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Advances in Coordination Polymers
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Advances in Coordination Polymers

A special issue of Polymers (ISSN 2073-4360).

Deadline for manuscript submissions: closed (30 November 2018) | Viewed by 47063

Special Issue Editors

Prof. Jhy-Der Chen

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Guest Editor
Department of Chemistry, Chung-Yuan Christian University, Chung-Li 320, Taiwan
Interests: inorganic chemistry; metal–metal bonded complexes; coordination polymer
Dr. Yung-Sheng Yen

E-Mail Website
Co-Guest Editor
Department of Chemistry, Chung Yuan Christian University, Chung-Li, Taiwan
Interests: organometallic chemistry and its application in potential materials; dye-sensitized solar cells; perovskite solar cells; optoelectronic sensors
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

This Special Issue focus on the current advances in coordination polymers. Coordination polymers are composed of metal ions and bridging organic ligands as primary constituents linked through covalent bonds and other weak chemical bonds to generate infinite assemblage type of networks. In the case of ordered structures, they can be named as coordination networks or metal-organic frameworks (MOFs). Coordination polymers have attracted a great attention not only due to their potential properties as novel zeolite-like materials for separation, ion exchange and catalysis, but also their intriguing structure and diverse topologies. The applications of structural transformations observed in coordination polymers are significant for sensors and switches.

Papers are sought that discuss the latest research in the area or summarize selected areas of the field. The scope of the Special Issue involves the synthesis, structural characterization, topologies, properties and applications of all type of coordination polymers. Of particular interests are the new structures and functions resulting from the synthesis of the materials featuring specific property, and new insights on the structure-property relationship leading to enhanced functionality.

Prof. Jhy-Der Chen
Guest Editor
Prof. Yung-Sheng Yen
Co-guest Editor

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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Polymers is an international peer-reviewed open access semimonthly journal published by MDPI.

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Keywords

  • Synthesis, structures and topology of coordination polymers
  • Structural transformation in coordination polymer
  • Coordination polymer for catalysis
  • Coordination polymer for optical sensing
  • Coordination polymer for gas capture and storage
  • Coordination polymer for energy transfer
  • Other application of coordination polymer

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Published Papers (11 papers)

