CRYSTAL STRUCTURE OF A NEW BISMUTH PERRHENATE Bi(Re0(4))3H(2)0
Monoaquatris(tetraoxorhenate (VII)) bismuth(III), Bi(Re0(4))3(H(2)0) was prepared by reaction of (BiO)2C0(3)/Bi2(C0(3))3 with concentrated HRe0(4) at room temperature. The pale yellow compound crystallize triclinic in the space group PI;, (No. 2); with two formula units per unit cell (a = 746.0(1) p...
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Autores principales: | , , , , |
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Lenguaje: | English |
Publicado: |
Sociedad Chilena de Química
2008
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Materias: | |
Acceso en línea: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072008000100008 |
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Sumario: | Monoaquatris(tetraoxorhenate (VII)) bismuth(III), Bi(Re0(4))3(H(2)0) was prepared by reaction of (BiO)2C0(3)/Bi2(C0(3))3 with concentrated HRe0(4) at room temperature. The pale yellow compound crystallize triclinic in the space group PI;, (No. 2); with two formula units per unit cell (a = 746.0(1) pm, b = 111. 1(2) pm, c = 990.5(2) pm, a = 100.99(3)°, p = 99.88(3)°, y = 100.17(3)° ). The main feature of the crystal structure is a distorted bicapped trigonal prism of Bi[(Re0(4))3;2 (Re0(4))2/2 (Re0(4))2/2 (H(2)0)], which are connected each other through [ReOJ-tetrahedra to form a three-dimensional network. In the titled compound, the cation Bi3+ is eightfold coordinated which agree with the tendency observed in other compounds of the family |
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