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This paper describes photoelectrochemical dehydrogenative cyclization of 2-arylbenzoic acid and 2-arylbenzamide in a PEC cell consisting of a mesoporous WO3 photoanode and Pt cathode. The cyclization reaction is effectively driven by this PEC system at room temperature with blue LED irradiation under external oxidant- and metal-free conditions, delivering a series of benzolactones and benzolactams in up to 95% isolated yields. Meanwhile, hydrogen is released as the only byproduct of this process. [ABSTRACT FROM AUTHOR]

Metal--organic frameworks (MOFs), an emerging class of highly ordered crystalline porous materials, possess structural tunability, high specific surface area, well-defined pores, and diverse pore environments and morphologies, making them suitable for various potential applications. Moreover, hydrogenbonded organic frameworks (HOFs), constructed from organic molecules with complementary hydrogen-bonding patterns, are rapidly evolving into a novel category of porous materials due to their facile mild preparation conditions, solution processability, easy regeneration capability, and excellent biocompatibility. These distinctive advantages have garnered significant attention across diverse fields. Considering the inherent binding affinity between MOFs and HOFs along with the fact that many MOF linkers can serve as building blocks for constructing HOFs, their combination holds promise in creating functional materials with enhanced performance. This feature paper provides an introduction to the interconversion between MOFs and HOFs followed by highlighting the emerging applications of MOF--HOF composites. Finally, we briefly discuss the current challenges associated with future perspectives on MOF--HOF composites. [ABSTRACT FROM AUTHOR]

In pursuit of global carbon neutrality, countries are intensifying their efforts to harness clean energy sources. Hydrogen emerges as a superior alternative to traditional fossil fuels and plays a crucial role in the global energy shift. Liquid Organic Hydrogen Carrier (LOHC) systems are lauded for their high hydrogen storage capacity, ease of handling, and safe and efficient transportation, positioning them as effective solutions for extensive hydrogen storage and international distribution. Nevertheless, the dehydrogenation of hydrogen-rich LOHCs is slow, requiring high temperatures and substantial energy inputs. Addressing these challenges by reducing energy demands and improving dehydrogenation rates is essential for advancing LOHC technology. This paper comprehensively examines various LOHC systems, focusing on the selection of carriers and dehydrogenation catalysts, and their dehydrogenation efficacy. It also highlights our recent contributions in photocatalytic LOHC and outlines future research directions to enhance LOHC technology. [ABSTRACT FROM AUTHOR]

Reductive elimination is a key step in Ni-catalysed cross-couplings, which is often considered to result in new covalent bonds. Due to the weak oxidizing ability of Ni(II) species, reductive eliminations from Ni(II) centers are challenging. A thorough mechanistic understanding of this process could inspire the rational design of Ni-catalysed coupling reactions. In this article, we give an overview of recent advances in the mechanistic study of reductive elimination from Ni(II) species achieved by our group. Three possible models for reductive elimination from Ni(II) species were investigated and discussed, including direct reductive elimination, electron density-controlled reductive elimination, and oxidation-induced reductive elimination. Notably, the direct reductive elimination from Ni(II) species often requires a high activation energy in some cases. In contrast, the electron density-controlled and oxidation-induced reductive elimination pathways can significantly enhance the driving force for reductive elimination, accelerating the formation of new covalent bonds. The intricate reaction mechanisms for each of these pathways are thoroughly discussed and systematically summarized in this paper. These computational studies showcase the characteristics of three models for reductive elimination from Ni(II) species, and we hope that it will spur the development of mechanistic studies of cross-coupling reactions. [ABSTRACT FROM AUTHOR]

