an indium tin oxide (ITO) substrate. The synergistic effect of the dual redox-active centers in the COF film, combined with its distinct crystallinity, significantly reduces the redox energy barrier, enabling the efficient modulation of 128 non-volatile conductive states in the Al/Ta-Cu3 COF/ITO memristor. Utilizing a convolutional neural network (CNN) based on these 128 conductance states, image recognition for ten representative campus landmarks was successfully executed, achieving a high recognition accuracy of 95.13 % after 25 training epochs. Compared to devices based on binary conductance states, the memristor with 128 conductance states exhibits a 45.56 % improvement in recognition accuracy and significantly enhances the efficiency of neuromorphic computing.

Dual Redox‐active Covalent Organic Framework‐based Memristors for Highly‐efficient Neuromorphic Computing

Organic memristors based on covalent organic frameworks (COFs) exhibit significant potential for future neuromorphic computing applications. The preparation of high‐quality COF nanosheets through appropriate structural design and building block selection is critical for the enhancement of memristor performance. In this study, a novel room‐temperature single‐phase method was used to synthesize Ta‐Cu3 COF, which contains two redox‐active units: trinuclear copper and triphenylamine. The resultant COF nanosheets were dispersed through acid‐assisted exfoliation and subsequently spin‐coated to fabricate a high‐quality COF film on an indium tin oxide (ITO) substrate. The synergistic effect of the dual redox‐active centers in the COF film, combined with its distinct crystallinity, significantly reduces the redox energy barrier, enabling the efficient modulation of 128 non‐volatile conductive states in the Al/Ta‐Cu3 COF/ITO memristor. Utilizing a convolutional neural network (CNN) based on these 128 conductance states, image recognition for ten representative campus landmarks was successfully executed, achieving a high recognition accuracy of 95.13% after 25 training epochs. Compared to devices based on binary conductance states, the memristor with 128 conductance states exhibits a 45.56% improvement in recognition accuracy and significantly enhances the efficiency of neuromorphic computing.

Covalent Transition Metal Borosilicides: Reaction Pathways in Molten Salts for Water Oxidation Electrocatalysis.

The properties of transition metal borides and silicides are intimately linked to the covalent character of the chemical bonds within their crystal structures. Bringing boron and silicon together within metal borosilicides can then engender different competing covalent networks and complex charge distributions. This situation results in unique structures and atomic environments, which can impact charge transport and catalytic properties. Metal borosilicides, however, hold the status of unusual exotic species, difficult to synthesize and with poor knowledge of their properties. Our strategy consists of developing a redox pathway to synthesize transition metal borosilicides in inorganic molten salts as high-temperature solvents. By studying the formation of Ni6Si2B, Co4.75Si2B, Fe5SiB2, and Mn5SiB2 with in situ X-ray diffraction, we highlight how new reaction routes, maintaining covalent structural building blocks, draw a general scheme of their formation. This pathway is driven by the covalence of the chemical bonds within the boron coordination framework. Next, we demonstrate high efficiency for water oxidation electrocatalysis, especially for Ni6Si2B. We ascribe the strongly increased resistance to corrosion, high stability, and electrocatalytic activity of the Ni6Si2B-derived material to three factors: (1) the two entangled boron and silicon covalent networks; (2) the ability to codope with boron and silicon an in situ generated catalytic layer; and (3) a rare electron enrichment of the transition metal by back-donation from boron atoms, previously unknown within this compound family. With this work, we then unveil a new chemical dimension for Earth-abundant water oxidation electrocatalysts by bringing to light a new family of materials.

Self-Assembly of Chiral Porous Metal-Organic Polyhedra from Trianglsalen Macrocycles.

