Thio- and selenosulfonato complexes of iron bearing aromatic and heterocyclic groups

被引:8
作者
El-khateeb, Mohammad [1 ]
Asali, Khalil J. [1 ]
Al-Noaimi, Mousa [2 ]
Al-Rabaee, Enas [1 ]
Awwadi, Firas F. [3 ]
Taher, Deeb [3 ]
Korb, Marcus [4 ]
Lang, Heinrich [4 ]
机构
[1] Jordan Univ Sci & Technol, Dept Chem, Irbid 22110, Jordan
[2] Hashemite Univ, Dept Chem, Zarqa 13115, Jordan
[3] Univ Jordan, Dept Chem, Amman 11942, Jordan
[4] Tech Univ Chemnitz, Inst Chem, D-09107 Chemnitz, Germany
关键词
Iron; Carbonyls; X-ray structure; Chalcogenosulfonate; Characterization; ORGANOMETALLIC SULFUR COMPLEXES; S-BONDED MONOTHIOCARBOXYLATES; CRYSTAL-STRUCTURE; CARBOXYLATE COMPLEXES; SELENOCARBOXYLATE; DERIVATIVES; REACTIVITY; MONO;
D O I
10.1016/j.ica.2014.07.021
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Various new thio-and selenosulfonato complexes of iron were synthesized by straight forward route. Treatment of the iron chalcogenides, (mu-E-x)[CpFe(CO)(2)](2) (E = S; x = 2-4, E = Se; x = 1) with sulfonyl chlorides produced the corresponding thio-or selenosulfonato complexes CpFe(CO)(2)ESO2Ar [Ar = 2-C4H3S (1), 5-C4H2SCl (2), 1,3-C6H4SO2Cl (3), 1,3-C6H4CO2H (4); E = S (a), Se (b)]. The dimers [CpFe(CO)(2) ESO2](2)(1,3-C6H4) (5) are obtained from the iron chalcogenides with 1,3-C6H4(SO2Cl) 2 in a 2:1 molar ratio. All of these new complexes have been characterized by IR, H-1, C-13 NMR spectroscopy, UV-Vis and elemental analysis. The X-ray structure of CpFe(CO)(2)ESO2-1,3-C6H4SO2Cl (3a) is determined. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:553 / 558
页数:6
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