Rational design of a covalently tethered dinuclear [MnII(N3O2)Cl(OH2)]22+ macrocyclic building block:: Synthesis, structure, and magnetic properties

被引：24

作者：

Wang, Jian

Slater, Brianna

Alberola, Antonio

Stoeckli-Evans, Helen

Razavi, Fereidoon S.

Pilkington, Melanie

机构：

[1] Brock Univ, Dept Chem, St Catharines, ON L2S 3A1, Canada

[2] Univ Jaume 1, Dept Quim Fis & Analit, Castellon de La Plana 12701, Spain

[3] Inst Microtech, CH-2009 Neuchatel, Switzerland

来源：

INORGANIC CHEMISTRY | 2007年 / 46卷 / 12期

关键词：

D O I：

10.1021/ic062212o

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A novel dimeric Mn-II complex {[Mn(N3O2)]Cl(OH2)}(2)2Cl (2) of a macrocyclic Schiff base ligand derived from the condensation of 2,2', 6,6'-tetraacetyl-4,4'-bipyridine with 3,6-dioxaoctane-1,8-diamine in the presence of a stoichiometric amount of MnII has been prepared and characterized. The X-ray analysis of 2 reveals that the two Mn ions assume a pentagonal-bipyramidal geometry, with the macrocycle occupying the pentagonal plane and the axial positions being filled by a halide ion and a H2O molecule. Magnetic susceptibility data (2-270 K) reveal the occurrence of weak antiferromagnetic interactions between covalently tethered Mn-II-Mn-II dimeric units.

引用

页码：4763 / 4765

页数：3

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