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Journal of Environmental Sciences 2025年第3期149卷 88-98页

作者： Shi-Ya Peng Ya-Di Yang Rong Tian Naihao Lu Jiangxi key laboratory of green chemistry College of Chemistry and Chemical EngineeringJiangxi Normal UniversityNanchang 330022China

A key characteristic to be elucidated,to address the harmful health risks of environmental perfluorinated alkyl substances(PFAS),is their binding modes to serum albumin,the most abundant protein in *** oxide-dimer acid(GenX or HFPO-DA)is a new industrial replacement for the widespread linear long-chain ***,the detailed interaction of new-generation short-chain PFAS with albumin is still ***,the binding characteristics of bovine serum albumin(BSA)to GenX were explored at the molecular and cellular *** found that this branched short-chain GenX could bind to BSA with affinity lower than that of legacy linear long-chain perfluorooctanoic acid(PFOA).Site marker competitive study and molecular docking simulation revealed that GenX interacted with subdomain IIIA to form BSA-GenX *** with its weaker affinity to albumin protein,the cytotoxicity of branched short-chain GenX was less susceptible to BSA binding compared with that of the linear long-chain *** contrast to the significant effects of strong BSA-PFOA interaction,the weak affinity of BSA-GenX binding did not influence the structure of protein and the cytotoxicity of *** detailed characterization and direct comparisons of serum albumin interaction with new generation short-chain GenX will provide a better understanding for the toxicological properties of this new alternative.

关键词： GenX Protein binding Albumin Cytotoxicity Risk assessment

A novel supramolecular assembly based on nor-seco-cucurbit[10]uril for spermine sensing and artificial light-harvesting

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Chinese Chemical Letters 2025年第1期36卷 262-266页

作者： Ran Cen Yan-Yan Tang Li-Xia Chen Zhu Tao Xin Xiao National key laboratory of green Pesticide State Key Laboratory of Green Pesticide and Agricultural BioengineeringMinistry of EducationKey Laboratory of Macrocyclic and Supramolecular Chemistry of Guizhou ProvinceGuizhou UniversityGuiyang 550025China

A supramolecular assembly composed of perylene diimide derivative(PDI-nm)and nor-secocucurbit[10]uril(ns-Q[10])was *** excellent host-guest interaction between PDI-nm and nsQ[10]prevented the aggregation-caused quenching(ACQ)effect of PDI-nm,resulting in a luminescent *** addition of spermine to the PDI-nm/ns-Q[10]assembly restored the ACQ of PDI-nm due to the competitive binding of spermine to ns-Q[10],which released *** assembly based on this principle showed ultra-high sensitivity for the detection of spermine with a detection limit as low as7.84×10^(-7)mol/L in aqueous solution and 3.69×10^(-7)mol/L in plasma ***,an artificial light-harvesting system based on this assembly was proposed,benefiting from its good luminescent *** red(Ni R)functioned as an acceptor loaded into assembly,and a highly efficient energy transfer process occurred from PDI-nm/ns-Q[10]to Ni R,with an efficiency up to 87%.

关键词： Nor-seco-cucurbituril Perylene diimide derivative Spermine Light-harvesting

Transition-metal-free isofunctional reaction of α,β-unsaturated ketones/nitriles

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Science China chemistry 2025年第2期68卷 499-504页

作者： Runyou Ye Jialin Ming Qinyue Tao Tian-Yu Gao Jian-Heng Ye Da-Gang Yu Xiangge Zhou key laboratory of green chemistry&Technology of Ministry of Education College of ChemistrySichuan UniversityChengdu 610064China Inner Mongolia key laboratory of Fine Organic Synthesis Inner Mongolia UniversityHohhot 010021China

Isofunctional reactions involving the cleavage of carbon-carbon double bonds(C=C)hold an important position in organic synthesis,as they allow for the restructuring of alkene carbon chains and enable the exchange of functional groups without introducing exogenous ***,these reactions are primarily divided into C=C/C=C metathesis and C=C/C=O metathesis,with most relying on the use of transition metal *** report herein a C=C/CH_(2) metathesis reaction that obviates the need for transition metals and directing groups,and is characterized by economic and straightforward *** reaction not only facilitates the replacement of nitriles with ketones,but also enables the replacement of ketones with nitriles,demonstrating great universality.