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Research

9 pages, 3181 KiB  
Article
Cobalt Nanoparticles Embedded into N-Doped Carbon from Metal Organic Frameworks as Highly Active Electrocatalyst for Oxygen Evolution Reaction
by Jitao Lu, Yue Zeng, Xiaoxue Ma, Huiqin Wang, Linna Gao, Hua Zhong and Qingguo Meng
Polymers 2019, 11(5), 828; https://doi.org/10.3390/polym11050828 - 8 May 2019
Cited by 43 | Viewed by 6157
Abstract
Cystosepiment-like cobalt nanoparticles@N-doped carbon composite named Co-NPs@NC with highly efficient electrocatalytic performance for oxygen evolution reaction was prepared from carbonization of N-doped Co-MOFs. The optimized Co-NPs@NC-600 shows overpotentials of 315 mV to afford a current density of 10 mA·cm−2. Meanwhile, the [...] Read more.
Cystosepiment-like cobalt nanoparticles@N-doped carbon composite named Co-NPs@NC with highly efficient electrocatalytic performance for oxygen evolution reaction was prepared from carbonization of N-doped Co-MOFs. The optimized Co-NPs@NC-600 shows overpotentials of 315 mV to afford a current density of 10 mA·cm−2. Meanwhile, the electrocatalys presents excellent long-term durability. The outstanding electrocatalytic performance can be attributed to the unique cystosepiment-like architecture with high specific surface area (214 m2/g), high conductivity of N-doped carbon and well-distributed active sites. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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12 pages, 5548 KiB  
Article
Hierarchical Ag Nanostructures Fabricated from Silver Coordination Polymers for Antibacterial Surface
by Jin-Song Jung, Su-Joung Ko, Hong-Beom Lee, Su-Bin Lee, Hyoung-Jun Kim and Jae-Min Oh
Polymers 2019, 11(1), 155; https://doi.org/10.3390/polym11010155 - 17 Jan 2019
Cited by 9 | Viewed by 3386
Abstract
A hierarchical silver nanostructure with improved antibacterial property was fabricated utilizing silver coordination polymer. Octadecanethiolate–silver polymer was synthesized to have a layered structure and was coated on silicon wafer by drop-casting method utilizing hydrophobic–hydrophobic interaction. Thus, the silver coordination polymer was calcined under [...] Read more.
A hierarchical silver nanostructure with improved antibacterial property was fabricated utilizing silver coordination polymer. Octadecanethiolate–silver polymer was synthesized to have a layered structure and was coated on silicon wafer by drop-casting method utilizing hydrophobic–hydrophobic interaction. Thus, the silver coordination polymer was calcined under reductive condition to produce zero-valent silver with a hierarchical nanostructure. X-ray diffraction patterns revealed that layered silver coordination polymer successfully transformed to hexagonal silver upon calcination. According to scanning electron and atomic force microscopy, silver coordination polymer with ~145.5 nm size was homogeneously coated on the surface before calcination, and it evolved micrometer-sized lumps and grooves which were composed of ~58.8 nm sized Ag nanoparticles. The hierarchical structure—micrometer lump/groove consisting of Ag nanoparticles—would be advantageous to kill bacteria; micrometer-grooves provide physical condition (pocket for bacteria capture) and the Ag nanoparticles from the neighboring lump endow chemical condition (antibacterial property of released Ag+). The antibacterial activity test on Escherichia coli via colony forming inhibitory assay indeed exhibited an improved antibacterial activity of hierarchical Ag nanostructure compared with the surface simply coated with Ag nanoparticles. From the line profile of atomic force microscopy, the bacterium trapped in the hierarchical Ag nanostructure was shown to interact intimately with Ag surface. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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19 pages, 6002 KiB  
