2018, Vol.47, No.6
719-722
Chalcogenation Reaction of Cyclic Digermenes#
2Graduate School of Natural Sciences, Nagoya City University, Yamanohata 1, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8501, Japan
719-722
Chalcogenation reactions of stable cyclic digermenes with elemental sulfur and selenium have been examined, resulting in the formation of [Ge2Ch2/3Cx] heterocycles, which should be a convenient procedure for the preparation of the cyclic tetrel chalcogenides. Thus, the [Ge2Ch3] heterocyclic compounds 5 were isolated for the first time, and the experimental data and theoretical calculations suggested the considerable delocalization of the lone pair on the chalcogen atoms.

Chalcogenation reactions of the stable cyclic digermenes with elemental sulfur and selenium have been examined, resulting in the formation of the [Ge2Ch2/3Cx] heterocycles, which should be a convenient procedure for the preparation of the cyclic tetrel chalcogenides. Thus, the [Ge2Ch3] heterocyclic compounds 5 were isolated for the first time, and the experimental data and theoretical calculations suggested the considerable delocalization of the lone pair on the chalcogen atoms.
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