4.7 Article

ST=22 [Mn10] Supertetrahedral Building-Block to Design Extended Magnetic Networks

期刊

INORGANIC CHEMISTRY
卷 50, 期 17, 页码 8580-8587

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ic201154n

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资金

  1. National Natural Science Foundation of China [20901027]
  2. Natural Science Foundation of Jilin Province [20080121]
  3. 111 project [B07016]
  4. University of Bordeaux
  5. ANR [NT09_469563]
  6. Region Aquitaine
  7. GIS Advanced Materials in Aquitaine (COMET Project)
  8. CNRS
  9. Ministerio de Ciencia e Innovacion
  10. Generalitat de Catalunya [CTQ2008-06670-C02-01, 2009SGR-1459]

向作者/读者索取更多资源

The controlled organization of high-spin complexes, eventually single-molecule magnets, is a great challenge in molecular sciences to probe the possibility to design sophisticated magnetic systems to address a large quantity of magnetic information. The coordination chemistry is a tool of choice to make such materials. In this work, high-spin S-T = 22 [Mn-10] complexes, such as [(Mn6Mn4II)-Mn-III(L-1)(6)(mu(4)-O)(4)(mu(3)-N-3)(4)(CH3CN)(11)-(H2O)]center dot(ClO4)(2)center dot(CH3CN)(8.5) (1), have been assembled using (i) 1,3-propanediol derivatives as chelating ligands to form the [Mn-10] core units and (ii) dicyanamide or azide anions as linkers to synthesize the first 2D and 3D [Mn-10] -based networks: [Mn-6(III)-Mn-4(II)(L-2)(6)(mu(3)-N-3)(4)(mu(4)-O)(4)(CH3OH)(4)(dca)(2)] (2) and [(Mn6Mn4II)-Mn-III(L-3)(6)(mu(3)-N-3)(4)(mu(4)-O)(4)(N-3)(2)]center dot(CH3OH)4 (3). The synthesis of these compounds is reported together with their single-crystal X-ray structures and magnetic properties supported by DFT calculations. In the reported synthetic conditions, the stability of the [Mn-10] complex is remarkably good that allows us to imagine many new materials combining these high-spin moieties and other diamagnetic but also paramagnetic linkers to design for example ordered magnets.

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