Angewandte Chemie (International ed. in English)最新文献_第10页

In-Built Compatible Electrode-Electrolyte Interphases for Quasi-Solid-State Li-SPAN Batteries. 准固态Li-SPAN电池的内置兼容电极-电解质界面。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-09-04 DOI: 10.1002/anie.202510624

Tao Zhang, Zhengyuan Shen, Xinhui Pan, Man Zhang, Tong Lian, Keqing Shi, Ji Qian, Li Li, Feng Wu, Renjie Chen

{"title":"In-Built Compatible Electrode-Electrolyte Interphases for Quasi-Solid-State Li-SPAN Batteries.","authors":"Tao Zhang, Zhengyuan Shen, Xinhui Pan, Man Zhang, Tong Lian, Keqing Shi, Ji Qian, Li Li, Feng Wu, Renjie Chen","doi":"10.1002/anie.202510624","DOIUrl":"https://doi.org/10.1002/anie.202510624","url":null,"abstract":"Lithium-sulfur batteries have been regarded as a promising candidate for next-generation energy storage systems owing to their high energy density and low cost. Sulfurized polyacrylonitrile (SPAN) as a cathode material has received wide interest due to the solid-solid conversion mechanism, while the Li-SPAN cell performance has been limited by the notorious issue of lithium metal anode. Developing solid-state electrolytes for lithium-sulfur batteries with favorable electrode-electrolyte compatibility is urgently desired. Herein, we demonstrate a dual-interface optimization strategy through in-situ polymerization interface construction, which synergistically enhances interfacial compatibility between the solid polymer electrolyte (SPE) and both the lithium metal anode and SPAN cathode. The initiator pre-buried in the SPE triggers the in-situ polymerization of 1,3-dioxolane (DOL) at the interface, thereby greatly reducing the electrode/electrolyte interfacial impedance. Additionally, the released fluoroethylene carbonate (FEC) into the poly-DOL interface could further reduce the impedance and enhance the interface stability during cycling, simultaneously preventing the dissolution of polysulfides, owing to the inorganic-rich and dense cathode electrolyte interphase formed on SPAN. As a result, the Li-SPAN cell could operate more than 200 cycles at 0.5C with a capacity retention of 90%. We believe that this strategy provides prospects for the development of high-energy solid-state lithium-sulfur batteries.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202510624"},"PeriodicalIF":16.9,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145002763","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Mechanistic Divergence in Sulfur-Ligated Iron(III)-Alkylperoxo Reactivity: Aldehyde Oxidation Prevails over Deformylation. 硫连接铁(III)-烷基过氧反应性的机理差异：醛氧化优于脱甲酰化。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-09-04 DOI: 10.1002/anie.202512839

Jagnyesh K Satpathy, Rolly Yadav, Payal Panwar, Vijaya Thangaraj, Maheswaran Shanmugam, Chivukula V Sastri, Sam P de Visser

