Chemical record最新文献_第6页

Ammonia as a Hydrogen Carrier: Advances in Storage, Catalytic Decomposition, Kinetics, and Techno-Economic Analysis 氨作为氢载体：储存、催化分解、动力学和技术经济分析的进展。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-22 Epub Date: 2026-06-29 DOI: 10.1002/tcr.70200

Jahril Nur Fauzan, Ahsan Ali, M. A. Shadab Siddiqui, Md. Delowar Hossain, Md. Abdul Aziz, Md. Hasan Zahir, Fahad Alam, M. Nasiruzzaman Shaikh

{"title":"Ammonia as a Hydrogen Carrier: Advances in Storage, Catalytic Decomposition, Kinetics, and Techno-Economic Analysis","authors":"Jahril Nur Fauzan, Ahsan Ali, M. A. Shadab Siddiqui, Md. Delowar Hossain, Md. Abdul Aziz, Md. Hasan Zahir, Fahad Alam, M. Nasiruzzaman Shaikh","doi":"10.1002/tcr.70200","DOIUrl":"10.1002/tcr.70200","url":null,"abstract":"A carbon-free energy system might use ammonia as a hydrogen carrier owing to its high hydrogen concentration, good liquefaction, and worldwide production and transportation infrastructure. Catalytic ammonia breakdown provides a CO2-free hydrogen-generating method, but high temperatures, catalyst deactivation, and expense restrict its practicality. This study covers important aspects of ammonia decomposition catalysts, including Ru-, Ni-, and Co-based systems supported by carbon, Al2O3, and perovskite oxides. To develop structure–activity connections and identify rate-limiting stages under various operating regimes, thermodynamic, kinetic, and fundamental reaction processes are examined. Ru-based catalysts, especially those supported on conductive carbons and tailored perovskites, are standards for low-temperature activity, but their high cost and stability prevent large-scale application. Combining Ni-based catalysts with Al2O3 or basic perovskite supports offers a good balance between activity, cost, and commercial practicality, making them the dominant non-noble alternatives. Due to strong metal–support interactions and alternate reaction routes, Co-based catalysts in perovskite formulations seem promising despite being inherently less active. Support chemistry, promoters, metal dispersion, and oxygen vacancies are discussed, along with low-temperature operation and scale-up problems and research prospects.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":"26 9","pages":""},"PeriodicalIF":8.9,"publicationDate":"2026-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148351105","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Catalyst-Free Aerobic Photooxidation: Mechanistic Pathways and Sustainability Perspectives 无催化剂有氧光氧化：机制途径和可持续性观点。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-22 Epub Date: 2026-06-29 DOI: 10.1002/tcr.70203

Hyena Suh, Sohyeon Kim, Boyoung Y. Park

{"title":"Catalyst-Free Aerobic Photooxidation: Mechanistic Pathways and Sustainability Perspectives","authors":"Hyena Suh, Sohyeon Kim, Boyoung Y. Park","doi":"10.1002/tcr.70203","DOIUrl":"10.1002/tcr.70203","url":null,"abstract":"Catalyst-free aerobic photooxidation represents an increasingly important strategy for visible-light-driven oxidative synthesis using molecular oxygen as the terminal oxidant. In these transformations, substrate excitation or electron donor–acceptor (EDA) interactions directly activate O2 through energy transfer, single-electron transfer, hydrogen-atom transfer, or EDA-mediated pathways, enabling diverse oxidative reactivity without external photocatalysts or stoichiometric oxidants. Despite rapid growth of this field, these reactions have largely been discussed as isolated transformations rather than as a unified oxidative platform governed by common photoactivation principles. This review provides a unified mechanistic and operational framework for catalyst-free aerobic photooxidation. Reported systems are organized into six major reaction classes, establishing recurring relationships between activation modes, oxygen-derived intermediates, and oxidative reactivity. The review further discusses sustainability and operational implications arising from solvent choice and reaction conditions. Together, these perspectives establish catalyst-free aerobic photooxidation as a conceptually unified platform for future sustainable oxidative synthesis.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":"26 9","pages":""},"PeriodicalIF":8.9,"publicationDate":"2026-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148351164","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Mimicking Natural Catalytic Systems: Design Inspired Beyond the Traditional Paradigm. 模仿自然催化系统：超越传统范式的设计灵感。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-16 DOI: 10.1002/tcr.70254

