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Coordination-driven control of nuclearity for tuning the near-infrared properties of a ball-shaped ruthenium complex 调节球形钌配合物近红外特性的核核协调驱动控制
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-21 DOI: 10.1039/d6cc05358k
Yuri Kimoto,Sari Ishikawa,Taniyuki Furuyama
The coordination-driven selective assembly of a ball-shaped ruthenium complex has been achieved. The choice of the metal salt controlled the assembly (monomer vs. heterotrinuclear). The resulting heterotrinuclear complex possessed a highly symmetrical propeller structure and exhibited red-shifted absorption band in the near-infrared region.
实现了配位驱动的球形钌配合物的选择性组装。金属盐的选择控制了组装(单体与杂三核)。得到的杂三核配合物具有高度对称的螺旋桨结构,并在近红外区表现出红移的吸收带。
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引用次数: 0
Precise Fabrication of Supported Zero-valent Nano-noble Metals via Reductant-Preset Cascade In-Situ Reduction: Nitroaromatics Reduction as Probe Reaction 用还原剂预置级联原位还原法精确制备负载型零价纳米贵金属:硝基芳烃还原为探针反应
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-21 DOI: 10.1039/d6cc05471d
Tianrui Deng,Xingye Zhao,Xue Zhao,Cuiyu Li,Yanjuan Zhao,Zhuo Zhao,Yicheng Zhang,Guangzhi Hu
Precise synthesis of noble metal nanoparticles is the key to cost reduction and efficiency enhancement, and this study has developed a ‘reductant preset cascade in-situ reduction’ strategy that achieves precise synthesis of supported noble metal nanoparticles through directed manipulation at the molecular level.
贵金属纳米颗粒的精确合成是降低成本和提高效率的关键,本研究开发了一种“还原剂预设级联原位还原”策略,通过分子水平上的定向操作实现了贵金属纳米颗粒的精确合成。
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引用次数: 0
Hydrogen-Bonded Supramolecular Liquid Crystals with Integrated Aggregation-Induced Emission and Room-Temperature Phosphorescence 具有聚集诱导发射和室温磷光的氢键超分子液晶
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-21 DOI: 10.1039/d6cc05916c
Shan Li,Yudong Cao,Yunle Lu,Smruti Ranjan Sahoo,Qingli Li,Xinyan Gu,Glib Baryshnikov,Danfeng Ye,Liangliang Zhu
A supramolecular hydrogen-bonding strategy converts a twisted non-mesogenic AIE luminogen into ordered smectic liquid crystals. The hydrogen-bond network acts as a conformation lock, planarizing excited states, enhancing intersystem crossing by two orders of magnitude, and activating room-temperature phosphorescence with an 8 ms lifetime.
一种超分子氢键策略将扭曲的非介晶AIE发光原转化为有序的近晶液晶。氢键网络作为构象锁,使激发态平面化,增强两个数量级的系统间交叉,并激活寿命为8毫秒的室温磷光。
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引用次数: 0
Disorder-Driven Dissolution: Cation Congruence in a High-Entropy Oxide Under Acidic Conditions 无序驱动的溶解:酸性条件下高熵氧化物中的阳离子同位
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-20 DOI: 10.1039/d6cc05475g
William J Deary,Gerald Bejger,Bailey L Miller,Lexie S Ibarra,Joshua Wright,Christina M Rost
High-entropy oxides offer tunable functional properties, yet their acidic dissolution is largely unexplored. We show that (MgCoNiCuZn)0.2O dissolves congruently in dilute nitric acid, releasing all five cations together. A physical mixture and a three-cation solid solution both dissolve incongruently, showing that a single phase alone does not ensure congruent release.
高熵氧化物具有可调的功能特性,但它们的酸性溶解在很大程度上尚未被探索。我们发现(MgCoNiCuZn)0.2在稀硝酸中完全溶解,同时释放所有五个阳离子。物理混合物和三阳离子固溶体都是不一致溶解的,这表明单独的单相不能保证一致释放。
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引用次数: 0
Characterization of Hydrogen Storage in Hydroquinone Clathrate using Terahertz Spectroscopy 对苯二酚包合物中储氢的太赫兹光谱表征
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-20 DOI: 10.1039/d6cc04354b
Katharine Bancroft,Johanna Kölbel,Michael T Ruggiero,Daniel M Mittleman
Hydroquinone clathrates are promising materials for solid-state hydrogen storage, yet, distinct spectroscopic characterization of H2 enclathration remains elusive. Here, we show that low-frequency (terahertz) vibrational spectroscopy, coupled with molecular simulations, reveals clear spectroscopic fingerprints of H2 clathrate formation in the α-hydroquinone polymorph, demonstrates an unexpected route to hydrogen incorporation.
对苯二酚包合物是一种很有前途的固态储氢材料,然而,氢包合物的光谱表征仍然难以实现。在这里,我们展示了低频(太赫兹)振动光谱,结合分子模拟,揭示了α-对苯二酚多晶中H2笼形物形成的清晰光谱指纹,展示了一个意想不到的氢结合途径。
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引用次数: 0
Hydrogen-bonded conjugated small molecules in organic electronics. 有机电子学中的氢键共轭小分子。
IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-20 DOI: 10.1039/d6cc05901e
Miriam Más-Montoya, David Curiel

Organic semiconductors have become highly important for next-generation electronic devices. However, further research is needed to enhance their charge-transport properties and long-term stability. These challenges largely originate from their solid-state structure, as organic semiconductors are molecular solids whose organisation is governed by very weak non-covalent interactions. Accordingly, the weakness of intermolecular interactions increases the chances of having structural disorder and generating defects, which detrimentally affect the performance of organic semiconductors. Therefore, controlling molecular organisation is a key objective. Hydrogen bonding is particularly effective for promoting solid-state self-assembly and gaining certain control over molecular organisation. The strength of hydrogen bonds, their directionality, and the broad range of functional groups and structures that can act as hydrogen-bond donors and acceptors have encouraged their rational incorporation into the molecular design of organic semiconductors. This Feature Article presents a review of the structural approaches developed to enhance the performance of materials based on small molecules through the integration of hydrogen-bond donor and acceptor sites within the conjugated framework. It also discusses the implementation of these materials in different types of electronic devices.

