Abstract
The reactions of dicyclopentadienylzirconium(IV) dichloride with bidentate aliphatic acid dihydrazide (LH2) derived from oxalic, succinic, and adipic acids (metal to ligand molar ratios 1 : 1 and 1 : 2, respectively) in anhydrous tetrahydrofuran in the presence of base led to the formation of the [Cp2Zr(L)] and [CpZr(LH)2Cl] complexes. The complexes were characterized by elemental analyses, electrical conductance, magnetic measurements and spectroscopic studies. These ligands appear to behave as bidentate chelate agents. All the complexes contain terminal amino or terminal hydrazinc nitrogen atoms with an unshared electron pair, enabling nucleophilic condensations. Therefore, the reactions of these complexes with β-diketones (acetylacetone, benzoylacetone, dibenzoylmethane, thenoyltrifluoroacetone) in the presence of glacial acetic acid have been studied viz., ring closure and formation of macrocyclic ligand (mac) complexes. Two types of cyclic products viz., [Cp2Zr(mac)] and [CpZr(Mac)Cl] were isolated. The spectral studies of these cyclic products are reported.
| Original language | English |
|---|---|
| Pages (from-to) | 27-35 |
| Number of pages | 9 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 321 |
| Issue number | 1 |
| DOIs | |
| State | Published - 24 Feb 1987 |
| Externally published | Yes |
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