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Sn4P3-decorated 2D N-doped carbon nanosheets as efficient polysulfide barriers for Li-S batteries. sn4p3修饰的二维氮掺杂碳纳米片作为Li-S电池的高效多硫化物屏障。
IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc02150b
Yawen Feng, Shunxian Yu, Xiaoxian Zhao, Junliang Xu, Zenghui Lin, Chuan Shi, Chaoyue Zhang, Shuangqiang Chen, Jianjun Song

The Sn4P3@NCS multifunctional separator suppresses polysulfide shuttling via van der Waals physical adsorption and Sn4P3/N-polar chemical anchoring, delivering a high discharge capacity of 1250 mA h g-1 at 0.2C, and of 753 mA h g-1 at 4C, and stable cycling performance under a sulfur loading of 3.8 mg cm-2.

Sn4P3@NCS功能分离器通过范德华物理吸附和Sn4P3/ n极性化学锚定抑制多硫化物的迁移,在0.2C和4C条件下具有1250 mA h g-1和753 mA h g-1的高放电容量,并且在3.8 mg cm-2的硫负荷下具有稳定的循环性能。
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引用次数: 0
Construction of balanced-transition AIE phototherapeutic agents based on fluorination strategy for prolonged triplet excited state lifetime 基于氟化策略延长三重态激发态寿命的平衡跃迁AIE光治疗剂的构建
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc02234g
Mengyan Tian, Xinyue Zhao, Shuai Zhao, Yaning Li, Ruofei Wang, Jun Guo, Pai Liu
To solve the competitive energy decay pathways in photodynamic therapy (PDT) and photothermal therapy (PTT), herein, we proposed a fluorination strategy of AIE photosensitizers (TPAN and TPAF) which exhibited high ROS generation and heat release. Innovatively, femtosecond transient absorption spectroscopy was emerged to verify the extension of triplet excited state lifetime induced by C-F bonds. In order to improve its hydrophilic and target ability, GSH-responsive nanogel HPCF was constructed, which presented controllable release of TPAF. In vivo experiments proved that HPCF-mediated PDT/PTT successfully downregulate heat shock proteins by reactive oxygen species and achieved synergetic phototherapy potential.
为了解决光动力治疗(PDT)和光热治疗(PTT)中存在的竞争性能量衰减途径,本文提出了一种具有高ROS生成和热释放能力的AIE光敏剂(TPAN和TPAF)的氟化策略。创新地,飞秒瞬态吸收光谱被提出来验证由C-F键引起的三重态激发态寿命的延长。为了提高其亲水性和靶向性,构建了gsh响应型纳米凝胶HPCF,其TPAF的释放是可控的。体内实验证明hpcf介导的PDT/PTT通过活性氧成功下调热休克蛋白,实现协同光疗潜能。
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引用次数: 0
A linear non-halogenated polymer donor via Suzuki-Miyaura coupling for organic solar cells. 通过Suzuki-Miyaura偶联的线性非卤化聚合物给体用于有机太阳能电池。
IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc00852b
Zhili Chen, Bingyan Yin, Baoqi Wu, Yuchuan Tian, Junyu Li, Xiang Gao, Zhiliang Huang, Zhitian Liu, Fei Huang, Yong Cao, Chunhui Duan

A novel linear non-halogenated polymer donor, PTTzP, with a simple structure was synthesized via Suzuki-Miyaura coupling. PTTzP exhibits comparable device performance (>12%) in organic solar cells (OSCs) when processed with halogenated and non-halogenated solvents, respectively. This achievement highlights the potential of PTTzP as an efficient and environmentally friendly polymer donor, enabling high-performance OSCs through entirely green synthesis and processing methods.

通过Suzuki-Miyaura偶联法合成了一种结构简单的线性非卤化聚合物给体PTTzP。PTTzP在有机太阳能电池(OSCs)中分别用卤化和非卤化溶剂加工时表现出相当的器件性能(>12%)。这一成就凸显了PTTzP作为高效环保聚合物供体的潜力,通过完全绿色的合成和加工方法实现高性能OSCs。
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引用次数: 0
Aggregation-induced emission-active indium complex as fluorescent turn-off chemosensor for perfluoroalkyl substances. 聚合诱导发光活性铟配合物作为全氟烷基物质的荧光关闭化学传感器。
IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc02424b
Oliver Baumeyer, Andrew Wu, Aastha Pandya, Peter Nelson, Patrick C Hillesheim, Matthias Zeller, Gia M Carignan, Jing Li, Daniel W Ki

We report a novel indium(III) chloride complex that exhibits aggregation-induced emission (AIE) and functions as a selective turn-off fluorescent chemosensor for perfluoroalkyl substances (PFAS). The complex shows strong blue-shifted luminescence quenching upon interaction with perfluoroheptanoic acid (PFHpA) and perfluorooctanoic acid (PFOA) due to stabilization of the ground state molecular orbitals relative to those of the excited state. The selectivity of these compounds for PFOA and PFHpA is also reflected in the dipole moment and thus emission intensity of this complex, hence, they represent promising platforms for sensing "forever chemicals".

