Cd(ii) coordination polymers constructed from bis(pyridyl) ligands with an asymmetric spacer in chelating mode and diverse organic dicarboxylates: syntheses, structural evolutions and properties. Issue 22 (8th May 2019)

• Record Type: Journal Article
• Authors: Zhu, Li-Na; Deng, Zhao-Peng; Ng, Seik Weng; Huo, Li-Hua; Gao, Shan
• Is Part Of: Dalton transactions. Volume 48:Issue 22(2019)
• Page Start: 7589
• Page End: 7601
• Publication Date: 2019-05-08
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c9dt00840c
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Thirteen Cd(ii ) complexes with diverse chain, (4, 4), (6, 3), (6 3 ), (6 5 ·8), 2-periodic (6, 3) layers, and diverse 3Dvma, irl, cds, eca nets have been synthesized. Abstract : Self-assembly of diverse Cd(ii ) metal salts, four organic dicarboxylic acids, and two flexible bis(pyridyl) ligands leads to the formation of thirteen complexes, namely, [Cd(L1)(C4 H4 O4 )] n (1 ), [Cd(L2)(C4 H4 O4 )0.5 ] n · n OH·8 n H2 O (2 ), [Cd(L1)(C4 H2 O4 )] n (3 ), [Cd(L1)(C4 H2 O4 )] n (4 ), [Cd2 (L2)(C4 H2 O4 )2 (H2 O)2 ] n · n H2 O (5 ), [Cd2 (L1)( m -BDC)2 (H2 O)2 ] n (6 ), [Cd2 (L2)( m -BDC)2 (H2 O)2 ] n (7 ), [Cd3 (L1)2 ( p -BDC)3 (H2 O)4 ] n ·2 n H2 O (8 ), [Cd(L2)( p -BDC)0.5 Cl] n (9 ), [Cd(L2)( p -BDC)0.5 (H2 O)] n · n (ClO4 )· n H2 O (10 ), [Cd3 (L2)2 ( p -BDC)(SO4 )2 (H2 O)6 ] n ·4 n H2 O (11 ), [Cd(L2)( p -BDC)] n · n H2 O (12 ) and [Cd(L2)( p -BDC)] n · n MeOH (13 ) (L1 = N, N ′-bis(pyridin-4-ylmethyl)propane-1, 2-diamine, L2 = N, N ′-bis(pyridin-3-ylmethyl)propane-1, 2-diamine, m -BDC 2− = m -benzene dicarboxylate dianion, p -BDC 2− = p -benzene dicarboxylate dianion), which have been characterized by elemental analysis, IR, TG, PL, and powder and single-crystal X-ray diffraction. The influence of different Cd(ii ) salts on the structure variations and properties has also been investigated. Complexes1 and3 present a (4, 4) layer motif accomplished by the interconnection of adjacent Cd(ii ) cations through L1 molecules and trans -conformational succinates or fumarates. In contrast, the cis -conformational succinates in complex2 only afford the formation of a chain structure. The L1 and L2 molecules in complexes4 and5 adopt the same coordination and join adjacent Cd(ii ) cations together with fumarates, giving rise to different 3D networks withvma andirl topologies. The same coordination mode of L1 and L2 in complexes6–8 joins adjacent Cd(ii ) cations together with aromatic dicarboxylates, leading to different (6 3 )(6 5 ·8), 2-periodic (6·3) and (4·4) layer motifs. The L2 molecules in complexes9–13 present different coordination modes and join adjacent Cd(ii ) cations together with p -BDC 2− dianions to form diverse (6·3) layer motifs, and different 3D networks withcds andeca topologies. Therefore, the diverse coordination modes of the bis(pyridyl) ligand and the feature of different organic dicarboxylate anions can effectively influence the topological structures of these complexes. Luminescence investigation reveals that the emission maximum of these complexes varies from 403 to 433 nm in the solid state at room temperature.