Igor V Komarov, Anastasiia Hurieva, Oleksandr Ishchenko, Oleksandr O Grygorenko

{"title":"Mimicking Natural Catalytic Systems: Design Inspired Beyond the Traditional Paradigm.","authors":"Igor V Komarov, Anastasiia Hurieva, Oleksandr Ishchenko, Oleksandr O Grygorenko","doi":"10.1002/tcr.70254","DOIUrl":"https://doi.org/10.1002/tcr.70254","url":null,"abstract":"Organocatalysis has undergone remarkable conceptual expansion over the past two decades, evolving from isolated early 20th century observations into a broad platform for designing structurally diverse and functionally sophisticated catalysts. While early developments were strongly influenced by straightforward analogies to natural enzymes, recent advances demonstrate that inspiration from biological catalysis can extend far beyond direct mimicry. This review covers representative examples in which chemists reinterpret, broaden, or strategically depart from enzymatic logic to achieve new reactivity and improved catalytic performance. We first examine organocatalysts derived from enzymatic cofactors, including thiamine-inspired carbene catalysts and pyridoxal-based systems, whose functions have been adapted for transformations not observed in nature. We then discuss catalysts engineered for efficient operation in aqueous media, followed by chemoenzymatic cascade processes. Further sections illustrate how organocatalysis can emulate biosynthetic logic in the construction of complex natural products. Finally, we highlight the reverse flow of inspiration, where organocatalytic concepts inform the design of engineered biocatalysts.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":" ","pages":"e70254"},"PeriodicalIF":8.9,"publicationDate":"2026-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148982464","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

High-Entropy Materials for Next-Generation Energy Systems: A Decade of Progress in Synthesis, Properties, and Applications. 用于下一代能源系统的高熵材料：合成、性质和应用的十年进展。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-15 DOI: 10.1002/tcr.70211

Saim Saher, Affaq Qamar, Chou Yong Tan, Walied Alfraidi, Kim Hung Mo, M Furjan, Xinwen Peng, Lee Ching Shya

{"title":"High-Entropy Materials for Next-Generation Energy Systems: A Decade of Progress in Synthesis, Properties, and Applications.","authors":"Saim Saher, Affaq Qamar, Chou Yong Tan, Walied Alfraidi, Kim Hung Mo, M Furjan, Xinwen Peng, Lee Ching Shya","doi":"10.1002/tcr.70211","DOIUrl":"https://doi.org/10.1002/tcr.70211","url":null,"abstract":"The transition to low-carbon energy systems is increasingly constrained by the intrinsic limitations of conventional materials, which often struggle to simultaneously deliver high catalytic activity, long-term stability, and operational durability. Over the past decade, high-entropy materials (HEMs) have emerged as a transformative materials-design paradigm that addresses these challenges by shifting from single-principal-element optimization to entropy-driven stabilization of multicomponent, highly disordered solid solutions. This review critically traces the evolution of functional HEMs from their metallurgical origins to their growing prominence in energy-related ceramic and ionic systems. We elucidate the thermodynamic foundations of the field, examining how the four core effects-high-entropy stabilization, severe lattice distortion, sluggish diffusion, and the cocktail effect-translate into tangible performance enhancements in electrochemical applications. Adopting a structure-centric framework, we highlight recent breakthroughs across key lattice families, including the suppression of cation segregation in high-entropy perovskite cathodes for solid oxide fuel cells, the expansion of redox windows in high-entropy layered double hydroxides for supercapacitors, and the precise electronic tuning of active sites in high-entropy spinels for nitrate reduction electrocatalysis. Furthermore, we assess advances in synthesis strategies, contrasting thermodynamically driven solid-state approaches with kinetically controlled solution-based routes essential for nanoscale engineering.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":" ","pages":"e70211"},"PeriodicalIF":8.9,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148975914","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Synthesis-Driven Structure-Property Correlations in Metal Oxytellurides for Emerging Device Applications. 新兴器件应用中金属氧碲化物的合成驱动结构-性质相关性。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-15 DOI: 10.1002/tcr.70251