关键词： isofunctional reaction transition-metal-free C=C cleavage base-promoted Michael addition

Research progress on piperidine-containing compounds as agrochemicals

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Chinese Chemical Letters 2025年第1期36卷 58-67页

作者： Wei Sun Anjing Liao Li Lei Xu Tang Ya Wang Jian Wu State key laboratory of green Pesticide Key Laboratory of Green Pesticide and Agricultural BioengineeringMinistry of EducationGuizhou UniversityGuiyang 550025China

Piperidine is a crucial pharmacophore and a special scaffold in the realm of drug *** flexibility increases the molecule’s capability to bind to the *** piperidine-containing compounds are distinguished by their remarkable activity,and are increasingly becoming a vital category of *** this review,the research progress of piperidines in the discovery of pesticides was updated according to their active *** structure-activity relationships(SARs),and mechanisms of action of piperidine-containing compounds were also *** article is meant to enable readers to quickly understand piperidines,while providing ideas for creating piperidines with novel structures and unique mechanisms of action.

关键词： Piperidine Agrochemicals Biological activity Structure-activity relationships Mechanism of action

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Trinuclear gold-catalyzed site-selective alkylation of peptides

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Science China chemistry 2025年第1期68卷 249-256页

作者： Qing-Yun Fang Chengyihan Gu Yinghan Chen Wencheng Yan Yong Liang Weipeng Li Chengjian Zhu Jie Han Jin Xie State key laboratory of Coordination chemistry Jiangsu Key Laboratory of Advanced Organic MaterialsChemistry and Biomedicine Innovation Center(ChemBIC)School of Chemistry and Chemical EngineeringNanjing UniversityNanjing 210023China green Catalysis Center College of ChemistryZhengzhou UniversityZhengzhou 450001China State key laboratory of Natural Medicines China Pharmaceutical UniversityNanjing 211198China

Selective modification of peptides has always been a challenging *** selective alkylation of peptides can alter the biological activity and physical properties of molecules,and it has gained significant research *** herein disclose an intriguing gold-catalyzed alkylation of peptides using bench-stable unactivated alkyl bromides under photoredox catalysis.A wide range of structurally diverse primary,secondary and tertiary alkyl bromides serve as effective coupling partners to precisely connect with theα-C(sp^(3))–H in glycine residue of *** protocol demonstrates an exceptionally broad scope for alkyl halides and excellent tolerance for a wide range of useful functional groups.A series of relay transformations to construct cyclic peptides,to proceed click reaction and to realize peptide fluorescence labeling further enhance its synthetic *** addition,mechanistic studies and density functional theory(DFT)calculations reveal an inner-sphere and subsequent outersphere single electron transfer(SET)mechanism.

关键词： gold catalysis peptide alkylation C-C coupling radical

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Synergistic enhancement of ion/electron transport by ultrafine nanoparticles and graphene in Li2FeTiO4/C/G nanofibers for symmetric Li-ion batteries

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Journal of Energy chemistry 2025年第02期101卷 42-51页

作者： Wenjie Ma Yakun Tang Yue Zhang Xiaohui Li Lang Liu Xueting Wang Yuliang Cao State key laboratory of chemistry and Utilization of Carbon Based Energy Resources Key Laboratory of Energy Materials Chemistry Ministry of Education College of Chemistry Xinjiang University College of chemistry and Molecular Sciences Hubei Key Laboratory of Electrochemical Power Sources Wuhan University

Low-cost Fe-based disordered rock salt（DRX） Li2FeTiO4is capable of providing high capacity(295 mA h g-1) by redox activity of cations(Fe2+/Fe4+and Ti3+/Ti4+) and anionic ***,DRX structures lack transport channels for ions and electrons,resulting in sluggish kinetics,poor electrochemical activity,and ***,graphene conductive carbon network permeated Li2FeTiO4（LFT/C/G） nanofibers are successfully prepared by a facile sol-gel assisted electrospinning *** Li2FeTiO4nanoparticles（2 nm） and one-dimensional（1D） structure provide abu ndant active sites and unobstructed diffu sion channels,accelerating ion *** addition,introducing graphene reduces the band gap and Li+diffusion barrier and improves the dynamic properties of Li2FeTiO4,thus achieving a relatively mild interfacial reaction and reversible redox *** expected,the LFT/C/1.0G cathode delivers a remarkable discharge capacity(238.5 mA h g-1),high energy density(508.8 Wh kg-1),and excellent rate capability(51.2 mA hg-1at 1.0 A g-1).Besides,the LFT/C/1.0G anode also displays a high capacity(514.5 mA h g-1at 500 mA g-1) and a remarkable rate capability(243.9 mA h g-1at 8 A g-1).Moreover,the full batteries based on the LFT/C/1.0G symmetric electrode demonstrate a reversible capacity of 117.0 mA h g-1after 100 cycles at 50 mA *** study presents useful insights into developing cost-effective DRX cathodes with durable and fast lithium storage.

