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[Mn6] under Pressure:A Combined Crystallographic and Magnetic Study

机译:在压力下[Mn6]:结晶和磁性研究

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While investigating the coordination chemistry of derivatized salicylaldoximes (R-saoH2) in the synthesis of Mn6 single-molecule magnets (SMMs) we found that the exchange between the metal centers was weak and typically only a few wavenumbers (< 1-2 cm~(-1)) in magnitude.Structurally distorting the molecule "internally" by deliberate chemical modification of the magnetic core (the twisting of the Mn-N-O-Mn moiety) allowed us to switch the exchange from antiferromagnetic to ferromagnetic,thus producing SMMs with ground states of S = 12 and greatly enhanced blocking temperatures.An alternative method of achieving such a switch is to exert "external" hydrostatic pressure.This is an attractive proposition since it offers the potential to provide detailed information about the relationship between structure and magnetic properties,especially if the magnetic studies can be coupled with high-pressure crystallography.
机译:在研究MN6单分子磁体(SMMS)的合成中研究衍生的水杨氧化氧基肟(R-SaOH2)的协调化学,我们发现金属中心之间的交换较弱,通常只有几个波数(<1-2cm〜( -1))幅度。通过刻意的化学改性,结构扭曲的分子“内部”磁芯(Mn-No-Mn部分的扭曲)使我们允许我们将交换从反铁磁对铁磁性切换,从而用地产生SMM S = 12的状态和大大增强的阻塞温度。实现这种开关的替代方法是施加“外部”静水压力。这是一个有吸引力的主张,因为它提供了提供有关结构和磁性之间关系的详细信息的有吸引力的主张 ,特别是如果磁性研究可以与高压晶体学结合。

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