Abstract
Geometries of several all-metal clusters with Zn 3 2− as the base are optimized within a B3LYP/6-311+G(d) level of theory. It is analyzed that the stability, bonding, reactivity and aromaticity patterns of such clusters often change drastically in the presence of counter cations like Li +, Na + or K + and/or through the substitution of Zn 3 2− units by Be 5 − or C 5H 5 − rings.
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