1.
Egyptian Journal of Chemistry. 1998; 41 (1-6): 97-108
in English
| IMEMR
| ID: emr-47900
ABSTRACT
Two forms of isatin isonicotinoyl hydrazone have been prepared. Analytical, t.g.a., electronic, i.r. and n.m.r. results show that the orange form [H.G.] is the anti-tautomer hydrazone whereas the yellow form [H.Y]. 1/2H[2]O is a mixture of imide-imidol of the syn one stabilized by H-bond through H-chelates. The complexes of Ti, Zr, Sn, Pt and Th with HG and HY were prepared and characterized using a variety of analytical, spectral and thermal measurements. The analytical data showed that 1:1 or 1:2 molar compounds were obtained. The title hydrazone behaved as a neutral or monobasic bidentate ligand coordinating through the azomethine N and isatin O or eventually as tridentate coordinating through O, N and pyridine N