Harry Adams, Neil A. Bailey, David E. Fenton, Michael B. Hursthouse, Wakako Kanda, Masatoshi Kanesato, K. M. Abdul Malik and Emily J. Sadler
The reactions of the diprotonated Schiff-base cryptand derived from
the bicyclocondensation of tris(2-aminoethyl)amine with
2,6-diacetylpyridine in the presence of acid and copper-(I)
and -(II) tetrafluoroborates have been studied. In the former
reaction a homodinuclear copper(I) complex of the neutral
cryptand was recovered whereas in the latter a homodinuclear
copper(II) complex of the bibracchial tetraimine Schiff-base
macrocycle in which one pyridinyl unit has been eliminated was the
product. The crystal structures of the two dinuclear complexes were
determined. The
CuI · ·
· CuI separation in the
cryptate complex is 6.25 Å and the
CuII · ·
· CuII separation in the
macrocyclic complex is ca. 4.6 Å.