压力下的元素周期表:不同的周期和外来化学

C. Gatti
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引用次数: 0

摘要

我们对化学的一般和可操作的概念,使我们能够描述和解释各种化合物的结构、键和反应性,本质上植根于它们构成元素性质的周期性。由于人们对原子电子结构的逐渐了解,周期性推动了元素周期表的提出和合理化。原子半径的周期性反映了原子最外层电子排布的周期性。原子半径的变化区分了化学性质,从而区分了元素固体及其化合物的结构和性质。然而,在外部压力下,这种完全合理的设想可能会发生巨大变化。当一个原子被压缩时,它的平均电子密度会增加,而它最外层的电子层是最容易被压缩的。在100千兆帕斯卡(GPa),也就是106个大气压下,原子半径沿周期表周期的变化变得不那么明显,在1000 GPa时,我们的经典周期性概念就完全消失了。在压力下,系统所做的压缩功所产生的能量加起来就是它的内能。有了这样的能量增益,系统可以到达势能面,否则将无法到达的区域。化学键的性质可能会发生变化,甚至是根本性的变化,以完全意想不到的性质为特征的新结构和键合模式,在能量上变得稳定,成为可能。例如,钠是一种银白色的高活性金属,它变成了完全透明的绝缘体,而硼则变成了部分离子固体元素相,因为电荷转移发生在不同簇状的硼原子群之间。当氦与钠形成稳定的化合物Na2He时,它令人难以置信的化学惰性最终下降。在适当的压力下,可以观察到具有不同寻常化学计量的化合物(Na3Cl2, Na2Cl, Na3Cl, NaCl3, NaCl7),尽管这些化合物的分子式如果在任何高中或大学考试中被学生提出会立即被拒绝,或者可能出现新的碳同素异形体,或者苯的芳香特性可能消失。这种新化学通常是通过从头算量子力学方法来预测的,并用最现代的化学键方法来解释和合理化。然而,在许多情况下,在硅中预期的化合物已经通过实验再现,通过使用金刚石砧细胞来合成它们,并使用各种原位仪器技术来适当地表征它们。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TAVOLA PERIODICA SOTTO PRESSIONE: UNA PERIODICITA' DIVERSA ED UNA CHIMICA ESOTICA
Our general and operative notion of chemistry, that enabling us to describe and interpret the structural, bonding and reactivity properties of the various compounds, is essentially rooted in the periodicity of properties of their constituting elements. Periodicity drove the path towards the proposition of the periodic table of elements and its rationalization thanks to the gradually acquired knowledge on the atomic electronic structure. Atomic radii periodicity mirrors the periodicity of the electronic configurations of the atoms’ outermost shell. The changes in atomic radii differentiate the chemical properties, hence the structures and properties of the elemental solids and of their compounds. Yet, under an external pressure, such a fully rationalized scenario may drastically change. When an atom is compressed, its average electron density increases and its outermost electronic shell is the easiest one to compress. At 100 Giga Pascal (GPa), that is at 106 atmospheres, the change of the atomic radius along a period of the Periodic Table becomes much less evident and at 1000 GPa our classical notion of periodicity is completely lost. Under pressure, the energy due to the compression work made on a system adds up to its internal energy. With such an energy gain the system may reach regions of the potential energy surface which would not be otherwise accessible. The chemical bond nature may change, even radically, and new structures and bonding patterns, characterized by totally unexpected properties, become energetically stable and possible. For instance, sodium, which is a silvery-white, highly reactive metal, becomes a fully transparent insulator, while boron is turned into a partially ionic solid elemental phase because charge transfer takes place between differently clustered groups of boron atoms. The incredible chemical inertness of helium finally falls as it forms a stable compound with sodium, Na2He. Under a suitable pressure, compounds with unusual stoichiometry (Na3Cl2, Na2Cl, Na3Cl, NaCl3, NaCl7) may be observed, despite their formula would be immediately rejected if proposed by a student at any high-school or university exam, or new carbon allotropes may appear or the aromatic character of benzene may vanish. This new chemistry is usually predicted through ab-initio quantum mechanical methods and interpreted and rationalized with the most modern chemical bonding approaches. However, compounds anticipated in silico have then be reproduced experimentally in many cases, by using diamond anvil cells to synthesize them and a variety of in situ instrumental techniques to characterize them properly.
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