A novel cyclic polysulfide, octathionane TbtCHS8 (7; Tbt = 2,4,6-tris[bis(trimethylsilyl)methyl]phenyl) was synthesized by thermal reaction of the corresponding diazomethane TbtCHN2 with cyclooctasulfur (S8) in benzene in the dark. Molecular structure of 7 was determined by X-ray crystallographic analysis and the geometry of the CS8 ring was compared with that of theoretically optimized cyclononasulfur (S9). Desulfurization of 7 by triphenylphosphine afforded the corresponding pentathiane TbtCHS5.
No takes yet. Share an insight, caveat, or question.
Takeda et al. (1995) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: