Publications by authors named "Changhai Yue"

Graphene oxide (GO) with its atomic thickness and abundant functional groups holds great potential in molecular-scale membrane separation. However, constructing high-speed and highly selective water transport channels within GO membranes remains a key challenge. Herein, sulfonato calix[n]arenes (SCn) molecules with a cavity structure, hydrophilic entrance, and hydrophobic wall were incorporated into GO interlayer channels through a layer-by-layer assembly approach to facilitate water permeation in a water/ethanol separation process.

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An unprecedented one-pot route to achieve highly regioselective 1-sulfur-functionalized 2-nitrogen-functionalized alkenes and 2-thiocyanate indolines from unsymmetrical ynamides (readily and generally available amides) using the commercially available inexpensive iodobenzene diacetate (PIDA) as the oxidant and potassium thiocyanate (KSCN) as the thiocyanate (SCN) source has been developed. The interconversion of thiocyanate (SCN) and isothiocyanate (NCS) groups simultaneously forms C-N and C-S bonds in this metal-free approach, while introducing important functional groups into homemade alkynes. A radical-chain mechanism, involving competing kinetically controlled chain transfer at the S atom and sterically-controlled chain transfer at the N atom of the thiocyanogen molecule in this mild approach, is proposed.

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Metal-organic frameworks (MOFs) are regarded as the next-generation, disruptive membrane materials, yet the straightforward fabrication of ultrathin MOF membranes on an unmodified porous support remains a critical challenge. In this work, we proposed a facile, one-step electrophoretic deposition (EPD) method for the growth of ultrathin zeolitic imidazole framework-8 (ZIF-8) membranes on a bare porous support. The crystallinity, morphology and coverage of ZIF-8 particles on support surface can be optimized via regulating EPD parameters, yet it is still difficult to ensure the integrity of a ZIF-8 membrane with the constant voltage mode.

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