期刊
INORGANICA CHIMICA ACTA
卷 448, 期 -, 页码 97-103出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2016.04.028
关键词
Carboranylalcohol; Chiral; Boron clusters; Fe-III; Magnetism
资金
- MEC [CTQ2013-44670-R, MAT2013-47869-C4-2-P]
- Generalitat de Catalunya [2014/SGR/00149]
- ICREA Funding Source: Custom
The reaction of iron(II) chloride with anti- or syn-1,2-bis{(pyridin-2'-yl) methanol}-1,2-dicarba-closododecaborane (anti- or syn-oCB-L1) afforded two new complexes, [Fe2Cl2(anti-oCB-L1(2))(2)] (1) or Fe2Cl3(syn-oCB-L1(2))(EtO)(H2O) (2), respectively. Both complexes were unambiguously characterized by means of X-ray structure analysis. Their solid state structures give evidence for the different coordination modes of the ligands. Both compounds are dinuclear FeIII complexes, however, whereas in complex 1 there are two anti-oCB-L1(2) ligands per molecular unit, in complex 2 only one syn-oCB-L1(2) is found. In complex 1, anti-oCB-L1(2) acts as a tetradentate N2O2-ligand affording a homochiral complex as a partial racemic mixture of Delta,Delta-[Fe2Cl2((RR)anti-oCB-L1(2))(2)] and Lambda,Lambda-[Fe2Cl2((SS)anti-oCB-L1(2))(2)]. In complex 2, syn-oCB-L1(2) behaves as a bis-bidentate NO ligand. Only complex 1 could be synthesized in good yield and as a pure phase and it has been therefore fully characterized by spectroscopic methods and the magnetic properties studied. (c) 2016 Elsevier B.V. All rights reserved.
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