A series of new “magic number” metal oxide clusters are described for the group V metals antimony and bismuth. Specific nonstatistical stoichiometries of M x O y cation and anion clusters are formed preferentially in the gas phase when oxidized metal is vaporized or when metal is vaporized and combined with gas phase oxygen (e.g., Bi 7 O 10 +, Bi 9 O 14 + ). Essentially the same stoichiometries are seen for antimony and bismuth analogues. The species produced in cluster growth are also produced preferentially by photodissociation of larger clusters. Localized covalent bonding schemes are suggested for these clusters, and polyhedral cage structures are proposed. The stoichiometries observed require a 3+ metal oxidation state in the small clusters, which shifts over to one or more 5+ metal atoms in larger clusters.
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France et al. (1997) studied this question.
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