New results are presented from a technique which appears capable of pr
oducing 'tailor-made' complexes from a variety of metals and ligands.
Data are presented for [Cu.({CH3}(2)CO)(n)](2+), [Cu.(C2H4)(n)](2+) an
d [Cu.(NH3)(n)](2+). Two of these, [Cu.({CH3}(2)CO)(n)](2+) and [Cu.(C
2H4)(n)](2+), conform to the expected pattern in terms of the most sta
ble co-ordination number and current views of bonding. However, the re
sults for [Cu.(NH3)(n)](2+) complexes do not fit any of the existing p
ictures of Cu(LI) solvated in concentrated ammonia. To account for thi
s observation, it is proposed that hydrogen bonding makes an important
secondary contribution to the solvation of Cu(II). (C) 1998 Elsevier
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