关键词： 1D structure Disordered rock salt Li2FeTiO4 Graphene Lithium-ion battery electrode Rapid ion/electron transport

The controlled oxidation states of the H4PMo11VO40 catalyst induced by plasma for the selective oxidation of methacrolein

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Chinese Chemical Letters 2025年第2期36卷 189-194页

作者： Gang Hu Chun Wang Qinqin Wang Mingyuan Zhu Lihua Kang School of chemistry and Chemical Engineering/State key laboratory Incubation Base for green Processing of Chemical Engineering Shihezi University College of chemistry&Chemical Engineering Yantai University

In this paper,low-temperature dielectric-blocked discharge plasma （DBD） was employed for the first time to treat silica-doped H4PMo11VO40（HPAV） catalysts (DBD（Ar/x）-MF-Catal) and apply them in the catalytic methacrolein （MAL） selective oxidation to produce methacrylic acid （MAA）.This work investigates in detail the controllable regulation of the concentration of oxidation states on silica-doped HPAV catalysts by adjusting the DBD discharge with controlled changes in voltage,current,treatment time,and treatment *** reports the intrinsic correlation between oxidation states and MAL oxidation *** research results indicated that the catalytic performance was related to the presence of oxygen vacancies and oxygen species (VO2+),and are the main reason for the selective oxidation of MAL to ***,the generation of oxygen vacancies and VO2+altered localized electrons,which resulted in the easier activation of *** calculations of DFT also proved the formation mechanism of oxygen vacancies and VO2+and electron properties on high-performance polymers,which elucidated the intrinsic influence of catalyst *** DBD（Ar/10）-MF-Catal catalysts with suitable VO2+and oxygen vacancy concentrations exhibited the highest catalytic performance with 90%MAL conversion and 70%MAA selectivity and showed good stability （500 h）.

关键词： Catalyst Dopant Methacrolein Methacrylic acid Oxygen vacancy Plasma

Recycling Fe and improving organic pollutant removal via in situ forming magnetic core-shell Fe_(3)O_(4)@CaFe-LDH in Fe(Ⅱ)-catalyzed oxidative wastewater treatment

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Journal of Environmental Sciences 2025年第1期147卷 523-537页

作者： Ting He Jie Sun Liangwei Deng Jialin Ming Changwei Hu key laboratory of green chemistry and Technology Ministry of EducationCollege of ChemistrySichuan UniversityChengdu 610064China Biogas Institute of Ministry of Agriculture and Rural Affairs Chengdu 610041China Inner Mongolia key laboratory of Fine Organic Synthesis Inner Mongolia UniversityHohhot 010021China

Due to its high efficiency,Fe(Ⅱ)-based catalytic oxidation has been one of the most popular types of technology for treating growing organic pollutants.A lot of chemical Fe sludge alongwith various refractory pollutantswas concomitantly produced,whichmay cause secondary environmental problemswithout proper *** here innovatively proposed an effective method of achieving zero Fe sludge,reusing Fe resources(Fe recovery=100%)and advancing organics removal(final TOC removal>70%)simultaneously,based on the in situ formation of magnetic Ca-Fe layered double hydroxide(Fe_(3)O_(4)@CaFe-LDH)***(Ca^(2+)and Fe^(3+))concentration(≥30 mmol/L)and their molar ratio(Ca:Fe≥1.75)were crucial to the success of the *** nano Fe_(3)O_(4)was designed to be involved in the Fe(Ⅱ)-catalytic wastewater treatment process,and was modified by oxidation intermediates/products(especially those with COO-structure),which promoted the co-precipitation of Ca^(2+)(originated from Ca(OH)_(2)added after oxidation process)and byproduced Fe^(3+)cations on its surface to in situ generate core-shell Fe_(3)O_(4)@*** oxidation products were further removed during Fe_(3)O_(4)@CaFe-LDH material formation via intercalation and *** applicable to many kinds of organicwastewater,such as bisphenol A,methyl orange,humics,and biogas *** prepared magnetic and hierarchical CaFe-LDH nanocomposite material showed comparable application performance to the recently reported *** work provides a new strategy for efficiently enhancing the efficiency and economy of Fe(Ⅱ)-catalyzed oxidative wastewater treatment by producing high value-added LDHs materials.