Prabhukrupa Chinmay Kumar, Soumya Pattnaik, Rohan Kumar Bisoi, Ramakanta Naik

{"title":"Synthesis-Driven Structure-Property Correlations in Metal Oxytellurides for Emerging Device Applications.","authors":"Prabhukrupa Chinmay Kumar, Soumya Pattnaik, Rohan Kumar Bisoi, Ramakanta Naik","doi":"10.1002/tcr.70251","DOIUrl":"https://doi.org/10.1002/tcr.70251","url":null,"abstract":"Metal oxytellurides (MOTs), a new class of mixed-anion oxychalcogenides with both O2- and Te2- ions, provide a highly tunable platform for next-generation electronic and energy devices. The structural chemistry of MOTs consists of the hard covalent oxide network with soft, polarizable telluride sublattice resulting in tunable electronic structures, adaptable coordination, and enhanced spin-orbit coupling. This Account aims to synthesize the structure-property relationships in MOTs with a unifying theme of how small deviations in anion order, composition, defect chemistry, and coordinated state can dramatically affect band structure, electron/hole transport, thermal transport, and electrochemical properties. Synthesis discussions focus on the importance of leveraging solid-state, flux-mediated, microwave-assisted, high-pressure, and topochemical transformations for phase stabilization, defect engineering, and particle/morphology control. The typical bandgap range across MOT families varies between ∼0.14 and 5.5 eV, and the highest reported thermoelectric figure of merit is ZT ≈ 1.06 for Te-substituted BiCuOTe. Structural models are analyzed with computational analysis, using density functional theory, giving insight into phase stability, defect preferences, and the consequent electronic structure evolutions. Guided by these models, descriptors, and computational predictions, select future directions are suggested for large-scale manufacture, compositional space exploration, property optimization, and commercialization of MOTs for thermoelectric, electrochemical, and optoelectronic devices.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":" ","pages":"e70251"},"PeriodicalIF":8.9,"publicationDate":"2026-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148975847","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Ligand-Controlled Selective Hydrosilylation of 1,3-Conjugated Dienes Catalyzed by Earth-Abundant Metals: Recent Advances. 稀土富集金属催化1,3-共轭二烯的配体控制选择性硅氢化反应研究进展。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-14 DOI: 10.1002/tcr.70252

Xiuling Wen, Wanyi Zhen, Sitong Guo, Chao Zhang, Hui Gao

引用次数: 0

Covalent Organic Frameworks-Based Hybrid Materials for Electrochemical Energy Storage: Advances in Supercapacitors and Batteries. 基于共价有机框架的电化学储能混合材料：超级电容器和电池的研究进展。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-14 DOI: 10.1002/tcr.70250

Basit Ali Khan, Syeda Rubab, Tongsheng Zhang, Farasat Haider, Manzar Abbas, Muhammad Muntazir Mehdi, Hasnain Ali, Fatima Zahra, Ali Junaid, Aftab Ahmad Khan