我们报道了一种新型氯化铟配合物,它表现出聚集诱导发射(AIE),并作为全氟烷基物质(PFAS)的选择性关闭荧光化学传感器。该配合物与全氟庚酸(PFHpA)和全氟辛酸(PFOA)相互作用时,由于基态分子轨道相对于激发态分子轨道的稳定,表现出强烈的蓝移发光猝灭。这些化合物对PFOA和PFHpA的选择性也反映在偶极矩和该复合物的发射强度上,因此,它们代表了有希望的传感“永远的化学物质”的平台。
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引用次数: 0
Pseudorotaxane monolayers of pillar[5]arene and linear fatty acids at the air-water interface. 柱状b[5]芳烃和线性脂肪酸在空气-水界面的假环紫杉烷单层。
IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc01040c
Masaki Ishii, Yuto Nakai, Yu Yamashita, Katsuto Onishi, Tan-Hao Shi, Nobutaka Shioya, Hideki Sakai, Takeshi Hasegawa, Tomoki Ogoshi, Katsuhiko Ariga, Taizo Mori

Pseudorotaxanes, which are formed by macrocyclic host molecules and linear guest molecules, show potential in molecular devices and surface applications. In this study, ethoxy-functionalized pillar[5]arene (P5A) and amphiphilic linear fatty acid guests were self-assembled into oriented monolayers at the air-water interface. The fatty acid structure dictates the monolayer formation: [2]pseudorotaxane-based, [3]pseudorotaxane-based and phase-separated monolayers. These findings provide insights into P5A-based pseudorotaxane monolayers, facilitating their integration into advanced functional materials.

