Four cobalt(II) coordination polymers based on a flexible N,N鈥?bis(3-pyridinecarboxamide)-1,6-hexane ligand: Modulation of crystal architectures through the substituent groups of isophthalates
文摘
Four cobalt(II) mixed ligand coordination polymers based on the flexible N,N鈥?bis(3-pyridinecarboxamide)-1,6-hexane (3-dpyh) and four isophthalates with different substituent groups, namely [Co(3-dpyh)(5-HIP)(H2O)3]路H2O (rong class="boldFont">1rong>), [Co(3-dpyh)(5-NIP)]路H2O (rong class="boldFont">2rong>), [Co(3-dpyh)(5-MIP)]路H2O (rong class="boldFont">3rong>) and [Co(3-dpyh)0.5(5-AIP)(H2O)]路2H2O (rong class="boldFont">4rong>), have been hydrothermally synthesized and structurally characterized (5-H2HIP = 5-hydroxyisophthalic acid, 5-H2NIP = 5-nitroisophthalic acid, 5-H2MIP = 5-methylisophthalic acid, 5-H2AIP = 5-aminoisophthalic acid). X-ray diffraction analyses reveal that complex rong class="boldFont">1rong> is a chain constructed from a [Co-3-dpyh]n meso-helical chain and 5-HIP anions, in which each 5-HIP anion adopts a monodentate mode coordinating to one Co(II) ion. The isostructural complexes rong class="boldFont">2rong> and rong class="boldFont">3rong> are assembled from 5-NIP and 5-MIP anions, respectively, featuring a 2D 3,5-connected network with the {42路67路8}{42路6} topology, in which the two carboxyl groups of dicarboxylates exhibit 渭1:畏1-畏1 and 渭2:畏1-畏1 modes. When the 5-AIP anion is utilized in rong class="boldFont">4rong>, a different 2D (3,4)-connected {42路63路8}{42路6} network is obtained, in which the two carboxyl groups of AIP exhibit 渭1:畏1-畏1 and 渭1:畏1-畏0 modes, and the N atom of AIP also coordinates to the Co(II) ion. The influence of the substituent groups of the isophthalates on the structures has been discussed in detail. The fluorescent, electrochemical and photocatalytic properties of complexes rong class="boldFont">1rong>-rong class="boldFont">4rong> have also been investigated.