Complexes of a hexa-nitrile dianion with neutral, chelating co-ligands: self-assembly, structure and magnetism |
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Authors: | Kutasi Anna M Turner David R Moubaraki Boujemaa Batten Stuart R Murray Keith S |
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Institution: | School of Chemistry, Monash University, Clayton, Vic. 3800, Australia. |
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Abstract: | Several new first-row transition-metal complexes have been synthesised by combining the polynitrile dianion HCTMCP(2-) (hexacyanotrimethylenecyclopropandiide) with neutral, chelating co-ligands; 2,2'-bipyridine, 1,10-phenanthroline and 3-(2-pyridyl)pyrazole. The products cover a remarkable range of species including mononuclear complexes, dimers, charge-separated species and coordination polymers. Complexes containing 2,2'-bipyridine take the form Mn(2,2'-bipy)(2)(HCTMCP)](2)·2MeOH (1) or M(2,2'-bipy)(3)](HCTMCP) (2Fe and 2Co) which are dimeric and charge-separated products, respectively. The products obtained using 1,10-phenanthroline were the discrete complex Co(HCTMCP)(1,10-phen)(2)(H(2)O)]·H(2)O·MeCN (3) and the 1D coordination polymer Mn(HCTMCP)(1,10-phen)(H(2)O)(MeOH)] (4). Complexes using the 3-(2-pyridyl)pyrazole co-ligand (pypzH) form similar 1D complexes to 4, namely Mn(pypzH)(HCTMCP)(MeOH)(H(2)O)] (5) and M(pypzH)(HCTMCP)(MeOH)(2)] (6Co and 6Fe), albeit with different hydrogen-bonding motifs between the chains. The polymeric HCTMCP complexes show weak to zero antiferromagnetic coupling between metal centres and thus no long-range ordering. |
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