Faculty Publications
Permanent URI for this communityhttps://idr.nitk.ac.in/handle/123456789/18736
Publications by NITK Faculty
Browse
5 results
Search Results
Item Magnetically retrievable nickel hydroxide functionalised AFe2O4 (A = Mn, Ni) spinel nanocatalyst for alcohol oxidation(Springer Nature, 2016) Bhat, P.B.; Badekai Ramachandra, B.R.Ultrasmall nickel hydroxide functionalised AFe2O4 (A = Mn, Ni) nanocatalyst was synthesized by traditional co-precipitation method and was examined for oxidation of aromatic alcohols to carbonyls using hydrogen peroxide as terminal oxidant. A very high surface area of 104.55 m2 g?1 was achieved for ferromagnetic MnFe2O4 and 100.50 m2 g?1 for superparamagnetic NiFe2O4, respectively. Efficient oxidation was observed due to the synergized effect of nickel hydroxide (bronsted base) on Lewis center (Fe) of the nanocatalyst. Catalyst recycling experiments revealed that the ultrasmall nanocatalyst can be easily recovered by external magnet and applied for nearly complete oxidation of alcohols for at least five successive cycles. Furthermore, the nickel hydroxide functionalised ultrasmall nanocatalyst exhibited higher efficiency for benzyl alcohol oxidation compared to Ni(OH)2, bare MnFe2O4 and NiFe2O4. Higher conversion rate was observed for nickel hydroxide functionalised NiFe2O4 compared to MnFe2O4. Ultrasmall magnetic nickel hydroxide functionalised nanocatalyst showed environmental friendly, greener route for the oxidation of alcohols without significant loss in activity and selectivity within successive runs. © 2015, The Author(s).Item 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.Item Enhanced photostability and optical nonlinearity of nickel and cobalt organometallic complexes(Elsevier B.V., 2019) Manjunatha, K.B.; Rajarao, R.; Poornesh, P.; Rudresha, B.J.; Umesh, G.; Badekai Ramachandra, B.R.Nonlinear optical and limiting properties of nickel, cobalt metal-organic complexes and ligand (L) {L = N,N?-o-phenylenebis (4-hyrdoxy-salicylideneimine)} were studied using Z-scan technique using Q-switched Nd: YAG laser with nanosecond pulses at 532 nm. The results reveal that metal complexes exhibit large negative nonlinear refractive index (n2) of the order of 10?11 esu. The metal complexes displays large nonlinearity than the ligand due to effective charge delocalization between metal ion and ligand. The magnitude of ground state absorption cross section is small compared to the effective excited-state absorption cross section implying the observed nonlinearity is due to reverse saturable absorption. Further, metal-organic complexes exhibit enhanced optical limiting behaviour at nanosecond laser pulses. © 2019 Elsevier B.V.Item 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.Item Significance of transition metal (Co, Ni and Zn) doping on the nano MnSe for high-performance supercapacitor electrode(Elsevier Ltd, 2024) Mascarenhas, F.J.; Rodney, J.D.; Kim, B.C.; Badekai Ramachandra, B.R.The demand for electrode materials in supercapacitors necessitates designs with exceptional performance, superior structure, and environmental sustainability, all while remaining affordable and abundantly available. This study introduces an economical hydrothermal synthesis method for producing MxMn1-xSe (M=Co / Ni / Zn) nanomaterials at varying concentrations (x = 0.0, 0.01, 0.02, and 0.03). Diverse characterization methods confirm the successful formation of nanomaterials. Among the materials studied, Co0.01Mn0.99Se nanoclusters exhibit superior performance as electrode materials for supercapacitors, delivering a specific capacitance of 421 F/g at 5 mV/s and 377 F/g at 1 A/g in a 5 M KOH solution. A two-electrode symmetric configuration was established utilizing Co0.01Mn0.99Se as the active material in a 5 M KOH electrolyte, yielding a notable specific capacitance of 73 F/g at 0.5 A/g. The maximum energy density and power density achieved are 20.44 Wh/kg and 2838 W/kg respectively. This configuration demonstrates the exceptional electrochemical performance and energy storage capabilities of Co0.01Mn0.99Se in a two-electrode system. Impressively, the symmetric cell maintains a significant 70% capacitance retention even after 5000 charge-discharge cycles. Considering these findings, the developed Co0.01Mn0.99Se emerges as a pivotal advancement, providing a robust framework for the development of cutting-edge energy conversion and storage technologies. © 2024 Elsevier B.V.