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Lyall R Hanton

Publications and source records attributed to Lyall R Hanton.

3 recordsLinked to original sources

Helices versus zigzag chains: one-dimensional coordination polymers of Ag(I) and Bis(4-pyridyl)amine.

Five one-dimensional coordination polymers were prepared by the reaction of a bent bridging ligand, bis(4-pyridyl)amine (bpa), with an extensive series of AgX salts (X = CF3SO3, PF6, ClO4, NO3). The 1D polymer networks formed with AgCF3SO3 (1), AgPF6 (2.MeCN), and AgClO4 (3.2MeCN) all incorporated MeCN and were found to adopt a zigzag arrangement. The networks formed with AgClO4 (4) and AgNO3 (5) did not contain any solvent and adopted a single-stranded helical arrangement. Two-dimensional H-bonding networks were formed for 1 and 3.2MeCN, with network topologies 4.8(2) and (4, 4), respectively, whereas three-dimensional H-bonded networks of helices were formed for 4, showing an (8, 3)-a network topology, and 5, showing the topology of the alpha-polonium net. The three-dimensional networks both exhibited 4-fold interpenetration. The NO3- anion in 5 appeared to be acting as a template for the 3D structure.

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Flexible ligands and structural diversity: isomerism in Cd(NO3)2 coordination polymers.

The ligands 1,4-bis(2-pyridylmethylsulfanylmethyl)benzene (L1) and 2,5-bis(2-pyridylmethylsulfanylmethyl)pyrazine (L2) were treated with Cd(NO3)2.4H2O in metal-to-ligand ratios of 1:1 and 2:1, respectively; L2 was also treated with CdCl2.2.5H2O in a 2:1 ratio. All products were found to be coordination polymers. The crystal structures of {[Cd(L1)(NO3)2].CH2Cl2}infinity (1a), {[Cd(L1)(NO3)2].4/3CH3CN}infinity (1b), {[Cd2(L2)(NO3)4].2CH3CN}infinity (2.2CH3CN), and {[Cd2(L2)Cl4].2CH2Cl2}infinity (3.2CH2Cl2) were determined. Compounds 1a and 1b were found to be conformational supramolecular isomers. The structure of 1b displayed topological isomerism with two isomeric polymer chains, 1b(1) and 1b(2), in the one crystal forming a single supramolecular array. The structure of 2.2CH(3)CN showed Cd2(L2) units linked together by nitrates bridging between the Cd(II) centers in a mode previously not seen in Cd(II) compounds. The overall structure of 3.2CH2Cl2 was found to be similar to that of 2.2CH3CN despite the presence of different anions and solvent molecules. Powder X-ray diffraction was used to investigate the nature of bulk preparations of compounds 1-3.

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