A dimeric Keggin polyoxometalate, [Cu(bpy)(μ2-OH)]4[(H2O)(bpy)2HPW11Cu2O39]2·2CH3CH2OH·10H2O (1), constructed from two dicopper(II)-substituted monovacant Keggin polyoxoanions bridged by a Cu4 cluster, has been hydrothermally synthesized. Magnetic analysis indicates predominantly an antiferromagnetic interaction between copper(II) centers. Compound 1 also shows very high catalytic activity for the esterification of phosphoric acid with equimolar lauryl alcohol to monoalkyl phosphate ester.
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http://dx.doi.org/10.1021/ic5000827 | DOI Listing |
Inorg Chem
June 2022
Department of Applied Chemistry, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.
A palladium-platinum bimetal complex containing a mono-lacunary α-Keggin-type polyoxotungstate is demonstrated. The bimetallic complex Cs{Pd(bpy)}[α-PWO{Pd(bpy)}{-Pt(NH)}]·12HO·2CHCN (bpy = 2,2'-bipyridine) () was synthesized by the reaction of CsK[α-PWO{Pt(NH)}]·10HO () with Pd(bpy)Cl in aqueous solution. The compound was characterized via elemental analysis, thermogravimetric/differential thermal analysis, and Fourier transform infrared, ultraviolet-visible, cold-spray ionization mass, and solution (H, C, and P) nuclear magnetic resonance spectroscopies.
View Article and Find Full Text PDFACS Appl Mater Interfaces
April 2022
Henan Key Laboratory of Polyoxometalate Chemistry, Institute of Molecular and Crystal Engineering, School of Chemistry and Chemical Engineering, Henan University, Kaifeng, Henan 475004, P. R. China.
A powerful approach to generate photocatalysts for the highly selective reduction of nitrobenzene using light as the driving force is a combination of photosensitizers and electron-storable components in a cooperative photocatalysis fashion. Herein, a new precious metal-free photocatalyst, , was prepared by incorporating a Zn-substituted monovacant Keggin polyanion [SiZnWO] and a photoactive organic bridging link 2,4,6-tri(4-pyridyl)-1,3,5-triazine (TPT) into a framework. In this structure, the direct coordination bond between [SiZnWO] and the TPT ligand and the π-π interactions between TPT molecules help separate and migrate photogenerated carriers, which improves the photocatalytic activity of .
View Article and Find Full Text PDFMolecules
October 2020
LAQV-REQUIMTE, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, 4169-007 Porto, Portugal.
Two quaternary ammonium catalysts based on the monovacant polyoxotungstate ([PWO], abbreviated as PW) were prepared and characterized. The desulfurization performances of the PW-based hybrids (of tetrabutylammonium and trimethyloctadecylammonium, abbreviated as TBA[PW] and ODA[PW], respectively), the corresponding potassium salt (KPWO, abbreviated as KPW) and the peroxo-compound (TBA-PO[WO(O)], abbreviated as TBA[PW]) were compared as catalysts for the oxidative desulfurization of a multicomponent model diesel (2000 ppm S). The oxidative desulfurization studies (ODS) were performed using solvent-free systems and aqueous HO as oxidant.
View Article and Find Full Text PDFInorg Chem
October 2018
Henan Key Laboratory of Polyoxometalate Chemistry, Institute of Molecule and Crystal Engineering, College of Chemistry and Chemical Engineering , Henan University, Kaifeng , Henan 475004 , PR China.
The facile one-step assembly reaction of NaWO·2HO, Sn(CH)Cl, RE(NO)·6HO and KTeO in the presence of dimethylamine hydrochloride as an organic solubilizing agent in acidic aqueous solution resulted in a family of dimethyltin-functionalized rare-earth (RE) incorporated tellurotungstates consisting of {B-α-TeWO} and {WO} mixed building units [HN(CH)]NaH[RE(OH)(B-α-TeWO)Sn(CH)(WO)]·18HO [RE = Er (1), Yb (2), Ho (3), Y (4)]. The most striking structural characteristic of 1-4 is that they all contain a novel tetrameric S-shaped [RE(OH)(B-α-TeWO)Sn(CH)(WO)] moiety simultaneously including two pentavacant Keggin [B-α-TeWO] and two monovacant Lindqvist [WO] fragments connected by RE and dimethyltin linkers. To the best of our knowledge, such dimethyltin-functionalized RE-containing tellurotungstates have not been reported before.
View Article and Find Full Text PDFDalton Trans
January 2015
Key Laboratory of Cluster Science, Ministry of Education of China, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry, Beijing Institute of Technology, Beijing 100081, People's Republic of China.
The solution chemistry of a series of mono-, di- and trilacunary Keggin silicotungstates was investigated by electrospray ionization mass spectrometry (ESI-MS) and general electrospray features especially for lacunary POMs are summarized. The reactions of vanadium incorporation into the lacunary structures were successfully monitored in real-time by a combination of ESI-MS and differential pulse voltammetry (DPV). It was found that all the reactions took place instantaneously and that a subtle speciation change occurred at prolonged reaction times for the pair of reactants, monovacant silicotungstate and sodium metavanadate, suggesting a conversion of mono- to divanadium substituted derivatives.
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