Metal-organic polyhedra (MOPs) can exhibit tunable porosity and functionality, suggesting potential for applications such as molecular separations. MOPs are typically constructed by the bottom-up multicomponent self-assembly of organic ligands and metal ions, and the final functionality can be hard to program. Here, we used trianglsalen macrocycles as preorganized building blocks to assemble octahedral-shaped MOPs. The resultant MOPs inherit most of the preorganized properties of the macrocyclic ligands, including their well-defined cavities and chirality. As a result, the porosity in the MOPs could be tuned by modifying the structure of the macrocycle building blocks. Using this strategy, we could systematically enlarge the size of the MOPs from 26.3 to 32.1 Å by increasing the macrocycle size. The family of MOPs shows experimental surface areas of up to 820 m2/g, and they are stable in water. One of these MOPs can efficiently separate the rare gases Xe from Kr because the prefabricated macrocyclic windows of MOPs can be modified to sit at the Xe/Kr size cutoff range.

Regioisomerism in Thienothiophene-Based Covalent Organic Frameworks─A Tool for Band-Gap Engineering.

The craft of tuning optical properties is well-established for crystalline inorganic and hybrid solids. However, a far greater challenge is to tune the optical properties of organic materials systematically by design. We now introduce a synthesis concept that enables us to alter the optical properties of crystalline covalent organic frameworks (COFs) systematically using isomeric structures of thienothiophene-based building blocks (T23/32T) combined with a variety of tetratopic aromatic amines, e.g., the Wurster moiety (W-NH2). This concept is demonstrated for the synthesis of COFs in bulk and film forms and provides highly crystalline and porous isomeric COFs featuring predesigned photophysical properties. The band gap of the framework can be tuned continuously and precisely by chemically doping the pristine W23TT COF with its related constitutional isomer building block. Density-functional theory investigations of COF model compounds indicate that the extent of π-conjugation is among the key characteristics enabling the band-gap engineering.

Diabetic Retinopathy: Current Understanding, Mechanisms and Treatment Strategies

Researchers have been assuming about the possible connection between the eye and the central nervous system (CNS) for a considerable amount of time. This is primarily due to the fact that the eye is considered to be an extension of the brain, which is a reasonable assumption. The neural tube is the beginning of both structures, and neurons are the building blocks of both structures. Retinal ganglionic cells, also known as RGCs, are a specific type of cell that are found in the retina. These cells are responsible for receiving light signals from the environment around them and then transmitting them to photoreceptors, which are involved in the process of vision. The retina, which is found inside the eye, is responsible for converting light into electrical impulses, which are then sent to the brain through the optic nerve. Glaucoma, age-related macular degeneration (AMD), and diabetic retinopathy are only few of the eye illnesses that can be caused by chronic progressive neurodegeneration of the retina, which is more prevalent in older people. It is the elderly who are most likely to be affected by these eye disorders; nevertheless, younger people are also susceptible to them and may experience permanent vision loss or a reduction in their eyesight. In most cases, neurodegenerative disorders that are characteristic of CSN are characterised by common symptoms and a cause that is only partially understood. Although certain risk factors have been identified, they do not account for all instances. On the other hand, according to a number of studies, several illnesses of the central nervous system (CNS), such as Alzheimer's disease (AD) and Parkinson's disease (PD), which are responsible for a significant amount of mortality and morbidity on a global scale, display distinctive alterations at the ocular level. It is helpful to be aware of potential linkages in order to have a better understanding of the mechanics on which onset occurs. In addition, experts have not yet reached a consensus regarding the factors that are responsible for these various disorders. In this overview, the symptoms of ocular illnesses are discussed in detail, with a particular focus on the interaction between the brain and the eye. At some point in the future, a more in-depth understanding could be of assistance in the development of innovative treatments that could help reduce or prevent blindness and improve quality of life.

