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Ligands with coordinating atoms are of much interest in inorganic chemistry.
Particularly, imines or azomethines, which are more commonly known as schiff bases, are
attracting attention as compounds for complex formation with metals. Magnetic
susceptibility, electronic absorption spectra, elemental analysis, molecular weight determination,
thermal analysis of many schiff bases and their complexes have been reported (Abel et al., 1971; Shehatta et al., 2001; and Abba et al., 2005). There are also several reports on their
biological properties such as antibacterial and antifungal activities (William 1972; and Campos et al., 1999). Particularly, schiff bases derived from the salicylaldehydes are
well-known polydendate ligands (Holm et al., 1996; and Tumer, 1999). It has been shown that
schiff base complexes derived from 4-hydroxysalicylaldehyde and amines have strong
anticancer activity (Narang and Singh, 1993). The salen complexes were found to be antifungal
active in most of the cases (Dharmaraj et
al., 2001; and Belaid et al., 2008).
Synthesis of schiff base complexes with transition metals (Kwiatkowski
and Kwiatkowski, 1980; and Costes, 1987) plays a vital role in bio-inorganic
chemistry due to their biomimitic properties. They mimic as metalloproteins
and metalloenzymes (Cotamagana et al., 1992; and Pandey et al., 1994) in which transition metals are bound to a macrocycle, such as a heme ring.
Generally, the metal complexes exhibit higher biological activity
compared to the parent ligand systems. Such
increased activity of the metal complexes is due to the lipophilic nature of the metal ions
in complexes (Guo et al., 2008). |