Hybrid water electrolysis (HWE) is a promising pathway for the simultaneous production of high-value chemicals and clean H2 fuel. Unlike conventional electrochemical water splitting, which relies on the oxygen evolution reaction (OER), HWE involves the anodic oxidation reaction (AOR). The AORs facilitate the conversion of organic or inorganic compounds at the anode into valuable chemicals, while the cathode carries out the hydrogen evolution reaction (HER) to produce H2. Recent literature has witnessed a surge in papers investigating various AORs with organic and inorganic substrates using a series of transition metal-based catalysts. Over the past two decades, metal–organic frameworks (MOFs) have garnered significant attention for their exceptional performance in electrochemical water splitting. These catalysts possess distinct attributes such as highly porous architectures, customizable morphologies, open facets, high electrochemical surface areas, improved electron transport, and accessible catalytic sites. While MOFs have demonstrated efficiency in electrochemical water splitting, their application in hybrid water electrolysis has only recently been explored. In recent years, a series of articles have been published; yet there is no comprehensive article summarizing MOFs for hybrid water electrolysis. This article aims to fill this gap by delving into the recent progress in MOFs specifically tailored for hybrid water electrolysis. In this article, we systematically discuss the structure–property–performance relationships of various MOFs utilized in hybrid water electrolysis, supported by pioneering examples. We explore how the structure, morphology, and electronic properties of MOFs impact their performance in hybrid water electrolysis, with particular emphasis on value-added chemical generation, H2 production, potential improvement, conversion efficiency, selectivity, faradaic efficiency, and their potential for industrial-scale applications. Furthermore, we address future advancements and challenges in this field, providing insights into the prospects and challenges associated with the continued development and deployment of MOFs for hybrid water electrolysis. [ABSTRACT FROM AUTHOR]

A highly efficient, practical and flexible two-step asymmetric synthesis of the β2-selective β-blocker ICI 118,551 is reported, allowing an unambiguous determination of the dependency of biological activity with optical activity, revealing the S,S-enantiomer to be the most potent. [ABSTRACT FROM AUTHOR]

The article "Retraction: PEG-nanotube liquid crystals as templates for construction of surfactant-free gold nanorods" published in Chemical Communications in 2018 has been retracted due to scientific misconduct. The retraction was recommended by the National Institute of Advanced Industrial Science and Technology (AIST) after discovering incorrect electron microscopy images in the paper. The first author, affiliated with AIST, was found responsible for the misconduct, leading to the retraction of the article. [Extracted from the article]

A highly selective and sensitive fluorescent sensor for Cd2+ in aqueous solution based on a lanthanide post-functionalized metal–organic framework was developed. [ABSTRACT FROM AUTHOR]

Efficient electrocatalysts are in great demand for renewable energy storage systems. Herein, we propose an ultrafast heating strategy to fabricate an efficient Ir/CP-UH catalyst for the oxygen evolution reaction (OER). Experimental results demonstrated that the ultrasmall Ir nanoparticles (≈1–3 nm) and clusters (<1 nm) were highly dispersed on the carbon paper support after a short thermal shock (∼5 s). The catalyst showed a low overpotential of 260 mV at 10 mA cm−2 and remarkable mass activity of about 13.8 times higher than that of the current state-of-the-art commercial Ir/C catalyst. This ultrafast heating strategy can also be applied to other catalyst systems for OER and other electrochemical reactions. [ABSTRACT FROM AUTHOR]

This paper shows a novel oxidative functionalization of α-amino ketones to yield the corresponding α-ketoamides and α-acylimidates. The reaction proceeds via oxygen delivery from water/alcohols in conjunction with an electron acceptor and 4-dimethylaminopyridine (DMAP). Mechanistic study indicates that DMAP exhibits a dual function of nucleophilic catalysis and proton abstraction. [ABSTRACT FROM AUTHOR]

In this paper, we provide a novel electrode switch (ES) method to improve the stability of the alkaline electrolyzer toward water splitting. The voltage of the alkaline electrolyzer consisting of commercial Ni mesh electrodes utilizing the ES mode exhibits extreme stability because highly active Ni oxide(hydroxide) with oxygen defects is in situ formed during the hydrogen evolution reaction (HER) polarization process. [ABSTRACT FROM AUTHOR]

