Catalytic Graphitization of Biocarbon for Lithium‐Ion Anodes: A Minireview

Catalytic Graphitization of Biocarbon for Lithium-Ion Anodes: A Minireview

Lithium-ion battery anodes are produced in a resource-intensive and polluting manner. This review focuses on biomass-derived graphitic anode materials for lithium-ion batteries that are advancing through innovation in thermochemical catalysis. Future research should focus more on electrochemical performance and less on the structural characteristics of the carbon materials.


Abstract

The demand for electrochemical energy storage is increasing rapidly due to a combination of decreasing costs in renewable electricity, governmental policies promoting electrification, and a desire by the public to decrease CO2 emissions. Lithium-ion batteries are the leading form of electrochemical energy storage for electric vehicles and the electrical grid. Lithium-ion cell anodes are mostly made of graphite, which is derived from geographically constrained, non-renewable resources using energy-intensive and highly polluting processes. Thus, there is a desire to innovate technologies that utilize abundant, affordable, and renewable carbonaceous materials for the sustainable production of graphite anodes under relatively mild process conditions. This review highlights novel attempts to realize the aforementioned benefits through innovative technologies that convert biocarbon resources, including lignocellulose, into high quality graphite for use in lithium-ion anodes.

Green Additives in Chitosan‐Based Bioplastic Films: Physical, Mechanical, and Chemical Properties

Green Additives in Chitosan-Based Bioplastic Films: Physical, Mechanical, and Chemical Properties

The Cover Feature shows bioplastic products generated from chitosan, a material derived from crustaceans, such as crabs. By exploring different green additives, such as glycerol and citric acid, chitosan-based ′plastic′ films were generated. The additives could be grouped by their uptake behavior, namely linear, non-linear, or crosslinking. Lower amounts of additives are deemed most practical, balancing the property enhancement with mechanical stability of the bioplastic films. Using spectroscopy, microscopy and chromatography, we show that the addition of these green additives enables the creation of a diverse range of chitosan-based plastic alternatives, offering alternatives to conventional plastics, ranging from soft flexible materials (e.g., cling film, and medical supplies) to hard, stiff plastics (e.g., bottles, and toys).More information can be found in the Research Article by K. B. Schnabl et al.


Deep Eutectic Solvents: An Eco‐friendly Design for Drug Engineering

Deep Eutectic Solvents: An Eco-friendly Design for Drug Engineering

The Front Cover highlights the deep eutectic solvent (DES)-optimized preparation through hydrogen bond acceptor and donor interactions between various molecules of pharmaceutical interest for personalized medicine. Indeed, the choice of the DES chemical components is influenced not only by their intrinsic properties but also by their intended therapeutic use after the components’ association. In the Review article, more insights regarding the different approaches to conveniently selecting the constituents of DESs, from physico-chemical concerns to engineered therapeutic eco-friendly materials, are raised. More information can be found in the Review by F. Oyoun et al.


5‐Ammonium‐4,4‐dimethylvaleryl (Amv) Group: Generation from Acryloyl Group through Decatungstate‐Catalyzed C(sp3)–H Addition and Removal by Base‐Triggered Cyclization

The 5-ammonium-4,4-dimethylvaleryl (Amv) group was generated by conversion of acryloyl group through decatungstatecatalyzed addition of C(sp3)–H bond of i-BuNH2·HCl under the irradiation of UV light (365 nm or 405 nm). Treatment of Amvprotected alcohols and anilines with aqueous Na2CO3 promoted the efficient deprotection of Amv. This is a unique method for the efficient removal of acryloyl groups from phenols, alcohols, and anilines. The selective removal of acryloyl groups through Amv in the presence of another acetyl or benzoyl group was demonstrated. The basetriggered intramolecular cyclization of Amv was monitored by the release of a fluorescent molecule, and it was found that cyclization by Na2CO3 was very rapid (within 1 min) and that some weak bases such as 2,6-lutidine are sufficient to promote cyclization.

Advances in Group VI Metals Catalysed Homogeneous Hydrogenation and Dehydrogenation Reactions

Transition metal catalysed homogeneous hydrogenation and dehydrogenation reactions for attaining plethora of organic scaffolds have evolved as a key domain of research in academia and industry. These protocols are atom-economic, greener, in line with the goal of sustainability, eventually pave the way for numerous novel environmentally benign methodologies. Appealing progress has been achieved in this realm of homogeneous catalysis utilizing noble metals. Owing to their high cost, less abundancy along with toxicity issues led the scientific community to search for sustainable alternatives. In this context, earth- abundant base metals have gained substantial attention culminating enormous progress in recent years, predominantly with pincer-type complexes of nickel, cobalt, iron, and manganese. In this regard, group VI chromium, molybdenum and tungsten complexes have been overlooked and remain underdeveloped despite their earth-abundancy and bio-compatibility. This review delineates a comprehensive overview in the arena of homogeneously catalysed (de)hydrogenation reactions using group VI base metals chromium, molybdenum, and tungsten till date. Various reactions have been described; hydrogenation, transfer hydrogenation, dehydrogenation, acceptorless dehydrogenative coupling, hydrogen auto transfer, along with their scope and brief mechanistic insights.

