Synthesis, spectral characterization and X-ray crystal structure of Fe(III) and Co(III) complexes with an acyclic Schiff base ligand

被引:6
|
作者
Sow, Mouhamadou Moustapha [1 ]
Diouf, Ousmane [1 ]
Gaye, Mohamed [1 ]
Sall, Abdou Salam [1 ]
Perez-Lourido, Paulo [2 ]
Valencia-Matarranz, Laura [2 ]
Castro, Goretti [2 ]
Caneschi, Andrea [3 ,4 ]
Sorace, Lorenzo [3 ,4 ]
机构
[1] Univ Cheikh Anta Diop, Dept Chem, Dakar, Senegal
[2] Univ Vigo, Fac Quim, Dept Quim Inorgan, Vigo 36310, Pontevedra, Spain
[3] Univ Florence, Dipartimento Chim U Schiff, I-50019 Sesto Fiorentino, FI, Italy
[4] Univ Florence, INSTM Res Unit, I-50019 Sesto Fiorentino, FI, Italy
关键词
Schiff base; Cobalt; Iron; Dinuclear complexes; Antiferromagnetic; SALEN COMPLEXES; COPPER(II) COMPLEXES; REACTIVITY; IRON(III); MONONUCLEAR; NICKEL(II); ANALOGS; BEARING; CU(II); SERIES;
D O I
10.1016/j.ica.2013.07.018
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two complexes of composition [Co(HL)(2)]center dot ClO4 center dot CH3OH (1) and [Fe2L3]center dot 0.38H(2)O (2) (H2L = 2-((2-(2-hydroxybenzylamino)ethylamino) methyl) phenol) have been synthesized and their structures have been characterized. The mononuclear cobalt complex 1 shows the metal ion Co(III) in an octahedral environment, being coordinated to two ligand molecules in a N4O2 core, remaining one of the two hydroxyl phenol groups of each ligand not deprotonated and uncoordinated. Instead, complex 2 is dinuclear, and each of the two metal centers is coordinated by one molecule ligand and other ligand molecule acts as bridge between the two metal centers, resulting a distorted N4O2 octahedral environment for each Fe(III) ion. In this case the two hydroxyl phenol groups of the ligand molecules are deprotonated and coordinated. Variable-temperature solid-state magnetic studies have been performed for compound 2. (C) 2013 Elsevier B.V. All rights reserved.
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页码:171 / 175
页数:5
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