The design, syntheses, co-ordination and electrochemical properties of novel multisite host molecules containing multiple benzo crown ether and ferrocenyl redox centres are described. The reaction of the macrocycle 2,8,14,20-tetraferrocenylpentacyclo[19.3.1.1.3,719,13.115,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17,19(26),21,23-dodecaen-4,6,10,12,16,18,22,24-octol 3 with propionic anhydride, benzoyl chloride or chlorocarbonylferrocene 6 gave new redox-active host molecules 4, 5 and 7 respectively. The acid-catalysed condensation of 15-formyl-2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecine with 1,3-dihydroxybenzene afforded a novel phenolic macrocycle 2,8,14,20-tetrakis(2,3,5,6,8,9,11,12-octahydro-1,4,7,10,13-benzopentaoxacyclopentadecin-15-yl)-pentacyclo[1.3.1.13,7.19,13.115,19]octacosa-1(25),3,5,7(28), 9,11,13(27),15,17,19(26),21,23-dodecaen-4,6,10,12,16,18,22,24-octol 14 which on reaction with propionic anhydride, benzoyl chloride, 6 or bromochloromethane gave respective host molecules 15, 16, 17 and 18(the latter being the first crown ether cavitand host), each containing four benzo-15-crown-5 moieties. Electrochemical studies show the four ferrocenyl redox centres present in 5 to undergo two one-electron oxidations at +0.58 and +0.67 V in dichloromethane. Redox-active host 17, containing eight ferrocenyl moieties, was found to undergo independent reversible one-electron oxidations in dichloromethane. High-field 1H NMR complexation studies reversible one-electron oxidations in dichloromethane. High-field 1H NMR complexation studies revealed hosts 16–18 to form solution complexes with bipyridinium guest species, exclusively at the host′s benzo crown ether binding site.