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A novel 3D Zn-based coordination polymer (NH 2 -LCU-110 , LCU names Liaocheng University) with the formula [Zn(L1)(bpea) n (H 2 L1 ​= ​2-aminoterephthalic acid, bpea ​= ​1,2-bis(4-pyridyl)ethane), was hydrothermally synthesized from a flexible nitrogen-containing carboxylic acid ligand with various coordination modes as main ligands and nitrogen-containing auxiliary ligand with different structures. NH 2 -LCU-110 demonstrates an interesting 5-fold interpenetrating diamond structure. Luminescence measurements reveal that this complex has obvious emission enhancement and quenching towards Al3+ and Cu2+, respectively. The mixed matrix membranes (MMMs) incorporating NH 2 -LCU-110 and poly(methyl methacrylate) (PMMA) as well as simple test papers were both prepared for potential application. The MMMs can quickly detect Al3+ and Cu2+ and the original emission could be regenerated by lifting from the analytical solutions, demonstrating its fast response and good selectivity. The sensing mechanism was investigated in details by various measurements and compared with isostructural complex LCU-110 without –NH 2 groups. All observations indicate that introduction of Lewis basic –NH 2 groups can enhance the intermolecular interactions between the frameworks of coordination polymers and sensing analytes (Al3+ and Cu2+). An amino-functionalized coordination polymer NH 2 -LCU-110 exhibits luminescence turn-on/off toward Al3+/Cu2+, and its mixed matrix membranes and test papers were prepared. [Display omitted] • An amino-functionalized coordination polymer was employed as a multiresponsive luminescence sensor. • NH 2 -LCU-110 exhibits luminescence turn-on and turn-off behavior toward Al3+ and Cu2+, respectively. • Mixed matrix membranes (MMMs) and test papers made the detection more simple and convenient. [ABSTRACT FROM AUTHOR]

A novel multifunctional coordination polymer {[Zn(HCOO) (bcbpy)Cl]·H 2 O} n (1) with multiple colour-changing has been synthesized from Zn(NO 3) 2 ·6H 2 O, and viologen ligand 1,1′-bis-((3-carboxylatobenzyl)-4,4′-bipyridinium) dichloride (H 2 bcbpy·2Cl). In coordination polymer (CP) 1 , bcbpy ligands bridge Zn2+ cations to form a 1D wave-like chain. CP 1 exhibited photochromic properties under xenon lamp and blue light irradiation while obtaining a structurally stable light product 1T. CP 1 thermochromic properties can also be observed during heating. 1 showed photo-controlled fluorescence properties during color rendering and decolorization, and its properties were studied. Interestingly, CP 1 can be deposited in filter paper by coating it with a solution of H 2 O. The filter paper can be used as a printing medium without ink. [Display omitted] • CP 1 was synthesized using viologen ligand 1,1′-bis-((3-carboxylatobenzyl)-4,4′-bipyridinium) dichloride (H 2 bcbpy·2Cl). • CP 1 exhibited photochromic properties under xenon lamp and blue light irradiation. • CP 1 obtaining a structurally stable light product 1T after irradiation. • CP 1 can be used as a good ink-free printing medium. [ABSTRACT FROM AUTHOR]

