Publications by authors named "Zhengguang Zhao"

In-plane heterostructures exhibit extraordinary chemical and electron transfer properties, which have received remarkable research attention. However, the synthesis of an in-plane MoC/MoO heterostructure has been rarely reported, and the deep investigation of the effect of its fine structure on reactivity is of great significance. Notably, the in-plane heterostructures endow the material with abundant grain boundaries, which facilitate the formation of surface acid sites and active oxygen species, thus contributing to the sensing performance.

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Article Synopsis
  • Pd-based materials are gaining attention for their excellent hydrogen (H) sensing performance, but the effects of metal support interaction (MSI) on this performance are not well understood.
  • A model material, Pd nanoparticle-decorated WO nanosheet, shows impressive H sensing abilities at low temperatures, particularly with a response rate of 40.63 at 10 ppm H.
  • The study uses DFT calculations to demonstrate that moderate MSI helps increase the mobility of surface O species and the optimal ratio of surface Pd-Pd species, enhancing the sensing performance by facilitating the desorption of PdH species at lower temperatures.
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Herein, we report a palladium-catalyzed relay Heck-type reaction of fluoroalkyl bromide and terminal alkenes. The reaction involves fluoroalkylation of alkenes and migration of double bonds via a 1,5-hydrogen atom transfer strategy. Through this method, a series of remote fluoroalkylated alkenes was obtained under mild conditions.

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Visible light-mediated cascade remote oxyfluoroalkylation of alkenes under mild conditions is developed for the first time. The key point of this transformation is the incorporation of alkene fluoroalkylation-initiated remote benzyl C-H bond activation via a 1,5-H shift in a highly controlled site-selective manner and Kornblum reaction with dimethyl sulfoxide as the oxidant. With this method, a broad array of fluoroalkyl groups were introduced into a double bond to produce 1,6-fluoroalkylated ketones at room temperature.

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A transition-metal-free and environmentally friendly synthesis method for bromobenzothiazines through tandem C-H amination/bromination was reported. This reaction contains both intramolecular C-H amination and site-selective electrophilic bromination of arenes with NaBr as the bromo source, PhI(OAc) or KSO as the oxidant, and HO as the only solvent.

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