Publications by authors named "Yong Ni"

The construction of three-dimensional nanocarbon structures with well-defined molecular dynamics is a challenging yet rewarding task in material science and supramolecular chemistry. Herein, we report the synthesis of two highly defective, nitrogen-doped molecular cylinders, namely MC1 and MC2, with a length of 1.4 nm and 2.

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π-Conjugated chiral shape-persistent molecular nanocarbons hold great potential as chiroptical materials, though their synthesis remains a considerable challenge. Here, we present a simple approach using Suzuki coupling of a [5]helicene building block with various aromatic units, enabling the one-pot synthesis of a series of chiral macrocycles with persistent figure-eight and Möbius shapes. Single-crystal structures of 7 compounds were solved, and 22 enantiomers were separated by preparative chiral HPLC.

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  • Radial and circular crack patterns are both visually attractive and important in various industrial applications, yet their formation mechanics, particularly involving channel fractures and delamination, are not fully understood.
  • The study shows that as the thickness of colloidal deposits increases beyond a certain point, the nature of crack patterns transitions from solely radial to a mix of radial and circular configurations, influenced by the colloidal volume fraction.
  • A phase-field fracture model is introduced to explain how thick deposits generate tensile stress that leads to the creation of circular cracks, providing new insights into designing micro-nano structures based on crack patterns.
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  • The text discusses the potential of organic radicals in creating color-changing materials that respond to external stimuli, highlighting their ability to easily dissociate and associate while changing colors.
  • It focuses on a new series of oxindolyl-based mono-radicals (OxRs) which were synthesized and studied, showing that they can spontaneously dimerize and change back to monomers via external factors like temperature and pressure.
  • The stability and properties of these mono-radicals are influenced by different substituents, allowing tailored responsiveness and opening avenues for developing materials that react to mechanical or temperature changes.
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Redox-active organic molecules have potential as electrode materials, but their cycling stability is often limited by the irreversible formation of σ-bonds from the radical intermediates. Herein, we present an effective approach to achieve high reversibility by using lone pair electrons to mediate intramolecular radical-radical coupling. Azatriangulenetrione () was examined as the anode in sodium-ion batteries, which displayed a reversible four-step, one-electron redox chemistry.

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  • ! The study aimed to assess the clinical importance of the CK-MB/total CK ratio, neutrophil/lymphocyte ratio (NLR), and red blood cell distribution width in patients with acute myocardial infarction (AMI). * ! A retrospective analysis of 196 AMI cases was compared to healthy controls, using statistical methods to identify risk factors and evaluate predictive values for AMI. * ! Findings revealed elevated serum CK-MB and NLR levels in AMI patients, indicating these markers may serve as useful diagnostic tools for identifying and assessing AMI. *
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Investigations of one-dimensional segmented heteronanostructures (1D-SHs) have recently attracted much attention due to their potentials for applications resulting from their structure and synergistic effects between compositions and interfaces. Unfortunately, developing a simple, versatile and controlled synthetic method to fabricate 1D-SHs is still a challenge. Here we demonstrate a stress-induced axial ordering mechanism to describe the synthesis of 1D-SHs by a general under-stoichiometric reaction strategy.

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Polycyclic hydrocarbons with diradical and polyradical characters usually display unique reactivities in ring-cyclization reactions. However, such reactions are rarely used to construct π-extended polycyclic aromatic hydrocarbons. Here, we describe the synthesis of an S-shaped doubly helical singlet diradicaloid compound and its facile transformation into an unprecedented circumchrysene via a two-stage ring cyclization, which includes: (1) an eletrocylization from diradicaloid precursor and (2) a Scholl reaction.

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Expanded azahelicenes, as heteroanalogues of helically chiral helicenes, hold significant potential for chiroptical materials. Nevertheless, their investigation and research have remained largely unexplored. Herein, we present the facile synthesis of a series of expanded azahelicenes NHn (n=1-5) consisting of 11, 19, 27, 35, and 43 fused rings, mainly by Suzuki coupling followed by Bi(OTf)-mediated cyclization of vinyl ethers.

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Article Synopsis
  • - The study focuses on a stable [10]cyclo-para-phenylmethine derivative (compound 1), analogous to [10]annulene, which allows for exploration of its conformations, electronic properties, and aromaticity.
  • - Compound 1 can easily be oxidized into several cations, each exhibiting unique conformations: a nearly planar rectangular structure for both 1 and its tetracation, while the radical cation shows a twisted configuration.
  • - Experimental and theoretical results reveal that 1 has localized aromaticity, while its dications (1a and 1b) display weak Möbius aromaticity and Hückel antiaromaticity, respectively; the tetracation shows
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Transparent bulk glass is highly demanded in devices and components of daily life to transmit light and protect against external temperature and mechanical hazards. However, the application of glass is impeded by its poor functional performance, especially in terms of thermal isolation and impact resistance. Here, a glass composite integrating the nacre-inspired structure and shear stiffening gel (SSG) material is proposed.

