Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/31351
Title: Supramolecular interactions in mononuclear iron(III) complex derived from a diamide ligand: Spectroscopic and electrochemical properties
Authors: Samanta, Suvendu
Dutta, Amit Kumar
Biswas, Papu
Keywords: Coordination chemistry;X-ray crystallography;Intermolecular hydrogen bonding;π–π stacking;Diamides;Iron
Issue Date: 13-Apr-2015
Abstract: The diamide ligand, 2,6-bis[(N-phenyl)amido]-4-methylphenol (HL), has been used to synthesize a mononuclear iron(III) complex [Fe(L)3]·DMF and characterized by elemental analyses, IR, UV–vis spectroscopy, cyclic voltammetry and finally by X–ray crystallography. X-ray diffraction analysis reveals that the complex crystallizes in the triclinic space group P-1(2) with a = 12.4923(15) Å, b= 13.5095(16), c = 19.296(2) Å, α = β = 86.451(2)°, γ = 66.5850(10)°, V = 2980.1(6) Å3 and Z = 2 with the central iron(III) ion in distorted octahedral geometry. The complex shows extensive intra- and intermolecular hydrogen bonding between each molecular units as well as solvent molecules giving rise to a two dimensional assembly. It also exhibits intermolecular π–π interaction between the aromatic rings with centroid distances of around 3.55 Å. In cyclic voltammetric studies, the iron(III) complex exhibits one quasi-reversible reduction at E1/2 = +0.046 V versus Ag/AgCl Ep = 0.092 V) due to a metal-centreed FeIII/FeII reduction.
Page(s): 478-483
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.54A(04) [April 2015]

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