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[2,2'-(2,6,9,13-Tetra-azatetra-decane-1,14-di-yl)diphenolato]iron(III) iodide.


ABSTRACT: The title Fe(III) complex, [Fe(C(22)H(32)N(4)O(2))]I, contains a six-coordinate FeN(4)O(2) cation in which the ligand is a reduced Schiff base resulting from the NaBH(4) reduction of the condensation product between salicylaldehyde and 1,5,8,12-tetra-azadodecane. In spite of the increased flexibility of the saturated backbone of the ligand compared to the Schiff base from which it was synthesized, the complex adopts a cis-FeN(4)O(2) conformation for the phenolic O-atom donors, which contrasts with the trans conformation adopted by the analogous ClO(4) (-) salt [Yisgedu et al. (2009 ?). J. Chem. Crystallogr.39, 315-319]. In addition to extensive N-H?I hydrogen bonding between the amine H atoms and the anion there is a weak C-H?I inter-action.

SUBMITTER: Assey G 

PROVIDER: S-EPMC2979518 | biostudies-literature | 2010 May

REPOSITORIES: biostudies-literature

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[2,2'-(2,6,9,13-Tetra-azatetra-decane-1,14-di-yl)diphenolato]iron(III) iodide.

Assey Gervas G   Butcher Ray J RJ   Gultneh Yilma Y   Yisgedu Teshome T  

Acta crystallographica. Section E, Structure reports online 20100526 Pt 6


The title Fe(III) complex, [Fe(C(22)H(32)N(4)O(2))]I, contains a six-coordinate FeN(4)O(2) cation in which the ligand is a reduced Schiff base resulting from the NaBH(4) reduction of the condensation product between salicylaldehyde and 1,5,8,12-tetra-azadodecane. In spite of the increased flexibility of the saturated backbone of the ligand compared to the Schiff base from which it was synthesized, the complex adopts a cis-FeN(4)O(2) conformation for the phenolic O-atom donors, which contrasts wi  ...[more]

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