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Syntheses and Crystal Structures of the Cluster Compounds A2[(W6Br3.0.CO;2-A/asset/equation/tex2gif-stack-1.gif?v=1&t=h5l3kt35&s=e74f1fc8be6246e083fc5deafc2f462f0248ae3a" class="inlineGraphic">)Br3.0.CO;2-A/asset/equation/tex2gif-stack-2.gif?v=1&t=h5l3kt35&s=76c2e86c2a8b850da7b366a5b8924d3b962ef395" class="inlineGraphic">] with A = K, Rb, Cs

✍ Scribed by Yue-Qing Zheng; Karl Peters; Yuri Grin; Hans Georg von Schnering


Publisher
John Wiley and Sons
Year
1998
Tongue
German
Weight
254 KB
Volume
624
Category
Article
ISSN
0372-7874

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✦ Synopsis


K 2 W 6 Br 14 (I), Rb 2 W 6 Br 14 (II), and Cs 2 W 6 Br 14 (III) were formed by reactions of W 6 Br 12 with the corresponding alkali metal bromides in evacuated silica tubes with a temperature gradient of 925 K/915 K. (I) crystallizes in the cubic space group Pn3 (no. 201), a = 13.808 A Ê , Z = 4, cP88. (II) crystallizes in the monoclinic space group C2/c (no. 15), a = 20.301 A Ê , b = 15.396 A Ê , c = 9.720 A Ê , b = 115.69°, Z = 4, mC88. (III) crystallizes in the trigonal space group P31c (no. 163), a = 10.180 A Ê , c = 15.125 A Ê , Z = 2, hP44. The crystal structures are composed of the isolated [(W 6 Br i 8 )Br a 6 ] 2± cluster anions and the alkali metal cations (d(W±W) = 2.635(2) A Ê , d(W±Br i ) = 2.624(4) A Ê , d(W±Br a ) = 2.595(4) A Ê ).

The shape of the anions is influenced by the crystal field symmetry, but the mean bond lengths are not changed by the cation size. The packing of the cluster anions corresponds to ccp pattern in (I) and hcp pattern in (II) and (III), respectively. The alkali metal cations in the octahedral holes are coordinated only by the Br a ligands while those in the tetrahedral and trigonal-bipyramidal cavities are surrounded by Br a and Br i ligands. The details will be discussed and compared with other structures.


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