Tetrathiophenalenyl Radical and its Disulfide-Bridged Dimer
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文摘

The presence of two disulfide groups in the tetrathiophenalenyl radical TTPLY leads to a highly delocalized spin distribution and the lowest cell potential ever observed for a monofunctional phenalenyl derivative. While the heteroatom substituents successfully block C−C bond formation, TTPLY nonetheless associates in the solid state to afford the hypervalent S−S-bonded dimer (TTPLY)2.

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