Coordination Chemistry Reviews最新文献

{"title":"New exploration of the effect of intracellular metal ions on tumor immunity","authors":"Zhaoran Wang ,&nbsp;Qiong Chen ,&nbsp;Xuejie Chen,&nbsp;Lin Lv,&nbsp;Wukun Liu","doi":"10.1016/j.ccr.2026.217594","DOIUrl":"10.1016/j.ccr.2026.217594","url":null,"abstract":"<div><div>Tumor occurrence and progression are intimately linked to immunity, so one strategy for the therapy of malignancies is the regulation of tumor immune environment. Despite the fact that metal ions are rarely noticed and are found in extremely small amounts in cells, they are crucial for many biological functions. It is noteworthy that intracellular metal ions significantly affect the immune system and the development of tumors. This review synthesizes current understanding of how intracellular metal ions influence multiple facets of immune function, including macrophage polarization, T cell activation, and cell death pathways such as ferroptosis and pyroptosis. Our primary focus is on the metal ions, including Ca²⁺, Mn²⁺, K⁺, Fe²⁺/Fe³⁺, Zn²⁺, Cu⁺ and Mg²⁺. It is worth mentioning that a few of these metal ions play a double-edged role in modulating tumor immunity, and they are deeply intertwined in several pivotal immunological pathways. Moreover, we reviewed a series of complexes that affect intracellular metal ions to influence tumor immunity. By elucidating the mechanism of intracellular metal ions regulating the immune response, this review focuses on the recent advances in metal ion-targeted therapeutic approaches, providing innovative strategies for improving tumor immunotherapy and addressing the limitations of existing cancer treatments.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217594"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076407","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Addressing the cold challenge: Advances in electrolyte design for low-temperature alkali-metal-ion batteries","authors":"Yunfei Wu ,&nbsp;Changzhu Huang ,&nbsp;Gaigai Duan ,&nbsp;Jingjiang Yang ,&nbsp;Yong Huang ,&nbsp;Zhao Liang ,&nbsp;Xiaoshuai Han ,&nbsp;Bin He ,&nbsp;Chunmei Zhang ,&nbsp;Shuijian He ,&nbsp;Shaohua Jiang","doi":"10.1016/j.ccr.2026.217655","DOIUrl":"10.1016/j.ccr.2026.217655","url":null,"abstract":"<div><div>With the overconsumption of traditional fossil energy and the increase of environmental pollution, the development of green renewable energy and energy storage technology is becoming more and more important, and alkali metal ion batteries have become a research hotspot. However, the performance of alkali metal ion batteries deteriorates at low temperatures, mainly due to the impeded ion transport in the electrolyte, high charge transport resistance at the electrode/electrolyte interface, and the instability of the solid electrolyte interphase layer. As an important part of the battery, the performance of the electrolyte is significantly affected by low temperature. Therefore, it is crucial to design the electrolyte suitable for low temperatures. When designing low temperature electrolytes, the selection of solvents, salts and additives needs to be considered. In conclusion, reasonable design of electrolyte composition can enhance the low temperature performance of alkali metal ion batteries. In the future, new electrolyte materials and formulations should be further explored to combine electrolyte chemistry improvement with electrode material optimization and electrolyte/electrode interaction tailoring to meet the demand for low-temperature energy storage, and to promote the development of green energy applications and global energy storage technology.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217655"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146185476","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Design concept and solar-to-energy applications of CuPbSbS3 from photovoltaics to photocatalysis","authors":"Yuhao Liu ,&nbsp;Xinjie Chen ,&nbsp;Gai Li ,&nbsp;Minghui Wang ,&nbsp;Miaomiao Yang ,&nbsp;Jing Li ,&nbsp;Xiaodong Shi ,&nbsp;Yonghao Xiao ,&nbsp;Fengyun Su ,&nbsp;Xinlong Tian","doi":"10.1016/j.ccr.2026.217656","DOIUrl":"10.1016/j.ccr.2026.217656","url":null,"abstract":"<div><div>The efficient solar-to-energy (STE) technique, relying on the advanced semiconductor materials, is critically important for addressing the global energy crisis. The ideal semiconductors for efficient STE conversion should exhibit high electronic dimensionality guided by the advanced concept. Herein, electronic dimensionality refers to the connectivity of atomic orbitals in the frontier electronic bands, which directly influence the charge transport anisotropy and carrier effective masses. The advanced three-dimensional (3D) electronic dimensionality enables the isotropic and efficient charge carrier transport, a feature of high-STE-performance semiconductors. Bournonite CuPbSbS₃, a recently emerging metal sulfide (MS) material, features the 3D electronic dimensionality, direct bandgap of approximately 1.3 eV, and defect-tolerant feature, rendering it a highly promising candidate for high-performance STE systems. This review begins by outlining the design principles and fundamental semiconductor characteristics of CuPbSbS₃, and then offers a comprehensive survey of its exploration process and applications across the STE spectrum, from photovoltaics to photocatalysis. Finally, perspective on the challenges and opportunities for future research on bournonite CuPbSbS₃ are provided.