Characterization of Functional Biohybrid Materials Based on Saccharomyces Cerevisiae Biomass

Biohybrid materials and engineered living materials (ELMs) are a dynamic field of research at the interface of material science and synthetic biology. Recently, microorganisms have been described as both functional and structural building blocks of such materials. Dry materials with bacteria as structural building block have previously not been investigated for their ability to retain catalytic activity. Herein, it is shown that Saccharomyces cerevisiae biomass can act as a structural building block in dry, macroscopic materials while simultaneously providing functionality. A benign method for the preparation of both coatings and free‐standing, flexible films is presented. Notably, free‐standing films can be prepared solely from biomass and plasticizers without the need for other additives. During the process, the integrity of the cells and the catalytic activity within is preserved, which is demonstrated by biocatalytic H2O2 degradation. The film‐forming properties of S. cerevisiae biomass and the influence of plasticizing and polymeric additives on the mechanical properties are investigated in detail and compared to related materials. The work presented is a first step toward new, mechanically strong microorganism‐based functional coatings and films.

A Tandem Ring Closure and Nitrobenzene Reduction with Sulfide Provides an Improved Route to an Important Intermediate for the Anti-Tuberculosis Drug Candidate Sutezolid.

Sutezolid is an in-development thiomorpholine derivative of the FDA-approved tuberculosis (TB) treatment linezolid. Current synthetic routes for preparing sutezolid start with thiomorpholine as a key structural building block; unfortunately, this material was identified as a major cost driver for the API, which will limit the potential uptake of this treatment in lower income regions. In this work, an alternative, lower-cost synthetic strategy to a known p-phenylenediamine intermediate to sutezolid has been demonstrated. The key step in this process is the construction of the thiomorpholine ring by a nucleophilic sulfide ring closure on an activated bis(2-hydroxyethyl)-functionalized aniline, which was in turn made by reaction of 3,4-difluoronitrobenzene and diethanolamine. This sulfide treatment has the added benefit of affecting a Zinin reduction of the nitro functional group, which alleviates the need for the transition metal reduction used in previous routes. After optimization, this key reaction was able to provide the desired aniline intermediate in yields between 65 and 80% and, after a standard charcoal treatment, purity of >94%. Initial demonstrations of the full 3-step strategy were successfully conducted on scales up to 100 g with overall yields of 53-68%. This preliminary work will serve as the foundation for a broader low-cost redesign of the sutezolid synthetic process.

Expanding the Reticular Chemistry Building Block Library toward Highly Connected Nets: Ultraporous MOFs Based on 18-Connected Ternary, Trigonal Prismatic Superpolyhedra.

The chemistry of metal-organic frameworks (MOFs) continues to expand rapidly, providing materials with diverse structures and properties. The reticular chemistry approach, where well-defined structural building blocks are combined together to form crystalline open framework solids, has greatly accelerated the discovery of new and important materials. However, its full potential toward the rational design of MOFs relies on the availability of highly connected building blocks because these greatly reduce the number of possible structures. Toward this, building blocks with connectivity greater than 12 are highly desirable but extremely rare. We report here the discovery of novel 18-connected, trigonal prismatic, ternary building blocks (tbb's) and their assembly into unique MOFs, denoted as Fe-tbb-MOF-x (x: 1, 2, 3), with hierarchical micro- and mesoporosity. The remarkable tbb is an 18-c supertrigonal prism, with three points of extension at each corner, consisting of triangular (3-c) and rectangular (4-c) carboxylate-based organic linkers and trigonal prismatic [Fe3(μ3-Ο)(-COO)6]+ clusters. The tbb's are linked together by an 18-c cluster made of 4-c ligands and a crystallographically distinct Fe3(μ3-Ο) trimer, forming overall a 3-D (3,4,4,6,6)-c five nodal net. The hierarchical, highly porous nature of Fe-tbb-MOF-x (x: 1, 2, 3) was confirmed by recording detailed sorption isotherms of Ar, CH4, and CO2 at 87, 112, and 195 K, respectively, revealing an ultrahigh BET area (4263-4847 m2 g-1) and pore volume (1.95-2.29 cm3 g-1). Because of the observed ultrahigh porosities, the H2 and CH4 storage properties of Fe-tbb-MOF-x were investigated, revealing well-balanced high gravimetric and volumetric deliverable capacities for cryoadsorptive H2 storage (11.6 wt %/41.4 g L-1, 77 K/100 bar-160 K/5 bar), as well as CH4 storage at near ambient temperatures (367 mg g-1/160 cm3 STP cm-3, 5-100 bar at 298 K), placing these materials among the top performing MOFs. The present work opens new directions to apply reticular chemistry for the construction of novel MOFs with tunable porosities based on contracted or expanded tbb analogues.