Membrane-based gas separation, characterized by a small footprint, low energy consumption and no pollution, has gained widespread attention as an environmentally friendly alternative to traditional gas separation. Metal–organic-frameworks (MOFs) are considered to be one of the most promising membrane-based gas separation materials because of their large specific surface area and high porosity. One of the hottest studies at the moment is how to utilize the characteristics of MOFs to prepare higher performance gas separation membranes. This paper provides a review of gas separation membranes used in recent years. Firstly, the synthesis methods of MOFs and MOF membranes are briefly introduced. Then, methods to improve the membrane properties of MOFs are described in detail, and include applications of lamellar MOFs, ionic liquid (IL) spin coating, functionalization of MOFs, defect engineering and mixed fillers. In addition, the challenges of MOF-based gas separation membranes are presented, including pore size, environmental disturbances, plasticization, interfacial compatibility, and so on. Finally, based on the current development status of the MOF membranes, the development prospects of MOF gas separation membranes are discussed. It is hoped to provide reliable and complete ideas for researchers to prepare high-performance gas separation membranes in the future. [ABSTRACT FROM AUTHOR]

Invisible inks have been applied for the secrecy of texts, symbols and binary images. Based on the photochromism of donor–acceptor Stenhouse adducts (DASAs) in the solid-state promoted by ester-containing molecules, we report the encryption of grayscale information by controlling the kinetics of photoisomerization. [ABSTRACT FROM AUTHOR]

Gallic acid, a natural phenolic compound, efficiently establishes surface complexes with liquid gallium leading to the formation of an aqueous gallium dispersion via sonication. The surface functionalised gallium particles thus obtained were easily impregnated into paper membranes that could be turned from insulating to conductive by pressure induced deformation of the embedded particles. [ABSTRACT FROM AUTHOR]

This work describes a highly active and stable acid activated carbon fibre and amorphous MoSx composite hydrogen evolution catalyst. The increased electrochemical-surface area is demonstrated to cause increased catalyst electrodeposition and activity. These composite electrodes also show an improved stability towards the mechanical degradation of the MoSx catalyst. [ABSTRACT FROM AUTHOR]

A novel dansyl-triazole-based fluorescent macrocycle with high Stokes shift and positive solvatochromism was developed. This is an excellent fluorescence sensor for selective detection of nitro-containing antibiotics and other nitro-heteroaromatics. Detection was possible in real samples/paper strips in submicromolar concentration. The interaction of the macrocycle with multiple proteins exhibited its bioactivity. [ABSTRACT FROM AUTHOR]

Ionic liquids (ILs) have emerged as a new class of materials, displaying a unique capability to self-assemble into micelles, liposomes, liquid crystals, and microemulsions. Despite evident interest, advancements in the controlled formation of amphiphilic ILs remain in the early stages. Taking inspiration from nature, we introduced the concept of lipid-like (or lipid-inspired) ILs more than a decade ago, aiming to create very low-melting, highly lipophilic ILs that are potentially bio-innocuous – a combination of attributes that is frequently antithetical but highly desirable from several application-specific standpoints. Lipid-like ILs are a subclass of functional organic liquid salts that include a range of lipidic side chains such as saturated, unsaturated, linear, branched, and thioether while retaining melting points below room temperature. It was observed in several homologous series of [Cnmim] ILs that elongation of N-appended alkyl chains to greater than seven carbons leads to a substantial increase in melting point (Tm) – which is the most characteristic feature of ILs. Accordingly, it is challenging to develop ILs with low Tm values while preserving their hydrophobicity and self-organizing properties. We found that two alternative Tm depressive approaches are useful. One of these is the replacement of the double bonds with thioether moieties in the alkyl chains, as detailed in several published papers detailing the chemistry of these ILs. Employing thiol–ene and thiol–yne click reactions is a facile, robust, and orthogonal method to overcome the challenges associated with the synthesis of alkyl thioether-functionalized ILs. The second approach involves replacing the double bonds with the cisoid cyclopropyl motif, mimicking the strategy used by certain organisms to modulate cell membrane fluidity. This discovery has the potential to greatly impact the utilization of lipid-like ILs in various applications, including gene delivery, lubricants, heat transfer fluids, and haloalkane separations, among others. This feature article presents a concise, historical overview, highlighting key findings from our work while offering speculation about the future trajectory of this de novo class of soft organic-ion materials. [ABSTRACT FROM AUTHOR]

