Synthesis and crystal structure of the mer-Fe(ReO4)3(H2O)3 complex

被引:0
|
作者
Mujica, C
Peters, K
Peters, EM
Carrillo, W
Von Schnering, HG
机构
[1] Univ Catolica Norte, Dept Quim, Antofagasta, Chile
[2] Max Planck Inst Festkorperforsch, D-70506 Stuttgart, Germany
来源
关键词
perrhenate ligand; iron complex; crystal structure; thermal stability; hydrogen bonding;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Triaquatris(tetraoxorhenato(VII) iron(III) [Triaquatris(perrhenato) iron(III)] has been synthesized from iron(III) hydroxide and perrhenic acid. The new compound crystallizes triclinically in the space group P (1) over bar (No. 2) with two formula units per unit cell (a = 775.2, b = 819.5, c = 1156.3 pm, alpha = 86.80 degrees, beta = 83.76 degrees and gamma = 64.97 degrees). The structure contains meridional configurated mer-Fe(ReO4)(3)(H2O)(3) complexes, which are interconnected via hydrogen bonding. The mean bond lengths are d(Fe-O) = 197 pm to the ReO4 ligands and d(Fe-O) = 203 pm to the water molecules. The three crystallographically different ReO4 tetrahedra are characterized by one long Re-O bond to the ligator oxygen atom (d = 175 pm) and three short ones (166-170 pm). The thermal decomposition starts at 400 K with the loss of water. Above 600 K the compound decomposes in several steps into solid iron(III) oxide and evaporating rhenium oxides.
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页码:161 / 166
页数:6
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