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- W2027335913 abstract "The crystal structures of [(CH3)2SS(CH3)]SbCl6(1), [(CH3S)3]SbCl6(2), and [(CH3Se)3]SbCl6(3) have been determined by X-ray crystallography at 170 K. Compound (1) is triclinic, space group P with a= 701.3(3), b= 1 415.1(8), c= 689.9(3) pm, α= 94.97(4), β= 91.19(4), γ= 91.43(4)°, Z= 2. Though (2) and (3) are analogous to each other and both are monoclinic, space group P21/c, they are not isomorphous. For (2), a= 1 395.3(4), b= 928.9(3), c= 1 145.2(4) pm, β= 94.31(3)°, Z= 4; for (3), a= 701.8(4), b= 1 970.7(9), c= 1 197.8(5) pm, β= 113.45(4)°, Z= 4. Each cation involves a three-co-ordinated chalcogen atom. The S–S bond length in (1) is relatively long while in (2) and (3) the chalcogen–chalcogen bonds have almost normal single bond lengths. (CH3)2SS(CH3)+ has an all-cis conformation with the approximate site symmetry Cs. The conformations of (CH3S)3+ and (CH3Se)3+ are fairly similar with the chain-end methyl groups in trans positions to each other. The packing of the ions is, however, different. This is also reflected by the drastically differing colours of these two compounds, (2) is practically colourless while (3) is deep red. In all three compounds the SbCl6– anion is almost a regular octahedron with Sb–Cl 236.1(1)–239.3(4) pm and Cl–Sb–Cl 88.4(1)–91.1(1)°. The Raman spectra of (2) and (3) are reported." @default.
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- W2027335913 date "1986-01-01" @default.
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- W2027335913 title "The crystal structures of the hexachloroantimonate salts of (CH3)2SS(CH3)+, (CH3S)3 +, and (CH3Se)3 +" @default.
- W2027335913 doi "https://doi.org/10.1039/dt9860001095" @default.
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