Three pentanuclear copper(
II) complexes,
[Cu
5
(OMe)
2
(CF
3
CO
2
)(pehp)
6
(Cl)] 1,
[Cu
5
(OMe)
2
(CF
3
CO
2
)(pehp)
6
(NO
3
)] 2 and
[Cu
5
(OH)(CF
3
CO
2
)
3
(pehp)
6
] 3, have been prepared via the solid-state
reaction of hydrated copper(
II) nitrate with the sodium salt
of the novel ligand, 6-(phenylethynyl)-2-pyridone (Hpehp) in the
presence of sodium trifluoroacetate. Crystal structural analysis at 220
K of 1–3 reveals capped-butterfly arrangements of the five copper
atoms with the two shortest
Cu · · ·

Cu vectors in 1 and 2 [3.024(6)–3.050(3) Å]
occurring between the caps and the wingtips while in 3 the
wingtip–cap distances are more asymmetric with one short [3.042(7)
Å] and one long [3.638(7) Å]
Cu · · ·

Cu vector. Mass spectroscopic studies of 1–3 show
fragmentation patterns consistent with the observed structures, while
magnetic studies of the complexes indicate antiferromagnetic exchange
coupling within the Cu
5
cores and
S = ½ ground states for all compounds. The
trifluoroacetate adduct of Hpehp,
Hpehp·0.5CF
3
CO
2
H was synthesised in three
steps from 2-bromo-6-benzyloxypyridine via
2-benzyloxy-6-(phenylethynyl)pyridine and the single crystal X-ray
structure of Hpehp was also determined.