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Stabilization of beryllium-containing planar pentacoordinate carbon species through attaching hydrogen atoms
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 CAl(n)Be(m)H(x)(q) (n + m = 5, q = 0, ±1, x = q + m − 1) (1a–9a) by attaching H atoms...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088823/ https://www.ncbi.nlm.nih.gov/pubmed/35558954 http://dx.doi.org/10.1039/c8ra07664b |
Sumario: | 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 CAl(n)Be(m)H(x)(q) (n + m = 5, q = 0, ±1, x = q + m − 1) (1a–9a) by attaching H atoms onto the Be atoms in CAl(4)Be, CAl(3)Be(2)(−), CAl(2)Be(3)(2−), and CAlBe(4)(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 CAl(3)Be(2)H (2a), CAl(2)Be(3)H(−) (4a), CAl(2)Be(3)H(2) (5a), and CAlBe(4)H(4)(+) (9a). They are the promising target for the experimental realization of species with a ppC. |
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