Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/70884
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Type: Journal article
Title: Pre-organisation or a hydrogen bonding mismatch; silver(I) diamide ligand coordination polymers versus discrete metallo-macrocyclic assemblies
Author: Abdul Kadir, M.
Clements, P.
Hanton, L.
Hollis, C.
Sumby, C.
Citation: Supramolecular Chemistry, 2012; 24(8):627-640
Publisher: Gordon Breach Sci Publ Ltd
Issue Date: 2012
ISSN: 1061-0278
1029-0478
Statement of
Responsibility: 
Maisara Abdul-Kadir, Philip R. Clements, Lyall R. Hanton, Courtney A. Hollis and Christopher J. Sumby
Abstract: The investigation of novel motifs to selectively complex anions is an area of considerable importance due to the significant environmental, biological and medicinal roles of anions. The synthesis of discrete metallo-macrocyclic compounds or coordination polymers displaying anion-binding pockets can generate specific anion receptors from relatively simple components. Here, we examine the self-assembly of a series of flexible diamide compounds L1–L5 with silver(I) metal salts. A new diamide ligand, 2,6-[N,N0-bis(di-(pyridin-2-yl)methyl)pyridine]-2,6-dicarboxamide (L5), with two chelating di-2- pyridylmethyl donor groups, was also prepared. Compounds L1–L3, lacking the pre-organising effect of a central 2,6-pyridine dicarboxamide core, form 1D coordination polymers {[Ag(L1)(CH3CN)](PF6)}n (6), {[Ag(L2)](NO3)•(H2O)]}n (7) and {[AgNO3(L3)]•(CH3OH)]}n (9) which in turn form 2D and 3D hydrogen-bonded networks through orthogonal hydrogen bonding. In one instance, L2 gives rise to a dinuclear metallo-macrocycle in the solid state, [Ag2(CF3CO2)2(L2)2][Ag2(m2- CF3CO2)2(L2)2] (8). Both diamide ligands L4 and L5 form dinuclear metallo-macrocycles, [Ag2(NO2)2(L4)2] (10) and [Ag2(L5)2](NO3)2•2CH3OH•2H2O (11), in solution and in the solid state. Where possible, all compounds were investigated in solution and their solid-state structures were determined using X-ray crystallography. This enabled the effect of competing supramolecular synthons, covalent MZL bonding and hydrogen bonding, to be examined by comparing the solution and solid-state behaviour of each metal–ligand combination.
Keywords: Metallo-supramolecular chemistry; coordination polymers; orthogonal interactions
Rights: © 2012 Taylor & Francis
RMID: 0020122049
DOI: 10.1080/10610278.2012.699052
Grant ID: http://purl.org/au-research/grants/arc/FT0991910
http://purl.org/au-research/grants/arc/DP0773011
Appears in Collections:IPAS publications
Environment Institute publications

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