Article
Synthesis, Structures and Electrochemical Properties of Lithium 1,3,5-Benzenetricarboxylate Complexes
by Pei-Chi Cheng, Bing-Han Li, Feng-Shuen Tseng, Po-Ching Liang, Chia-Her Lin and Wei-Ren Liu
Polymers 2019, 11(1), 126; https://doi.org/10.3390/polym11010126 - 12 Jan 2019
Cited by 4 | Viewed by 3748
Abstract
Four lithium coordination polymers, [Li3(BTC)(H2O)6] (1), [Li3(BTC)(H2O)5] (2), [Li3(BTC)(μ2-H2O)] (3), and [Li(H2BTC)(H2O)] (4) [...] Read more.
Four lithium coordination polymers, [Li3(BTC)(H2O)6] (1), [Li3(BTC)(H2O)5] (2), [Li3(BTC)(μ2-H2O)] (3), and [Li(H2BTC)(H2O)] (4) (H3BTC = 1,3,5-benzenetricarboxylatic acid), have been synthesized and characterized. All the structures have been determined using single crystal X-ray diffraction studies. Complexes 1 and 2 have two-dimensional (2-D) sheets, whereas complex 3 has three-dimensional (3-D) frameworks and complex 4 has one-dimensional (1-D) tubular chains. The crystal-to-crystal transformation was observed in 1–3 upon removal of water molecules, which accompanied the changes in structures and ligand bridging modes. Furthermore, the electrochemical properties of complexes 3 and 4 have been studied to evaluate these compounds as electrode materials in lithium ion batteries with the discharge capacities of 120 and 257 mAhg−1 in the first thirty cycles, respectively. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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13 pages, 3352 KiB  
Article
A Three-Dimensional Nickel(II) Framework from a Semi-Flexible Bipyrimidyl Ligand Showing Weak Ferromagnetic Behavior
by Shin-Shan Dong and Chen-I Yang
Polymers 2019, 11(1), 119; https://doi.org/10.3390/polym11010119 - 11 Jan 2019
Cited by 6 | Viewed by 2984
Abstract
A semi-flexible bipyrimidyl ligand, 5,5′-bipyrimidin (bpym), was used for the self-assembly of a transition metal coordination polymer, resulting in the formation of a nickel(II) compound, [Ni(Br)2(bpym)2]n (1) with a three-dimemsional (3D) structure. Single-crystal X-ray analysis showed [...] Read more.
A semi-flexible bipyrimidyl ligand, 5,5′-bipyrimidin (bpym), was used for the self-assembly of a transition metal coordination polymer, resulting in the formation of a nickel(II) compound, [Ni(Br)2(bpym)2]n (1) with a three-dimemsional (3D) structure. Single-crystal X-ray analysis showed that compound 1 crystallizes in the monoclinic space group C2/c and the structure represents a 3D (4,4)-connected bbe topological framework constructed of nickel(II) ions, twisted cis-μ-bpym and planar trans-μ-bpym groups. Magnetic characterization revealed that 1 shows antiferromagnetic coupling between the pyrimidyl-bridged Ni(II) ions along with weak ferromagnetism due to spin canting with a magnetic ordering below Tc = 3.4 K. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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13 pages, 2801 KiB  
Article
Synthesis and Structural Characterization of a Series of One-Dimensional Heteronuclear Dirhodium-Silver Coordination Polymers
by Paula Cruz, Estefania Fernandez-Bartolome, Miguel Cortijo, Patricia Delgado-Martínez, Rodrigo González-Prieto, José L. Priego, M. Rosario Torres and Reyes Jiménez-Aparicio
Polymers 2019, 11(1), 111; https://doi.org/10.3390/polym11010111 - 10 Jan 2019
Cited by 6 | Viewed by 3143
Abstract
Herein, we describe the preparation of heteronuclear dirhodium-silver complexes by reaction between molecular Rh(II)-Rh(II) compounds [Rh2(μ-O2CR)4L2] (R = Me, Ph (1), CH2OEt (2); L = solvent molecules) with paddlewheel [...] Read more.