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217656"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146098425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Solid-state NMR characterization of weak interactions in molecular crystals","authors":"Chiara Sabena ,&nbsp;Chiara Rosso ,&nbsp;Téodor Iftemie ,&nbsp;Roberto Gobetto ,&nbsp;David L. Bryce ,&nbsp;Michele R. Chierotti","doi":"10.1016/j.ccr.2026.217610","DOIUrl":"10.1016/j.ccr.2026.217610","url":null,"abstract":"<div><div>Weak non-covalent interactions, including hydrogen bonds, π–π stacking, and the diverse family of σ-hole interactions (halogen, chalcogen, pnictogen, tetrel, osme, and matere bonds), govern the structure, stability, and properties of molecular crystals. Solid-state Nuclear Magnetic Resonance (SSNMR) spectroscopy provides an unparalleled means of probing these interactions at the atomic level by directly sensing local electronic environments, independent of long-range order. This review surveys recent advances (approximately since 2020) in SSNMR methodologies for detecting, characterizing, and quantifying weak interactions in molecular solids. Particular emphasis is placed on developments in high-field and ultrafast magic-angle spinning (MAS) instrumentation, as well as novel pulse sequences that enhance access to key nuclei involved in non-covalent bonding. SSNMR observables, such as chemical shifts, dipolar and <em>J</em> couplings, quadrupolar parameters, and relaxation rates, are shown to provide quantitative insight into the interaction strength, geometry, and dynamics of hydrogen-bonded, π-stacked, and σ-hole-bonded systems. The review also discusses the synergistic integration of SSNMR with diffraction (single-crystal and powder X-ray diffraction, electron diffraction) and computational methods (Crystal Structure Prediction, DFT calculations, molecular dynamics simulations, machine learning models), yielding a multidimensional framework for elucidating structure–property relationships in both crystalline and disordered materials. Special attention is devoted to complex environments such as multicomponent crystals, host–guest assemblies, and amorphous dispersions. Looking ahead, continued advances in ultrahigh-field instrumentation, pulse-sequence design, and NMR crystallography promise to transform SSNMR from a diagnostic into a predictive tool for supramolecular chemistry and crystal engineering, bridging microscopic interactions with macroscopic material behaviour.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217610"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146072752","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Molecularly imprinted catalysts for pollutants degradation: principle, process, application, toxicological effect, and prospect","authors":"Zhimin Liu,&nbsp;Rong Fan,&nbsp;Yuanyuan Wan,&nbsp;Xiaolan Zhang,&nbsp;Shihan Gao,&nbsp;Zhigang Xu","doi":"10.1016/j.ccr.2026.217629","DOIUrl":"10.1016/j.ccr.2026.217629","url":null,"abstract":"<div><div>Environmental pollutants, often present at low concentrations and pose a serious threat to ecological security. Traditional treatment techniques are constrained by poor selectivity, low efficiency and high susceptibility to interference from complex matrices. Molecular imprinting technology (MIT), characterized by exceptional selectivity in specific recognition and a simplified yet precise fabrication process, is increasingly emerging as a promising tool in the environment monitoring field. By integrating with various catalytic factors, molecularly imprinted catalysts (MICs) offer an effective solution to this challenge. This review systematically summarizes the underlying principles of photocatalysis, electrocatalysis, and enzyme-mimicking catalysis in MICs. Furthermore, it highlights the recent advances in various forms of MICs and their practical applications in pollutant degradation for the first time. The potential toxicity and environmental impact of MICs materials and their degradation products are also critically evaluated. This work aims to inspire novel applications of MIT in catalysis, offer methodological insights into the effective removal of persistent pollutants, and provide a forward-looking perspective to encourage further exploration by emerging researchers in this interdisciplinary field.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217629"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146072748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Optical probes for redox imaging: A comparative review of fluorescent, bioluminescent, and chemiluminescent strategies for in vivo sensing of ROS, RNS, and RSS","authors":"Yuhan Wang ,&nbsp;Xiaoyu Li ,&nbsp;Zhangdong Wang ,&nbsp;Peng Wang ,&nbsp;Zhen Chen ,&nbsp;Jing Yang","doi":"10.1016/j.ccr.2026.217628","DOIUrl":"10.1016/j.ccr.2026.217628","url":null,"abstract":"<div><div>Reactive oxygen species (ROS), reactive nitrogen species (RNS), and reactive sulfur species (RSS), when overproduced during sustained inflammatory responses, cause oxidative stress and contribute to various acute and chronic diseases. Monitoring these molecules is crucial for understanding pathological mechanisms and evaluating therapeutic effects. This review provides a systematic comparison of fluorescent, bioluminescent, and chemiluminescent probes for <em>in vivo</em> imaging of ROS, RNS and RSS in inflammatory diseases. Over the past decade, each modality has developed distinct advantages: fluorescence offers high-resolution real-time visualization, bioluminescence enables deep-tissue imaging with ultra-low background, and chemiluminescence allows direct, excitation-free detection of redox activity. To clarify this landscape, we employ a “building-block” logic to dissect the design principles and evolutionary trajectories of these probes. Focusing on inflammation and related disease models, we highlight the transformative potential of bioluminescent and chemiluminescent probes for real-time monitoring of oxidative stress. This work provides a structured guide for selecting and innovating optical probes in redox biology.