The possibility of metal coordination in oxazolinyl phenols has allowed the
preparation of new chiral metal-containing liquid crystals in which the st
ereogenic center is located in the rigid mesogenic core. By using (S)-beta
-amino alcohols as chiral starting materials for the synthesis of the oxazo
line ligands, two types of complex have been prepared: (i) mononuclear copp
er(II) complexes and (ii) dinuclear orthopalladated organometallic compound
s with either nonplanar (acetato-bridged) or planar (chloro-bridged) geomet
ries. The synthesis and structural characterization of all of these compoun
ds are described. The formation of a single diastereoisomer with a trans co
nfiguration in nonplanar palladium(H) complexes has been confirmed by H-1 N
MR, spectroscopy. The complexes mainly show SA mesomorphism, although when
they are used as chiral dopants in a matrix with the phase sequence N-S-A-S
-C they induce a cholesteric mesophase. The presence of stereogenic centers
lying out of the coordination plane in a rigid environment must account fo
r the formation of the helical cholesteric mesophase over broad temperature
ranges.