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The First Row Anomaly and Recoupled Pair Bonding in the Halides of the Late p-Block Elements

机译:p块晚期元素的卤化物中的第一行异常和重耦合对键合

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摘要

The dramatic differences between the properties of molecules formed from the late p-block elements of the first row of the periodic table (N–F) and those of the corresponding elements in subsequent rows is well recognized as the first row anomaly. Certain properties of the atoms, such as the relative energies and spatial extents of the ns and np orbitals, can explain some of these differences, but not others.In this Account, we summarize the results of our recent computational studies of the halides of the late p-block elements. Our studies point to a single underlying cause for many of these differences: the ability of the late p-block elements in the second and subsequent rows of the periodic table to form recoupled pair bonds and recoupled pair bond dyads with very electronegative ligands. Recoupled pair bonds form when an electron in a singly occupied ligand orbital recouples the pair of electrons in a doubly occupied lone pair orbital on the central atom, leading to a central atom-ligand bond. Recoupled pair bond dyads occur when a second ligand forms a bond with the orbital left over from the initial recoupled pair bond.Recoupled pair bonds and recoupled pair bond dyads enable the late p-block elements to form remarkably stable hypervalent compounds such as PF5 and SF6 and lead to unexpected excited states in smaller halides of the late p-block elements such as SF and SF2. Recoupled pair bonding also causes the Fn–1X–F bond energies to oscillate dramatically once the normal valences of the central atoms have been satisfied. In addition, recoupled pair bonding provides a lower-energy pathway for inversion in heavily fluorinated compounds (PF3 and PF2H, but not PH2F and PH3) and leads to unusual intermediates and products in reactions involving halogens and late p-block element compounds, such as (CH3)2S + F2.Although this Account focuses on the halides of the second row, late p-block elements, recoupled pair bonds and recoupled pair bond dyads are important in the chemistry of p-block elements beyond the second row (As, Se, and Br) and for compounds of these elements with other very electronegative ligands, such as OH and O. Knowledge of recoupled pair bonding is thus critical to understanding the properties and reactivity of molecules containing the late p-block elements beyond the first row.
机译:由元素周期表第一行(N-F)的晚期p嵌段元素形成的分子的性质与后续行中相应元素的性质之间的显着差异被公认是第一行异常。原子的某些性质(例如ns和np轨道的相对能量和空间范围)可以解释其中的一些差异,而不能解释其他差异。在此帐户中,我们总结了最近对氢的卤化物进行计算研究的结果。后期的p块元素。我们的研究指出了造成这些差异的一个根本原因:元素周期表第二行和后续行中后期的p嵌段元素形成具有非常负电性配体的重耦合对键和重耦合对键二元体的能力。当单个占据的配体轨道中的电子将中心原子上的双重占据的孤对轨道中的电子对重新耦合时,会形成重新耦合的对键,从而形成中心原子-配体键。当第二个配体与最初的再结合对键留下的轨道形成一个键时,就会发生再结合对键二重体。再结合对键和再结合对键二重体使后期的p-嵌段元素能够形成非常稳定的高价化合物,例如PF5和SF6并在晚期p嵌段元素(如SF和SF2)的较小卤化物中导致意外的激发态。一旦满足中心原子的正常化合价,重新耦合的对键也会导致Fn-1X-F键的能量剧烈振荡。此外,再结合对键合为重氟化物(PF3和PF2H,但不包括PH2F和PH3)的转化提供了较低的能量途径,并导致涉及卤素和较晚的p嵌段元素化合物的反应中产生异常的中间体和产物,例如(CH3)2S + F2。尽管此帐户着眼于第二行的卤化物,但后期的p嵌段元素,重新偶联的对键和重新偶联的成对双键在第二行以外的p嵌段元素的化学反应中很重要(As, (Se和Br),以及这些元素与其他非常带负电的配体(例如OH和O)的化合物。因此,重新配对键的知识对于理解第一行以外含晚期p嵌段元素的分子的性质和反应性至关重要。

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