Abstract

Four new coordination polymers, namely, {[Cd(btmx)(BTEC)0.5(H2O)]·H2O}n (1), {[Cd(btmx)1.5(1,2,4-HBTC)]·(H2O)2}n (2), {[Co(btmx)(HBTC)]·2H2O}n (3) and [Co(btmx)(1,4-BDC)]n (4) (btmx = 1,4-bis(1,2,4-triazol-1-ylmethyl)-2,3,5,6-tetramethylbenzene, H4BTEC = 1,2,4,5-benzenetetracarboxylic acid, 1,2,4-H3BTC = 1,2,4-benzenetricarboxylic acid, 1,3,5-H3BTC = 1,3,5-benzenetricarboxylic acid and 1,4-H2BDC = 1,4-benzenedicarboxylic acid) have been obtained under hydrothermal conditions and characterized structurally. Complex 1 is a 3D 3-fold interpenetrating (4,4)-connected net with (4·64·8)(42·62·82) topology. Complex 2 displays a 2D cabinet-like structure with infinite 1D double Cd–btmx chains. Complex 3 possesses a 3D 3-fold interpenetrating 4-connected framework with 66-dia topology. Complex 4 exhibits a (4,6)-connected 3D pillar-layered structure with point symbol of (44·62)(44·610·8). The structural differences of these complexes demonstrate that the flexible ligand btmx and aromatic polycarboxylate anions play critical roles in the formation of the resulting frameworks. Furthermore, the photoluminescent properties of 1 and 2 have been studied in the solid state at room temperature.

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