The advent of two-dimensional nanomaterials, a revolutionary class of materials, is marked by their atomic-scale thickness, superior aspect ratios, robust mechanical attributes, and exceptional chemical stability. These materials, producible on a large scale, are emerging as the forefront candidates in the domain of membrane-based gas separation. The concept of defect engineering in 2D nanomaterials has introduced a novel approach in their application for membrane separation, offering an effective technique to augment the performance of these membranes. Nonetheless, the development of customized microstructures in gas separation membranes via defect engineering remains nascent. Hence, this review is designed to serve as a comprehensive guide for the application of defect engineering in 2D nanomaterial-based membranes. It delves into the most recent developments in this field, encompassing the synthesis methodologies of defective 2D nanomaterials and the mechanisms underlying gas transport. Special emphasis is placed on the utilization of defect-engineered 2D nanomaterial-based membranes in gas capture applications. Furthermore, the paper encapsulates the burgeoning challenges and prospective advancements in this area. In essence, defect engineering emerges as a promising avenue for enhancing the efficacy of 2D nanomaterial-based membranes in gas separation, offering significant potential for advancements in membrane-based gas separation technologies. [ABSTRACT FROM AUTHOR]

DNA nanostructures are easy to design and construct, have good biocompatibility, and show great potential in biosensing and drug delivery. Numerous distinctive and versatile DNA nanostructures have been developed and explored for biomedical applications. In addition to DNA nanostructures that are completely assembled from DNA, composite DNA nanostructures obtained by combining DNA with other organic or inorganic materials are also widely used in related research. The CRISPR/Cas system has attracted great attention as a powerful gene editing technology and is also widely used in biomedical diagnosis. Many researchers are committed to exploring new possibilities by combining DNA nanostructures with CRISPR/Cas systems. These explorations provide support for the development of new detection methods and cargo delivery pathways, provide inspiration for improving relevant gene editing platforms, and further expand the application scope of DNA nanostructures and CRISPR/Cas systems. This paper mainly reviews the design principles and biomedical applications of CRISPR/Cas combined with DNA nanostructures based on the types of DNA nanostructures. Finally, the application status, challenges and development prospects of CRISPR/Cas combined with DNA nanostructures in detection and delivery are summarized. It is expected that this review will enable researchers to better understand the current state of the field and provide insights into the application of CRISPR/Cas systems and the development of DNA nanostructures. [ABSTRACT FROM AUTHOR]

The direct conversion of methane to hydrogen and high-value hydrocarbons under mild conditions is an ideal, carbon-neutral method for utilizing natural gas resources. Compared with traditional high-temperature thermal catalytic methods, using clean light energy to activate inert C–H bonds in methane can not only significantly reduce the reaction temperature and avoid catalyst deactivation, but also surpass the limitations of thermodynamic equilibrium and provide new reaction pathways. This paper provides a comprehensive review of developments in the field of photocatalytic non-oxidative conversion of methane (PNOCM), while also highlighting our contributions, particularly focusing on catalyst design, product selectivity, and the underlying photophysical and chemical mechanisms. The challenges and potential solutions are also evaluated. The goal of this feature article is to establish a foundational understanding and stimulate further research in this emerging area. [ABSTRACT FROM AUTHOR]

