Chemical record最新文献

pH has been considered one of the paramount factors in bodily functions because most cellular tasks exclusively rely on precise pH values. In this context, the current techniques for pH sensing provide us with the futuristic insight to further design therapeutic and diagnostic tools. Thus, pH-sensing (electrochemically and optically) is rapidly evolving toward exciting new applications and expanding researchers’ interests in many chemical contexts, especially in biomedical applications. The adaptation of cutting-edge technology is subsequently producing the modest form of these biosensors as wearable devices, which are providing us the opportunity to target the real-time collection of vital parameters, including pH for improved healthcare systems. The motif of this review is to provide insight into trending tech-based systems employed in real-time or in-vivo pH-responsive monitoring. Herein, we briefly go through the pH regulation in the human body to help the beginners and scientific community with quick background knowledge, recent advances in the field, and pH detection in real-time biological applications. In the end, we summarize our review by providing an outlook; challenges that need to be addressed, and prospective integration of various pH in vivo platforms with modern electronics that can open new avenues of cutting-edge techniques for disease diagnostics and prevention.

The cover picture shows the progress in the skeletal editing of the isatin scaffold in the last decade (2013-2023). A series of ring-expansion reactions for the construction of high-value heterocycles (quinolines, quinolones, polycyclic quinazolines, medium-sized compounds), as well as a variety of ring-opening strategies for the generation of the 2-(azoly)anilines by cleavage of the C−C bond and the C−N bond are revealed. More details can be found in article number e202400024 by Tiantian Zhang and Huangdi Feng (DOl: 10.1002/tcr.202400024.

Functionalized nanoporous heteropoly acids (HPAs) have garnered significant attention in recent years due to their enhanced surface area and porosity, as well as their potential for low-cost regeneration compared to bulk materials. This review aims to provide an overview of the recent advancements in the synthesis and applications of functionalized HPAs. We begin by introducing the fundamental properties of HPAs and their unique structure, followed by a comprehensive overview of the various approaches employed for the synthesis of functionalized HPAs, including salts, anchoring onto supports, and implementing mesoporous silica sieves. The potential applications of functionalized HPAs in various fields are also discussed, highlighting their boosted performance in a wide range of applications. Finally, we address the current challenges and present future prospects in the development of functionalized HPAs, particularly in the context of mesoporous HPAs. This review aims to provide a comprehensive summary of the recent progress in the field, highlighting the significant advancements made in the synthesis and applications of functionalized HPAs.

In the last past twenty years, research on luminescent platinum (II) complexes has been intensively developed for useful application such as organic light emitting diodes (OLEDs). More recently, new photoluminescent complexes based on diazine ligands (pyrimidine, pyrazine, pyridazine, quinazoline and quinoxaline) have been developed in this context. This review will summarize the photophysical properties of most of the phosphorescent diazine Pt(II) complexes described in the literature and compare the results to pyridine analogues whenever possible. Based on the emission color, and the photoluminescence quantum yield (PLQY) values, the relationship between structure modification, and photophysical properties are highlighted. Tuning of emission color, quantum yields in solution and solid state and, for some complexes, aggregation induced emission (AIE) or thermally activated delayed fluorescence (TADF) properties are described. When emitting OLEDs have been built from diazine Pt(II) complexes, the external quantum efficiency (EQE) values and luminance for different emission wavelengths and in some cases, chromaticity coordinates obtained from devices, are given. Finally, this review highlights the growing interest in studies of new luminescent diazine Pt(II) complexes for OLED applications.

Isatins have been widely used in the preparation of a variety of heterocyclic compounds, where the skeletal editing of isatins has shown significant advantages for the construction of diverse heterocycles. This review highlights the progress made in the last decade (2013−2023) in the skeletal editing of the isatin scaffold. A series of ring expansion reactions for the construction of quinoline skeleton, quinolone skeleton, polycyclic quinazoline skeleton, medium-sized ring skeleton, as well as a series of ring opening reactions for the generation of 2-(azoly)aniline skeleton by the cleavage of C−C bond and C−N bond are highlighted. It is hoped that this review will provide some understanding of the chemical transformations of isatins and contribute to the further realization of its molecular diversity.

