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- W2016047020 abstract "An ionic crystal [Cr3O(OOCCF3)6(H2O)3]3[α-PW12O40]·8CH3COCH3·8H2O·CHCl3 [Ia] was synthesized by the complexation of a fluorine-substituted macrocation with a phosphododecatungstate. Compound Ia possessed a layered structure with an interlayer distance of ca. 3.5 Å, and the inner surface of the layer was decorated with CF3 groups of the macrocations. The solvent molecules (acetone and chloroform) spontaneously desorbed and exchanged with water under an ambient atmosphere and a hydrated phase [Cr3O(OOCCF3)6(H2O)3]3[α-PW12O40]·25H2O [Ib] was formed. The water molecules were partially desorbed by the treatment of Ibin vacuo or under a dry N2 or He flow at 298–303 K, and [Cr3O(OOCCF3)6(H2O)3]3[α-PW12O40]·15H2O [Ic] was formed. The powder XRD pattern of Ic well agreed with that calculated for Ia, showing that the structure was maintained after the exchange and partial desorption of guests. Compound Ic sorbed CO2 and unsaturated hydrocarbons, while saturated hydrocarbons such as ethane and methane were almost excluded despite the similar kinetic diameters. Acetylene/methane, CO2/methane, and ethylene/ethane sorption ratios were 13, 15, and 4.9, respectively, at 198 K and 100 kPa. Typical Monte Carlo-based optimized geometries of acetylene and CO2 showed different alignments in the structure of Ic despite the similar amounts of sorption and molecular sizes. Acetylene and CO2 were aligned mainly parallel and perpendicular, respectively, to the layer, which is probably due to the differences in the electron density distributions of the HOMO orbitals." @default.
- W2016047020 created "2016-06-24" @default.
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- W2016047020 date "2013-01-01" @default.
- W2016047020 modified "2023-10-15" @default.
- W2016047020 title "Highly selective sorption and unique packing geometries of unsaturated hydrocarbons and CO2 in a fluorine-substituted organic–inorganic ionic crystal" @default.
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- W2016047020 doi "https://doi.org/10.1039/c3dt51458g" @default.
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