Faculty Publications

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    Single-step oxidative homocoupling of aryl Grignard reagents via Co(II), Ni(II) and Cu(II) Complexes under air
    (John Wiley and Sons Ltd Southern Gate Chichester, West Sussex PO19 8SQ, 2014) Bhat, A.P.I.; Badekai Ramachandra, B.R.
    A simple catalytic system of direct synthesis for the symmetrical biaryls using catalytic amounts of Co(II), Ni(II) and Cu(II) complexes has been developed. The reaction system involves in situ synthesis of Grignard reagents. The complexes, containing bidentate Schiff base and dmit (2-thioxo-1,3-dithiole- 4,5-dithiolate) ligands, were compatible with diverse functionalities and afford a high yield of biaryls in a single step, proving to be promising catalysts in homocoupling reactions. Atmospheric oxygen is used as an oxidant which renders a green, simple and economical catalytic route. Copyright © 2014 John Wiley & Sons, Ltd.
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    Immobilized magnetic nano catalyst for oxidation of alcohol
    (Elsevier, 2015) Bhat, P.B.; Rajarao, R.; Sahajwalla, V.; Badekai Ramachandra, B.R.
    Covalent attachment of Schiff base on magnetic nanoparticles yielded good selectivity for oxidation of alcohols. The ferromagnetic interaction in the complex added comprehensive advantage in enhancing the catalytic activity of the nanocatalyst. A greener approach for alcohol oxidation was achieved in solventless method with good yield (>78%). Leaching experiments confirmed a strong interaction between magnetic support and complex. The catalyst showed significant conversion even after 5 catalytic runs. © 2015 Elsevier B.V. All rights reserved.
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    Air-Stable Cobalt(II) and Nickel(II) Complexes with Schiff Base Ligand for Catalyzing Suzuki–Miyaura Cross-Coupling Reaction
    (Pleiades journals, 2018) Ansari, R.M.; Kumar, L.M.; Badekai Ramachandra, B.R.
    The Co(II) complex [Co{C6H4–1,2-(N=CH–C6H4O)2}] (I) and Ni(II) complex [Ni{C6H4–1,2-(N=CH–C6H4O)2}] (II) with Schiff base of o-phenylenediamine and salicylaldehyde have been synthesized. The structure of the ligand and its complexes were derived on the basis of various techniques such as elemental analysis, mass, FT-IR, electronic spectra and magnetic susceptibility. From the Singal crystal X-ray diffraction (SCXRD) analysis techniques (CIF file CCDC no. 1498772 (II)), it has been confirmed that the Schiff base ligand (L), coordinates to the metal ion in a tetradentate fashion through the nitrogen and oxygen atom. In addition, the square planar geometry of Ni(II) complex also has been confirmed from SCXRD. Electronic spectra, mass spectra, and magnetic susceptibility measurements reveal square planar geometry for the Co(II) complex. Synthesized complexes were used in cross-coupling of arylhalides with phenylboronic acid. The transformation offers products in good yields using 0.02 mmol catalysts loading, thereby proving the efficiency of the complexes as catalysts for Suzuki–Miyaura reaction. © 2018, Pleiades Publishing, Ltd.
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    Copper complex with N-,O- architecture grafted graphene oxide nanosheet as a heterogeneous catalyst for Suzuki cross coupling reaction
    (Taiwan Institute of Chemical Engineers, 2019) Anuma, S.; Mishra, P.; Badekai Ramachandra, B.R.
    We report a straight forward synthesis of a heterogeneous catalyst by covalently immobilizing copper Schiff base complex on the surface of amino functionalized graphene oxide (AGO) for the Suzuki coupling of substituted aryl halides with arylboronic acids. The as-synthesized complex and subsequent catalyst were characterized for their structural features using suitable techniques. The analysis confirmed that the Cu bound to Schiff base (L) ligand via bi(N-,O-) linkage and Cu-L immobilization on AGO was due to its amino functionality. The catalyst exhibited excellent yield of 94% for Suzuki coupling reactions as analyzed by gas chromatography. The catalyst was recycled for 5 successive reactions with insignificant loss in efficiency. ICP-AES analysis showed the catalyst retained 87.5% of its active metal center after 5th iteration. High yield, environmentally benign, easy work-up procedure, easy separation of catalyst and mild reaction conditions are some of the important facets this catalyst offer. © 2018 Taiwan Institute of Chemical Engineers
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    Thermally stable complexes of Fe(III), Co(II), Ni(II) and Cu(II) with Schiff base derived from 4-aminoacetophenone and salicylaldehyde
    (Springer, 2022) Ansari, R.M.; Ramakrishna, D.; Badekai Ramachandra, B.R.
    The Schiff base ligand 1-(4-((2-hydroxybenzylidene)amino)phenyl)ethan-1-one, obtained from 4-aminoacetophenone and salicylaldehyde, and its complexes with Fe(III), Co(II), Ni(II) and Cu(II) have been synthesized. These complexes were characterized by FTIR spectroscopy, elemental, and SCXRD analysis. FTIR spectra of complexes show the bidentate coordination of metal ions with ligands where O and N are electron-donating sites of the azomethine group. The electronic absorption spectra of these complexes show the characteristics of absorption bands involved in the Fe, Co, and Ni complexes due to their π→π*, n→π* transitions. Further, the geometry of the complexes was deduced from the calculated magnetic moment values and single crystal XRD analysis. Graphical abstract: A Schiff base derived from the condensation reaction between 2-aminoacetophenone and salicylaldehyde was involved in the formation of four different metal complexes, i.e., with Nickel, Cobalt, Iron, and Copper. The synthetic route to forming these complexes followed an easy process, and the complexes were obtained in good yields.[Figure not available: see fulltext.] © 2022, Indian Academy of Sciences.