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ABSTRACT: Synthesis, crystal structure as well as IR- and Raman-spectroscopic properties of the new ternary azidoaurates(III) A[Au(N3)4] (A = K, Rb, Cs) are reported. The translucent orange-red compounds were prepared by reaction of the respective binary azides with HAuCl4 in aqueous solutions at room temperature. The crystal structures determined by single crystal X-ray diffraction methods are monoclinic (C2/c (No. 15), K/Rb/Cs[Au(N3)4]: a = 1049.30(9) pm / 1033.93(10) pm / 1011.9(8) pm, b = 1047.52(8) pm / 1064.20(11) pm / 1093.8(8) pm, c = 776.97(7) pm / 809.79(8) pm / 858.4(6) pm, β = 91.220(5)° / 90.322(5)° / 92.72(5)°) and provide the first examples for azidoaurates with mono-atomic cations. The unusual reduction of the lattice parameter a with increasing cation size in the isotypic series is discussed in detail. IR- and Raman-spectroscopic measurements show strongly covalent gold-nitrogen contacts, a bonding situation which is further supported by quantum chemical calculations and ELF-analyses.
Zeitschrift für anorganische Chemie 07/2006; 632(10‐11):1671 - 1680.