{"title":"Mechanistic Divergence in Sulfur-Ligated Iron(III)-Alkylperoxo Reactivity: Aldehyde Oxidation Prevails over Deformylation.","authors":"Jagnyesh K Satpathy, Rolly Yadav, Payal Panwar, Vijaya Thangaraj, Maheswaran Shanmugam, Chivukula V Sastri, Sam P de Visser","doi":"10.1002/anie.202512839","DOIUrl":"https://doi.org/10.1002/anie.202512839","url":null,"abstract":"Metalloenzymes activate molecular oxygen within their catalytic cycles to generate a reactive species capable of substrate transformation. In many iron-containing enzymes, it is a high-valent iron(IV)-oxo complex that is synthesized from an iron(III)-alkylperoxo intermediate, although direct observation and characterization of such species have remained elusive, leaving their mechanistic role uncertain. To address this gap in our understanding, we present here the synthesis, comprehensive characterization, and reactivity of a novel thioether-ligated iron(III)-alkylperoxo complex supported by the ligand 2-((2-(pyridin-2-yl)ethyl)thio)-N,N-bis(pyridin-2-ylmethyl)ethan-1-amine. Characterization was done using UV-vis spectroscopy, resonance Raman spectroscopy, electron paramagnetic resonance spectroscopy, and electrospray ionization mass spectrometry. Reactivity studies reveal that this complex exhibits electrophilic oxidation of model substrates, including dimethylsulfide, triphenylphosphine, and cyclohexanecarboxaldehyde. Notably, the latter substrate reacts via the unusual aldehyde C─H bond abstraction leading to cyclohexanecarboxylic acid, which is explained by favorable aldehyde C─H abstraction transition states due to stabilizing interactions between the ligand framework and the substrate. Moreover, the reaction is initiated with a homolytic O─O bond cleavage in the iron(III)-alkylperoxo group that yields a reactive iron(IV)-oxo species that mediates substrate oxidation. To our knowledge, this work represents the first example of a mononuclear low-spin (S = ½) nonheme iron(III)-alkylperoxo complex displaying such unprecedented electrophilic reactivity.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202512839"},"PeriodicalIF":16.9,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145002743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Multifunctional Binding Interface Drives Near-Unity CO Selectivity in Acidic CO₂ Electrolysis. 多功能结合界面驱动酸性CO2电解中近乎统一的CO选择性。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-09-04 DOI: 10.1002/anie.202514111

Zhengyuan Li, Yuting Xu, Xing Li, Gregory D Y Foley, Dian-Zhao Lin, Lingyu Zhang, Krish N Jayarapu, Long Chen, Carter S Gerke, Andong Liu, Anmol Mathur, Zhiyao Qi, Lavanya Gupta, Van Sara Thoi, Fanglin Che, Yayuan Liu

{"title":"Multifunctional Binding Interface Drives Near-Unity CO Selectivity in Acidic CO2 Electrolysis.","authors":"Zhengyuan Li, Yuting Xu, Xing Li, Gregory D Y Foley, Dian-Zhao Lin, Lingyu Zhang, Krish N Jayarapu, Long Chen, Carter S Gerke, Andong Liu, Anmol Mathur, Zhiyao Qi, Lavanya Gupta, Van Sara Thoi, Fanglin Che, Yayuan Liu","doi":"10.1002/anie.202514111","DOIUrl":"https://doi.org/10.1002/anie.202514111","url":null,"abstract":"The electrocatalytic carbon dioxide (CO2) reduction is challenged by the parasitic hydrogen evolution reaction (HER) especially in acidic media. Here, we elaborate that redox-active isoindigo, acting as a multifunctional co-catalyst, can pre-activate CO2-bound intermediates and suppress HER upon the synergistic effects of Lewis acid-base adduct formation, intramolecular hydrogen-bond interaction, and interfacial water structure modulation. Modifying a silver catalyst with isoindigo substantially decreases the energy barrier for CO2-to-*COOH conversion, which is regarded as the potential-limiting step of carbon monoxide production. Accordingly, superior catalytic performances are obtained at pH 2, where Faradaic efficiencies surpass 99% at industrial-relevant current densities. Moreover, we find that assembling an additional polyamine-coated layer in front of gas flow channels improves CO2 transport to the catalyst layer, optimizing the trade-off of conversion and selectivity at low flow rates.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202514111"},"PeriodicalIF":16.9,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145002761","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Tibor Szilvási.

