The reaction of the fourfold functionalized [3.3][3.3]metacyclophane 8
with tosylamide monosodium salt leads to a new deltaphane in quantita
tive yield. An X-ray analysis confirms the belt-shaped structure of 3.
Moreover, a series 10-15 of well-soluble belt-shaped macrocycles with
up to 21 interconnected benzene rings were detected. The intermediate
[3.3][3.3]metacyclophane 4 shows remarkably short distances to enclos
ed toluene, one toluene molecule acting twice as a pi acceptor and onc
e as a pi donor. Competition experiments with benzene demonstrate the
dependence of conformational behaviour on the solvent.