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Persulfuranes are hypervalent organosulfur compounds where sulfur has an expanded valence beyond the typical octet, reaching a dectet or dodecet. These compounds are classified as (10-S-4) for pentacoordinate sulfuranes or (12-S-6) for hexacoordinate persulfuranes, indicating the number of electrons shared by sulfur and the number of ligands, respectively. They adopt specific geometric structures, such as trigonal bipyramidal for sulfuranes, where lone pairs occupy equatorial positions. Due to their expanded valence, persulfuranes are relatively unstable and tend to extrude ligands to return to an octet state. However, some acyclic and cyclic dialkyloxysulfuranes can be stable at room temperature and are useful in organic synthesis.1

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