Herein, we describe the preparation of heteronuclear dirhodium-silver complexes by reaction between molecular Rh(II)-Rh(II) compounds [Rh2(μ-O2CR)4L2] (R = Me, Ph (1), CH2OEt (2); L = solvent molecules) with paddlewheel structure and PPh4[Ag(CN)2]. One-dimensional coordination polymers of (PPh4)n[Rh2(μ-O2CR)4Ag(CN)2]n (R = Me (3), Ph (4), CH2OEt (5)) formula have been obtained by replacement of the two labile molecules in the axial positions of the paddlewheel structures by a [Ag(CN)2]− bridging unit. The crystal structures of 3–5 display a similar arrangement, having anionic chains with a wavy structure and bulky (PPh4)+ cations placed between the chains. The presence of the (PPh4)+ cations hinders the existence of intermolecular Ag-Ag interactions although several C-H····π interactions have been observed. A similar reaction between [Rh2(μ-O2CCMe3)4(HO2CCMe3)2] and PPh4[Ag(CN)2] led to the molecular compound (PPh4)2{Rh2(μ-O2CCMe3)4[Ag(CN)2]2} (6) by replacement of the axial HO2CCMe3 ligands by two [Ag(CN)2]− units. The trimethylacetate ligand increases the solubility of the complex during the crystallization favouring the formation of discrete heteronuclear species. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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15 pages, 3205 KiB  
Article
White-Light-Emitting Decoding Sensing for Eight Frequently-Used Antibiotics Based on a Lanthanide Metal-Organic Framework
by Mingke Yu, Xu Yao, Xinyu Wang, Yuxin Li and Guangming Li
Polymers 2019, 11(1), 99; https://doi.org/10.3390/polym11010099 - 9 Jan 2019
Cited by 23 | Viewed by 4591
Abstract
Developing multi-selective luminescence sensing technology to differentiate serial compounds is very important but challenging. White-light-emitting decoding sensing based on lanthanide metal-organic frameworks (Ln-MOFs) is a promising candidate for multi-selective luminescence sensing application. In this work, three isomorphic Ln-MOFs based on H3dcpcpt [...] Read more.
Developing multi-selective luminescence sensing technology to differentiate serial compounds is very important but challenging. White-light-emitting decoding sensing based on lanthanide metal-organic frameworks (Ln-MOFs) is a promising candidate for multi-selective luminescence sensing application. In this work, three isomorphic Ln-MOFs based on H3dcpcpt (3-(3,5-dicarboxylphenyl)-5-(4-carboxylphenl)-1H-1,2,4-triazole) ligand, exhibiting red, blue, and green emission, respectively, have been synthesized by solvothermal reactions. The isostructural mixed Eu/Gd/Tb-dcpcpt is fabricated via the in-situ doping of different Ln3+ ions into the host framework, which can emit white light upon the excitation at 320 nm. It is noteworthy that this white-light-emitting complex could serve as a convenient luminescent platform for distinguishing eight frequently-used antibiotics: five through luminescence-color-changing processes (tetracycline hydrochloride, yellow; nitrofurazone, orange; nitrofurantoin, orange; sulfadiazine, blue; carbamazepine, blue) and three through luminescence quenching processes (metronidazole, dimetridazole, and ornidazole). Moreover, a novel method, 3D decoding map, has been proposed to realize multi-selective luminescence sensing applications. This triple-readout map features unique characteristics on luminescence color and mechanism. The mechanism has been systematically interpreted on the basis of the structural analysis, energy transfer and allocation process, and peak fitting analysis for photoluminescence spectra. This approach presents a promising strategy to explore luminescent platforms capable of effectively sensing serial compounds. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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13 pages, 3236 KiB  
Article
