Building Fe(iii) clusters with derivatised salicylaldoximes

Abstract

The syntheses, structures and magnetic properties of nine new iron complexes containing salicylaldoxime (saoH(2)) or derivatised salicylaldoximes (R-saoH(2)), [Fe(3)O(OMe)(Ph-sao)(2)Cl(2)(py)(3)].2MeOH (1.2MeOH), [Fe(3)O(OMe)(Ph-sao)(2)Br(2)(py)(3)].Et(2)O (2.Et(2)O), [Fe(4)(Ph-sao)(4)F(4)(py)(4)].1.5MeOH (3.1.5MeOH), [Fe(6)O(2)(OH)(2)(Et-sao)(2)(Et-saoH)(2)(O(2)CPh)(6)] (4), [HNEt(3)](2)[Fe(6)O(2)(OH)(2)(Et-sao)(4)(O(2)CPh(Me)(2))(6)].2MeCN (5.2MeCN), [Fe(6)O(2)(O(2)CPh)(10)(3-(t)But-5-NO(2)-sao)(2)(H(2)O)(2)].2MeCN (6.2MeCN), [Fe(6)O(2)(O(2)CCH(2)Ph)(10)(3-(t)But-sao)(2)(H(2)O)(2)].5MeCN (7.5MeCN), {[Fe(6)Na(3)O(OH)(4)(Me-sao)(6)(OMe)(3)(H(2)O)(3)(MeOH)(6)].MeOH}n (8.MeOH) and [HNEt(3)](2)[Fe(12)Na(4)O(2)(OH)(8)(sao)(12)(OMe)(6)(MeOH)(10)] (9) are discussed. The predominant building block appears to be the triangular [Fe(3)O(R-sao)(3)](+) species which can self-assemble into more elaborate arrays depending on reaction conditions. An interesting observation is that the R-saoH(-)/R-sao(2-) ligand system tends to adopt coordination modes similar to carboxylates. The most unusual molecule is the [Fe(4)F(4)] molecular square, 3. While Cl(-) and Br(-) appear to act only as terminal ligands, the F(-) ions bridge making a telling impact on molecular structure and topology.