Bi-Nuclear Metal Complexes of 2,6-Bis(1,4,7-triazacyclonon-1-yl-methylene)pyridine with Zinc(ii), Copper(ii), and Nickel(ii)
Campbell J. Coghlan A C , Eva M. Campi A , Craig M. Forsyth B , Roy W. Jackson A and Milton T. W. Hearn A B D
+ Author Affiliations
- Author Affiliations
A Centre for Green Chemistry, Monash University, Clayton, Vic. 3800, Australia.
B School of Chemistry, Monash University, Clayton, Vic. 3800, Australia.
C Current address: School of Chemistry and Physics, Centre for Advanced Nanomaterials, The University of Adelaide, Adelaide, SA 5005, Australia.
D Corresponding author. Email: milton.hearn@monash.edu
Australian Journal of Chemistry 68(7) 1115-1121 https://doi.org/10.1071/CH14618
Submitted: 15 October 2014 Accepted: 24 November 2014 Published: 11 February 2015
Abstract
The coordination chemistry of 2,6-bis(1,4,7-triazacyclonon-1-ylmethyl)pyridine (Lpyx, 1) has been investigated and shown to yield bi-nuclear metal complexes in the presence of zinc(ii), copper(ii), or nickel(ii) ions. The reaction of (Lpyx)·7HCl (2) with Zn(NO3)2 gave the monomeric [Zn2(μ-Cl)2(Lpyx)(H2O)](ClO4)2 (3) in which the ligand encapsulates a Zn2(μ-Cl)2 moiety. Similar treatment of 2 with Cu(NO3)2 gave a bi-nuclear complex cation which exists as a 1 : 1 co-crystal {[Cu(Cl)(Lpyx)Cu(μ-Cl)(Cl)](BF4)(H2O)}2 and {[Cu(Cl)(Lpyx)Cu(μ-Cl)(H2O)](BF4)2(H2O)}2 (4) with two discrete CuII centres bridged by the Lpyx ligand and dimerised through an unsymmetrical Cu2(μ-Cl)2 interaction. Similarly, reaction of 2 with Ni(NO3)2 also gave a dimeric complex {[Ni(Cl)(μ-Cl)(Lpyx)Ni(NO3)(H2O)](PF6)}2 (5) containing two discrete NiII centres with dimerisation occurring through a symmetrical Ni2(μ-Cl)2 interaction. In all cases, the Lpyx ligand binding is unsymmetrical between the two metal centres being tridentate to one and tetradentate to the other through an additional coordination of the pyridyl linker.
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