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-09-04 DOI: 10.1002/anie.202518924

Tibor Szilvási

引用次数: 0

Rare Mononuclear Lithium-Carbene Complex for Atomic Layer Deposition of Lithium Containing Thin Films. 用于含锂薄膜原子层沉积的稀有单核锂-碳烯配合物。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-09-04 DOI: 10.1002/anie.202513066

Jorit Obenlüneschloß, Nils Boysen, Karl Rönnby, Arbresha Muriqi, Volker Hoffmann, Carlos Abad, Detlef Rogalla, Ulrike Brokmann, Edda Rädlein, Michael Nolan, Anjana Devi

{"title":"Rare Mononuclear Lithium-Carbene Complex for Atomic Layer Deposition of Lithium Containing Thin Films.","authors":"Jorit Obenlüneschloß, Nils Boysen, Karl Rönnby, Arbresha Muriqi, Volker Hoffmann, Carlos Abad, Detlef Rogalla, Ulrike Brokmann, Edda Rädlein, Michael Nolan, Anjana Devi","doi":"10.1002/anie.202513066","DOIUrl":"https://doi.org/10.1002/anie.202513066","url":null,"abstract":"Lithium is the core material of modern battery technologies and fabricating the lithium-containing materials with atomic layer deposition (ALD) confers significant benefits in control of film composition and thickness. In this work, a new mononuclear N-heterocyclic carbene (NHC) stabilized lithium complex, [Li(tBuNHC)(hmds)], is introduced as a promising precursor for ALD of lithium-containing thin films. Structural characterization is performed, comparing density functional theory (DFT) and single-crystal X-ray diffraction (SC-XRD), confirming a rare mononuclear structure. Favorable thermal properties for ALD applications are evidenced by thermogravimetric analysis (TGA). The compound exhibits a low melting point, clean evaporation, and its volatility parameters are encouraging compared to other lithium precursors. ALD trials using [Li(tBuNHC)(hmds)] with ozone demonstrate its effectiveness in depositing LiSixOy films. The ALD process exhibits a saturated growth per cycle (GPC) of 0.95 Å. Compositional analysis using Rutherford backscattering spectrometry/nuclear reaction analysis (RBS/NRA), X-ray photoelectron spectrometry (XPS), and glow discharge optical emission spectrometry (GD-OES), confirms the presence of lithium and silicon in the expected ratios. This work not only presents a new ALD precursor but also contributes to the understanding of lithium chemistry, offering insights into the intriguing coordination chemistry and thermal behavior of lithium complexes stabilized by NHC ligands.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202513066"},"PeriodicalIF":16.9,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145002769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Selective Catalysis-Mediated Interface to Stabilize Antimony Atom-Cluster Anode for Robust Potassium-Ion Batteries. 稳健钾离子电池中稳定锑原子簇阳极的选择性催化介面。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-09-04 DOI: 10.1002/anie.202511870

Song Chen, Fangrui Yu, Hongli Deng, Wei Chen, Hongtao Sun, Jian Zhu, Bingan Lu

{"title":"Selective Catalysis-Mediated Interface to Stabilize Antimony Atom-Cluster Anode for Robust Potassium-Ion Batteries.","authors":"Song Chen, Fangrui Yu, Hongli Deng, Wei Chen, Hongtao Sun, Jian Zhu, Bingan Lu","doi":"10.1002/anie.202511870","DOIUrl":"https://doi.org/10.1002/anie.202511870","url":null,"abstract":"Controlling the electrode-electrolyte interfacial behavior is crucial for achieving a high-quality solid electrolyte interphase (SEI) and ensuring sustainable battery performance. Here, we propose a selective catalysis strategy to stabilize antimony atom-cluster (SbSA-AC) anode/electrolyte interface for robust potassium-ion batteries (PIBs). Specifically, the electrode featuring SbSA-AC in porous carbon (SbSA-AC/PC) as \"electrocatalyst\" unduly catalyzes the reduction of the dimethyl ether-based electrolyte, resulting in loose SEI layer and rapid capacity decay. While in triethyl phosphate-based electrolyte, the SbSA-AC/PC selectively catalyzes the preferential decomposition of anions and the polymerization of solvent molecules, leading to a bilayer SEI with inner inorganic-rich components and an outer elastic polyphosphate layer, which improve the interface stability and electrochemical performance. Thus, the SbSA-AC/PC maintains a long-term stability over 12 months and demonstrates long-cycling stability over 4000 cycles with a capacity retention of 96%. This research establishes a correlation between electrode/electrolyte interactions and SEI characteristics, providing a new insight for advanced interface engineering in high-performance PIBs and beyond.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202511870"},"PeriodicalIF":16.9,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145002720","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Distinct Hole and Electron Transport Anisotropy in Ambipolar Nickel Dithiolene-Based Semiconductor. 双极性镍基半导体中不同空穴和电子输运各向异性。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-09-03 DOI: 10.1002/anie.202512609