Nanoarchitectonics, as a post-nanotechnology concept, constructs functional materials and structures using nanounits of atoms, molecules, and nanomaterials as materials. With the concept of nanoarchitectonics, asymmetric structures, and hierarchical organization, rather than mere assembly and organization of structures, can be produced, where rational physical and chemical communications will lead to the development of more advanced functional materials. Layer-by-layer assembly can be a powerful tool for this purpose, as exemplified in this feature paper. This feature article explores the possibility of constructing advanced functional systems based on recent examples of layer-by-layer assembly. We will illustrate both the development of more basic methods and more advanced nanoarchitectonics systems aiming towards practical applications. Specifically, the following sections will provide examples of (i) advancement in basics and methods, (ii) physico-chemical aspects and applications, (iii) bio-chemical aspects and applications, and (iv) bio-medical applications. It can be concluded that materials nanoarchitectonics based on layer-by-layer assembly is a useful method for assembling asymmetric structures and hierarchical organization, and is a powerful technique for developing functions through physical and chemical communication. [ABSTRACT FROM AUTHOR]

Given the rising lithium-ion battery retirement trend, there is a pressing need for a sustainable, cost-effective, versatile, and industrially viable positive active powder reprocessing method. The current treatment methods require significant amounts of acids, reducing agents, and other additives, resulting in increased treatment expenses and detrimental environmental consequences. This paper proposes a synergistic redox strategy, based on thermodynamic calculations of potential self-promoting reactions in mixed LFP/NCM systems, for the recovery of spent LFP and NCM batteries without the need for additional agents in a milder acidic atmosphere. In this cooperative redox strategy, the spontaneous extraction and oxidation of Fe2+ to Fe3+ took place within the acidic solution atmosphere encapsulating LFP. Simultaneously, NCM underwent further reduction, yielding Ni2+ and Fe2+, thereby enabling the proficient dissolution and segregation of lithium and transition metal ions. The leaching rate of lithium, nickel, cobalt and manganese was close to 100% when the reaction was carried out at 20 °C for 40 min. The final raw material was reprepared into a battery with a capacity of 168.8 mA h g−1 at 1C, and the cycle retention rate was 76.78% after 300 cycles. Regenerating FPO into LFP cathode material achieves closed-loop recycling of all elements and generates 12% higher profits compared to separate processes. Our method proposes a zero-additive battery recycling process and successfully explains the intrinsic redox process. [ABSTRACT FROM AUTHOR]

The current review describes different annulation strategies reported with electrophilic benzannulated heterocycles for accessing heteroacenes. For the past two decades, the chemistry of electrophilic benzannulated heterocycles was extensively investigated, and several dipolar cycloadditions, metal and organo-catalyzed transformations were introduced for the generation of fused heterocycles. In this review, we have collected all the reports where the annulation of electrophilic benzannulated heterocycles results in a fully aromatic system, viz. heteroacenes with tri-, tetra-, and pentacyclic rings. We reviewed every paper on the synthesis of fused heterocycles that was accessible and categorized the review into several parts based on the electrophilic benzannulated heterocycle used in the heteroacene synthesis such as electrophilic indole, electrophilic benzothiophene, and so forth. The generality and mechanistic postulates of each methodology are highlighted. In addition, we have also tried to feature the advantages or shortcomings of each method and have mentioned the possible applications of these methodologies for accessing heteroacenes for material applications. [ABSTRACT FROM AUTHOR]

In this paper, benzo-fused cyclic carbonates were designed and synthesized as a new type of precursor of π-allylpalladium zwitterionic intermediates, and were applied in Pd-catalyzed diastereo- and enantioselective (4+3) cycloaddition with C,N-cyclic azomethine imines, leading to various biologically important 1,3,4-benzoxadiazepine derivatives in 43–99% yields with 6 : 1 to >20 : 1 dr and up to 95% ee. [ABSTRACT FROM AUTHOR]

Homopurine strands are known to form antiparallel triplexes stabilized by G*G and A*A Hoogsteen pairs, which have two hydrogen bonds. But there has been no report on the parallel triplex formation of homopurine involving both adenosine and guanosine to the duplex. In this paper, we first report parallel triplex formation between a homopurine serinol nucleic acid (SNA) strand and an RNA/SNA duplex. Melting profiles revealed that the parallel SNA:RNA*SNA triplex was remarkably stable, even though the A*A pair has a single hydrogen bond. An L -acyclic threoninol nucleic acid (L -aTNA) homopurine strand also formed a stable parallel triplex with an L -aTNA/RNA duplex. [ABSTRACT FROM AUTHOR]

