ALEKHA KUMAR SUTAR
Articles written in Journal of Chemical Sciences
Volume 126 Issue 6 November 2014 pp 1695-1705 Regular Articles
In the present investigation, a new synthetic route for a novel recyclable free [3-MOBdMBn-Ni] and polystyrene-anchored [P-3-MOBdMBn-Ni] nickel complexes is presented. The free and polymer-anchored metal complexes were synthesized by the reaction of nickel (II) with one molar equivalent of unsupported N N′-bis (2-Hydroxy-3-methoxybenzaldehyde) 4-Methylbenzene-1,2-diamine (3-MOBdMBn) or polymersupported (P-3-MOBdMBn) Schiff-base ligand in methanol under nitrogen atmosphere. The advantages of these polymer-supported catalysts are the low cost of catalyst and recyclability up to six times, due to easy availability of materials and simple synthetic route. The higher efficiency of complexation of nickel on the polymer-anchored 3-MOBdMBn Schiff base than the unsupported analogue is another advantage of this catalyst system. The structural study reveals that nickel(II) complex of 3-MOBdMBn is square planar in geometry. The catalytic activity of nickel complex towards the oxidation of phenol was investigated in the presence of hydrogen peroxide. Experimental results indicate that the reactivity of P-3-MOBdMBn-Ni was dramatically affected by the polymer support compared to free 3-MOBdMBn-Ni. The rates of oxidation (R$_p$) for unsupported and supported catalysts are 1.37 × 10-6 mole dm-3 s-1 and 2.33 × 10-6 mole dm-3 s-1 respectively.
Volume 128 Issue 6 June 2016 pp 883-891 Regular Article
Salicylaldimine copper complex has been synthesized and its reactivity for the ring-opening polymerization(ROP) of lactide has been studied. This monomeric copper complex was prepared by the reaction ofcopper(II) solution with one molar equivalent of salicylaldimine Schiff-base ligand in methanol under nitrogenatmosphere. This copper complex has been characterized by different spectroscopic methods, which showedsquare planar geometry. The molecular structure of the salicylaldimine Schiff-base has been determined byX-ray diffraction studies. The complex was tested as the initiator for the ring-opening polymerization of lactide,with variation in diamine group in ligand. The rate of polymerization is dependent on the diamine groupin the following order: ethylene > propylene > phenyl. The salicylaldimine copper complex allows controlledring-opening polymerization as indicated by the linear relationship between the percentage conversion and thenumber-average molecular weight. On the basis of literature reports, a mechanism for ROP of lactide has beenproposed.
Volume 132 All articles Published: 22 January 2020 Article ID 0025
In the present study, the cobalt (II) complex [Co-HMBED] has been prepared and characterized by spectrochemical techniques, which confirmed its square planar structure. The catalytic activity of the cobalt complex was evaluated towards solvent-free conversion of CO2 and styrene oxide into cyclic styrene carbonate and polymerization of lactide
Volume 133, 2021
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