Multi-responsive fluorescent covalent organic framework based on phenanthro[9,10-d]imidazole moiety for relayed detection of Cu2+/Al3+ followed by PO43− and its applications

Designation and application of the luminescent COFs remains a tough challenge and imperative task because of their limited building block structure, the unavailable raw material, the tedious modification process, or the onefold sensing function. Herein, a fluorinated fluorescent covalent organic framework containing a phenanthro[9,10-d]imidazole moiety [TFPB-PI(F)–COF] had been successfully designed for Cu2+ and Al3+ detection relayed by PO43−. TFPB-PI(F)–COF serves as a highly sensing platform with the superior selectivity toward Cu2+ and Al3+ based on the coordination interaction and the chelation enhancement quenching (CHEQ) effect, and the detection limits are 2.3 and 4.2 nmol L−1, respectively. Subsequently, accompanied with the gradual introduction of PO43−, TFPB-PI(F)–COF@M (Cu2+ and Al3+) complex is wrecked due to electrostatic attraction with the detection limit of 10 nmol L−1, led to the fluorescent recovery of TFPB-PI(F)–COF. Furthermore, the reversible fluorescent performance by the mode of “on–off–on” is perfect. Besides, the established relayed method can be successfully employed for the analysis of Cu2+ and Al3+ in environmental water samples with recoveries of 96.00–104.63 % and RSD <4.62 %. Moreover, the fluorescent images for the visual detection of Cu2+ is also fabricated in living HeLa cells, which provides a modest contribution and an effective platform to the biological analysis.

Revolutionizing Construction - Harnessing the Power of Brick Kiln Dust as a Sustainable Cement Alternative

Abstract: The concrete industry stands as the preeminent colossus within the realm of industrial domains. The building and construction industry, a primary contributor to environmental issues, is constantly seeking innovative approaches to enhance sustainability. Bricks forming the building block of the building structures are being manufactured worldwide. A substantial volume of fine particle dust is produced during the production step in the form of leftovers. This dust is the by-product of firing clay bricks at high temperature and the residual ash of the induced fuel. Brick Kiln dust poses environmental challenge due to disposal complexities. Commonly, the only established method of disposal is through land-filling, which can contribute to environmental concerns. This experimental investigation explores the transformative potential of utilizing Brick Kiln Dust as sustainable alternative to convention cement. BKD, obtained from a kiln situated in District Budgam, Jammu and Kashmir, was incorporated into concrete mixes at varying proportions (5%, 10%, 15%, 20%, and 25%) as a replacement for cement. Through the use of rigorous testing on mix samples, this study examined the effect of BKD on concrete workability as well as compressive and split tensile strength. The results were compared to identify the optimal dosage for achieving a balance between reduced cement consumption and maintaining structural integrity. The results showed that adding BKD not only significantly decreased the amount of cement used, but also demonstrated that it was a workable and sustainable substitute. This research not only addresses the environmental concern associated with BKD but also contributes to the ongoing efforts to develop sustainable construction practices.

Two Short-Wave UV Antimony(III) Sulfates Exhibiting Large Birefringence.

In the present work, we have successfully obtained two new UV antimony-based sulfates, NH4Sb(SO4)2 and Ca2Sb2O(SO4)4, by a conventional hydrothermal method. Interestingly, both compounds share similar structural building blocks, such as SbO4 seesaws and SO4 tetrahedra, yet they endow discrepant birefringence values measured at 546 nm with values of 0.150 and 0.114, respectively, owing to the different distortions of the SbO4 groups with SCALP electrons. Moreover, both compounds display large band gaps (4.32 and 4.43 eV, respectively), so they can be used as short-wavelength UV birefringent materials. Moreover, NH4Sb(SO4)2 is a noncentrosymmetric compound, showing a frequency doubling effect of 0.2 × KDP. Detailed structural analyses and calculations confirm the source of superior optical performance and the reasons for the different birefringence of the two compounds. This work provides ideas for the following discovery of antimony-based optical materials with excellent properties.

