Publications by authors named "Liancheng He"

Most C-H bond activations of natural gas alkanes rely on transition metal complexes. Activations by using main-group systems have been reported but required heating or photo-irradiation under high atmospheric pressure with rather low regioselectivity. Here we report that Lewis acid-carbene adducts facilely undergo oxidative additions to C-H bonds of ethane, propane and n-butane with high selectivity under room temperature and atmospheric pressure.

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Graph Convolutional Networks (GCNs) have shown remarkable performance in processing graph-structured data by leveraging neighborhood information for node representation learning. While most GCN models assume strong homophily within the networks they handle, some models can also handle heterophilous graphs. However, the selection of neighbors participating in the node representation learning process can significantly impact these models' performance.

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This work describes a Lewis-acid-coordination strategy to efficiently enhance the electrophilicity of a carbene beyond structural modification. A hybrid BCF-DAC is formed by the coordination of a Lewis acid, B(CF) (BCF), to an ,'-diamidocarbene (DAC), possessing superior low LUMO energy that is indicated by theoretical calculation. This endows the hybridized carbene with a unique reactivity that speeds up the activation of the sp-hybridized C-H bond of toluene and the [2+1] cycloaddition with CH.

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Article Synopsis
  • The study focuses on creating a new 3D metal-organic framework (Cd-MOF) designed specifically for capturing lead ions (Pb(II)) from water, which is crucial for environmental safety.
  • Cd-MOF demonstrates impressive performance with a maximum adsorption capacity of 845.55 mg/g for Pb(II), surpassing many other similar materials.
  • The material not only boasts excellent stability and recycling potential but also operates through a spontaneous endothermic adsorption process, highlighting its effectiveness for industrial applications in lead capture and recovery.
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Tryptophan regulates and participates in various physiological systems in the human body, and its excessive intake has harmful effects. Therefore, detecting and monitoring tryptophan in water and distinguishing it from other amino acids are necessary. In addition to their excellent luminescence, coordination polymer-based sensors have good stability and high sensitivity and selectivity for sensing applications.

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In this study, we reported the covalent post-synthetic modification (PSM) of a luminescent complex to achieve aggregation-induced emission (AIE), prepared using the Schiff base reaction of TPE-CHO and HLC-NH2, denoted by HLC-NH2-TPE. HLC-NH2 formed a 2D luminescent complex which was constructed using 4,4'-diamino-[1,1'-biphenyl]-2,2'-dicarboxylic acid and zinc ions a solvothermal reaction. HLC-NH2-TPE inherited the luminescence properties of HLC-NH2 and exhibited noticeable AIE properties in response to environmental viscosities and temperature changes.

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Using multifunctional organic ligands with multiple acidic groups (carboxylate and sulfonate groups) to synthesize metal-organic frameworks (MOFs) bearing effective H-bond networks is a promising strategy to obtain highly proton conductive materials. In this work, a highly stable two-dimensional MOF, [CuCu(μ-OH)(HO)(L)(HL)]·3HO (denoted as ; HL = 6-sulfonaphthalene-1,4-dicarboxylic acid) containing mixed-valence [CuCu(μ-OH)] subunits, was successfully prepared. It exhibited excellent stability and temperature- and humidity-dependent proton conduction properties.

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