Interaction of the trilacunary Keggin polyanions [A-α-XW9O34](10-) (X = Si(IV), Ge(IV)) with Co(II) and phosphate ions in aqueous, basic media and under mild heating leads to the formation of the tetrameric, Co16-containing heteropolytungstates [{Co4(OH)3PO4}4(A-α-XW9O34)4](32-) (X = Si(IV), Ge(IV)). Both polyanions were characterized in the solid state by single-crystal X-ray diffraction, IR spectroscopy, and thermogravimetric and elemental analyses. Furthermore, the electrochemical and magnetic properties of these isostructural polyanions were investigated.
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http://dx.doi.org/10.1021/ic500298u | DOI Listing |
Chemistry
May 2019
Institut für Chemie, Technische Universität Berlin, Fakultät II, Strasse des 17. Juni 124, 10623, Berlin, Germany.
The E. coli siderophore enterobactin, the strongest Fe chelator known to date, forms hexacoordinate complexes with Si , Ge , and Ti . Synthetic protocols have been developed to prepare non-symmetric enterobactin analogues with varying denticities.
View Article and Find Full Text PDFInorg Chem
April 2016
Institut für Anorganische Chemie, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany.
We investigated computationally the α-, γ-, and β-isomeric structures, relative stabilities, and the electronic and basicity properties of magnetic [V(IV)14E8O50](12-) (hereafter referred to as {V14E8}) heteropolyoxovanadates (heteroPOVs) and their heavier chalcogenide-substituted [V(IV)14E8O42X8](12-) ({V14E8X8}) derivatives for E = Si(IV), Ge(IV), and Sn(IV) and X = S, Se, and Te. We used density functional theory (DFT) with scalar relativistic corrections in combination with the conductor-like screening model of solvation. The main purpose of this investigation is to introduce the structure-property relations in heteroPOVs as well as to assist the synthesis and molecular deposition of these molecular vanadium-oxide spin clusters on surfaces.
View Article and Find Full Text PDFInorg Chem
July 2015
†Department of Life Sciences and Chemistry, Jacobs University, P.O. Box 750 561, 28725 Bremen, Germany.
The tetrameric, multi-Fe(III)-containing polyoxotungstates [Fe14O6(OH)13(P2W15O56)4](31-) (1) and [Na2Fe14(OH)12(PO4)4(A-α-XW9O34)4](20-) (X = Si(IV) (2), Ge(IV) (3)) have been successfully synthesized under conventional reaction conditions in aqueous, slightly acidic (1), or basic (2 and 3) media. Polyanions 1-3 were characterized in the solid state by single-crystal X-ray diffraction, IR spectroscopy, thermogravimetric analysis, and magnetic studies, and in solution by electrochemistry.
View Article and Find Full Text PDFPhys Chem Chem Phys
May 2015
Institute of Functional Material Chemistry, Key Laboratory of Polyoxometalate Science of Ministry of Education, Faculty of Chemistry, Northeast Normal University, Changchun 130024, P. R. China.
Quantum chemical calculations were performed to explore the structural and electronic properties of the two polyoxoaurates, [Au(III)4As(V)4O20](8-) (Au4As4) and [Au(III)4Se(IV)4O16](4-) (Au4Se4), known to date, and a number of hypothetical polyoxoaurate derivatives comprising heteroatoms different from arsenic and selenium (namely, Si, Ge and P). In addition, the interactions of [Au(III)4X4Om](n-) (X = As, Se) with alkali-metal cations (Li(+), Na(+), K(+) and Rb(+)) are also analysed. The studies suggest that the geometry structure, electronic properties and nucleophilicity of oxygen atoms of these polyoxoaurates are tuned by the size or electronegativity of the heteroatoms (Si, Ge, P, As and Se).
View Article and Find Full Text PDFInorg Chem
May 2014
School of Engineering and Science, Jacobs University, P.O. Box 750 561, 28725 Bremen, Germany.
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