Abstract
The stepwise syntheses of large [4+4] electron-rich
thiamacrocycles, which aim at fullerene complexation, were performed using
two types of building blocks, viz. 1,4-bis(bromomethyl)benzene or
its dibutoxylated analogue and 4,5-bis(2-cyanoethylsulfanyl)-1,3-dithiole-2-thione.
Alternatively, a multicomponent mixture of thiamacrocycles, ranging
in size from [2+2] to [6+6] units,
was generated by the direct reaction of bis(tetraethylammonium)
bis(thioxo-1,3-dithiole-4,5-dithiol)zincate with 1,4-bis(bromomethyl)-2,5-dibutoxybenzene,
and the individual macrocycles were successfully separated.
Key words
alkylation - arenes - atropoisomerism - macrocycles - thiols
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