Synthesis of Styrene-Allylchloride Copolymer Supported Cobalt(II) Schiff Base Complex and Its Catalytic Activity

Abstract

Abstract N,N′-bis(acetylacetone)o-phenylenediamine cobalt (II) Schiff base complex and its polymer bound analogue have been prepared and characterized for their structure and catalytic activity. To prepare heterogenized analogue of the cobalt (II) complex, a new crosslinked functional polymeric beads were prepared by suspension copolymerization of styrene (48.97 mmol, 5.1 g), allylchloride (48.97 mmol, 3.746 g) and divinylbenzene (1.50 mmol, 0.195 g) in the presence of azobisisobutyronitrile (9.0×10−4 mmol, 0.15 g) as initiator at 25±0.1°C under inert atmosphere. The beads of variable crosslinked densities were prepared by varying the amount of divinylbenzene in a reaction mixture from 0.80–2.00 mmol. The beads prepared with 1.5 mmol of divinylbenzene contained 4.90 mmol (0.367 g) of allylchloride as found with the chlorine content in the beads. These beads have shown optimum degree of swelling (4.83%) and maximum attachment of N,N′-bis(acetylacetone)o-phenylenediamine Schiff base (1.96 mmol g−1 of beads). These beads have also shown maximum loading of cobalt (II) ions on polymer anchored Schiff base (1.37 mmol g−1 of beads). The spectral and magnetic measurements have suggested a square planar structure for cobalt (II) complex both in homogeneous and heterogeneous state. The heterogenized cobalt (II) complex has shown an enhanced rate of decomposition of hydrogen peroxide with low activation energy (42.37 kJ mol−1) in comparison to a homogenized complex (63.59 kJ mol−1). The rate of decomposition has been found to be directly proportional to the concentration of hydrogen peroxide and cobalt (II) complex. A suitable rate expression has been derived for the decomposition of hydrogen peroxide. Keywords: AllylchlorideStyreneO-phenylenediamineHeterogeneous catalysisCopolymerization Acknowledgments The authors are thankful to I.I.T. Roorkee for providing infrastructural facilities to carry out these investigations. Mr. H. K. Abdulkadir is thankful to ICCR, New Delhi, India, for the award of a fellowship.