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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >A charge-transfer salt magnet based on a non-cyanocarbon acceptor, 1,4,9,10-anthracenetetrone and decamethylferrocene
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A charge-transfer salt magnet based on a non-cyanocarbon acceptor, 1,4,9,10-anthracenetetrone and decamethylferrocene

机译:基于非氰基碳氢化合物受体,1,4,9,10-蒽酮和十甲基二茂铁的电荷转移盐磁体

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摘要

The charge-transfer (CT) salt apporach to the synthesis of magnetic solids has been shown to be an attractive and general route to the creation of new families of molecule-based magnetic solids. It is based on reactions between building block donors and acceptors, where new candidates forthe latter role can be readily identified by their shape and by their electrochemical properties. In particular, acceptors should be flat (to facilitate stacking) and exhibit reversible electrochemical reduction at potentials that are not too negative (for promoting the creation of the radical anion). For tunately, these same criteria have previously been used to idetntify one-electron acceptors for the synthesis of CT salt conductors. Although one such molecule, 1,4,9,10-anthracenetetrone has not yielded good organic metals in its reactions with alkali metals or tetrathiafulvalene and related molecules, it was found to give a magnet (T_C = 3 K) in its reaction with decamethylferrocene. Frequency-dependent ac susceptibility measurements indicate glassiness. Significantly, this result shows that nitrile functional groups onthe acceptor are not necessary to obtain magnetic ordering in CT salts.
机译:电荷转移(CT)盐用于合成磁性固体的方法已被证明是创建基于分子的磁性固体新家族的一种有吸引力的通用途径。它基于结构单元供体和受体之间的反应,其中后一种作用的新候选物可以通过其形状和电化学性质轻松确定。特别是,受体应该是平坦的(以促进堆积),并且在不太负的电势下表现出可逆的电化学还原(以促进自由基阴离子的产生)。显然,这些相同的标准先前已被用来识别用于合成CT盐导体的单电子受体。尽管一个这样的分子1,4,9,10-蒽酮在与碱金属或四硫富瓦烯及相关分子的反应中未产生良好的有机金属,但发现在与十甲基二茂铁的反应中产生了磁体(T_C = 3 K) 。频率相关的交流磁化率测量表明呈玻璃状。显着地,该结果表明受体上的腈官能团对于获得CT盐中的磁性有序不是必需的。

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