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During bottom trawl surveys carried out between 20132021, 52 specimens (33.854.0 mm SL) of Egglestones bumblebee goby Egglestonichthys bombylios were collected at a depth of 1.

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The study of through-space electronic coupling in π-conjugated systems remains an underexplored area. In this work, we present the facile synthesis of two isomeric macrocycles (1 and 2) bridged by [2,2]paracyclophane (pCp) and based on thiophene. The structures of these macrocycles have been confirmed through X-ray crystallographic analysis.

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Homogeneous wrinkles and localized patterns are ubiquitous in nature and are useful for a wide range of practical applications. Although various strain-driven surface instability modes have been extensively investigated in the past decades, understanding the coexistence, coevolution, and interaction of wrinkles and localized patterns is still a great challenge. Here, we report on the formation and evolution of coexisting wrinkle and ridge patterns in metal films deposited on poly(dimethylsiloxane) (PDMS) substrates by uniaxial compression.

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Layered inorganic material, with large-area interlayer surface and interface, provides an essential material platform for constructing new configuration of functional materials. Herein, a layered material pillared with nanoclusters realizing high temperature thermal insulation performance is demonstrated for the first time. Specifically, systematic synchrotron radiation spectroscopy and finite element calculation analysis show that ZrO nanoclusters served as "pillars" to effectively produce porous structures with enough boundary defect while maintaining the layered structure, thereby significantly reducing solid state thermal conductivity (≈0.

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Background & Aims: Hepatic ischemia-reperfusion injury is a significant complication of partial hepatic resection and liver transplantation, impacting the prognosis of patients undergoing liver surgery. The protein proprotein convertase subtilisin/kexin type 9 (PCSK9) is primarily synthesized by hepatocytes and has been implicated in myocardial ischemic diseases. However, the role of PCSK9 in hepatic ischemia-reperfusion injury remains unclear.

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Twisted polyarenes with persistent chirality are desirable but their synthesis has remained a challenge. In this study, we present a "one-pot" synthesis of 1,2:8,9-dibenzozethrene (DBZ) and its vertically fused dimers and trimers using nickel-catalyzed cyclo-oligomerization reactions. X-ray crystallographic analysis confirmed highly twisted helical structures that consist of equal parts left- and right-handed enantiomers.

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We report a facile synthesis of diindeno-fused dibenzo[a,h]anthracene derivatives (DIDBA-2Cl, DIDBA-2Ph, and DIDBA-2H) with different degrees of non-planarity using three substituents (chloro, phenyl, and hydrogen) of various sizes. The planarization of their cores, as evidenced by the decreased end-to-end torsional angles, was confirmed by X-ray crystallography. Their enhanced energy gaps with twisting were investigated by a combination of spectroscopic and electrochemical methods with density functional theory, which showed a transition from singlet open-shell to closed-shell configuration.

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Architected two-dimensional (2D) lattice materials consisting of elastic beams are appealing because of their tunable sign of Poisson's ratio. A common belief is that such materials with positive and negative Poisson's ratios display anticlastic and synclastic curvatures, respectively, when bent in one direction. Here, we show theoretically and demonstrate experimentally that this is not true.

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The research on aromaticity has mainly focused on monocyclic [n]annulene-like systems or polycyclic aromatic hydrocarbons. For fully π-conjugated multicyclic macrocycles (MMCs), the electronic coupling between the individual constitutional macrocycles would lead to unique electronic structures and aromaticity. The studies on MMCs, however, are quite limited, presumably due to the great challenges to design and synthesize a fully π-conjugated MMC molecule.

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Receptor-interacting protein kinase 1 (RIPK1) contributes to necroptosis. Our previous study showed that pharmacological or genetic inhibition of RIPK1 protects against ischemic stroke-induced astrocyte injury. In this study, we investigated the molecular mechanisms underlying RIPK1-mediated astrocyte injury in vitro and in vivo.

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Chiral shape-persistent molecular nanocarbons are promising chiroptical materials; their synthesis, however, remains a big challenge. Herein, we report the facile synthesis and chiral resolution of a double-stranded figure-eight carbon nanobelt 1 in which two [5]helicene units are fused together. Two synthetic routes were developed, and, in particular, a strategy involving Suzuki coupling-mediated macrocyclization followed by Bi(OTf) -catalyzed cyclization of vinyl ether turned out to be the most efficient.

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