Constructing nanoscale coordination polymers (CPs) with different micro- or nanoscale morphologies and sizes is crucial for the functionalization of CPs-based heterogeneous catalysts. Herein, surfactant polyvinylpyrrolidone (PVP), surface-supported frameworks (filter paper or Ni foam), and Co-based CPs (1), [Co 2 (pdpa)(py) 4 (H 2 O)] n (H 4 pdpa ​= ​5,5'-(pentane-1,2-diyl)-bis(oxy)diisophthalic; py ​= ​pyridine)) were employed to develop highly ordered micro- or nanoscale CPs, achieving microscale 1a (without surface-supported framework) and nanoscale 1b-c (filter paper and Ni foam as surface-supported frameworks for 1b and 1c , respectively). Furthermore, the catalytic performance of nanoscale 1c with spheric particles for the tandem conversion reactions of aromatic nitriles and diamines into imidazoline or tetrahydropyrimidine frameworks was much more prominent than that of large scale 1 , microscale 1a , and nanoscale 1b because of the easily accessible catalytic active sites in the nanoscale spheric particles, which offered a functionalizable platform for the tandem reactions by minimizing the diffusion distance but did little for their activity. By introducing surfactant and surface-supported frameworks, different morphologies and particle sizes of Co-based CPs with micro- or nanoscale 1a-c were constructed and were used as efficient heterogeneous catalysts to execute tandem conversion reactions. [Display omitted] • A new Co-based CPs was constructed under solvothermal conditions. • Co-based CPs with different morphologies and particle sizes were obtained. • The catalytic performance of all the prepared particles for tandem reactions was conducted. [ABSTRACT FROM AUTHOR]

Multistimuli responsive materials based on the viologen coordination polymers have attracted much interest in the past few years due to the increasing demand for smart materials. In this paper, based on a viologen ligand 1-(3-carboxybenzyl)- 4,4′-bipyridinium chloride (Hcbbpy) and zinc(II) ion, a new crystalline complex, namely, {[Zn(cbbpy)Cl 2 ]·H 2 O} n (1) has been designed and synthesized. In complex 1 , every cbbpy ligand as a bridge links two Zn2+ ions via carboxylate O atom and pyridine N atom to extend to a 1D zigzag chain. The 1D chains are extended to 3D supramolecular structure through π···π stacking and hydrogen bonding. More importantly, 1 exhibits fast photochromic behaviors in response to UV and X-ray due to the formation of viologen radicals. Complex 1 also shows photo-modulated luminescence property in the solid state. In addition, complex 1 can be deposited on filter paper and displays the potential application as inkless print material. [Display omitted] • A new viologen complex was successfully synthesized and characterized. • Complex 1 shows fast response to UV light and X-ray irradiation. • Complex 1 can be deposited on filter paper and displays as inkless print material. [ABSTRACT FROM AUTHOR]

[Display omitted] • 1D MWO 4 (M = Mn, Co, Cd) nanomaterials were synthesized by electrospinning method. • CoWO 4 nanotubes exhibited superior efficiency in degrading BPA under UV–Vis–NIR light. • The wide-spectrum responses mechanism for MWO 4 (M = Mn, Co, Cd) were explained by DFT. Broadening the absorption region to near-infrared (NIR) light is critical for the photocatalysis due to the larger proportion and stronger penetration of NIR light in solar energy. In the present paper, one-dimensional (1D) MWO 4 (M = Mn, Co, and Cd) materials synthesized by electrospinning technique, were studied by combining the density functional theory (DFT) with experiment results, which possessed the enhanced light absorption capability within the range of 200–2000 nm. It was proved that in the ultraviolet–visible (UV–Vis) region, the absorption bands of CoWO 4 and MnWO 4 samples were attributed to the metal-to-metal charge transfer mechanism, while the absorption of CdWO 4 sample may be referable to the ligand-to-metal charge transfer mechanism. In the near-infrared (NIR) region, the absorption of CoWO 4 and MnWO 4 primarily originated from the d-d orbital transitions of Mn2+ and Co2+. The photocatalytic experimental results showed that the degradation rates for bisphenol A (BPA) over CoWO 4 , MnWO 4 , and CdWO 4 photocatalysts under UV–Vis/NIR light irradiation for 140 min/12 h were 78.8 %/75.9 %, 23.8 %/21.3 %, 12.8 %/8.7 %, respectively. This research offers the novel insights into the precise construction of tungstate catalytic systems and contributes to the advancement of UV–Vis–NIR full spectrum photocatalytic technology, and lays a foundation for a cleaner and more environmental-friendly future. [ABSTRACT FROM AUTHOR]