有机半导体在下一代电子器件中变得非常重要。然而,需要进一步的研究来提高它们的电荷输运性能和长期稳定性。这些挑战很大程度上源于它们的固态结构,因为有机半导体是分子固体,其组织受非常弱的非共价相互作用支配。因此,分子间相互作用的薄弱增加了结构紊乱和产生缺陷的机会,这对有机半导体的性能产生不利影响。因此,控制分子组织是一个关键目标。氢键在促进固态自组装和获得对分子组织的一定控制方面特别有效。氢键的强度,它们的方向性,以及可以作为氢键供体和受体的官能团和结构的广泛范围,鼓励它们合理地纳入有机半导体的分子设计中。本文介绍了通过在共轭框架内结合氢键供体和受体位点来提高基于小分子的材料性能的结构方法。它还讨论了这些材料在不同类型的电子设备中的实现。
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引用次数: 0
A viscosity-associated fluorescence turn-on probe for rapid local and topical tumor visualization 一种用于快速局部和局部肿瘤可视化的黏度相关荧光开启探针
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-20 DOI: 10.1039/d6cc05627j
Zhengyumeng Zhu,Zhirun Xu,Yanji Sun,Xiangzhou Liu,Weidong Lv,Yanyan Huang,Huihui Xu,Fang Hu
IR720 is a viscosity-associated near-infrared fluorescence turn-on probe that brightens in glycerol-rich media. It produces rapid cell-associated signals and allows imaging of pulmonary metastases and topically treated intestinal tumors. Exploratory limited proteolysis mass spectrometry identifies peptide-level changes in tumor tissue after IR720 exposure.
IR720是一种粘度相关的近红外荧光开启探针,在富含甘油的介质中变亮。它能产生快速的细胞相关信号,并能对肺转移瘤和局部治疗的肠道肿瘤进行成像。探索性有限蛋白水解质谱法鉴定IR720暴露后肿瘤组织中肽水平的变化。
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引用次数: 0
A B←N framework for highly selective adsorption of toluene 高选择性吸附甲苯的A B←N框架
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-20 DOI: 10.1039/d6cc05536b
Xiang-Shuai Li,Yizhou WANG,Herman H-Y. Sung,Ian Duncan Williams,Yangjian Quan
Differentiating toluene (Tol) from xylene isomers is critical yet challenging in industry due to their nearly identical physicochemical properties. Here, we report the design of a B←N framework that exhibits high adsorption selectivity for Tol over xylenes. Single-crystal X-ray diffraction analyses of the host–guest complexe and DFT calculation reveal that the selectivity stems from precise size matching and electronic complementarity.
由于甲苯与二甲苯异构体的物理化学性质几乎相同,因此在工业中区分甲苯(Tol)是至关重要的,但也是具有挑战性的。在这里,我们报道了一种对Tol在二甲苯上具有高吸附选择性的B←N框架的设计。主客体配合物的单晶x射线衍射分析和DFT计算表明,选择性源于精确的尺寸匹配和电子互补。
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引用次数: 0
Biomimetic Hollow Ferriporphyrin Porous Aromatic Frameworks for Boosted Electrooxidation Nitrogen to Nitrate 仿生空心铁卟啉多孔芳香骨架促进氮电氧化制硝态氮
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-20 DOI: 10.1039/d6cc06313f
Bingyue Yang,Ping Li,Pengfei Yuan,Jiaxi Zhang,Hongming He,Bin Li,Cheng-Peng Li,Chunju Li
This study reports hollow ferriporphyrin porous aromatic frameworks with distinct morphologies. The hollow FeP-PAF exhibits a high NO3− yield of 2232.3 µmol h−1 gcat.−1 and a Faradaic efficiency of 80.5%, which are higher than its counter FeP-PAF powder and ferriporphyrin molecule.
本研究报道了具有不同形态的空心铁卟啉多孔芳香框架。FeP-PAF的NO3−产率高达2232.3µmol h−1 gcat。−1,法拉第效率为80.5%,高于其对应物FeP-PAF粉末和铁卟啉分子。
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引用次数: 0
A hydrogen-bonded aramide cage for selective CO adsorption 一种用于选择性CO吸附的氢键芳纶笼
IF 4.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pub Date : 2026-10-20 DOI: 10.1039/d6cc05693h
Xirui Wang,Xinnan Chen,Yimin Cai,Wen Feng,Lihua Yuan,Xiaowei Li
An aramide organic cage was synthesized using intramolecular hydrogen-bond preorganization of oligoaramide foldamer precursors. The cage exhibits a CO2-derived BET surface area of 706 m² g⁻¹ and preferential CO2 adsorption over C2H2, N2 and CH4, with a reverse CO2/C2H2 IAST selectivity of 104, highlighting its potential for selective gas capture.
采用分子内氢键预组织方法合成了一种芳酰胺有机笼。笼子里展品CO2-derived打赌表面面积706 m²g⁻¹和优惠二氧化碳吸附在乙炔,N2和CH4,反向二氧化碳/乙炔IAST 104年选择性,突出其潜在的选择性气体捕获。
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引用次数: 0
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Chemical Communications
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