Synthesis and characterization of an unprecedented water-soluble tris-functionalized Anderson-type polyoxometalate
Autor: | Hongli Jia, Qi Li, Yongge Wei, Yunshen Zhang, Yi-Chao Huang |
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Rok vydání: | 2020 |
Předmět: |
Tris
Aqueous solution 010405 organic chemistry Hydrogen bond Ligand Organic Chemistry Synthon 010402 general chemistry 01 natural sciences 0104 chemical sciences Analytical Chemistry Inorganic Chemistry chemistry.chemical_compound chemistry Polyoxometalate Polymer chemistry Proton NMR Molecule Spectroscopy |
Zdroj: | Journal of Molecular Structure. 1219:128555 |
ISSN: | 0022-2860 |
DOI: | 10.1016/j.molstruc.2020.128555 |
Popis: | A water-soluble single-sided tris-functionalized Anderson-type polyoxometalate (POM) with counter ammonium cations, (NH4)2{[NH3C(CH2O)3]Cr(OH)3Mo6O18}·5H2O(1), has been synthesized by a hydrothermal reaction of parent Anderson-type POMs, [NH4]3[Cr(OH)6Mo6O18] (CrMo6) and tris ligand (HOCH2)3CNH2·HCl (Tris) in aqueous solution. Single-crystal X-ray diffraction analysis has revealed that compound 1 crystallizes in triclinic space group P-1. Each asymmetric unit contains one protonated single-side tris-functionalized Anderson-type POMs anion cluster, {[NH3C(CH2O)3]Cr(OH)3Mo6O18}2- (CrMo6-tris-NH3), and two NH4+ counter cations and five crystallized H2O solvent molecules, which can assemble into a layer-by-layer structure via hydrogen bonding interactions. Furthermore, compound 1 was characterized by elemental analysis, FT-IR, 1H NMR, UV–Vis and TGA. Such a water-soluble tris-functionalized POM with the remote amino reactive group has not been reported before and it may serve as a valuable synthon for further post-functionalization in aqueous solution. |
Databáze: | OpenAIRE |
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