[MnIII6MnIINaI2], [MnIII3MnIINaI], and [MnIII3] Clusters Derived from Schiff Bases: Syntheses, Structures, and Magnetic Properties

被引:1
作者
Lohr, Johannes [1 ,2 ]
Font-Bardia, Merce [3 ]
Mayans, Julia [1 ,4 ]
Escuer, Albert [1 ,4 ]
机构
[1] Univ Barcelona, Dept Quim Inorgan & Organ, Seccio Quim Inorgan, Marti i Franques 1-11, Barcelona 08028, Spain
[2] Inst Solar Energy Res Hamelin, D-31860 Emmerthal, Germany
[3] Univ Barcelona, CCiTUB, Ctr Cient & Tecnol, Dept Mineral Cristal log & Diposits Minerals & Uni, Barcelona 08028, Spain
[4] Univ Barcelona, Inst Nanociencia & Nanotecnol IN2UB, Barcelona 08028, Spain
关键词
manganese; crystal structure; mixed valence; chirality; magnetic properties; HEPTANUCLEAR MANGANESE COMPLEXES; CRYSTAL-STRUCTURES; CD SPECTRA; COORDINATION; (NAMNMN3III)-MN-II; NUCLEARITY; OXIDATION; FAMILY; SERIES; IODO;
D O I
10.3390/magnetochemistry10100076
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of manganese halides with polydentate Schiff bases obtained by the condensation of 3-ethoxysalicylaldehyde and different amino alcohols, resulting in a NO3 set of donors, yielded a series of manganese clusters with {MnIII6MnIINa2}, {MnIII3MnIINa}, and {MnIII3} metallic cores. The influence of the ligand substituents and the halide on the final nuclearity has been studied. Analysis of their static magnetic behaviour confirms the ground states of 19/2 for the {MnIII6MnIINa2} complexes, 7/2 for the {MnIII3MnIINa} clusters, and 12/2 for the triangular {MnIII3} systems, and a weak field induced a slow relaxation of the magnetization for the trinuclear complexes.
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页数:13
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