The development of sensors for the detection of triacetone triperoxide (TATP) has attracted great attention. Here, we constructed a low-cost, portable, reusable, visible paper-based fluorescent sensor for the sensitive detection of TATP via vapor sampling. Under optimized conditions, the fluorescent film showed a high sensitivity to TATP with a detection limit of lower than 0.5 μg mL−1 in air. The linear range of the response is from 0.5 to 8.0 μg mL−1. In addition, the paper-based sensor exhibited high selectivity to TATP. The presence of potential interferents showed little effect on sensing. Moreover, sensing is fully reversible. Fortunately, the test can also be conducted in a visualized way. [ABSTRACT FROM AUTHOR]

A nanozyme-like colorimetric sensing strategy based on persulfate activation on Co-based metal – organic frameworks is developed for biomolecule detection in solution and on paper strips. By switching from H2O2 activation on nanozymes to catalytic persulfate activation, this general strategy provides higher sensitivity, faster speed, and wider application ranges for detection. [ABSTRACT FROM AUTHOR]

In this work, by installing a free-rotating benzene ring to suppress the intermolecular π–π stacking effect in the aggregated state, a naphthalimide-derived hypochlorite (ClO−) fluorescent probe, Probe A, with the aggregation-caused quenching (ACQ) effect was successfully transformed into Probe B possessing typical aggregation-induced emission (AIE) characteristics. The experimental results indicated that Probe B with good selectivity and a low detection limit (LOD) of 0.02 µM can also exhibit a significant ratiometric fluorescence color change from cyan to dark blue within 2 min in a nearly pure water solvent system after the addition of ClO−. Finally, by virtue of the good photophysical properties and ClO− sensing performance, Probe B and the Probe B loaded portable test paper were successfully applied to live cell imaging and the naked eye recognition of ClO−, respectively. [ABSTRACT FROM AUTHOR]

The article "Retraction: Enhancement of the photocatalytic activity of rhenium(I) complexes by encapsulation in light-harvesting soft nanotubes" published in Chemical Communications in 2017 has been retracted due to incorrect electron microscopy images in Fig. 2b and c. The errors in the scale bars of the images were found to be approximately 6 and 2 times longer than the actual lengths, leading to inconsistencies with the description of the nanotubes' diameter sizes. The retraction was recommended by the National Institute of Advanced Industrial Science and Technology (AIST) due to scientific misconduct by the first author, Naohiro Kameta, who was solely responsible for the errors. [Extracted from the article]

The landmark 1954 J. Chem. Soc. paper by Craig et al. exploring the role of d-orbitals in chemical bonding is discussed. This paper set the agenda for discussions that continue until the present about topics in inorganic chemistry such as hypervalency, arguably the most significant bonding phenomenon to differentiate the chemistry of the 2p main group elements from their heavier congeners. [ABSTRACT FROM AUTHOR]

Polyimide covalent organic frameworks (PI-COFs) are outstanding functional materials for electrochemical energy conversion and storage owing to their integrated advantages of the high electroactive feature of polyimides and the periodic porous structure of COFs. Nevertheless, only anhydride monomers with C2 symmetry are generally used, and limited selectivity of electron-deficient monomers has become a major obstacle in the development of materials. The introduction of polycyclic aromatic hydrocarbons (PAHs) is a very effective method to regulate the structure–activity relationship of PI-COFs due to their excellent stability and electrical properties. Over the past two years, various star-shaped electron-deficient PAH building blocks possessing different compositions and topologies have been successfully fabricated, greatly improving the monomer selectivity and electrochemical performances of PI-COFs. This paper systematically summarizes the recent highlights in PI-COFs based on these building blocks. Firstly, the preparation of anhydride (or phthalic acid) monomers and PI-COFs related to different star-shaped PAHs is presented. Secondly, the applications of these PI-COFs in energy conversion and storage and the corresponding factors influencing their performance are discussed in detail. Finally, the future development of this meaningful field is briefly proposed. [ABSTRACT FROM AUTHOR]