Masatoshi Ito, Tomoko Fujino, Toshiki Higashino, Mafumi Hishida, Hatsumi Mori

{"title":"Distinct Hole and Electron Transport Anisotropy in Ambipolar Nickel Dithiolene-Based Semiconductor.","authors":"Masatoshi Ito, Tomoko Fujino, Toshiki Higashino, Mafumi Hishida, Hatsumi Mori","doi":"10.1002/anie.202512609","DOIUrl":"https://doi.org/10.1002/anie.202512609","url":null,"abstract":"Understanding anisotropic charge transport in molecular semiconductors is crucial for device optimization, yet its intricate dependence on orbital-specific intermolecular interactions and molecular packing remains a challenge, especially in ambipolar systems. In ambipolar semiconductors, where both holes and electrons participate in conduction, distinct molecular orbitals prompt a critical inquiry: can orbital variations result in coexisting yet distinct anisotropic transport properties within a single component? We confirm this possibility by demonstrating that the air-stable nickel dithiolene, Ni(4OPr), exhibits such behavior. Despite its herringbone stacking implying a two-dimensional electronic structure, Ni(4OPr) uniquely exhibits distinct intermolecular interactions for hole (HOMO-to-HOMO; HOMO = highest occupied molecular orbital) and electron (LUMO-to-LUMO; LUMO = lowest unoccupied molecular orbital) transport. Crucially, this leads to highly anisotropic hole transport pathways, while electron pathways are remarkably isotropic, demonstrating a stark contrast in their transport anisotropies. Leveraging the high crystallinity, grazing-incidence wide-angle X-ray scattering (GIWAXS) determined in-plane molecular orientation. This enabled experimental verification of distinct anisotropic hole and electron transport, directly governed by orbital-specific intermolecular interactions, in an ambipolar molecular semiconductor. Our findings, demonstrating coexisting yet distinct anisotropic transport properties for both carriers within a single component, significantly advance the understanding of ambipolar molecular semiconductors and broaden their scope for future device applications.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202512609"},"PeriodicalIF":16.9,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144995019","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Acid-Alkaline Double Electrolytes for High-Energy Aqueous Proton Batteries. 高能质子水电池用酸碱双电解质。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-08-31 DOI: 10.1002/anie.202514026

Ziyue Li, Fengmei Wang, Jinyu Yang, Xinjie Li, Mingxu Wang, Pengfei Zhang, Mochou Liao, Jiafeng Ruan, Sainan Luo, Junjie Chi, Xuelian Qu, Ruohan Jiang, Zihao Zhang, Chaoxin Wu, Dalin Sun, Fang Fang, Fei Wang

