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Article type: Research Article
Authors: Lashanizadegan, Maryam | Sarkheil, Marzieh
Affiliations: Department of Chemistry, Faculty of Sciences, Alzahra University, Tehran, Iran
Note: [] Corresponding author: Maryam Lashanizadegan, Department of Chemistry, Faculty of Sciences, Alzahra University, P. O. Box 1993893973, Tehran, Iran. Tel.: +98 21 88041344; Fax: +98 21 88041344; E-mail: [email protected]
Abstract: The Schiff base ligands trans-N,N′-bis[benzylidene]cyclohexane-1,2-diamine (L1) and trans-N,N′-bis [cinnamalidene]cyclohexane-1,2-diamine (L2) were synthesized. The reaction of L1 with MCl2.xH2O (M = Co, Zn, Ni, Cu) in ethanol, undergoes partial hydrolysis of the imino bond and results bidentate ligand (L1′) which immediately formed the complexes [ML1′Cl2] with N2 coordination sphere. L2 reacts with MCl2.xH2O (M = Co, Zn) in ethanol and gives complexes [ML2Cl2]. The reaction of L2 with MCl2.xH2O (M = Ni, Cu) in ethanol undergoes hydrolysis of the imino bond and [M (DACH)Cl2] complexes are formed. The ligands and complexes were analyzed by elemental analysis, UV-VIS, FT-IR, 1H NMR, GC/MS and luminescence properties. The ligands and complexes display intra-ligand (π–π*) fluorescence in the solid state at room temperature.
Keywords: (±)trans-1,2-diaminocyclohexane, hydrolysis, fluorescence, Schiff base
DOI: 10.3233/MGC-130086
Journal: Main Group Chemistry, vol. 12, no. 1, pp. 15-23, 2013
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