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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: The flexible zirconium tetraphosphonate coordination polymer 1 is a very robust coordination polymer because it can be regenerated in H- form using strong acid solutions and ri-exchanged several times without hydrolysis and loss of crystallinity.
Abstract: The flexible zirconium tetraphosphonate coordination polymer with formula Zr(O3PCH2)2N-C6H10-N(O3CH2P)2X2–xH2+x·nH2O (X = H, Li, Na, K, 0 < x < 1, 4 < n < 7.5) (1) possesses an open framework structure with 1D cavities decorated with polar and acids P═O and P—OH groups. 1 has been fully protonated by adding HCl and then subjected to several acid–base ion-exchange reactions with alkaline metals hydroxides. 1 is a very robust coordination polymer because it can be regenerated in H- form using strong acid solutions and ri-exchanged several times without hydrolysis and loss of crystallinity. The flexibility of 1 has been also studied by means of TDXD (temperature dependent X-ray diffraction) evidencing remarkable phase transformations that lead to a different disposition of the water molecules. These transformations also influence the accessibility of the cations on the P–OH groups placed inside the channels and thus the ion-exchange properties. The dependence of the proton conductivity properties on these ph...

83 citations

Journal ArticleDOI
TL;DR: Using reversible polymerization and depolymerization reactions in a single crystal state, the structural frameworks switched between nonporous hexanuclear clusters and porous double-zigzag chains; the magnetic behaviors switched between paramag netism and metamagnetism, respectively.
Abstract: Using reversible polymerization and depolymerization reactions in a single crystal state, we achieved a reversible transformation from a nanocluster to a coordination polymer During the interconversion, the structural frameworks switched between nonporous hexanuclear clusters and porous double-zigzag chains; the magnetic behaviors switched between paramagnetism and metamagnetism, respectively The microporous framework, which had 1D channels 19 A × 36 A in size, exhibited selective gas adsorption of H2 and CO2 over N2

83 citations

Journal ArticleDOI
TL;DR: The self-assembly of metallosupramolecules from reactions of flexible 2-pyridyl ligands and silver salts is described, and the examination of its solution shows that this coordination polymer is formed via the solution-based discrete metallocyclic species.
Abstract: The self-assembly of metallosupramolecules from reactions of flexible 2-pyridyl ligands and silver salts is described. When 1,3-bis(2-pyridyl)propane (L1), tris[(2-pyridyl)methyl]methane (L2), and 1,3-bis(2-pyridyl)-2-tolylpropane (L3) are used in combination with silver ions, novel discrete metallocyclic complexes are formed in crystals. Moreover, the self-assembly of 1,3-bis(2-pyridyl)-2-phenylpropane (L4) with silver nitrate yields a coordination polymer. The examination of its solution shows that this coordination polymer is formed via the solution-based discrete metallocyclic species.

83 citations

Journal ArticleDOI
TL;DR: Cyano-mediated interaction of the alternating high-spin Mn(II) centers and low-spin Ru(III) centers in {Mn[Ru(acac)2 (CN)2 ]2 }n (Hacac=acetylacetone) results in long-range ferromagnetic ordering below 3.6 K.
Abstract: Cyano-mediated interaction of the alternating high-spin Mn(II) centers and low-spin Ru(III) centers in {Mn[Ru(acac)2 (CN)2 ]2 }n (Hacac=acetylacetone) results in long-range ferromagnetic ordering below 3.6 K. This novel Mn(II) Ru(III) coordination polymer, which has a diamond-like structure, was constructed from [Ru(acac)2 (CN)2 ](-) and Mn(2+) ions.

83 citations

Journal ArticleDOI
Lin-Wei Zhang1, Yu Zhang1, Yong-Fan Cui1, Meng Yu1, Wen-Kui Dong1 
TL;DR: In this paper, a 3-EtO salamo H2L with nickel acetate tetrahydrate, lanthanide nitrate hexahydrate (Ln = Sm and Tb) and terephthalic acid (H2bdc) was synthesized.

83 citations


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