{"title":"Covalent Organic Frameworks-Based Hybrid Materials for Electrochemical Energy Storage: Advances in Supercapacitors and Batteries.","authors":"Basit Ali Khan, Syeda Rubab, Tongsheng Zhang, Farasat Haider, Manzar Abbas, Muhammad Muntazir Mehdi, Hasnain Ali, Fatima Zahra, Ali Junaid, Aftab Ahmad Khan","doi":"10.1002/tcr.70250","DOIUrl":"https://doi.org/10.1002/tcr.70250","url":null,"abstract":"The growing global energy demand and the need for sustainable energy technologies have accelerated the development of advanced electrochemical energy storage systems. Covalent organic frameworks, class of crystalline porous polymers formed through reversible covalent bonding, have emerged as promising materials for energy storage applications. Their tunable porosity, high surface area, structural diversity, and high chemical stability make them attractive electrode materials for supercapacitors and rechargeable batteries. This review highlights recent advances in COF-based composites and their enhanced electrochemical performance in different energy storage devices. Particular emphasis is given to rational design strategies in which COFs are combined with conductive polymers, carbon-based nanomaterials, and metal oxides. These hybrid structures help overcome the inherent limitations of pristine COFs, such as low electrical conductivity and limited redox activity. The relationship between structure, properties, and electrochemical performance of COF-based electrodes is critically discussed for batteries and supercapacitors. Key performance parameters, including specific capacity, rate capability, and cycling stability, are systematically analyzed. Despite significant progress, several challenges remain, with scalable synthesis methods, cost-effectiveness, and long-term stability. Upcoming research should focus on the development of multifunctional COF composites, environmentally friendly synthesis approaches, and the application of machine learning techniques to accelerate the optimization of high-performance energy storage materials.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":" ","pages":"e70250"},"PeriodicalIF":8.9,"publicationDate":"2026-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148966917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Designing Zinc- and Cadmium-Based Luminescent Metal-Organic Frameworks for Antibiotic Detection: Structure-Function Relationships, Sensing Mechanisms, and Future Perspectives. 设计用于抗生素检测的锌和镉基发光金属有机框架：结构-功能关系，传感机制和未来展望。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-11 DOI: 10.1002/tcr.70241

Deepak Kumar Pandey, Aman K K Bhasin, K K Bhasin, Ahmad Husain, Girijesh Kumar

{"title":"Designing Zinc- and Cadmium-Based Luminescent Metal-Organic Frameworks for Antibiotic Detection: Structure-Function Relationships, Sensing Mechanisms, and Future Perspectives.","authors":"Deepak Kumar Pandey, Aman K K Bhasin, K K Bhasin, Ahmad Husain, Girijesh Kumar","doi":"10.1002/tcr.70241","DOIUrl":"https://doi.org/10.1002/tcr.70241","url":null,"abstract":"The widespread presence of antibiotic residues in environmental and food systems poses serious risks to ecological safety and accelerates antimicrobial resistance, creating an urgent need for rapid, selective, and sensitive detection methods. This review highlights the recent advances in Zn(II)- and Cd(II)-based metal-organic frameworks (MOFs) as luminescent sensing platforms for antibiotic monitoring. Owing to their diverse structures, tunable porosity, and versatile coordination chemistry, these MOFs enable efficient detection of various antibiotic classes, including tetracyclines, sulfonamides, fluoroquinolones, nitrofurans, nitroimidazoles, amphenicols, β-lactams, and cephalosporins. Key design strategies, such as ligand engineering, pore-environment modulation, metal-node selection, and hybrid framework construction, are discussed in relation to sensing performance. Particular emphasis is placed on structure-property relationships governing selectivity, sensitivity, and detection limits. Major fluorescence sensing mechanisms, including photoinduced electron transfer (PET), Förster resonance energy transfer (FRET), inner filter effect (IFE), aggregation-induced emission (AIE), and intramolecular charge transfer (ICT), are critically compared. The review further addresses challenges related to framework stability, selectivity, and real-sample applicability, while outlining future directions involving multifunctional sensors, portable detection devices, and artificial intelligence (AI)-assisted MOF design. Overall, this review provides practical guidelines for the rational development of next-generation Zn- and Cd-based MOF sensors for antibiotic detection.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":" ","pages":"e70241"},"PeriodicalIF":8.9,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148929172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Artificial Interfacial Protective Layers for Zinc Anodes in Aqueous Zinc-Ion Batteries: Design Principles and Stabilization Mechanisms. 水锌离子电池中锌阳极的人工界面保护层：设计原理和稳定机制。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-09 DOI: 10.1002/tcr.70248

