1018810-30-4Relevant articles and documents
A new class of binuclear and trinuclear iron-sulfur clusters derived from bis[bis(trimethylsilyl)amido]iron(II)
Pryadun, Ruslan,Holm
, p. 3366 - 3370 (2008)
The compound Fe[N(SiMe3)2]2 is shown to be a useful precursor to dinuclear and trinuclear iron-sulfur-silylamido complexes by reaction with thiols or thiols and sulfur in tetrahydrofuran (THF) or toluene. Reaction with 1 equiv of p-tolylthiol affords [Fe2(μ 2-S-p-tol)2(N(SiMe3)2) 2(THF)2] (1); with 0.5 equiv of adamantane-1 -thiol, [Fe2(μ2-S-1-Ad)(μ2-N(SiMe 3)2)(N(SiMe3)2)2] (2) is formed. The clusters [Fe3(μ3-Q)(μ2-SR) 3(N(SiMe3)2)3] are available by three methods: (i) self-assembly in the systems Fe[N(SiMe3) 2]2/RSH/S or Se [Q = S, R = p-tol (3) and 1-Ad (5)]; (ii) reaction of 1 with Q = S or Se to yield 3 or [Fe3Se(S-p-tol) 3(N(SiMe3)2)3] (4); (iii) reaction of 2 with 1-AdSH and S to give 5. Structures of 1-5 are presented. Complexes 1 and 2 contain planar Fe2S2 and Fe2SN rhombs. Clusters 3-5 contain a mixed-valence Fe3Q(SR)3 core with trigonal (cuboidal) geometry. Of known iron-sulfur clusters, these most closely resemble previously reported [Fe3S(S-R-S)3]2- stabilized by bidentate thiolate ligands. Complexes 1-5, together with a small set of recently described clusters of nuclearities 2, 4, and 8, constitute a new class of iron-sulfur-silylamido clusters. Complexes 3-5 constitute a new structure type of mixed-valence iron-sulfur clusters.