Two mixed-ligand copper(II) complexes [{Cu(L1)(l1,3-N3)}{Cu(L)(l1,3-N3)(l1,1-N3)}]n (1) [HL1 = 1-(Northo- hydroxyacetophenimino)-2,2-dimethyl-aminoethane; L = 2-(dimethylamino)-ethylamine] and [{Cu(L2)(l1,3-N3)}{Cu(L)(l1,3-N3)(l1,1-N3)}]n (2) [HL2 = 1-(N-5-methoxy-ortho-hydroxyacetophenimino)- 2,2-dimethyl-aminoethane] have been formed upon addition of aqueous solution of sodium azide to a methanolic solution of copper nitrate trihydrate and corresponding Schiff-base ligands. The ligands, HL1 and HL2 undergo partial hydrolysis of their imine bond during the course of reaction. Both the complexes contain single end-to-end (l1,3) azido bridged 1D infinite chains (rail) which propagate parallel to the crystallographic b-axis; neighboring chains are interconnected by pairs through double asymmetric end-on (l1,1) azido bridges (rung) to yield a ladder-like structure. In both complexes, rungs (end-on azido bridges) do not connect copper centers of the chains like in a regular ladder; instead they connect only the alternating copper sites of the 1D chain. In a chain the coordination environment around copper(II) ions are not the same: while the {Cu(L1)(l1,3-N3)} and {Cu(L2)(l1,3-N3)} moieties have a penta-coordinated copper(II) center, the copper(II) ion of the neighboring {Cu(L1)(l1,3-N3)(l1,1-N3)} or {Cu(L2)(l1,3- N3)(l1,1-N3)} moiety has an octahedral coordination environment. The variable temperature (2–300 K) magnetic susceptibility measurements showed that the magnetic interaction between the metal centers in complexes 1 and 2 is dominantly antiferromagnetic. The results of magnetic model are in good agreement with the experimental data.

Ladder-like azido-bridged copper(II) complexes: Synthesis, X-ray structure and magnetic Study / C., Adhikary; R., Sen; J. P., Tuchagues; S., Chaudhuri; Ianelli, Sandra; Solzi, Massimo; S., Koner. - In: INORGANICA CHIMICA ACTA. - ISSN 0020-1693. - 362:(2009), pp. 5211-5218. [10.1016/j.ica.2.009.09032]

Ladder-like azido-bridged copper(II) complexes: Synthesis, X-ray structure and magnetic Study

IANELLI, Sandra;SOLZI, Massimo;
2009-01-01

Abstract

Two mixed-ligand copper(II) complexes [{Cu(L1)(l1,3-N3)}{Cu(L)(l1,3-N3)(l1,1-N3)}]n (1) [HL1 = 1-(Northo- hydroxyacetophenimino)-2,2-dimethyl-aminoethane; L = 2-(dimethylamino)-ethylamine] and [{Cu(L2)(l1,3-N3)}{Cu(L)(l1,3-N3)(l1,1-N3)}]n (2) [HL2 = 1-(N-5-methoxy-ortho-hydroxyacetophenimino)- 2,2-dimethyl-aminoethane] have been formed upon addition of aqueous solution of sodium azide to a methanolic solution of copper nitrate trihydrate and corresponding Schiff-base ligands. The ligands, HL1 and HL2 undergo partial hydrolysis of their imine bond during the course of reaction. Both the complexes contain single end-to-end (l1,3) azido bridged 1D infinite chains (rail) which propagate parallel to the crystallographic b-axis; neighboring chains are interconnected by pairs through double asymmetric end-on (l1,1) azido bridges (rung) to yield a ladder-like structure. In both complexes, rungs (end-on azido bridges) do not connect copper centers of the chains like in a regular ladder; instead they connect only the alternating copper sites of the 1D chain. In a chain the coordination environment around copper(II) ions are not the same: while the {Cu(L1)(l1,3-N3)} and {Cu(L2)(l1,3-N3)} moieties have a penta-coordinated copper(II) center, the copper(II) ion of the neighboring {Cu(L1)(l1,3-N3)(l1,1-N3)} or {Cu(L2)(l1,3- N3)(l1,1-N3)} moiety has an octahedral coordination environment. The variable temperature (2–300 K) magnetic susceptibility measurements showed that the magnetic interaction between the metal centers in complexes 1 and 2 is dominantly antiferromagnetic. The results of magnetic model are in good agreement with the experimental data.
2009
Ladder-like azido-bridged copper(II) complexes: Synthesis, X-ray structure and magnetic Study / C., Adhikary; R., Sen; J. P., Tuchagues; S., Chaudhuri; Ianelli, Sandra; Solzi, Massimo; S., Koner. - In: INORGANICA CHIMICA ACTA. - ISSN 0020-1693. - 362:(2009), pp. 5211-5218. [10.1016/j.ica.2.009.09032]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2299211
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