Abstract
The salts Cs4[Re6S8(OH)6]·6H2O (1) and Cs4[Re6Se8(OH)6]·8H2O (2) were obtained by the reactions of Re6S8Br2 and Re6Se8Br2 with a CsOH melt with further solution of the products in water and crystallization of 1 and 2 from the aqueous solutions. The structure of the compounds was established by X-ray single crystal diffraction analysis. Compound 1 crystallizes in the orthorhombic space group Pbca with unit cell parameters a = 14.175(2) Å, b = 11.321(2) Å, c = 17.503(2) Å, V = 2808.5(7) Å3, Z = 4, d calc = 5.003 g/cm3; compound 2 crystallizes in the triclinic space group \(P\bar 1\) with unit cell parameters a = 9.020(4) Å, b = 9.127(4) Å, c = 10.289(4) Å, α = 79.589(7)°, β = 75.829(7)°, γ = 72.186(7)°, V = 776.8(6) Å3, Z = 1, d calc = 5.402 g/cm3.
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Original Russian Text Copyright © 2007 by K. A. Brylev, Yu. V. Mironov, S.-J. Kim, and V. E. Fedorov
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Translated from Zhurnal Strukturnoi Khimii, Vol. 48, No. 6, pp. 1183–1188, November–December, 2007.
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Brylev, K.A., Mironov, Y.V., Kim, SJ. et al. Crystal structures of the octahedral rhenium cluster compexes Cs4[Re6S8(OH)6]·6H2O and Cs4[Re6Se8(OH)6]·8H2O. J Struct Chem 48, 1118–1123 (2007). https://doi.org/10.1007/s10947-007-0179-5
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DOI: https://doi.org/10.1007/s10947-007-0179-5