TY - JOUR
T1 - Synthesis, crystal structure and catecholase activity of a Ni(II) complex derived from a tetradentate Schiff base ligand
AU - Basu, Pradipta Kumar
AU - Mitra, Merry
AU - Ghosh, Amrita
AU - Thander, Latibuddin
AU - Lin, Chia Her
AU - Ghosh, Rajarshi
N1 - Publisher Copyright:
© 2014 Indian Academy of Sciences.
PY - 2014/11
Y1 - 2014/11
N2 - A new nickel(II) complex [Ni(L)] (1) [H2L = 1,1′-(1E,1′E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)dinaphthalen-2-ol] was synthesized and X-ray crystallographically characterized. 1 crystallizes in orthorhombic crystal system with Cmc21 space group. The unit cell dimensions of the crystal are a = 30.6345(4) Å, b = 8.45340(10) Å, c = 7.75180(10) Å. Structural analysis reveals a tetradentate chelation behaviour of the dianionic ligand H2L having a distorted square planar geometry around Ni(II) with NiN2O2 chromophore in 1. The title complex 1 behaves as an effective catalyst towards oxidation of 3,5-ditertiarybutyl catechol (3,5-DTBC) in acetonitrile to its corresponding quinone derivative in air. The reaction follows first-order reaction kinetics with rate constant 4.28 × 10-5 min -1. The reaction follows Michaelis-Menten enzymatic kinetics with a turnover number of (K c a t ) 140.72 h-1 in acetonitrile. [Figure not available: see fulltext.]
AB - A new nickel(II) complex [Ni(L)] (1) [H2L = 1,1′-(1E,1′E)-(propane-1,3-diylbis(azan-1-yl-1-ylidene))bis(methan-1-yl-1-ylidene)dinaphthalen-2-ol] was synthesized and X-ray crystallographically characterized. 1 crystallizes in orthorhombic crystal system with Cmc21 space group. The unit cell dimensions of the crystal are a = 30.6345(4) Å, b = 8.45340(10) Å, c = 7.75180(10) Å. Structural analysis reveals a tetradentate chelation behaviour of the dianionic ligand H2L having a distorted square planar geometry around Ni(II) with NiN2O2 chromophore in 1. The title complex 1 behaves as an effective catalyst towards oxidation of 3,5-ditertiarybutyl catechol (3,5-DTBC) in acetonitrile to its corresponding quinone derivative in air. The reaction follows first-order reaction kinetics with rate constant 4.28 × 10-5 min -1. The reaction follows Michaelis-Menten enzymatic kinetics with a turnover number of (K c a t ) 140.72 h-1 in acetonitrile. [Figure not available: see fulltext.]
KW - Catecholase activity
KW - Nickel(II)
KW - Schiff base
KW - X-ray structure
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U2 - 10.1007/s12039-014-0742-5
DO - 10.1007/s12039-014-0742-5
M3 - Article
AN - SCOPUS:84921754281
SN - 0974-3626
VL - 126
SP - 1635
EP - 1640
JO - Journal of Chemical Sciences
JF - Journal of Chemical Sciences
IS - 6
ER -