In this paper, the synthesis of a novel tetra-phenol π-extended dihydrophenazine is reported. The obtained derivative presents marked reducing properties in the excited state and was exploited as an organo-photocatalyst in dehalogenation and C–C bond formation reactions. These results underline the great potential of functionalized π-extended dihydrophenazines as organo-photocatalysts. [ABSTRACT FROM AUTHOR]

As an emerging functional material, liquid metal–hydrogel composites exhibit excellent biosafety, high electrical conductivity, tunable mechanical properties and good adhesion, thus providing a unique platform for a wide range of flexible electronics applications such as wearable devices, medical devices, actuators, and energy conversion devices. Through different composite methods, liquid metals can be integrated into hydrogel matrices to form multifunctional composite material systems, which further expands the application range of hydrogels. In this paper, we provide a brief overview of the two materials: hydrogels and liquid metals, and discuss the synthesis method of liquid metal–hydrogel composites, focusing on the improvement of the performance of hydrogel materials by liquid metals. In addition, we summarize the research progress of liquid metal–hydrogel composites in the field of flexible electronics, pointing out the current challenges and future prospects of this material. [ABSTRACT FROM AUTHOR]

This paper describes the design and synthesis of a conjugate, which is composed of a percarboxylated water-soluble pillar[6]arene and three fluorescent pyrene chromophores on alternating methylene bridges. The optical characteristics are investigated. This conjugate is capable of encapsulating polycationic guest spermine, which results in an enhancement in the fluorescence intensity of pyrene. This host–pyrene conjugate is used for direct sensing of spermine, which shows selectivity towards a variety of biological analytes. The detection of spermine is demonstrated in live cells. [ABSTRACT FROM AUTHOR]

Phenolic compounds are ubiquitous in nature because of their unique physical and chemical properties and wide applications, which have received extensive research attention. Phenolic compounds represented by tannic acid (TA) play an important role at the nanoscale. TA with a polyphenol hydroxyl structure can chemically react with organic or inorganic materials, among which metal–phenolic networks (MPNs) formed by coordination with metal ions and polyphenol derivatives formed by interactions with organic matter, exhibit specific properties and functions, and play key roles in photo(electro)catalysis. In this paper, we first introduce the fundamental properties of TA, then summarize the factors influencing the properties of MPNs and structural transformation of polyphenol-derived materials. Subsequently, the functions of MPNs and polyphenol derivatives in photo(electro)catalysis reactions are summarized, encompassing improving interfacial charge carrier separation, accelerating surface reaction kinetics, and enhancing light absorption. Finally, this article provides a comprehensive overview of the challenges and outlook associated with MPNs. Additionally, it presents novel insights into their stability, mechanistic analysis, synthesis, and applications in photo(electro)catalysis. [ABSTRACT FROM AUTHOR]

Sequential peptide coupling plays a central role in chemical protein synthesis. This paper describes a new peptide derivative, peptide-aminothiazoline (At), whereof the C-terminus is functionalized with 2-aminothiazoline. Peptide-At streamlined the sequential peptide ligation in a one-pot manner and demonstrated the convergent synthesis of a circular protein and homogeneous glycoproteins. [ABSTRACT FROM AUTHOR]

Nickel-based electrocatalysts for the oxygen evolution reaction (OER) show the disadvantages of low activity and poor stability. In this paper, an FeNi alloy is wrapped by an amino-modified MOF-5-derived N-doped carbon layer to address these problems. Additionally, the improvement resulting from Fe doping of NiOOH catalysts is theoretically supported. [ABSTRACT FROM AUTHOR]