Biomass resources are often disposed of inefficiently and it causes environmental degradation. These wastes can be turned into bio-products using effective conversion techniques. The synthesis of high-value bio-products from biomass adheres to the principles of a sustainable circular economy in a variety of industries, including agriculture. Recently, fluorescent carbon dots (C-dots) derived from biowastes have emerged as a breakthrough in the field, showcasing outstanding fluorescence properties and biocompatibility. The C-dots exhibit unique quantum confinement properties due to their small size, contributing to their exceptional fluorescence. The significance of their fluorescent properties lies in their versatile applications, particularly in bio-imaging and energy devices. Their rapid and straight-forward production using green/chemical precursors has further accelerated their adoption in diverse applications. The use of green precursors for C-dot not only addresses the biomass disposal issue through a scientific approach, but also establishes a path for a circular economy. This approach not only minimizes biowaste, which also harnesses the potential of fluorescent C-dots to contribute to sustainable practices in agriculture. This review explores recent developments and challenges in synthesizing high-quality C-dots from agro-residues, shedding light on their crucial role in advancing technologies for a cleaner and more sustainable future.

The assembly of cluster nodes through linker molecules has been successfully implemented to enhance the material stability. However, the specific reasons behind its success remain to be resolved. This cover image shows such a present situation on the assembly of silver cluster. See the Review by Sourav Biswas, and and Yuichi Negishi (DOl: 10.1002/tcr.202400052.

The exploration of individual nanoclusters is rapidly advancing, despite stability concerns. To address this challenge, the assembly of cluster nodes through linker molecules has been successfully implemented. However, the linking of the cluster nodes itself introduces a multitude of possibilities, especially when additional factors come into play. While this method proves effective in enhancing material stability, the specific reasons behind its success remain elusive. In our laboratory, we have undertaken extensive studies on Ag cluster-assembled materials. So, here our goal is to establish a model system that allows for the discernment of various factors, eliminating unnecessary complexities during the linking approach. So, we hope that the systematic discourse presented in here will contribute significantly to future endeavors, helping to set clear priorities, and provide solutions to concerns that arise when working with a model system.

Hydrogen gas is a prominent focus in pursuing renewable and clean alternative energy sources. The quest for maximizing hydrogen production yield involves the exploration of an ideal photocatalyst and the development of a simple, cost-effective technique for its generation. Iron titanate has garnered attention in this context due to its photocatalytic properties, affordability, and non-toxic nature. Over the years, different synthesis routes, different morphologies, and some modifications of iron titanate have been carried out to improve its photocatalytic performance by enhancing light absorption in the visible region, boosting charge carrier transfer, and decreasing recombination of electrons and holes. The use of iron titanate photocatalyst for hydrogen evolution reaction has seen an upward trend in recent times, and based on available findings, more can be done to improve the performance. This review paper provides a comprehensive overview of the fundamental principles of photocatalysis for hydrogen generation, encompassing the synthesis, morphology, and application of iron titanate-based photocatalysts. The discussion delves into the limitations of current methodologies and present and future perspectives for advancing iron titanate photocatalysts. By addressing these limitations and contemplating future directions, the aim is to enhance the properties of materials fabricated for photocatalytic water splitting.

Presented here is a personal account of how the ideas and concepts underlying the design and construction of coordination polymers/MOFs developed historically - from the earliest conjectures in the 1970’s about the possibility of using pre-organized building blocks to construct targeted polymeric structures, to the initial experimental implementation of these ideas in the mid-80’s and to the introduction of the name MOFs in the 90’s. The early exploratory work with pre-organized building blocks described in this article paved the way for the subsequent explosion of research activity in the CP/MOF area and for the generation of an essentially unlimited range of designed coordination polymer structures promising a variety of useful properties.