Abstract

Two novel three-dimensional (3D) copper(II) complexes [Cu3(3-bpcb)(1,2-BDC)2(μ2-OH)2] (1) and [Cu2(3-bpcb)1.5(SIP)(μ3-OH)]·H2O (2), based on a rigid bis-pyridyl-bis-amide ligand [3-bpcb=N,N′-bis(3-pyridinecarboxamide)-1,4-benzene] and two different polycarboxylates [1,2-H2BDC=1,2-benzenedicarboxylic acid, NaH2SIP=sodium 5-sulfoisophthalic acid] have been prepared under hydrothermal conditions. Single crystal X-ray diffraction analysis shows that complex 1 exhibits a 4-nodal mixed (3,4,4,5)-connected 3D structure with the (3·4·5)2(3·42·5·86)2(32·8·92·10)(42·82·102) Schläfli symbol, which is constructed from two-dimensional (2D) Cu(II)-μ2-OH-3-bpcb layers (3-bpcb: μ4-bridging coordination mode via two pyridyl nitrogen and two carbonyl oxygen atoms) and the 1,2-BDC bridging ligands. Complex 2 is also a 3D coordination polymer constructed from the μ2-bridging 3-bpcb ligands (via two pyridyl nitrogen atoms) and the 2D Cu(II)-μ3-OH-SIP sheets containing tetranuclear copper clusters, showing a novel 3-nodal (5,6,6)-connected (33·43·53·63·72·8)(33·43·53·6)(33·46·54·62) topology. The differences between the final 3D structures for complexes 1 and 2 might be attributed to the different aromatic polycarboxylates and the bis-pyridyl-bis-amide ligand with different coordination modes. Moreover, the electrochemical behavior of complex 1 and the fluorescence properties of the complexes 1–2 have been investigated.

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