Step-by-Step Strategy from Achiral Precursors to Polyoxometalates-Based Chiral Organic–Inorganic Hybrids

Using two types of triol ligands, several novel asymmetrically triol-functionalized Anderson organic hybrids have been efficiently synthesized in high purity and good yields via a convenient two-step esterification reaction. These organic–inorganic hybrids are chiral and can be spontaneously resolve...

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Veröffentlicht in:Inorganic chemistry 2015-03, Vol.54 (6), p.2551-2559
Hauptverfasser: Zhang, Jiangwei, Luo, Jianhui, Wang, Pingmei, Ding, Bin, Huang, Yichao, Zhao, Zhenlin, Zhang, Jin, Wei, Yongge
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Sprache:eng
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Zusammenfassung:Using two types of triol ligands, several novel asymmetrically triol-functionalized Anderson organic hybrids have been efficiently synthesized in high purity and good yields via a convenient two-step esterification reaction. These organic–inorganic hybrids are chiral and can be spontaneously resolved with suitable solvents. Their molecular and crystal structures have been confirmed by single-crystal X-ray diffraction studies. Stable solid-state chirality of the corresponding enantiopure crystals has also been confirmed definitively by CD spectra. Interestingly, these organic–inorganic hybrids possess a layer-by-layer structure, forming solvent-accessible nanoscale chiral channels via a 1D infinite helical chain substructure. TGA measurements indicated that the species of the central heteroatoms significantly effects the stability of these compounds.
ISSN:0020-1669
1520-510X
DOI:10.1021/ic502622k