Supramolecular patterns of cationic and neutral Ni(ii) complexes from the interplay of hydrogen-bonding, stacking interactions and metal-coordination motifs

• Published in: CrystEngComm 2012-01, Vol.14 (20), p.6492-6502
• Main Authors: Kounavi, Konstantina A., Moushi, Eleni E., Manos, Manolis J., Papatriantafyllopoulou, Constantina, Tasiopoulos, Anastasios J., Nastopoulos, Vassilios
• Format: Article
• Language: English
• Subjects: Arrays; Assembly; Cations; Clusters; Hydrogen bonding; Ligands; Self assembly; Transition metals
• ISSN: 1466-8033; 1466-8033
• DOI: 10.1039/c2ce25704a

In an effort to explore the way in which the chemical subunits of crystal structures of transition metal complexes are put together in periodic ordered arrays in the solid state vianoncovalent interactions, an investigation on a series of 13 nickel(ii) complexes has been carried out. The complexes were isolated from the general Ni super(II)/X super(-)/L or HL' [X super(-) = Cl super(-), Br super(-), I super(-), NO sub(3) super(-), NO sub(2) super(-), ClO sub(4) super(-); L = 1-methyl-4,5-diphenylimidazole, and HL' = 4,5-diphenylimidazole] reaction system. A single-crystal diffraction analysis shows that, independently of the ligand used, most of the complexes contain the rigid square planar [NiL sub(4)] super(2+) (1-5) or [Ni(HL') sub(4)] super(2+) (6-10) cation, which seems to have an impact on the self-assembly process by adopting a structure-directing role: the supramolecular assembly is organized around the rigid bulky cations viainteractions with the surrounding counterion/solvent clusters in each individual structure. The components of the clusters, i.e.OH super(-)/H sub(2)O (1), [NiCl sub(4)] super(2-)/ EtOH (2), Br super(-)/H sub(2)O (3), NO sub(3) super(-)/MeOH (4), ClO sub(4) super(-)/Me sub(2)CO (5), Cl super(-)/H sub(2)O (6), Br super(-)/MeCN (7), I super(-)/Me sub(2)CO/H sub(2)O (8), NO sub(3) super(-)/EtOH/ H sub(2)O (9), and ClO sub(4) super(-)/Me sub(2)CO (10), are held tightly together by strong or weak hydrogen bonding. The structure-directing action of the cations is accomplished viaweak C-H...O/Cl/Br super(-), pi ... pi and C-H... pi interactions (for L-containing complexes) or strong recurring N-H.../Cl super(-)/Br super( -)/I super(-)/O motifs dominating the molecular self-assembly together with weak interactions (for HL'-containing complexes). The variety of the stereochemistries observed among the studied compounds (square planar, 1-10; tetrahedral, 11 and 12; octahedral, 13) seems to advocate the choice of nickel as an interesting candidate in metallosupramolecular research.