{"title":"Acid-Alkaline Double Electrolytes for High-Energy Aqueous Proton Batteries.","authors":"Ziyue Li, Fengmei Wang, Jinyu Yang, Xinjie Li, Mingxu Wang, Pengfei Zhang, Mochou Liao, Jiafeng Ruan, Sainan Luo, Junjie Chi, Xuelian Qu, Ruohan Jiang, Zihao Zhang, Chaoxin Wu, Dalin Sun, Fang Fang, Fei Wang","doi":"10.1002/anie.202514026","DOIUrl":"https://doi.org/10.1002/anie.202514026","url":null,"abstract":"Aqueous proton batteries offer a promising energy storage solution due to their inherent safety, rapid ion mobility, and low cost. However, their performance is largely constrained by water's limited electrochemical stability, restricting operating voltage and energy density. This study addresses this challenge by introducing an innovative acid-alkaline double electrolyte configuration to achieve high-voltage aqueous proton batteries. Employing a high-anodic-limit acidic catholyte (7 M H3PO4) and a low-cathodic-limit alkaline anolyte (6 M KOH), separated by a proton exchange membrane (PEM), significantly expands the full battery's electrochemical stability window (ESW) to 2.91 V. Cobalt-doped Prussian blue (CoCuHCF) was selected as the cathode due to its superior proton kinetics and cycling durability, while benzo[c]cinnoline (BCC) was identified as an optimal anode via combined theoretical analysis and experimental validation. Consequently, the battery delivered exceptional electrochemical performance, achieving a high energy density of 329.6 Wh kg-1 at 1 A g-1, a remarkable power density of 14788.3 W kg-1 at 10 A g-1, and excellent cycling stability with 98.3% capacity retention after 1000 cycles. The proposed acid-alkaline double electrolyte strategy provides efficient and valuable guidance for advancing aqueous energy storage technologies.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202514026"},"PeriodicalIF":16.9,"publicationDate":"2025-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144985950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Programmable Circularly Polarized Electroluminescence Through Stereocontrol of Chiral Liquid-Crystalline Co-Assemblies. 手性液晶共组装体立体控制的可编程圆极化电致发光。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-08-31 DOI: 10.1002/anie.202515032

Yu Zhang, Pengxiang Wang, Zhenhao Jiang, Dong Li, Hang Li, Yixiang Cheng

{"title":"Programmable Circularly Polarized Electroluminescence Through Stereocontrol of Chiral Liquid-Crystalline Co-Assemblies.","authors":"Yu Zhang, Pengxiang Wang, Zhenhao Jiang, Dong Li, Hang Li, Yixiang Cheng","doi":"10.1002/anie.202515032","DOIUrl":"https://doi.org/10.1002/anie.202515032","url":null,"abstract":"Circularly polarized organic light-emitting diodes (CP-OLEDs) are essential to prospective 3D displays and advanced polarized lighting systems. The rational design of programmable circularly polarized electroluminescence (CP-EL) materials with a large electroluminescence dissymmetry factor (gEL) remains a great challenge and is still in its preliminary exploration phase. In this work, two aggregation induced emission active (AIE-active) chiral inducers with different dihedral angles of binaphthalene (S-/R-1 and S-/R-2) and achiral acrylate-based liquid crystalline polymer (LCP) (PyP) were chosed to construct chiral co-assemblies through an intermolecular chirality induction mechanism. Interestingly, as the dihedral angle of the AIE-active binaphthyl inducer decreased from obtuse to acute angle, the resulting co-assemblies (S-/R-2-PyP) could emit inverted and amplified CP-EL signals compared with S-/R-1-PyP after annealing. Significantly, the (S-/R-2)0.1-(PyP)0.9-based CP-OLEDs displayed remarkable blue CP-EL (λEL = 480 nm, Lmax = 14860 cd m-2) with a record |gEL| value of up to 0.18 in chiral co-assembled CP-OLEDs to date. This work describes the first observation of dynamic CP-EL with tunable signal direction and intensity through stereocontrol of AIE-active chiral inducers in LCP co-assembled films, providing a valuable guidance for realizing programmable CP-EL.","PeriodicalId":520556,"journal":{"name":"Angewandte Chemie (International ed. in English)","volume":" ","pages":"e202515032"},"PeriodicalIF":16.9,"publicationDate":"2025-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144985268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

A Water Soluble and Solid-State Molecular Solar Thermal (MOST) System as Renewable Solar Fuel. 水溶性固态分子太阳能热（MOST）系统作为可再生太阳能燃料。

IF 16.9

Angewandte Chemie (International ed. in English) Pub Date : 2025-08-31 DOI: 10.1002/anie.202514349

Sara Hernáez-Troya, Nil Sanosa, Alberto Giménez-Gómez, Ví Pozo-Gavara, Diego Sampedro, Ignacio Funes-Ardoiz

引用次数: 0