关键词： CaFe layered double hydroxide Fe(Ⅱ)-catalytic oxidation Fe recycling Magnetic nanomaterial in situ formation Fe_(3)O_(4)modification

Potassium-modified carbon nitride photocatalyzed-aminoacylation of N–sulfonyl ketimines

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Chinese Chemical Letters 2025年第2期36卷 406-411页

作者： Cailing Wu Shaojie Wu Qifei Huang Kai Sun Xianqiang Huang Jianji Wang Bing Yu Collaborative Innovation Center of Henan Province for green Manufacturing of Fine Chemicals Key Laboratory of Green Chemical Media and ReactionsMinistry of Education School of Chemistry and Chemical Engineering Henan Normal University College of chemistry Zhengzhou University School of chemistry & Chemical Engineering Liaocheng University

The development of innovative and sustainable catalytic strategies for organic synthesis is a pivotal aspect of advancing material science and chemical *** research presents a new catalytic method for the aminoacylation of N–sulfonyl ketimines by utilizing a potassium-doped graphite-like carbon nitride （g-C3N4） *** method not only enhances the catalytic efficiency and broadens the light absorption spectrum of g-C3N4but also significantly reduces the recombination rate of electronhole pairs,thereby increasing the reaction yield and ***,our approach facilitates the synthesis of aminoacylated N-heterocycles,expanding the applicability of potassium-modified g-C3N4in photocatalytic organic synthesis.A notable accomplishment of this study is the unprecedented generation of carbamoyl radicals via heterogeneous photocatalysis,which can be easily recycled after *** advancement highlights the capability of potassium-doped g-C3N4（namely K-CN） as an advanced heterogeneous photocatalyst for the formation of complex organic compounds.

关键词： Amides Aminoacylation K+-modified carbon nitride Oxamic acids Photocatalysis

Upcycling of polyphenylene oxide into 2,6-dimethyl aniline via depolymerization and amination over a Pt/CeO_(2) catalyst

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Science China chemistry 2025年第2期68卷 520-525页

作者： Shengchao Jia Wenke Zhao Xiaohui Liu Yong Guo Yanqin Wang State key laboratory of green Chemical Engineering and Industrial Catalysis Research Institute of Industrial CatalysisSchool of Chemistry and Molecular EngineeringEast China University of Science and TechnologyShanghai 200237China Shanghai key laboratory of Functional Materials chemistry School of Chemistry and Molecular EngineeringEast China University of Science and TechnologyShanghai 200237China

Upcycling of plastic waste into N-containing compound is a novel and attractive strategy for its disposal and will opens up a promising direction for the production of value-added ***,an efficient strategy for the depolymerization-amination of polyphenylene oxide(PPO)into 2,6-dimethyl aniline is developed over a simple Pt/CeO_(2) *** C–O linkages of PPO can be selectively broken,producing 2,6-dimethyl phenol and then hydrogenated and aminated to 2,6-dimethyl cyclohexylamine over the Pt/CeO_(2) ***,2,6-dimethyl aniline was produced with high selectivity through the dehydrogenation of 2,6-dimethyl cyclohexylamine in the same *** can be used as the hydrogen-acceptor in the dehydrogenation step and enhance the selectivity of target *** N-containing compound,2,6-dimethyl aniline,is obtained and separated after HCl ***,the Pt/CeO_(2) catalyst exhibit remarkable stability and can sustainably catalyze the synthesis of 2,6-dimethyl aniline in several cycles.

关键词： PPO depolymerization-amination 2,6-dimethyl aniline Pt/CeO_(2)