Faculty Publications
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Item One-step synthesis of biaryls under mild conditions(Wiley-VCH Verlag, 2013) Bhat, A.P.I.; Inam, F.; Badekai Ramachandra, B.A one-step synthesis of symmetrical biaryls was developed and uses a nickel(III) complex containing a Schiff base and dithiolate ligands as a catalyst for the homocoupling of in situ generated Grignard reagents. The coupling reaction was performed at room temperature with molecular oxygen as the oxidant, which renders the reaction energy-efficient and environmentally friendly. The catalytic methodology is compatible with diverse functionalities, including chlorido, nitro, nitrile, and heteroatoms, and provides biaryls in appreciable yields. A practical, room-temperature nickel(III) catalytic system has been developed for the synthesis of biaryls in one step from the homocoupling of in situ generated Grignard reagents. The use of molecular oxygen as the oxidant makes the system environmentally friendly. The reaction system is compatible with diverse functionalities and affords biaryls in appreciable yields. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.Item Cobalt pincer complex catalyzed Suzuki-Miyaura cross coupling – A green approach(Elsevier B.V., 2017) Kumar, L.M.; Badekai Ramachandra, B.A series of cobalt complexes with tridentate pincer ligands were synthesized to study their catalytic activity in Suzuki-Miyaura coupling reactions. Cobalt complexes, C-1, C-2, C-3 bearing asymmetrical PNCOP pincer ligand [C6H4-1-(NHPPh2)-3-(OPPh2)] (L-1) and symmetrical PNCNP, PNNNP pincer ligands [C6H4-2,6-(NHPPh2)2] (L-2) and [C5H3N-2,6-(NHPPh2)2] (L-3) were synthesized by the reaction of diphenylchlorophosphine with m-aminophenol, m-phenylenediamine and 2,6-diaminopyridine respectively in a 1:2 ratio in the presence of triethylamine as a base and tetrahydrofuran as solvent media. The synthesized complexes were examined for their C-C coupling efficiency in cross-coupling between phenyl boronic acid and para substituted bromobenzenes. Effect of variation of the ligand on the catalytic activity of cobalt pincer complex was explored based on the coupling yields. It is observed that as the number of ‘N’ atoms increases in the side arm of the ligand, the donating ability of the ligand increases which leads to the increased catalytic activity of the complex. The symmetrical PNNNP pincer complex (C-3) was found to be more effective as a catalyst among the complexes synthesized and reported in the present study. © 2016 Elsevier B.V.Item Iron pincer complex and its graphene oxide composite as catalysts for Suzuki coupling reaction(Elsevier B.V., 2019) Kumar, L.M.; Mishra, P.; Badekai Ramachandra, B.R.We report the synthesis of Fe-NCN pincer complex as homogenous catalyst and its composite by immobilizing the complex on amino functionalized graphene oxide as a heterogeneous catalyst for Suzuki coupling reactions. Both the complex and the composite were employed in catalyzing the Suzuki-Miyaura cross-coupling reaction between the aryl halide and phenyl boronic acid in acetonitrile solvent media with Cs2CO3 as a base. Effect of substitution over aryl halide was also investigated. Immobilization of the pincer complex had advantageous recovery and reuse of the catalyst as compared to its homogenous analog with no significant decrease in the catalytic efficiency. © 2018 King Saud University