Abstract
The crystal and molecular structures of Ni(II) complexes with two tridentate anthracene-containing Schiff bases are reported. The Schiff bases were prepared by condensation of 9-anthraldehyde with diethylenetriamine (adien) and with dipropylenetriamine (adipn). Complexes synthesized from Ni(O2CCH3)2·4H2O and the ligands (1 : 1 mol ratio) crystallize from methanol as [Ni(adien)(O2CCH3)2(H2O)] (1) and [Ni(adipn)(O2CCH3)2]·2CH3OH (2·2CH3OH) in space groups P21/n and P212121, respectively. In 1, the distorted octahedral N3O3 coordination sphere around the metal ion is formed by the meridional N3-donor adien, two mutually trans unidentate acetates and one water molecule. The N3O3 coordination sphere constituted by the N3-donor adipn, one unidentate acetate and one bidentate acetate in 2 can be best described as trigonal bipyramidal. The secondary amine-N of adipn, the O-atom of the unidentate acetate and the midpoint of the two O-atoms of the bidentate acetate occupy the three equatorial positions and two imine-N atoms of adipn lie in axial sites. In the crystal lattice, molecules of 1 exist as discrete dimers due to intermolecular hydrogen bonding and π–π interactions. In contrast, self-assembly of 2 via intermolecular π–π interactions leads to a one-dimensional supramolecular structure.
Acknowledgements
Financial assistance for this work was provided by the Council of Scientific and Industrial Research (CSIR), New Delhi (Grant No. 01(1880)/03/EMR-II to S. Pal). We thank the University Grants Commission (UGC), New Delhi for the facilities provided under the Universities with Potential for Excellence program. X-ray crystallographic studies were performed at the National Single Crystal Diffractometer Facility, School of Chemistry, University of Hyderabad (funded by the Department of Science and Technology, New Delhi). Mr. V. K. Muppidi and Mr. C. P. Pradeep thank the CSIR and the UGC, respectively for research fellowships.
Notes
†Present address: Vice Chancellor, Goa University, Goa 403 206, India