The spiral of plants and soil in the cycle of life

This is not an article, but rather an account of a meeting that took place between two naturalists who had not seen each other for a few years and who freely exchanged their doubts and matured lines of thought. It is a provocative dialogue between the author of this article and Sandro Pignatti on natural evolution, considering the soil as a living matrix in which recycling of organic matter (including DNA) takes place. We can also interpret it as an attempt to merge the points of view of vegetation and soil ecologists, in order to revive the discussion on natural evolution. We think we understand it, but we don’t. We discussed the following topics: 1) the relationship between phytosociology and plant ecology; 2) the soil as an individual or as an ecosystem’s digestive machinery; 3) the hypothesis of a complemental geological (long-term) flow of DNA fragments in relation to the recycling process that takes place in the soil. Past and recent research in the fields of biology and evolution highlights a functional and primordial collaboration between living beings in the exploitation of natural resources. In this process that ultimately is life, soil plays a crucial role because it is cyclically and progressively renewed and enriches the sources of structural building blocks. The purpose of this story is to encourage us to reflect on the meaning of life, considering the functional contribution of death, which we perhaps mistakenly call “biodegradation”.

Thermal Property of Fullerene Fibers: One-DimensionalMaterial with Exceptional Thermal Performance.

The recent groundbreaking achievement in the synthesis of large-sized single crystal C60 monolayer, which is covalently bonded in a plane using C60 as building blocks. The asymmetric lattice structure endows it with anisotropic phonon modes and conductivity. If these C60 are arranged in form of 1D fiber, the improved manipulation of phonon conduction along the fiber axis could be anticipated. Here, thermal properties of C60-fiber, including thermal transfer along the C60-fiber axis and across the interlayer interface are investigated using molecular dynamic simulations. Taking advantage of the distinctively hollow spherical structure of C60 building blocks, the spherical structure deformation and encapsulation induced thermal reduction can be up to 56% and 80%, respectively. By applying external electronic fields in H2O@C60 model, its thermal conductivity decreases up to 60%, which realizes the contactless thermal regulation. ln particular, the thermal rectification phenomenon is discovered by inserting atoms/molecules in C60 with a rational designed mass-gradient, and its maximum thermal rectification factor is predicted to ≈45%. These investigations aim to achieve effective regulation of the thermal conductivity of C60-fibers. This work showcases the potential of C60-fiber in the realms of thermal management and thermal sensing, paving the way to C60-based functional materials.

Die Serie caesiumhaltiger Thioarsenate(V) der Lanthanoide vom Formeltyp Cs3 Ln[AsS4]2 mit Ln = La–Nd und Sm

