2014
DOI: 10.1002/ejic.201402818
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Unexpected Strong Antiferromagnetic Interaction in [CuCyclam][Ni(1,2‐benzenedithiolate)2]2

Abstract: IntroductionIn recent decades, researchers have attempted to construct and investigate new molecule-based magnetic materials; this has resulted in numerous new findings such as organic ferromagnets, [1] single-molecule magnets, [2] singlechain magnets, [3] magnetically controlled conductivities, [4] and chiral magnets.[5] However, although magnetic molecules can exhibit many of the aforementioned interesting properties, the application and investigation of these materials has been quite limited because of the… Show more

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Cited by 3 publications
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“…Such ring fusion increases molecule planarity and enhances orbital overlap, thus maximizing electron delocalization into the organic ligands. Many fused-ring dithiolene systems have been studied, including the fusion of benzene, functionalized benzene, thiophene, ,, pyridine, quinoxaline, , and other heterocyclic systems. The incorporation of such fused-ring systems allows synthetic modification of the resulting materials via substituents and heteroatoms on the fused-ring units, allowing a great deal of diversity in the resulting dithiolene systems and the potential to finely tune both the electronic structures and solid-state arrangements. In addition, fused benzene analogues containing additional disulfide pairs have also allowed the generation of extended one- and two-dimensional dithiolene-based coordination polymers. , …”
Section: Introductionmentioning
confidence: 99%
“…Such ring fusion increases molecule planarity and enhances orbital overlap, thus maximizing electron delocalization into the organic ligands. Many fused-ring dithiolene systems have been studied, including the fusion of benzene, functionalized benzene, thiophene, ,, pyridine, quinoxaline, , and other heterocyclic systems. The incorporation of such fused-ring systems allows synthetic modification of the resulting materials via substituents and heteroatoms on the fused-ring units, allowing a great deal of diversity in the resulting dithiolene systems and the potential to finely tune both the electronic structures and solid-state arrangements. In addition, fused benzene analogues containing additional disulfide pairs have also allowed the generation of extended one- and two-dimensional dithiolene-based coordination polymers. , …”
Section: Introductionmentioning
confidence: 99%