Shuo Liu, Shaohua Luo, Jun Cong, Qi Sun, Shengxue Yan, Jing Guo

{"title":"Artificial Interfacial Protective Layers for Zinc Anodes in Aqueous Zinc-Ion Batteries: Design Principles and Stabilization Mechanisms.","authors":"Shuo Liu, Shaohua Luo, Jun Cong, Qi Sun, Shengxue Yan, Jing Guo","doi":"10.1002/tcr.70248","DOIUrl":"https://doi.org/10.1002/tcr.70248","url":null,"abstract":"Aqueous zinc-ion batteries (AZIBs) are promising for large-scale energy storage owing to their high safety, low cost, abundant Zn resources, and environmental compatibility. However, Zn metal anodes suffer from interfacial instability in aqueous electrolytes, including dendrite growth, hydrogen evolution, corrosion/passivation, and insulating by-products, which impair reversible Zn2+ plating/stripping and cycling durability. Artificial interfacial protective layers offer an effective route to stabilize Zn anodes by integrating protective and regulatory functions at the Zn/electrolyte interface. This review summarizes the failure mechanisms of Zn anodes and the design principles of artificial interphases, emphasizing homogenized Zn2+ flux and electric-field distribution, suppression of active water and side reactions, and improved ionic conductivity and interfacial stability. The compositions, fabrication methods, mechanisms, advantages, and limitations of inorganic, organic/polymeric, and organic-inorganic hybrid interphases are discussed. Finally, current challenges, including molecular-level mechanism identification, long-term structural stability, practical-condition evaluation, and scalable fabrication, are highlighted. A mechanism-oriented framework linking interfacial composition, Zn2+ transport, desolvation, water activity regulation, electric-field homogenization, and structural adaptability is proposed to guide advanced Zn-anode protection.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":" ","pages":"e70248"},"PeriodicalIF":8.9,"publicationDate":"2026-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148918478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

From Barrier Disruption to Precision Skin Interface Engineering: Next-Generation Transdermal Drug Delivery. 从屏障破坏到精确皮肤界面工程：新一代透皮给药。

IF 8.9 2区化学

Chemical record Pub Date : 2026-09-09 DOI: 10.1002/tcr.70249

Cong-Zheng Zhou, Xin-Yu Lin, Shou-Shan Yu, Sheng-Lin Qiao

{"title":"From Barrier Disruption to Precision Skin Interface Engineering: Next-Generation Transdermal Drug Delivery.","authors":"Cong-Zheng Zhou, Xin-Yu Lin, Shou-Shan Yu, Sheng-Lin Qiao","doi":"10.1002/tcr.70249","DOIUrl":"https://doi.org/10.1002/tcr.70249","url":null,"abstract":"Transdermal drug delivery (TDD) is reemerging as a clinically attractive route for noninvasive therapy, driven by the growing demand for alternatives to repeated injection and by the rapid development of materials capable of regulating transport across the skin. By avoiding gastrointestinal degradation and hepatic first-pass metabolism, TDD can provide prolonged drug exposure, reduce peak-to-trough fluctuations in plasma concentration, and improve adherence in long-term treatment. Its broader implementation, however, is still constrained by the exceptional barrier function of the stratum corneum, which severely limits the passive transport of hydrophilic molecules, charged species, and macromolecular therapeutics. In this review, we critically discuss the structural basis of the skin barrier and summarize the evolution of TDD strategies from conventional chemical permeation enhancement and device-assisted physical disruption to nanocarrier-mediated, biomimetic, and intelligent bio-delivery systems. Particular emphasis is placed on the mechanistic logic that connects carrier composition, interfacial interactions, skin microenvironment remodeling, and therapeutic performance. Representative examples are analyzed to highlight both opportunities and translational bottlenecks. Finally, we outline future directions in multimodal delivery, pathology-adapted design, standardized evaluation, and scalable manufacturing, which will be essential for transforming TDD from a permeability enhancement technology into a precision-regulated therapeutic platform.","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":" ","pages":"e70249"},"PeriodicalIF":8.9,"publicationDate":"2026-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148918503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0