Structural studies have confirmed that it is possible to exploit the relati
vely low nucleophilicity of the "external" amino substituents on the Co-III
complex of 1,8-diaminosarcophagine ("sarcophagine" = sar = 3,6,10,13,16,19
-hexaazabicyclo[6.6.6]-icosane) in acylation and alkylation reactions leadi
ng to a variety of functionalized cage amine complexes. With the appropriat
e choice of solvent, all these reactions can be conducted with high efficie
ncy, and the new complexes display properties foreshadowing the application
of cage systems in, for example, electroactive polymers.