Hisham, N.A.I. and Hadi, H.A. and Ali, Hapipah Mohd and Khaledi, H. (2012) Coordination modes of two flexidentate salicylaldimine ligands derived from N-(3-aminopropyl)morpholine toward zinc and copper. Journal of Coordination Chemistry, 65 (17). pp. 2992-3006. ISSN 0095-8972, DOI https://doi.org/10.1080/00958972.2012.708412.
Full text not available from this repository.Abstract
Two flexidentate Schiff-base ligands condensed from salicylaldehyde or 5-chlorosalicylaldehyde with N-(3-aminopropyl)morpholine were prepared in situ and reacted with Zn(II) and Cu(II) salts. Upon complexation, the Schiff bases underwent deprotonation at hydroxyl to act as mono-anionic ligands. When a ligand : metal ratio of 2 : 1 was applied, the deprotonated Schiff bases coordinated metal ions through phenolate and imine in a square-planar or tetrahedral geometry. In contrast, 5-chlorosalicylaldimine reacted with the metal ions in a 1 : 1 ratio to form complexes wherein morpholine nitrogen also participates in an N,N,O-tridentate coordination mode. The structures of the complexes were characterized by spectroscopic methods and single-crystal X-ray diffraction.
| Item Type: | Article |
|---|---|
| Funders: | UNSPECIFIED |
| Additional Information: | Department of Chemistry, Faculty of Science Building, University of Malaya, 50603 Kuala Lumpur, MALAYSIA |
| Subjects: | Q Science > QD Chemistry |
| Divisions: | Faculty of Science > Department of Chemistry |
| Depositing User: | Miss Malisa Diana |
| Date Deposited: | 19 Mar 2013 00:13 |
| Last Modified: | 30 Jan 2019 01:28 |
| URI: | http://eprints.um.edu.my/id/eprint/5141 |
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