RESUMO
Two unprecedented examples of cluster organic frameworks (TBA)3Cu[V6O13(L)2]2·4DEF (2) (TBA)Ag[V6O13(L)2] solvent (3) (TBA = tetrabutylammonium, H3L = tris(hydroxymethyl)-4-picoline, DEF = N, N'-diethylformamide) based on Lindqvist-type polyoxometalate (POM) secondary building units (SBUs) have been constructed successfully. Compounds 2 and 3 are the second cases of cluster organic frameworks based on Lindqvist-type POM cluster SBUs. Furthermore, the cluster organic framework of 2 exhibits efficient electrocatalytic activity and strong durability in oxygen reduction reaction.
RESUMO
A new approach to prepare heterometallic cluster organic frameworks has been developed. The method was employed to link Anderson-type polyoxometalate (POM) clusters and transition-metal clusters by using a designed rigid tris(alkoxo) ligand containing a pyridyl group to form a three-fold interpenetrated anionic diamondoid structure and a 2D anionic layer, respectively. This technique facilitates the integration of the unique inherent properties of Anderson-type POM clusters and cuprous iodide clusters into one cluster organic framework.
RESUMO
In the title compound, [Fe(C(5)H(3)N(2)O(4))(2)](n), each Fe atom lies on a centre of symmetry, in an octahedral coordination environment consisting of two chelate rings [Fe-N = 2.154 (3) A and Fe-O = 2.180 (3) A] and two carboxylate O atoms [Fe-O = 2.111 (2) A] from imidazole-4,5-dicarboxylate ligands. Extensive hydrogen-bonding interactions exist between layers constructed of Fe(4) squares, forming tunnels along the a axis with large voids.