[Display omitted] • Coordination of four metal ions with the chelator APP and functionalized carbon nanotubes leads to supramolecular polymers as electrode material. • MWCNT-APP-Fe integrates the functions of each component in supramolecular polymer. • Dual energy storage mechanism boosters the high capacity and rate capability for MWCNT-APP-Fe-based supercapacitor. In this paper, we prepared the supramolecular polymers (MWCNT-APP-s) with a dual energy storage mechanism as the electrode materials by the coordination of four transition metal ions with the small molecule chelator (APP) and functionalized carbon nanotubes, respectively. Among four MWCNT-APP-s, MWCNT-APP-Fe has the characteristics of moderate micropore/mesopore, significant hydrophobicity, redox property and functional groups. Interestingly, the redox reaction of Fe3+/Fe2+ and -C N-/-C N- transformation give MWCNT-APP-Fe an energy storage basis of pseudocapacitance, while MWCNTs and the micro/mesopore structure in MWCNT-APP-Fe provide a double-layer energy storage platform. As expected, on base of the dual energy storage mechanism, the symmetric supercapacitor assembled with MWCNT-APP-Fe has a higher specific capacity (Cs, 421 F g−1 at 1 mV s−1) as well as a long-lasting stability of 94.8% capacity retention with 99% Coulombic efficiency after 10,000 cycles at 20 mV s−1. More notably, the relevant aqueous Zn2+ hybrid supercapacitor provides a high capacity (Cm) of 191 mAh g−1 at 0.5 A g−1 and a long duration of over 2000 cycles at 50 A g−1, with a capacity retention of 92.4%. In summary, MWCNT-APP-Fe with a dual energy storage mechanism enables a potential application as an electrode material for high-performance supercapacitor. [ABSTRACT FROM AUTHOR]

This work reports a universal strategy that functionalizes various metal–organic frameworks by endogenous bioenzyme of glucose oxidase, which achieves monodispersity and water-stability. We further integrate it as a highly efficient nanoplatform for cancer synergistic therapy. Generation of large amounts of reactive oxygen species induces cell apoptosis, and further guarantees good therapeutic effect and anti-migration performance. [Display omitted] The agglomeration of metal–organic frameworks (MOFs) has long been a problem, and achieving stable monodispersity in water remains a great challenge. This paper reports a universal strategy that functionalizes MOFs by using an endogenous bioenzyme namely glucose oxidase (GOx), to achieve stable water monodispersity, and integrates it as a highly efficient nanoplatform for cancer synergistic therapy. Phenolic hydroxyl groups in GOx chain confers robust coordination interactions with MOFs, which not only endows stable monodispersion in water, but also provides many reactive sites for further modification. Silver nanoparticles are uniformly deposited onto MOFs@GOx to achieve high conversion efficiency from near-infrared light to heat, resulting in an effective starvation and photothermal synergistic therapy model. In vitro and in vivo experiments confirm excellent therapeutic effect at very low doses without using any chemotherapeutics. In addition, the nanoplatform generates large amounts of reactive oxygen species, induces heavy cell apoptosis, and demonstrates the first experimental example to effectively inhibit cancer migration. Our universal strategy enables stable monodispersity of various MOFs via GOx functionalization and establishes a non-invasive platform for efficient cancer synergistic therapy. [ABSTRACT FROM AUTHOR]

