Abstract

In the crystal of the title compound, [Cd2Na2(C2H3O2)2(C21H24N2O4)2]·0.67C2H6O, the doubly deprotonated Schiff base ligand N,N′,O,O′-chelates to the CdII cation, which is also O,O′-chelated by the acetate ion. Two Cd–Schiff base units are connected to two Na+ atoms to form the tetra­nuclear complex, in which the Cd2+ and Na+ cations show distorted octa­hedral coordinations. The asymmetric unit consists of half a tetra­nuclear mol­ecule (lying on an inversion center) and a full tetra­nuclear mol­ecule (lying on a general position) along with a lattice ethanol mol­ecule, which links to the coordinating acetate ion via an O—H⋯O hydrogen bond. In the crystal, the propyl and ethyl groups of the complex mol­ecule are disordered over two positions in a 1:1 ratio; the ethyl group of the lattice ethanol mol­ecule is also equally disordered over two positions.

Highlights

  • In the crystal of the title compound, [Cd2Na2(C2H3O2)2(C21H24N2O4)2]0.67C2H6O, the doubly deprotonated Schiff base ligand N,N0,O,O0 -chelates to the CdII cation, which is

  • Two Cd–Schiff base units are connected to two Na+ atoms to form the tetranuclear complex, in which the Cd2+ and Na+ cations show distorted octahedral coordinations

  • The asymmetric unit consists of half a tetranuclear molecule and a full tetranuclear molecule along with a lattice ethanol molecule, which links to the coordinating acetate ion via an O—H O hydrogen bond

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Summary

Introduction

In the crystal of the title compound, [Cd2Na2(C2H3O2)2(C21H24N2O4)2]0.67C2H6O, the doubly deprotonated Schiff base ligand N,N0 ,O,O0 -chelates to the CdII cation, which is Two Cd–Schiff base units are connected to two Na+ atoms to form the tetranuclear complex, in which the Cd2+ and Na+ cations show distorted octahedral coordinations. The asymmetric unit consists of half a tetranuclear molecule (lying on an inversion center) and a full tetranuclear molecule (lying on a general position) along with a lattice ethanol molecule, which links to the coordinating acetate ion via an O—H O hydrogen bond. Absorption correction: multi-scan (SADABS; Sheldrick, 1996)

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Conclusion

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