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217628"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076406","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Design and Engineering of Metal-Organic Frameworks for Energy Conversion and Environmental Remediation","authors":"K. Aravinthkumar ,&nbsp;S. Gokul Eswaran ,&nbsp;Shuchen Hsieh ,&nbsp;Shuling Hsieh ,&nbsp;A. Santhana Krishna Kumar ,&nbsp;C. Raja Mohan","doi":"10.1016/j.ccr.2026.217582","DOIUrl":"10.1016/j.ccr.2026.217582","url":null,"abstract":"<div><div>Recent technological advancements, rising energy crises, and environmental pollution have prompted the development and synthesis of innovative materials for efficient energy conversion and water purification in order to fulfil society's clean energy and water needs. A variety of pollutants have grown more persistent in aquatic environments. The inappropriate use of dyes and antibiotics, as well as their inadequate digestion in organisms, results in their discharge into aquatic habitats, which has harmed human health. Therefore, effective removal of textiles and pharmaceuticals, especially dyes and antibiotics, from wastewater and polluted water bodies is of significant interest to research communities across the world. Besides, the depletion of fossil fuels increases the demand for renewable energy sources. Since solar energy is the most abundant and endless energy source, it provides an environmentally friendly alternative to fossil fuels. Metal-organic frameworks (MOFs), which are porous crystalline hybrid materials formed by the linkage of metal centers (clusters) and organic linkers (organic ligands), have been identified as a highly active research domain for more than a decade due to their wide range of applications as photocatalytic and photovoltaic. In the present research domain, the research community has been drawn to emerging MOFs by their distinctive properties, which include a large surface area, controllable morphologies, tunable porosities, layer-by-layer design, high-quality crystalline products, outstanding inorganic-organic nature, and incredible diversity in functionalities. In this review, the latest developments in the use of MOFs and their derivatives in a variety of solar cell technologies, such as dye-sensitized, perovskite, and organic solar cells, are methodically described. These MOF-based photovoltaic systems have shown remarkable potential for enhancing sunlight-to-electricity conversion efficiency and improving stability. In addition, the utilization of MOFs and their derivatives as photocatalysts is a highly effective approach for breaking down dye and antibiotic residues in water. Key improvements and modifications, such as stronger interfacial contact, enhanced light harvesting, and improved charge separation, have been emphasized to develop potent photocatalysts that significantly enhance the removal of dyes and antibiotics. The environmental factors influencing photocatalytic degradation activity, such as photocatalyst concentration, pollutant concentration, solution pH, light intensity, reaction temperature, Fenton reagent, and scavengers, were thoroughly discussed, assisting in the design of an ideal photoreactor with high photocatalytic efficiency and a cost-effective process. Furthermore, the remaining significant challenges in the aforementioned domains are addressed, and potential future research endeavours in the development of MOFs are also outlined.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217582"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076408","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Covalent organic frameworks based dual-emission materials for ratiometric fluorescence sensing: A review on design strategies, mechanisms, and applications","authors":"Ming-Yue Wang ,&nbsp;Jing Zeng ,&nbsp;Yue-Fan Lai ,&nbsp;Lei-Jiao Peng ,&nbsp;Dan-Dan Wang ,&nbsp;Min-Min Wang ,&nbsp;Mei-ling Yang ,&nbsp;Yue Lan ,&nbsp;Jia-Qi Hu ,&nbsp;Feng-Qing Yang ,&nbsp;Die Gao","doi":"10.1016/j.ccr.2026.217638","DOIUrl":"10.1016/j.ccr.2026.217638","url":null,"abstract":"<div><div>Covalent organic frameworks (COFs), characterized by high specific surface area, tunable pore structures, and excellent stability, provide an ideal platform for developing high-performance ratiometric fluorescence sensors. By measuring the intensity ratio of two emission signals, these sensors offer built-in self-calibration, overcoming the limitations of single-signal probes affected by environmental interference, and thus improving sensitivity, selectivity, and reliability in detecting trace analytes in complex samples. This review systematically outlines construction strategies for dual-emission COF-based ratiometric sensors, such as intrinsic backbone dual-emission, doping-induced dual-emission, and hybrid/heterostructure-induced dual-emission. For each approach, advantages, limitations, and development directions are discussed. Key structural factors (e.g. topology, π–π stacking, donor–acceptor motifs, pore environment, and crystallinity) and their roles in integrating luminescent units are discussed