Single-crystal-to-single-crystal (SCSC) transformation provides a good platform for obtaining new functional coordination polymers. In this study, we demonstrate a violent and rapid structural transformation between two d10 coordination polymers (CPs). The complex 1 [Zn(3,5-thbzc) 2 (C 2 H 6 O) 2 ] transformed into the complex 2 {[Zn(3,5-thbzc) 2 (H 2 O) 2 ]·C 3 H 7 NO·2H 2 O} (where t = tbutyl, hbzc− = 2-Hydroxybenzoato) triggered by deionized water under standard temperature and pressure conditions in solid state. The transformation reaction was confirmed using single-crystal XRD, PXRD and SEM. The results showed that complex 1 adopts a bidentate chelate six-coordination mode, and complex 2 adopts a monodentate four-coordination mode. SEM clearly showed that complex 2 was in the form of random nanowire clusters, suggesting that their transformation required degradation of the entire crystal structure. UV–Vis–NIR spectra were used to calculate the band gaps of complexes 1 and 2 , which demonstrated wide-bandgap semiconductor-like materials with ∼3.2 eV band gap widths. The results of dielectric studies of complex 1 revealed that it possessed a medium dielectric constant (κ = 6.08 at 1 kHz), while complex 2 displayed an even higher dielectric constant (κ = 7.97 at 1 kHz) at room temperature. Interestingly, parent complex 1 exhibited a small ladder-like dielectric anomaly at 188 °C, while progeny complex 2 did not. This paper describes a new strategy for preparing adjustable functional dielectric materials. Through solid-state transformation triggered by deionized water, the parent bidentate six-coordination complex 1 generates the progeny monodentate four-coordination complex 2. This transformation process involves the cleavage and regeneration of coordination bonds. Complex 2 has a high dielectric constant due to the substitution of water ligands. [Display omitted] • Ligand-substituted SCSC transformation between complexes 1 and 2 was triggered by deionized water. • The transformation process involves the cleavage and regeneration of coordination bonds. • The coordination number of Zn2+ changes from six-coordination to four-coordination. • The introduction of H 2 O ligands can significantly improve the dielectric constants of Zn-CPs. • Complex 1 shows a ladder-like dielectric anomaly at 188 °C. [ABSTRACT FROM AUTHOR]

Abstract This paper explains the crystal structure analysis of Ag(I) coordination polymers based on 4-Amino-3-halobenzonitrile ligands. Three coordination polymers of general formula [Ag(L x)]NO 3 , where X = Cl(1), I(3) and [Ag 2 (L x)][NO 3 ] 2 , where X = Br(2), were synthesized and characterized by single crystal X-ray crystallography. The effect of changing the single halogen atom of 4-Amino-3-halobenzonitrile on the crystal packing of a series of Ag(I) coordination polymers was studied. Our results revealed that N-H···O hydrogen bonds play important role in the crystal packing. Nanoparticles of these coordination polymers were also synthesized by ultrasonic irradiation of (1) , (2) and (3) , and characterized using different analytical techniques. Graphical abstract In this paper, we investigated the synthesis and characterization of three new Silver (I) coordination polymers containing 4-Amino-3- halobenzonitrile ligands with different halogen substituents. Herein, Compounds 1, 2 and 3 were synthesized by reaction of AgNO3 with LCl, LBr and LI respectively. These compounds are completely characterized by the elemental analysis, FT-IR spectroscopy and single crystal X-ray crystallography. fx1 [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) have been widely used in filed of electrochemistry. Compared with traditional inorganic porous materials, the polyvalent pyridinecarboxylic acid ligands have many advantages which contains more active sites, flexible coordination mode, adjustable structure. Therefore, it becomes good choice for constructing MOFs materials with excellent performance. In this paper, a novel MOF was synthesized by pyridine polycarboxylic acid ligand and CoCl 2 ·6H 2 O using solvothermal method. The physicochemical properties were characterized by FT-IR, powder diffraction and thermogravimetry. Single crystal X-ray diffraction reveal that MOF-1 crystallizes in monoclinic system with P 2 1 / C space group. The central Co2+ ions have a dual core structure with 5 and 6 coordination, respectively. The carboxyl groups show two kinds of coordination modes μ 2 : η1: η1 and μ 2 : η1: η2, and the pyridine N atoms also coordinate to form a three-dimensional network structure. Electrochemical experiments show that MOF-1 has a lower overpotential (339.4 mV) and Tafel slope (65.3 mV·dec−1) with higher ECSA and better OER kinetics. A large number of exposed active sites indicate that the MOF has higher potential as catalyst for oxygen evolution reaction. [Display omitted] • A Co-MOFs based on pyridine polycarboxylic acid ligand were prepared by a simple hydrothermal method. • Electrochemical test show that the MOFs has a lower overpotential and Tafel slope with higher ECSA and better OER kinetics. • MOFs exhibit a porous three-dimensional network structure. [ABSTRACT FROM AUTHOR]

