(Me3SiCH2)3(Me3SiC≡)W←O=PMe3 (1), an adduct between (Me3SiCH2)3W≡CSiMe3 (2) and O=PMe3, reacts with O2 to give O=W(OSiMe3)(CH2SiMe3)3 (3) and CO2. Reaction of 2 with H2O yields 3 and the trimer [(μ-O)W(CH2SiMe3)2(=O)(THF)]3 (4). In the reaction of D2O with 2, 3-d(n) and methane isotopologues CH2D2, CHD3 and CD4 have been observed.
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http://dx.doi.org/10.1039/c3cc46014b | DOI Listing |
J Colloid Interface Sci
January 2025
Henan Key Laboratory of Polyoxometalate Chemistry, School of Energy Science and Technology, Henan University, Zhengzhou 450046, PR China. Electronic address:
Due to the limited active sites and poor conductivity, the application of tungsten disulfide (WS) in alkaline water electrolysis remains a challenge. Herein, Ni-WS nanosheet arrays were in situ grown on the carbon fiber paper (Ni-WS/CFP) as an electrocatalyst for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline media, and the introduction degree of Ni can be regulated by adjusting the electrodeposition time. When the electrodeposition time is 3 min, Ni ions are doped into the lattice of WS, and by prolonging the electrodeposition time to 10 min, the nickel disulfide (NiS) crystal phase is generated to form NiS@WS heterojunction.
View Article and Find Full Text PDFSmall
January 2025
Department of Chemistry and Life Science, Yokohama National University, Yokohama, 240-8501, Japan.
Hydrogen spillover, particularly when involving "interparticle" hydrogen spillover, offers a unique opportunity to enhance catalytic efficiency by remote activation of surface acidity. Building on this concept, this study aims to investigate physically mixed alumina-supported platinum nanoparticles (Pt/AlO) and zirconia-supported tungsten oxide (WO/ZrO) in promoting the direct synthesis of cumene from benzene and propane at 300 °C. The reaction with Pt/AlO alone afforded propylene as the only product, indicating the successive reaction route of Pt-catalyzed dehydrogenation of propane, followed by acid-catalyzed alkylation.
View Article and Find Full Text PDFACS Omega
January 2025
State Key Joint Laboratory of Environment Simulation and Pollution Control, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Selective catalytic reduction of nitrogen oxides (NO ) by ammonia (NH-SCR) over supported vanadium catalysts is a commercial technology for NO abatement in combustion exhaust. The addition of tungsten oxide (WO) significantly enhances the performance of supported vanadium catalysts (VO/TiO), but the mechanism underlying this enhancement remains controversial. In this study, we employed combined operando spectroscopy (DRIFTS-UV-vis-MS) to investigate the dynamic state of active sites (acid sites and redox sites) on VO-WO/TiO during the NH-SCR reaction.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Hydrogen spillover is an important process in catalytic hydrogenation reactions, facilitating H activation and modulating surface chemistry of reducible oxide catalysts. This study focuses on the unveiling of platinum-induced hydrogen spillover on monoclinic tungsten trioxide (γ-WO), employing ambient pressure X-ray photoelectron spectroscopy, density functional theory calculations and microkinetic modeling to investigate the dynamic evolution of surface states at varied temperatures. At room temperature, hydrogen spillover results in the formation of W and hydrogen intermediates (hydroxyl species and adsorbed water), facilitated by Pt metal clusters.
View Article and Find Full Text PDFInorg Chem
January 2025
MOE Key Laboratory of Cluster Science, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing 102488, China.
A novel antimonotungstate (AT)-based heterometallic framework {[Er(HO)][Fe(Hpdc)(B-β-SbWO)]}·50HO (, Hpdc = pyridine-2,5-dicarboxylic acid) was obtained through a synergistic strategy of in situ-generated transition-metal-encapsulated polyoxometalate (POM) building units and the substitution reaction. Its structural unit is composed of a tetra-Fe-substituted Krebs-type [Fe(Hpdc)(B-β-SbWO)] subunit and two [Er(HO)] cations. This subunit can be regarded as a product of carboxylic oxygen atoms of Hpdc ligands replacing active water ligands in the [Fe(HO)(B-β-SbWO)] species.
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