to explain how they collectively influence dual-emission performance and stability. Common construction challenges and corresponding mitigation strategies are also summarized to enhance sensor reliability and efficiency. The review further elaborates on relevant sensing mechanisms, including excited-state intramolecular proton transfer (ESIPT) and Förster resonance energy transfer (FRET), as well as summarizes the interrelationships of construction strategy-response mode-sensing mechanism. Performance advantages and recent applications in environmental monitoring, food safety, and biomedical analysis are highlighted. Despite their promise, practical use of these sensors still faces challenges in signal controllability and environmental adaptability. Based on current limitations, this review suggests future directions: precise control and mechanistic study of dual-emission behavior, enhancing signal reliability in real samples and enabling device integration, and data-driven material design for performance optimization. Through collaborative advances, dual-emission COF-based sensors are expected to evolve into versatile detection platforms for environmental, clinical, and food safety applications, promoting the practical adoption of next-generation sensing technologies.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217638"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076409","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Unveiling the versatility and reactivity of N-heterocyclic carbene complexes with metal and non-metal fluorides: a comprehensive review","authors":"Evelin Gruden,&nbsp;Gašper Tavčar","doi":"10.1016/j.ccr.2026.217604","DOIUrl":"10.1016/j.ccr.2026.217604","url":null,"abstract":"<div><div>N-Heterocyclic carbenes (NHCs) have become cornerstone ligands in modern coordination and main-group chemistry, yet their interactions with metal and non-metal fluorides have long remained underexplored because many fluorides are poorly soluble and often difficult to handle. This review surveys the synthesis, structures, and reactivity of all structurally characterized NHC complexes and adducts containing the NHC-M-F fragment reported from the advent of isolable NHCs (1991) through mid-2025. Across 33 elements spanning the s-, p-, d-, and f-blocks, we compile 458 reported compounds, including 277 crystallographically authenticated species, and organize the field by element group and oxidation state. Emphasis is placed on practical synthetic entry points: direct coordination to soluble fluoride sources, transmetalation and synthon strategies, dehydrofluorination routes from fluoride salts, fluorination of pre-formed halide, hydride, or organo precursors, and redox-driven fluoride formation. We highlight how ligand sterics and electronics (including CAAC and related carbenes) govern stability and speciation. Comparative analysis of NHC–M and M–F metrics, typical geometries, and ¹⁹F NMR ranges reveals periodic trends and recurring structural motifs, providing a unified reference framework for designing new NHC-stabilized fluoride compounds and leveraging their distinctive reactivity.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217604"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146076454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Organic dyes and dye derivatives for advanced electrochemical energy storage: a review of sustainable and emerging materials","authors":"Chen Xiao ,&nbsp;Dan Shao ,&nbsp;Igor Zhitomirsky ,&nbsp;Guanjie He ,&nbsp;Kaiyuan Shi","doi":"10.1016/j.ccr.2026.217659","DOIUrl":"10.1016/j.ccr.2026.217659","url":null,"abstract":"<div><div>This review addresses the growing demand for sustainable energy technologies by exploring the rapid advancements in organic dyes for aqueous-based electrochemical energy storage (AEES). By examining their functional groups, structural properties, and solvation behavior, we explore the mechanisms that govern their electrochemical behavior in aqueous environments. Organic dyes enhance interfacial charge transport via proton-electron coupled exchange. Their electrochromic behavior allows for versatile applications in AEES systems. The review systematically categorizes prominent dyes- including anthraquinone, azo, nitro, triphenylmethane, and heterocyclic compounds and highlights their redox mechanisms and electrochemical properties. Advanced analytical techniques, such as UV–Vis, Raman, FTIR, and NMR spectroscopy, provide critical insights into structure-function relationships. Investigations into aqueous solubility, ion coordination effects, and interfacial interactions emphasize the multifunctional potential of these materials. Challenges, including the irreversible transformation and shuttling effect, are addressed in dye-containing electrolytes. Additionally, the incorporation of organic dyes with conductive polymers and carbon-based additives, such as graphene and carbon nanotubes, improves charge storage and electrochemical stability. The review highlights the crucial role of organic dyes and their derivatives for AEES applications. It outlines future research directions, emphasizing the need for interdisciplinary collaboration and innovative engineering approaches to enhance their sustainability and electrochemical performance.</div></div>","PeriodicalId":289,"journal":{"name":"Coordination Chemistry Reviews","volume":"555 ","pages":"Article 217659"},"PeriodicalIF":23.5,"publicationDate":"2026-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146109822","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}