Abstract

Ten coordination polymers constructed from divalent metal salts, polycarboxylic acids, and bis-pyridyl-bis-amide ligands with different donor atom positions and flexibility are reported. They were structurally characterized by single-crystal X-ray diffraction. The ten coordination polymers are as follows: (1) {[Ni(L1)(3,5-PDA)(H2O)3]·2H2O}n (L1 = N,N′-di(3-pyridyl)suberoamide, 3,5-H2PDA = 3,5-pyridinedicarboxylic acid); (2) {[Ni2(L1)2(1,3,5-HBTC)2(H2O)4]·H2O}n (1,3,5-H3BTC = 1,3,5-benzenetricarboxylic acid); (3) {[Ni(L2)(5-tert-IPA)(H2O)2]·2H2O}n (L2 = N,N′-di(3-pyridyl)adipoamide, 5-tert-H2IPA = 5-tert-butylisophthalic acid); (4) [Ni(L3)1.5(5-tert-IPA)]n (L3 = N,N′-di(4-pyridyl)adipoamide); (5) [Co(L1)(1,3,5-HBTC)(H2O)]n; (6) {[Co3(L1)3(1,3,5-BTC)2(H2O)2]·6H2O}n; (7) [Cu(L4)(AIPA)]n (L4 = N,N′-bis(3-pyridinyl)terephthalamide, H2AIPA = 5-acetamido isophthalic acid); (8) {[Cu(L2)0.5(AIPA)]·MeOH}n; (9) {[Zn(L4)(AIPA)]·2H2O}n; and (10) {[Zn(L2)(AIPA)]·2H2O}n. Complex 1 forms a 1D chain and 2 is a two-fold interpenetrated 2D layer with the sql topology, while 3 is a 2D layer with the hcp topology and 4 shows a self-catenated 3D framework with the rare (42·67·8)-hxg-d-5-C2/c topology. Different Co/1,3,5-H3BTC ratios were used to prepare 5 and 6, affording a 2D layer with the sql topology and a 2D layer with the (4·85)2(4)2(83)2(8) topology that can be further simplified to an hcp topology. While complex 7 is a 2D layer with the (42·67·8)(42·6)-3,5L2 topology and 8 is a 2-fold interpenetrated 3D framework with the pcu topology, complexes 9 and 10 are self-catenated 3D frameworks with the (424·64)-8T2 and the (44·610·8)-mab topologies, respectively. The effects of the identity of the metal center, the ligand isomerism, and the flexibility of the spacer ligands on the structural diversity of these divalent coordination polymers are discussed. The luminescent properties of 9 and 10 and their photocatalytic effects on the degradation of dyes are also investigated.

Highlights

  • Owing to the interesting structures of coordination polymers (CPs) and their potential applications in magnetism, luminescence, catalysis, gas storage, and sensing, CPs have been extensively studied and discussed by scientists during recent years [1,2,3,4]

  • Through the self-assembly process, the coordination of spacer ligands to the metal ions may lead to the formation of infinite one-dimensional (1D), two-dimensional (2D), or three-dimensional (3D) CPs

  • We have shown that reactions of the flexible N,N′di(3-pyridyl)suberoamide (L1) with Cu(II) salts in the presence of the isomeric phenylenediacetic

Read more

Summary

Introduction

Owing to the interesting structures of coordination polymers (CPs) and their potential applications in magnetism, luminescence, catalysis, gas storage, and sensing, CPs have been extensively studied and discussed by scientists during recent years [1,2,3,4]. Through the self-assembly process, the coordination of spacer ligands to the metal ions may lead to the formation of infinite one-dimensional (1D), two-dimensional (2D), or three-dimensional (3D) CPs. Judicial choice of the metal-ion template and spacer ligands with diverse functionalities and flexibility may form well-defined frameworks. We have shown that reactions of the flexible N,N′di(3-pyridyl)suberoamide (L1) with Cu(II) salts in the presence of the isomeric phenylenediacetic. The bis-pyridyl-bis-amide (bpba) ligands are intriguing ligands that can be tailored to prepare. Most of the bpba ligands are flexible,

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call