This document is a back cover advertisement for Chemical Communications, a journal that aims to advance careers in science by providing professional recognition. The advertisement encourages readers to apply for professional registers or chartered status to gain recognition and unlock their career potential. It also features research from Professor Shashank Deep's laboratory at the Indian Institute of Technology Delhi, discussing the inhibition of fibril formation by polyphenols and its potential implications for neurodegenerative diseases. The document also mentions another article in the journal about the detection of Escherichia coli using a paper device. [Extracted from the article]

ChemComm Chemical Communicationsrsc. li/ chemcomm ISSN 1359- 7345 COMMUNICATION Yangyang Chang, Meng Liu et al . Amplification- free detection of Escherichia coli using an acidic deoxyribozyme- based paper device Volume 60 Number 53 7 July 2024 Pages 6693– 6826 EES Catalysis GOLD Exceptional research on energy and environmental catalysis Open to everyone. Impactful for all Registered charity number: 207890 rsc. li/ EESCatalysis Fundamental questions Elemental answers OPEN ACCESS [Extracted from the article]

Designing counter electrodes (CEs) with high efficiency and understanding the mechanism of dye-sensitized solar cells (DSSCs) are still challenges. In this paper, we synthesized K-doped molybdenum disulfide (K-MoS2) with few layers and it has a great enhancement effect on the electrocatalytic activity compared to pure MoS2 CE and reference Pt CE. A dual electron-path model is proposed to explain the mechanism, which is supported by first-principles calculations. When an electron in MoS2 is transferred to the triiodide, the K atoms can act as an electron reservoir to provide another electron in a short time to improve the catalytic activity. So the proposed dual-electron effect in this paper is helpful to understand the charge transfer mechanism on the interfaces of these CEs and may be crucial for obtaining high photoelectric efficiencies in DSSCs. [ABSTRACT FROM AUTHOR]

Benefiting from a high overpotential of the competitive hydrogen evolution reaction with a carbon paper cathode, the desired electrochemical reduction of imines was achieved with high faradaic efficiency by using H2O as a H-source. With this sustainable atom-economic strategy, a series of potentially versatile amines were obtained in medium-to-high yields (49–86%). [ABSTRACT FROM AUTHOR]

Electrocatalytic nitrate reduction reaction (NitRR) is an energy-saving and environmentally benign approach to synthesizing ammonia under ambient conditions. However, the development of noble metal-free catalysts with high activity and selectivity is still a significant challenge. In this study, uniformly dispersed amorphous CoBx nanoparticles supported on carbon paper were synthesized VIA a simple wet chemical reduction method. As an efficient nitrate reduction electrocatalyst, CoBx exhibited a maximum faradaic efficiency of 94.00 ± 1.67% and a yield rate of up to 0.787 ± 0.028 mmol h−1 cm−2 for ammonia production. The enhanced NitRR performance could be attributed to a partial electron transfer from B to Co, which is necessary for optimizing the adsorption energies of the reaction intermediates and facilitating electron transport. Thus, selective and cost-effective electroreduction of nitrates to ammonia can be achieved using CoBx nanoparticles. [ABSTRACT FROM AUTHOR]

A fluorescent probe for phenylhydrazine detection was developed with aldehyde as the recognition group and good selectivity towards phenylhydrazine over hydrazine, hydroxylamine and other amines was observed. Its application in real water samples and fast visualization of phenylhydrazine using a probe-loaded paper strip were demonstrated. [ABSTRACT FROM AUTHOR]

The powerful strategy of “intracellular click reaction” was used to retain a chemical Ca2+ indicator in the cytosol. Specifically, a novel clickable Ca2+ indicator “N3-fura-2 AM” was coupled with dibenzylcyclooctyl-modified biomacromolecules via copper-free click reaction in living cells and Ca2+ oscillation was observed for an extended period of time. [ABSTRACT FROM AUTHOR]

A method using ink-jet printing for constructing multi-enzyme systems was proposed, in which a precisely defined enzyme ratio and two-dimensional distribution was obtained by the preset 'color' values. The applications of the print-on-paper multi-enzyme systems were exemplified by the detection of glucose and the design of an enzyme-enabled two-dimensional code. [ABSTRACT FROM AUTHOR]