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Coordination polymer

About: Coordination polymer is a research topic. Over the lifetime, 11988 publications have been published within this topic receiving 212219 citations.


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TL;DR: In this article, a novel coordination polymer [Co3(btec)(C2O4)(H2O)2]n (1; btec = 1,2,4,5-benzenetetracarboxylate) has been hydrothermally synthesized and characterized by IR, XPS, XRPD, TG analysis and single-crystal X-ray diffraction.
Abstract: A novel coordination polymer [Co3(btec)(C2O4)(H2O)2]n (1; btec = 1,2,4,5-benzenetetracarboxylate) has been hydrothermally synthesized and characterized by IR, XPS, XRPD, TG analysis and single-crystal X-ray diffraction. The structural analysis reveals that 1 exhibits a new three-dimensional metal-organic framework constructed from two-dimensional parallel interpenetrating networks based on trinuclear cobalt cluster building blocks. Such interpenetrating composite networks in 1 represent the first example in the {M-btec} (M = transition metal) system. Variable-temperature magnetic susceptibility measurements indicate an antiferromagnetic behavior in 1. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

87 citations

Journal ArticleDOI
TL;DR: Reversible construction of a nanoporous framework from a nonporous framework has been found in the zinc(II) coordination polymer with 4,4'-oxybis(benzoate) (oba).
Abstract: Reversible construction of a nanoporous framework from a nonporous framework has been found in the zinc(II) coordination polymer with 4,4'-oxybis(benzoate) (oba). [Zn(2)(oba)(2)(dmf)(2)].2DMF (1), which has 1 nm scale channels, transforms to the nonporous coordination polymer [Zn(oba)(H(2)O)] (2) with the loss of the open framework. Compound 2 on treatment with DMF reversibly yields nanoporous compound 1.

86 citations

Journal ArticleDOI
TL;DR: In this article, a two-dimensional morphology characterizes the nanoflakes obtained in the bottom-up synthesis of a single-crystalline coordination polymer, Ni(HO)[Ni(CN)]×x HO.
Abstract: A two-dimensional morphology characterizes the nanoflakes that are obtained in the bottom-up synthesis of a single-crystalline coordination polymer, Ni(HO)[Ni(CN)]×x HO. The 10 nm-thick nanoflakes are well-dispersed in solution and have a very high accessible surface area (240 m g). Thermal treatment leads to nanoporous NiO with retention of the original flake morphology.

86 citations

Journal ArticleDOI
TL;DR: The results indicate that the donor inclusion has little effect on its antiferromagnetic behavior, whereas dehydration of the compound decreases the strength of the magnetic exchange couplings and results in a change of the antiferromeagnetic transition temperature from 14.7 to 9.8 K.
Abstract: A multifunctional pillared-layer porous coordination polymer, {[Mn(2)(Bpybc)(ox)(2)]8 H(2)O}(n), has been constructed based on a flexible viologen derivative, 1,1'-bis(4-carboxybenzyl)-4,4'-bipyridinium dichloride (H(2)BpybcCl(2)), and an oxalate (ox) coligand. Single-crystal X-ray analysis reveals that the compound possesses multichannels with dimensions of about 6.1x6.6 A along the [110] and [-110] directions and 4.2x7.6 A along [100], and a void space of about 41.4 %. Hydrogen adsorption measurements at 77 K and 1 atm indicate that the compound exhibits a hydrogen uptake of 0.71 wt %. Owing to the incorporation of bipyridinium acceptor units, the compound can selectively accommodate aromatic donors into its nanosized pores based on charge-transfer interactions in an elastic way, and afford a specific color to different guests. Furthermore, the effect of perturbation exerted by the guest molecules on its magnetic properties has been investigated. The results indicate that the donor inclusion has little effect on its antiferromagnetic behavior, whereas dehydration of the compound decreases the strength of the magnetic exchange couplings and results in a change of the antiferromagnetic transition temperature from 14.7 to 9.8 K.

86 citations

Journal ArticleDOI
TL;DR: A single-crystal X-ray diffraction study demonstrates the ability of the unsymmetrical cyclobutane 3,4'-tpcb to self-assemble with Cu(II) ions in [Cu(2)(hfac)(4)(3, 4'-tPCb)](∞) (where hfac is hexafluoroacetylacetonate) to form a solvated 1D coordination polymer.
Abstract: Metallogels form from Cu(II) ions and tetratopic ligand rctt-1,2-bis(3-pyridyl)-3,4-bis(4-pyridyl)cyclobutane. The tetrapyridyl cyclobutane has been synthesized in the organic solid state. The gel forms with a variety of counteranions and gels water. The hydrogel is thixotropic and is composed of nanoscale metal-organic particles (NMOPs), a high surface area of which likely accounts for the gelation of the polar aqueous medium. A shear stress profile of the thixotropic hydrogel gave a yield value of 8.33 Pa. A novel combination of atomic force microscopy (AFM) and scanning transmission X-ray microscopy (STXM) is used to assess the densities of individual NMOPs. A density of 1.37 g/cm(3) has been determined. A single-crystal X-ray diffraction study demonstrates the ability of the unsymmetrical cyclobutane 3,4'-tpcb to self-assemble with Cu(II) ions in [Cu(2)(hfac)(4)(3,4'-tpcb)](∞) (where hfac is hexafluoroacetylacetonate) to form a solvated 1D coordination polymer.

85 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023152
2022360
2021576
2020657
2019663
2018688