Paddlewheel SBU based Zn MOFs: Syntheses, Structural Diversity, and CO2 Adsorption Properties
by Ting-Ru Lin, Cheng-Hua Lee, Yi-Chen Lan, Shruti Mendiratta, Long-Li Lai, Jing-Yun Wu, Kai-Ming Chi and Kuang-Lieh Lu
Polymers 2018, 10(12), 1398; https://doi.org/10.3390/polym10121398 - 17 Dec 2018
Cited by 6 | Viewed by 5586
Abstract
Four Zn metal–organic frameworks (MOFs), {[Zn2(2,6-ndc)2(2-Pn)]·DMF}n (1), {[Zn2(cca)2(2-Pn)]·DMF}n (2), {[Zn2(thdc)2(2-Pn)]·3DMF}n (3), and {[Zn2(1,4-ndc)2(2-Pn)]·1.5DMF}n (4), were [...] Read more.
Four Zn metal–organic frameworks (MOFs), {[Zn2(2,6-ndc)2(2-Pn)]·DMF}n (1), {[Zn2(cca)2(2-Pn)]·DMF}n (2), {[Zn2(thdc)2(2-Pn)]·3DMF}n (3), and {[Zn2(1,4-ndc)2(2-Pn)]·1.5DMF}n (4), were synthesized from zinc nitrate and N,N′-bis(pyridin-2-yl)benzene-1,4-diamine (2-Pn) with naphthalene-2,6-dicarboxylic acid (2,6-H2ndc), 4-carboxycinnamic acid (H2cca), 2,5-thiophenedicarboxylic acid (H2thdc), and naphthalene-1,4-dicarboxylic acid (1,4-H2ndc), respectively. MOFs 1–4 were all constructed from similar dinuclear paddlewheel {Zn2(COO)4} clusters and resulted in the formation of three kinds of uninodal 6-connected non-interpenetrated frameworks. MOFs 1 and 2 suit a topologic 48·67-net with 17.6% and 16.8% extra-framework voids, respectively, 3 adopts a pillared-layer open framework of 48·66·8-topology with sufficient free voids of 39.9%, and 4 features a pcu-type pillared-layer framework of 412·63-topology with sufficient free voids of 30.9%. CO2 sorption studies exhibited typical reversible type I isotherms with CO2 uptakes of 55.1, 84.6, and 64.3 cm3 g−1 at 195 K and P/P0 =1 for the activated materials 1′, 2′, and 4′, respectively. The coverage-dependent isosteric heat of CO2 adsorption (Qst) gave commonly decreased Qst traces with increasing CO2 uptake for all the three materials and showed an adsorption enthalpy of 32.5 kJ mol−1 for 1′, 38.3 kJ mol−1 for 2′, and 23.5 kJ mol−1 for 4′ at zero coverage. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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15 pages, 5247 KiB  
Article
Sometimes the Same, Sometimes Different: Understanding Self-Assembly Algorithms in Coordination Networks
by Y. Maximilian Klein, Alessandro Prescimone, Mariia Karpacheva, Edwin C. Constable and Catherine E. Housecroft
Polymers 2018, 10(12), 1369; https://doi.org/10.3390/polym10121369 - 11 Dec 2018
Cited by 7 | Viewed by 2720
Abstract
The syntheses and characterizations of three new ligands containing two 4,2′:6′,4″-tpy or two 3,2′:6′,3″-tpy metal-binding domains are reported. The ligands possess different alkyloxy functionalities attached to the central phenylene spacer: n-pentyloxy in 3, 4-phenyl-n-butoxy in 4, benzyloxy in [...] Read more.
The syntheses and characterizations of three new ligands containing two 4,2′:6′,4″-tpy or two 3,2′:6′,3″-tpy metal-binding domains are reported. The ligands possess different alkyloxy functionalities attached to the central phenylene spacer: n-pentyloxy in 3, 4-phenyl-n-butoxy in 4, benzyloxy in 5. Crystal growth under ambient conditions has led to the formation of {[Co(NCS)2(3)]·0.8C6H4Cl2}n and {[Co(NCS)2(4)]·1.6H2O·1.2C6H4Cl2}n, with structures confirmed by single crystal X-ray diffraction. Both the cobalt(II) center and ligand 3 or 4 act as 4-connecting nodes and both {[Co(NCS)2(3)]·0.8C6H4Cl2}n and {[Co(NCS)2(4)]·1.6H2O·1.2C6H4Cl2}n possess a 3D cds net despite the fact that 3 and 4 contain two 4,2′:6′,4″-tpy and two 3,2′:6′,3″-tpy units, respectively. Taken in conjunction with previously reported data, the results indicate that the role of the alkyloxy substituent is more significant than the choice of 4,2′:6′,4″- or 3,2′:6′,3″-tpy isomer in determining the assembly of a particular 3D net. The combination of Co(NCS)2 with 5 resulted in the formation of the discrete molecular complex [Co(NCS)2(MeOH)2(5)2]·2CHCl3·2MeOH in which 5 acts as a monodentate ligand. The pendant phenyls and both coordinated and non-coordinated 4,2′:6′,4″-tpy units are involved in efficient π-stacking interactions. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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16 pages, 4713 KiB  