Abstract Cesium-containing thioarsenates(V) of lanthanoids with the composition Cs3 Ln[AsS4]2 can be prepared for Ln = La–Nd and Sm by the oxidation of the lanthanoid metals in the presence of orpiment (As2S3), cesium sesquisulfide (Cs2S3) and elemental sulfur (S). The reaction mixtures were handled under argon atmosphere and heated in fused silica ampoules to a moderate reaction temperature of 500 °C. Single crystals of this Cs3 Ln[AsS4]2 series appear as yellowish, transparent rods that are not stable to moist air and water. Their monoclinic crystal structure was determined from single-crystal X-ray diffraction data. The cesium-containing thioarsenates(V) Cs3 Ln[AsS4]2 with Ln = La–Nd and Sm crystallize isotypically with Rb3Sm[PS4]2 in the non-centrosymmetric monoclinic space group P21 with Z = 2. The lattice parameters range between a = 997–1015 pm, b = 699–703 pm, c = 1192–1195 pm and β = 90.2–90.4°. There are two crystallographically different As5+ cations and one unique Ln 3+ cation present, all coordinated by sulfur anions. Tetrahedral [AsS4]3− anions form two functionally different units working either as bridging units between three Ln 3+ cations or as terminal ligands for Ln 3+. [LnS8]13− polyhedra form ∞ 1 { [ Ln S 2 / 2 v S 6 / 1 t ] 11 − } ${}_{\infty }^{1}\left\{{[\mathit{Ln}{\mathrm{S}}_{2/2}^{\mathrm{v}}{\mathrm{S}}_{6/1}^{\mathrm{t}}]}^{11-}\right\}$ chains propagating along [010], which are separated by Cs+ cations with coordination numbers as high as C.N. = 9, 10 and 11. Surprisingly, the eighth interatomic distance d(Ln–S3) does not follow the lanthanoid contraction, but increases with decreasing ionic radius, changing the coordination polyhedron of Ln 3+ from a bicapped to a monocapped trigonal prism upon the transition from Nd to Sm, and causing a structural break in the crystal structure of this series. The results of Raman spectroscopic measurements on single crystals of Cs3La[AsS4]2 have confirmed the presence of [AsS4]3− tetrahedra as structural building blocks.

Self-Assembly in Curved Space: Ordering, Defect and Entropy

Self-assembly of nanoscale objects is of essential importance in materials science, condensed matter physics, and biophysics. Curvature modifies the principles and sequence of self-assembly in Euclidean space, resulting in unique and more complex structures. Understanding self-assembly behavior in curved space is not only instrumental for designing structural building blocks and assembly processes from a bottom-up perspective but is also critically important for delineating various biological systems. In this review, we summarize efforts made to unveil the physical nature of self-assembly in curved space through experiments and simulations. First, we outline the differences in the physical nature of self-assembly between curved space and Euclidean space by presenting relevant results of experiments and simulations. Second, we explore the principles of self-assembly in curved space at multiple scales and interactions, elucidating important factors that govern the self-assembly process from the perspectives of confinement and structural building blocks. Finally, we enumerate practical applications and control strategies for self-assembly in curved space and outline the challenges and prospects in this field. We hope that this review will encourage further efforts toward fundamental research and broaden the potential applications of designed assemblies in curved space.

Microwave-assisted synthesis of polyoxometalate-Dy2O3 monolayer nanosheets and nanotubes.

Two-dimensional (2D) materials have shown unique chemical and physical properties; however, their synthesis is highly dependent on the layered structure of building blocks. Herein, we developed monolayer Dy2O3-phosphomolybdic acid (PMA) nanosheets and nanotubes based on microwave synthesis. Microwave-assisted synthesis with high-energy input gives a faster and dynamically driven growth of nanomaterials, resulting in high-purity nanostructures with a narrow size distribution. The reaction times of the nanosheets and nanotubes under microwave synthesis are significantly reduced compared with oven-synthesis. Dy2O3-PMA nanosheets and nanotubes exhibit enhanced activity and stability in photoconductance, with higher sensitivities (0.308 μA cm-2 for nanosheets and 0.271 μA cm-2 for nanotubes) compared to the individual PMA (0.12 μA cm-2) and Dy2O3 (0.025 μA cm-2) building blocks. This work demonstrates the promising application potential of microwave-synthesized 2D heterostructures in superconductors and photoelectronic devices.

Spontaneous and Selective Macrocyclization in Nitroaldol Reaction Systems.

Through a dynamic polymerization and self-sorting process, a range of lowellane macrocycles have been efficiently generated in nitroaldol systems composed of aromatic dialdehydes and aliphatic or aromatic dinitroalkanes. All identified macrocycles show a composition of two repeating units, resulting in tetra-β-nitroalcohols of different structures. The effects of the building block structure on the macrocyclization process have been demonstrated, and the influence from the solvent has been explored. In general, the formation of the lowellanes was amplified in response to phase-change effects, although solution-phase structures were, in some cases, favored.