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UNUSUALLY STRONG INTRAMOLECULAR MAGNETIC COUPLING IN A CHROMIUM HYDRIDE CLUSTER

机译:氢化铬团簇中异常强的分子内磁耦合

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MOLECULES With large spins, and associated large magnetic moments, are potential building blocks for magnetic materials(1). To make such molecules, spin-carrying metal ions can be assembled into polynuclear complexes, but the coupling between the spins is usually antiferromagnetic, leading to antiparallel alignment(2). Magnetic coupling leading to parallel alignment occurs only rarely, and even then is usually too weak for the alignment to persist at ambient temperatures(3-14). Here we report the synthesis of a tetranuclear chromium hydride cluster With a ground state of non-zero spin (spin quantum number S = 7/2), in which the intramolecular magnetic coupling is so strong that the magnetic alignment is not disturbed appreciably even at room temperature. This ground state cannot be explained either by simple parallel or antiparallel alignment of spins, but can be understood in terms of antiparallel alignment of three Cr(III) moments with one Cr(II) moment, These findings indicate that hydride ligands can mediate extremely strong magnetic exchange interactions between metal ions, and that metal hydrides may therefore be promising components for the construction of molecular magnetic materials. [References: 33]
机译:分子具有大的自旋以及相关的大磁矩,是磁性材料的潜在构成要素(1)。为了制造这种分子,可以将自旋载金属离子组装成多核络合物,但自旋之间的耦合通常是反铁磁性的,从而导致反平行排列(2)。导致平行对准的磁耦合很少发生,即使这样,通常也太弱了,无法在环境温度下保持对准(3-14)。在这里,我们报告了具有非零自旋(自旋量子数S = 7/2)的基态的四核氢化铬簇的合成,其中分子内的磁耦合非常强,即使在90°C时,磁取向也不会受到明显干扰。室内温度。该基态不能通过自旋的简单平行或反平行排列来解释,而是可以通过三个Cr(III)力矩与一个Cr(II)力矩的反平行排列来理解。这些发现表明氢化物配体可以介导非常强的因此,金属离子与金属氢化物之间的磁性交换相互作用可能是分子磁性材料构建的有希望的成分。 [参考:33]

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