Article
Bimetallic Gold-Silver Nanoparticles Supported on Zeolitic Imidazolate Framework-8 as Highly Active Heterogenous Catalysts for Selective Oxidation of Benzyl Alcohol into Benzaldehyde
by Lili Liu, Xiaojing Zhou, Yongmei Yan, Jie Zhou, Wenping Zhang and Xishi Tai
Polymers 2018, 10(10), 1089; https://doi.org/10.3390/polym10101089 - 1 Oct 2018
Cited by 34 | Viewed by 5031
Abstract
The metal-organic zeolite imidazolate framework-8 (ZIF-8) supported gold-silver bimetallic catalysts with a core-shell structure (Au@Ag/ZIF-8 and Ag@Au/ZIF-8) and cluster structure (AuAg/ZIF-8) were successfully prepared by the deposition-redispersion method. Energy dispersive X-ray spectroscopy (EDS) elemental mapping images displayed that in the Au@Ag/ZIF-8 catalyst, Ag [...] Read more.
The metal-organic zeolite imidazolate framework-8 (ZIF-8) supported gold-silver bimetallic catalysts with a core-shell structure (Au@Ag/ZIF-8 and Ag@Au/ZIF-8) and cluster structure (AuAg/ZIF-8) were successfully prepared by the deposition-redispersion method. Energy dispersive X-ray spectroscopy (EDS) elemental mapping images displayed that in the Au@Ag/ZIF-8 catalyst, Ag atoms were deposited on an exposed Au surface, and core-shell structured Au@Ag particles with highly dispersed Ag as the shell were formed. Additionally, the XPS investigation at gold 4f levels and silver 3d levels indicated that the Au and Ag particles of Au@Ag/ZIF-8, Ag@Au/ZIF-8, and AuAg/ZIF-8 were in a zero valence state. Among the resultant catalysts obtained in this study, Ag@Au/ZIF-8 catalysts showed the highest catalytic activity for the selective oxidation of benzyl alcohol, followed by AuAg/ZIF-8 and Au@Ag/ZIF-8. The turnover frequency (TOF) values were in the order of Ag@Au/ZIF-8 (28.2 h−1) > AuAg/ZIF-8 (25.0 h−1) > Au@Ag/ZIF-8 (20.0 h−1) at 130 °C within 1 h under 8 bar O2 when using THF as solvent. The catalysts of Au@Ag/ZIF-8 and Ag@Au/ZIF-8 with core–shell structures have higher benzaldehyde selectivities (53.0% and 53.3%) than the AuAg/ZIF-8 catalyst (35.2%) in the selective oxidation of benzyl alcohol into benzaldehyde. The effect of the solvent, reaction temperature, reaction time, and reaction pressure on benzyl alcohol conversion and benzaldehyde selectivity in benzyl alcohol selective oxidation over Au@Ag/ZIF-8, Ag@Au/ZIF-8, and AuAg/ZIF-8 were also investigated. All of the catalysts showed excellent performance at 130 °C under 8 bar O2 within 1 h when using THF as the solvent in the selective oxidation of benzyl alcohol to benzaldehyde. Moreover, the catalysts can be easily recycled and used repetitively at least four times. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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18 pages, 2815 KiB  
Article
Sponge-Like Water De-/Ad-Sorption versus Solid-State Structural Transformation and Colour-Changing Behavior of an Entangled 3D Composite Supramolecuar Architecture, [Ni4(dpe)4(btc)2(Hbtc)(H2O)9]·3H2O
by Chih-Chieh Wang, Szu-Yu Ke, Kuan-Ting Chen, Ning-Kuei Sun, Wei-Fang Liu, Mei-Lin Ho, Bing-Jyun Lu, Yi-Ting Hsieh, Yu-Chun Chuang, Gene-Hsiang Lee, Shi-Yi Huang and En-Che Yang
Polymers 2018, 10(9), 1014; https://doi.org/10.3390/polym10091014 - 11 Sep 2018
Cited by 8 | Viewed by 3890
Abstract
