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Synthesis of a Neutral Mixed-Valence Diferrocenyl Carborane for Molecular Quantum-Dot Cellular Automata Applications

机译:用于分子量子点自动机应用的中性混合价二茂铁碳硼烷的合成

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摘要

The preparation of 7-Fc(+)-8-Fc-7,8-nido-[C2B9H10](-) (Fc(+)FcC(2)B(9)) demonstrates the successful incorporation of a carborane cage as an internal counteranion bridging between ferrocene and ferrocenium units. This neutral mixed-valence Fe-II/Fe-III complex overcomes the proximal electronic bias imposed by external counterions, a practical limitation in the use of molecular switches. A combination of UV/Vis-NIR spectroscopic and TD-DFT computational studies indicate that electron transfer within Fc(+)FcC(2)B(9)(-) is achieved through a bridge-mediated mechanism. This electronic framework therefore provides the possibility of an all-neutral null state, a key requirement for the implementation of quantum-dot cellular automata (QCA) molecular computing. The adhesion, ordering, and characterization of Fc(+)FcC(2)B(9)(-) on Au(111) has been observed by scanning tunneling microscopy.
机译:7-Fc(+)-8-Fc-7,8-nido- [C2B9H10](-)(Fc(+)FcC(2)B(9))的制备证明了碳硼烷笼的成功结合二茂铁和二茂铁单元之间的内部抗衡阴离子桥接。这种中性的混合价Fe-II / Fe-III络合物克服了外部抗衡离子施加的近端电子偏压,这是在使用分子开关时的实际限制。 UV / Vis-NIR光谱和TD-DFT计算研究的结合表明,Fc(+)FcC(2)B(9)(-)中的电子转移是通过桥介导的机制实现的。因此,该电子框架提供了实现全中性零状态的可能性,这是实现量子点细胞自动机(QCA)分子计算的关键要求。 Fc(+)FcC(2)B(9)(-)在Au(111)上的粘附,排序和表征已通过扫描隧道显微镜观察到。

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