Abstract
The reactions of HL1 [2-((2-(benzylthio)phenylimino)methyl)phenol] and HL2 [3-((2-(benzylthio)phenylimino)methyl)-2-hydroxy-5-methylbenzaldehyde] separately with Cu(OAc)2·H2O afforded new Cu(II) complexes [Cu(L1)(OAc)] (1) and [Cu(L2)2] (2), respectively. These are characterized by microanalytical data and spectroscopic studies. UV–vis spectra of the complexes show intense low-energy transitions ∼ 420 nm which are ligand to metal charge transfer (LMCT) transitions. The single-crystal X-ray structures were determined for 1 and 2. Reactions of [Cu(L1)(OAc)] (1) with , SCN– and
show the replacement of weakly coordinated acetate yielding [Cu(L1)(N3)], [Cu(L1)(SCN)] and [Cu(L1)(NO2)], respectively. Unequivocal characterization of the substituted products has been done by single-crystal X-ray study of [Cu(L1)(N3)]. HL2 and its Cu(II) complex exhibited low-intensity emission bands at ∼575 nm upon excitation at 375 nm and at 420 nm, respectively. Redox properties of the complexes were determined electrochemically. Density functional theory (DFT) computations have been carried out to explain the spectroscopic and redox properties of the complexes.
Acknowledgements
Special thanks to Professor Surajit Chattopadhyay, University of Kalyani, for his valuable suggestions throughout this study. The financial support from University Grants Commission is gratefully acknowledged (under Minor Research Project, Sanction No. F.PSW/067/2011-12). The necessary laboratory and infrastructural facility are provided by the Department of Chemistry, Kandi Raj College and Department of Chemistry, University of Kalyani.