An entangled composite compound, [Ni4(dpe)4(btc)2(Hbtc)(H2O)9]·3H2O (1), where H3btc = 1,3,5-benzenetricarboxylic acid and dpe = 1,2-bis(4-pyridyl)ethane, has been synthesized and structurally characterized. Single-crystal structural determination reveals that compound [...] Read more.
An entangled composite compound, [Ni4(dpe)4(btc)2(Hbtc)(H2O)9]·3H2O (1), where H3btc = 1,3,5-benzenetricarboxylic acid and dpe = 1,2-bis(4-pyridyl)ethane, has been synthesized and structurally characterized. Single-crystal structural determination reveals that compound 1 consists of four coordination polymers (CPs), with two two-dimensional (2D) (4,4) layered metal-organic frameworks (MOFs) of [Ni(dpe)(Hbtc)(H2O)] and [Ni(dpe)(btc)(H2O)]− anion, and two one-dimensional (1D) polymeric chains of [Ni(dpe)(btc)(H2O)3]− anion and [Ni(dpe)(H2O)4]2+ cation, respectively. The three-dimensional (3D) supramolecular architecture of 1 is constructed via the inter-penetration of inter-digited, double-layered, 2D rectangle-grid MOFs by two 1D coordination polymeric chains, and tightly entangled together via the combination of inter-CPs π–π stacking and hydrogen bonding interactions. The ad-/de-sorption isotherms of 1 for water displays a hysteresis profile with a maximum adsorption of 17.66 water molecules of per molecule unit at relative P/P0 < 0.89. The reversible de-/re-hydration processes in 1 monitored by cyclic water de-/ad-sorption TG analysis and PXRD measurements evidence a sponge-like water de-/ad-sorption property associated with a thermal-induced solid-state structural transformation. The magnetic property of 1 suggests that the ferromagnetic coupling might refer to a stronger inter-Ni(II) interaction, which could be along the btc3− or Hbtc2− ligands; the antiferromagnetic coupling corresponding to the weaker inter-Ni(II) interactions, which could be the dpe ligands for the 2D framework. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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14 pages, 3864 KiB  
Article
Metal(II) Coordination Polymers Derived from Mixed 4-Imidazole Ligands and Carboxylates: Syntheses, Topological Structures, and Properties
by Wei-Dong Li, Jia-Le Li, Xing-Zhe Guo, Zhi-You Zhang and Shui-Sheng Chen
Polymers 2018, 10(6), 622; https://doi.org/10.3390/polym10060622 - 6 Jun 2018
Cited by 11 | Viewed by 4299
Abstract
Four new metal–organic coordination polymers [Cu(L)(mpa)]·3H2O (1), [Co(L)(mpa)]·H2O (2), [Zn(L)(mpa)]·H2O (3), and [Cd(L)(mpa)(H2O)]·H2O (4) were synthesized by reactions of the corresponding metal(II) salts based on [...] Read more.
Four new metal–organic coordination polymers [Cu(L)(mpa)]·3H2O (1), [Co(L)(mpa)]·H2O (2), [Zn(L)(mpa)]·H2O (3), and [Cd(L)(mpa)(H2O)]·H2O (4) were synthesized by reactions of the corresponding metal(II) salts based on mixed ligands of 1,4-di(1H-imidazol-4-yl)benzene (L) and 4-methylphthalic acid (H2mpa), respectively. The structures of the complexes were characterized by elemental analysis, FT-IR spectroscopy, and single-crystal X-ray diffraction. Compound 1 exhibits a binodal 4-connected three dimensional (3D) architecture with (65·8)-CdSO4 topology, while complexes 2 and 3 are isostructural and have two-dimensional (2D) layer structure with (4, 4) sql topology based on the binuclear metal subunits. Complex 4 has the same 2D layer structure with (4, 4) sql topology as complexes 2 and 3, but the inclined interpenetration of parallel sets of layers result in the formation with 2D + 2D → 3D framework. The activated sample 1 shows selective CO2 uptake over N2. The photoluminiscent properties together with quantum yield (QY) and luminescence lifetime are also investigated for complexes 3 and 4 in the solid state at room temperature. Full article
(This article belongs to the Special Issue Advances in Coordination Polymers)
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