Stabilization of beryllium-containing planar pentacoordinate carbon species through attaching hydrogen atoms

被引:0
|
作者
Zhao X.-F. [1 ]
Bian J.-H. [1 ]
Huang F. [3 ]
Yuan C. [1 ]
Wang Q. [2 ]
Liu P. [2 ]
Li D. [2 ]
Wang X. [4 ]
Wu Y.-B. [1 ,2 ]
机构
[1] Key Laboratory of Materials for Energy Conversion and Storage of Shanxi Province, Institute of Molecular Science, Shanxi University, Taiyuan
[2] State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, 27 South Taoyuan Road, Taiyuan, 030001, Shanxi
[3] College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, 88 East Culture Road, Jinan, 250014, Shandong
[4] Department of Chemistry, University of Colorado Denver, Campus Box 194, P.O. Box 173364, Denver, 80217-3364, CO
基金
中国国家自然科学基金;
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D O I
10.1039/C8RA07664B
中图分类号
学科分类号
摘要
The diagonal relationship between beryllium and aluminum and the isoelectronic relationship between BeH unit and Al atom were utilized to design nine new planar and quasi-planar pentacoordinate carbon (ppC) species CAlnBemHx q (n + m = 5, q = 0, ±1, x = q + m − 1) (1a-9a) by attaching H atoms onto the Be atoms in CAl4Be, CAl3Be2 −, CAl2Be3 2−, and CAlBe4 3−. These ppC species are σ and π double aromatic. In comparison with their parents, these H-attached molecules are more stable electronically, as can be reflected by the more favourable alternative negative-positive-negative charge-arranging pattern and the less dispersed peripheral orbitals. Remarkably, seven of these nine molecules are global energy minima, in which four of them are kinetically stable, including CAl3Be2H (2a), CAl2Be3H− (4a), CAl2Be3H2 (5a), and CAlBe4H4 + (9a). They are the promising target for the experimental realization of species with a ppC. © The Royal Society of Chemistry.
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页码:36521 / 36526
页数:5
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