Issue 16, 1985

Hexasilabenzene (Si6H6). An ab initio theoretical study of its aromaticity and relative stability

Abstract

Ab initio calculations show that hexasilabenzene has approximately half the aromatic stabilization energy of benzene, and lies very close in stability to its valence Si6H6 isomers, this being in sharp contrast with the fact that benzene is by far the most stable C6H6 isomer.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1121-1122

Hexasilabenzene (Si6H6). An ab initio theoretical study of its aromaticity and relative stability

S. Nagase, T. Kudo and M. Aoki, J. Chem. Soc., Chem. Commun., 1985, 1121 DOI: 10.1039/C39850001121

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