Abstract
We report on the synthesis and crystal structure of the octaammine calcium(II) halides [Ca(NH3)8]Br2, and [Ca(NH3)8]I2, which were synthesized by the reaction of the respective calcium( II) halides with dry liquid ammonia. The compounds form colorless crystals which crystallize isotypically at 123 K with Z = 4 in the orthorhombic space group Pnma with a = 12:0478(3), b = 7:4406(2), c = 15:7216(4) Å, V = 1409:33(6) Å3 for the bromide, and a = 12:1113(4), b = 7:7706(3), c = 16:7145(6) Å, V = 1573:0(1) Å3 for the iodide. Instead of the expected tetragonal antiprism for the eightfold-coordinated Ca2+ ions, we observed a coordination polyhedron best described as a twofold capped trigonal prism. After evaporation of the liquid ammonia and warming of [Ca(NH3)8]I2 to room temperature, [Cu(NH3)6]I2 was obtained as a colorless powder. The hexaammine calcium(II) iodide crystallizes isotypically to [Mn(NH3)6]I2 (CaF2 type) in the cubic space group Fm3̅m with a = 11:18580(6) Å, V = 1399:59(1) Å3, Z = 4 at 293 K
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