Abstract

Some five-coordinated cobalt(III) complexes were synthesized and characterized using elemental analysis, 1 H NMR and IR spectra. The formation constants and the thermodynamic parameters were measured spectrophotometrically for the 1:1 adduct formation of [Co(Chel)(PBu 3 )]ClO 4 .H 2 O where Chel = cd3OMesalen, cd4OMesalen, cd5OMesalen: methyl-2-{[1-methyl-2-(2-hydroxy-3-, 4-, 5-methoxyphenyl)methylidynen-itrilo]ethyl}amino-1-cyclopentene-dithiocarboxylate, as acceptors, with some linear and cyclic amines as donors, in different solvents at constant ionic strength (I = 0.1 M NaClO 4 ), and at various temperatures (T = 283-313 K). The results revealed that the formation constants of the Co(III) Schiff base complexes toward a given amines donor are as follow: [Co(cd4OMesalMeen)(PBu 3 )] + > [Co(cd3OMesalMeen)(PBu 3 )] + > [Co(cd5OMesalMeen)(PBu 3 )] + . The trend of the formation constants of the donors (amines) toward a given cobalt(III) complex is as follow: Im > 4-MeIm > BzIm and n-butylamine > sec-butylamine > tert-butylamine. Also the effect of the solvents on the formation constants of a given cobalt(III) Schiff base complex toward a given donor are as follow: CH 3 CN > DMF > EtOH. The ligands and their cobalt complexes have been screened for their antibacterial activities. All the free Schiff base ligands exhibit higher antibacterial activity than the cobalt(III) complexes. KEY WORDS : Cobalt (III) Schiff base complex, Thermodynamic parameters, Amines, Antibacterial activity Bull. Chem. Soc. Ethiop. 2016 , 30(2), 209-220. DOI: http://dx.doi.org/10.4314/bcse.v30i2.5

Highlights

  • For a long time tetradentate Schiff base complexes of transition metal ions have attracted many researchers interest in the field of coordination chemistry [1,2,3,4]

  • Though a large number of papers have appeared on metal complexes with Schiff base derived from aromatic aldehydes and substituted amines with N4 and N2O2 coordination sphere [5,6,7,8], only few publications exist on Schiff bases containing sulfur donor ligands

  • Following our earlier studies on the coordination behavior, here we report the formation constants for three Co(III) Schiff base complexes with three cyclic amine donors Im, 4-MeIm and BzIm

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Summary

INTRODUCTION

For a long time tetradentate Schiff base complexes of transition metal ions have attracted many researchers interest in the field of coordination chemistry [1,2,3,4]. This paper describes thermodynamic studies of five coordinated cobalt(III) complexes in equilibrium with amines as the sixth ligand in ethanol, CH3CN and DMF as solvents. Yield: 56%; m.p.: 301 oC; 1H NMR (400 MHz, DMSO-d6, r.t., TMS, δ ppm): 0.85 (3H, d, Me), 1.28-1.62 (9H, t, P-CH3), 1.94-2.03 (18H, m, P(CH2)3), 2.54 (2H, m, H4'), 2.96 (3H, s, SMe), 3.04-3.20 (4H, m, H3',5'), 3.65 (2H, d, Hen), 3.86 (3H, s, OMe), 4.42 (1H, m, Hen), 6.74 (1H, dd, H4), 6.80 (1H, d, H5), 6.91 (1H, d, H6), 8.56 (1H, s, CH=N); IR (KBr, cm-1): 456 (νCo-N), 579 (νCo-O), 737 (νC-S), 1094 (νClO4), 1180 (νC-S+νC-N), 1246 (νC-O), 1444 (νC=C aromatic), 1607, 1614 (νC=N), 2930 (νC-H), 3420 (νO-H); UV-Vis (DMF) Found: C, 48.34, H, 7.32, N, 3.64, S, 8.58%

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