3D geometrically frustrated magnets assembled by transition metal ion and 1,2,3-triazole-4,5-dicarboxylate as triangular nodes

Three new chiral metal-organic frameworks, (H2NMe2)[M(tzdc)]center dot 0.5H(2)O [M=Co(II) (1), Mn(II) (2)] and (NH4)[ Mn(tzdc)]center dot 2.6H(2)O (3) (tzdc(3-) = 1,2,3-triazole-4,5-dicarboxylate), have been solvothermally synthesized. In the frameworks of 1-3, the ratio of metal and tzdc(3-) is 1 : 1. Each metal ion is chelated by three tzdc(3-) ligands, and each tzdc(3-) connects three metal ions, resulting in three-dimensional, 3-connected anionic frameworks. 1 and 2 are isomorphous, and both crystallize in the cubic space group P2(1)3. With the template of H2NMe2+ cations, the frameworks of 1 and 2 have a well-known, porous (10,3)-a network. In contrast, 3 can be obtained by replacing the H2NMe2+ with smaller NH4+ cations, which leads to a significant topological change to a unique uniform etd (8,3) network as well as the change of the space group to P6(1). Magnetic studies show dominated antiferromagnetic interactions in 1-3 with theta = -46.8(1), -22.3(1) and -25.8(1) K for 1, 2 and 3, respectively. Due to the triangular arrangement of the metal centres, geometrically spin-frustrated magnetism is a characteristic behaviour of 1-3. For 1, spin-glassy behaviour with a freezing temperature T-f of 2.4 K was distinctly observed, and an empirical factor f = | theta |/T-f approximate to 20 > 10 indicates strong spin-frustration effect. For both 2 and 3, no obvious long-range magnetic ordering and/or spin-glassy behaviour was observed down to 2.0 K, which might indicate the f values in them being also larger than 10. By contrast, the observed spin-glassy behaviour above 2.0 K in 1 is probably due to the stronger magnetic anisotropy of Co( II) ion and the stronger antiferromagnetic interactions in 1.