Crystal Structure and Thermal Behavior of Cs2[B4O5(OH)4]3H2O
β Scribed by M. Touboul; N. Penin; G. Nowogrocki
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 202 KB
- Volume
- 143
- Category
- Article
- ISSN
- 0022-4596
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β¦ Synopsis
The crystal structure of synthetic Cs 2 [B 4 O 5 (OH) 4 ]3H 2 O was determined from single-crystal X-ray diffraction data. The compound is monoclinic, space group P2 1 /c; the unit cell parameters are aβ«)2(424.8Ψβ¬ A s , bβ«)3(873.11Ψβ¬ A > , cβ«)5(061.31Ψβ¬ A > , β«Ψβ¬ 92.06(3)Β°; Zβ«.4Ψβ¬ The crystal structure was solved from 6355 reflections until Rβ«;920.0Ψβ¬ it contains isolated [B 4 O 5 (OH) 4 ] 2Ψ polyanions separated by free water molecules and Cs Ψ ions. Although its formula is the same as that of the tincalconite Na 2
which contains only two isolated water molecules. In the cesium and the potassium borates, the [B 4 O 5 (OH) 4 ] 2Ψ anions have not a two-fold axis as in the tincalconite; the shorthand notations of these two kinds of anions shall be noted as: 4: 2 Ψ2T in the first two borates and 4:( ΨT) 2 in the tincalconite, and T being triangular and tetrahedral borons, respectively.Cs 2 [B 4 O 5 (OH) 4 ]3H 2 O indexed X-ray powder diffraction pattern is given. The dehydration of this borate occurs in two close steps and leads to an amorphous phase; this process is well explained considering the structure and especially the change in the Cs Ψ coordination during the heating.
π SIMILAR VOLUMES
The crystal structure of synthetic Rb 2 [B 4 O 5 (OH) 4 ] ' 3.6H 2 O has been established from single-crystal X-ray di4raction data. It crystallizes in the orthorhombic space group Pbcn with a unit cell of dimensions a β«Ψβ¬ 11.276(5) A s , b β«Ψβ¬ 13.097(14) A s , c β«Ψβ¬ 16.751(5) A s ; V β«Ψβ¬ 2474(3) A
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