Epoxide/CO2 cycloaddition reaction catalyzed by Indium Chloride Complexes Supported by Constrained Inden Schiff‐Base Ligands

Cyclic carbonates have received significant interests for uses as reagents, solvents, and monomers. The coupling reaction of epoxides with carbon dioxide (CO2) to produce cyclic carbonate is an attractive route which can significantly reduce greenhouse gas emissions and environmental hazards. Herein, a series of five indium chloride complexes supported by inden Schiff-base ligands were reported along with four X-ray crystal structures. The constrained five-membered rings were added to the ligands to enhance the coordination of epoxides to the In metal. From the catalyst screening, In inden complex having tert-butyl substituents and propylene backbone in combination with tetrabutylammonium bromide (TBAB) exhibited the highest catalytic activity (TON up to 1017) for propylene oxide/CO2 coupling reaction with >99% selectivity for cyclic carbonate under solvent-free conditions. In addition, the catalyst was shown to be active at atmospheric pressure of CO2 at room temperature. The catalyst system can be applied to various internal and terminal epoxide substrates to exclusively produce the corresponding cyclic carbonates.

Design of novel balanced COX inhibitors based on natural anti‐inflammatory ascidian metabolites and celecoxib

The serious adverse effects caused by non-selective and selective cyclooxygenase-2 (COX-2) inhibitors remain significant concerns for current anti-inflammatory drugs. In this study, we present the design and synthesis of a novel series of celecoxib analogs incorporating a hydrazone linker, which were subjected to in silico analysis to compare their binding poses with those of clinically used nonsteroidal anti-inflammatory drugs (NSAIDs) against COX-1 and COX-2. The synthesized analogs were evaluated for their inhibitory activity against both COX enzymes, and compound 6m, exhibiting potent balanced inhibition, was selected for subsequent in vitro anti-inflammatory assays. Treatment with 6m effectively suppressed the NF-κB signaling pathway in lipopolysaccharide (LPS)-stimulated murine RAW264.7 macrophages, resulting in reduced expression of pro-inflammatory factors such as inducible nitric oxide synthase (iNOS), COX-2, tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), IL-1β, as well as decreased production of prostaglandin E2 (PGE2), nitric oxide (NO), and reactive oxygen species (ROS). However, 6m has no effect on the MAPK signaling pathway. Therefore, due to its potent in vitro anti-inflammatory activity coupled with lack of cytotoxicity, 6m represents a promising candidate for further development as a new lead compound targeting inflammation.

DABCO‐Promoted Bicyclization/Rearrangement Reaction Synthesis of Tetrasubstituted Furans and Furo[3,4‐d]pyrimidine‐2,4‐diones from 1,4‐Enediones

A DABCO-promoted bicyclization/rearrangement reaction has been developed for the synthesis of tetrasubstituted furans from 1,4-enediones at room temperature. This transformation involves aza-Michael addition, intramolecular bicyclization, and rearrangement processes. In addition, the 4-ureidofuran-3-carboxylate ester products can further be converted to furo[3,4-d]pyrimidine-2,4-diones through intramolecular substitution cyclization under heating conditions.

Fe‐Based Metal‐Organic Frameworks: From Various Synthesis, Diverse Structures to Multifunctional Applications


Fe-Based Metal-Organic Frameworks: From Various Synthesis, Diverse Structures to Multifunctional Applications

This review comprehensively summarizes the various structures of Fe-MOFs, along with recent research progress on their synthesis and multifunctional applications in gas storage and separation, catalysis, bioimaging, and magnetism.


Comprehensive Summary

Iron-based metal-organic frameworks (Fe-MOFs) have attracted extensive interest from researchers due to their tunability, favorable properties, and chemical versatility. Compared with conventional porous materials, Fe-MOFs exhibit better performance in a wide variety of applications. Herein, the structures of Fe-MOFs are summarized to explore potential structures based on isoreticular chemistry, as well as the recent research progress in their synthesis and multifunctional applications. The rapid development of Fe-MOFs has broadened the application range of Fe-MOFs, and a brief description of Fe-MOF applications in gas storage and separation, catalysis, bioimaging, and magnetism is outlined, with the aim to expand the prospects of Fe-MOFs in more practical applications.