假环紫杉烷是由大环宿主分子和线性客体分子形成的,在分子器件和表面应用方面具有很大的潜力。在这项研究中,乙氧基功能化的柱状[5]芳烃(P5A)和两亲线性脂肪酸主体在空气-水界面自组装成定向单层。脂肪酸结构决定了单层的形成:[2]伪紫杉烷基单层,[3]伪紫杉烷基单层和相分离单层。这些发现为p5基假环紫杉烷单层膜的研究提供了新的见解,促进了它们与先进功能材料的整合。
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引用次数: 0
Energetics of Carboxylate-Metal Bonds in Polymetallic Rings 多金属环中羧酸-金属键的能量学
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc01911g
Niklas Geue, Tim Renningholtz, George F. S. Whitehead, Grigore A. Timco, Cristina Trujillo, Perdita Barran, Richard E. P. Winpenny
Using collision-induced dissociation mass spectrometry and density functional theory, we assess the energetics of polymetallic [Cr7NiF8(O2CR)16]- anions in vacuo, showing how the carboxylate influences the ring stability. We find the best correlation with the enthalpic contribution to the computed proton affinity of the isolated carboxylates, demonstrating how the stability of polymetallic rings can be predicted in silico.
利用碰撞诱导解离质谱和密度泛函理论,我们评估了真空中多金属[Cr7NiF8(O2CR)16]-阴离子的能量学,显示了羧酸盐如何影响环的稳定性。我们发现与分离羧酸盐的质子亲和力的焓贡献的最佳相关性,证明了如何在硅中预测多金属环的稳定性。
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引用次数: 0
Schottky barrier modulation via calcium hydroxide nanoparticles on g-C3N4/Ti3C2 for overall photocatalytic applications 氢氧化钙纳米粒子在g-C3N4/Ti3C2上的肖特基势垒调制在全光催化中的应用
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc01620g
Zeeshan Asghar, Jawad Ahmad Jrar, Alauddin N/A, Faheem K. Butt, Kewang Zheng, Yong Cai Zhang, Nian-Tzu Suen, Jianhua Hou
In this work, a novel 2D g-C3N4/Ca(OH)2/Ti3C2 heterojunction was synthesized via a one-step thermal method to enhance photocatalytic efficiency. With a 2.44 eV band gap and improved porosity, it enables stronger visible light absorption. Calcium hydroxide enhances structural integrity, while oxygen and nitrogen vacancies optimize charge separation and Schottky barrier modulation. This photocatalyst achieves a CO evolution rate of 205.3 μmol g-1 h-1, H2 evolution of 17300 μmol g-1 h-1, and 99.7% MB and 99.2% TC removal. This strategy advances sustainable energy and environmental remediation.
本文采用一步热法合成了一种新型的二维g-C3N4/Ca(OH)2/Ti3C2异质结,以提高光催化效率。具有2.44 eV的带隙和改进的孔隙率,可以实现更强的可见光吸收。氢氧化钙增强了结构的完整性,而氧和氮空位优化了电荷分离和肖特基势垒调制。该光催化剂CO析出速率为205.3 μmol g-1 h-1, H2析出速率为17300 μmol g-1 h-1,对MB和TC的去除率分别为99.7%和99.2%。这一战略促进了可持续能源和环境补救。
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引用次数: 0
Halogenase-mimicking Selective Chlorination of Unactivated C–H bonds by a Fe-complex 模拟卤素酶的铁络合物对未活化C-H键的选择性氯化反应
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc02614h
Himangshu Kuiry, Anish Gangopadhyay, Bittu Chandra, Sayam Sen Gupta
In this study, we report a selective aliphatic C–H bond chlorination mediated by Fe-bTAML (bTAML: biuret-modified tetraamido macrocyclic ligand) using sodium hypochlorite as the chlorine source. The reaction predominantly yields chlorinated products over hydroxylated ones across various unactivated C–H bonds in acetonitrile-water medium. The formation of rearranged chlorinated products in norcarane and the absence of stereo-retention in cis-dimethylcyclohexane suggest the involvement of a long-lived, cage-escaped carbon radical intermediate. UV-Vis and EPR spectroscopic analyses confirm the presence of [FeV(O)-(NO2)bTAML]- (2) as the reactive intermediate. The 3°:2° selectivity in hydrocarbons, kinetic isotope effect (KIE), and product formation profile indicate hydrogen atom abstraction (HAA) by [FeV(O)-(NO2)bTAML]- (2) as the rate-determining step.
在本研究中,我们报道了以次氯酸钠为氯源,Fe-bTAML (bTAML:双缩脲修饰的四氨基大环配体)介导的选择性脂肪族C-H键氯化反应。在乙腈-水介质中,通过各种未活化的C-H键,主要产生氯化产物而不是羟基化产物。内甲烷中重排氯化产物的形成和顺式二甲基环己烷中立体保留的缺失表明了长寿命的笼状逃逸碳自由基中间体的参与。紫外可见光谱和EPR光谱分析证实了[FeV(O)-(NO2)bTAML]-(2)作为反应中间体的存在。碳氢化合物的3°:2°选择性、动力学同位素效应(KIE)和产物形成剖面表明,[FeV(O)-(NO2)bTAML]-(2)的氢原子萃取(HAA)是决定速率的步骤。
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引用次数: 0
Mechanochromic Luminescence in Copper Nanoclusters: Resolving Structural Transitions through Microcrystal Electron Diffraction 铜纳米团簇的机械致变色发光:通过微晶电子衍射解析结构跃迁
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc02594j
Harshita Nagar, Subrata Duary, Vivek Yadav, Amoghavarsha Ramachandra Kini, Sudhadevi Antharjanam, Tomas Base, Anirban Som, Brent Lane Nannenga, T. Pradeep
MicroED reveals insights into mechanochromic luminescence in copper nanoclusters, demonstrating structural transitions from crystalline to amorphous state upon grinding, with restoration of crystallinity following solvent exposure. Luminescence switching occurs due to reversible amorphization-recrystallization rather than chemical changes, providing critical design principles for such stimuli-responsive materials.
MicroED揭示了铜纳米团簇的机械致变色发光,展示了在研磨时从晶体到无定形的结构转变,以及在溶剂暴露后结晶度的恢复。发光开关的发生是由于可逆的非晶化-再结晶而不是化学变化,这为这种刺激响应材料提供了关键的设计原则。
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引用次数: 0
Pillar[5]arene-based ionic single crystals formed by dual self-assemblies through host-guest and ionic interactions for iodine capture 柱状[5]芳烃基离子单晶通过主-客体相互作用和离子相互作用形成的双自组装用于碘捕获
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2025-06-11 DOI: 10.1039/d5cc02200b
Ting Zhang, Lulu Wang, Hui Li, Mingxia Sun, Jia Chen, Shuzhe Guan, Hongdeng Qiu
This study reports the first preparation of an ionically crosslinked pillar[5]arene single-crystal material (DMIBP5-NA) featuring a unique dual self-assembly structure. The material demonstrates excellent adsorption performance toward iodine vapor with an equilibrium adsorption capacity reaching 3.28 g/g.
本研究首次制备了具有独特双自组装结构的离子交联柱[5]芳烃单晶材料(DMIBP5-NA)。该材料对碘蒸气具有良好的吸附性能,平衡吸附容量达到3.28 g/g。
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引用次数: 0
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Chemical Communications
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