Urease may rapidly hydrolyze urea, causing a significant amount of ammonia to be released and decreasing the efficacy of urea fertilizers. However, urease inhibitors (UIs) can inhibit the interaction between urease and urea so that ammonium nitrogen can be absorbed by crops for a long time. In this paper, we developed and fabricated two Cu-based coordination polymers (Cu-CPs) to function as UIs by combining two aromatic carboxylic acids and a bis-pyridine-bis-amide ligand, which demonstrate outstanding urease inhibitory efficacy. Cu-CP-1 exhibits a pronounced inhibitory effect on the inhibitory activity of jack bean urease while the semi-inhibitory concentration (IC 50) value was 0.74 ± 0.01 μM, whereas the IC 50 value of Cu-CP-2 was 4.77 ± 0.51 μM. Furthermore, inhibitory activity against urease, kinetic, molecular docking, and comparisons of the title Cu-CPs and other complex-based materials have been comprehensively investigated. More importantly, the oxygen atoms of μ 2 -OH and –COO play important roles in urease inhibition activity. The structure–function relationship were further discussed which indicates that Cu-CPs can be used as a kind of UIs. By using different O-donor second auxiliary ligands, we have designed and synthesized two Cu-based CPs to operate as urease inhibitors which show excellent urease inhibitory activity. [Display omitted] • The development of UIs has been a matter of great concern to researchers. • Two Cu-CPs have been synthesized by using diverse O-donor ligands. • The Cu-CPs are served as UIs and show excellent urease inhibitory activity. • Inhibitory activity, kinetic, molecular docking of the Cu-CPs have been studied. [ABSTRACT FROM AUTHOR]

To search for more high-performance crystalline proton conducting materials and to accelerate the related research progress, in this paper, a one-dimensional coordination polymer (CP), [Co(BBOT) 2 (H 2 O) 3 ·2H 2 O] n (1) (H 2 BBOT = N-benzoyl-N′-(4-benzoxy)thiourea) was firstly prepared by solvent volatilization approach. Subsequently, the thermal, H 2 O and chemical stabilities of the CP were tested and its high structural stability was confirmed. Furthermore, in 1 , a stable solid three-dimensional framework can be constructed by intermolecular H-bonds and stacking interactions between phenyl units. Then, utilizing the AC impedance determination, the dependence of the proton conductivity of this CP on temperature and humidity in the water vapor environment was explored and the positive correlation was verified. Excitingly, the optimized proton conductivity of this compound under specific test conditions (100 °C/98 % relative humidity) can be as high as 10−4 S/cm, being in the forefront of similar crystalline solid materials. Finally, according to the value of activation energy and the characteristics of crystal structure, we speculate on the proton conduction mechanism. Proton conductivity of a CP under variable humidity and temperatures was explored. Its highest proton conductivity can attain up to 10−4 S/cm, and its proton-conduction mechanism was speculated. [Display omitted] • One carboxylate-based Co(II) coordination polymer was prepared. • Its structure was characterized by single-crystal X-ray diffraction. • Its water-assisted proton conduction was explored. • The proton-conducting mechanism was speculated. [ABSTRACT FROM AUTHOR]

In this paper, two unique 3D MOFs, namely, {[Cd 5 (L) 2 (H 2 O) 16 ]·4H 2 O} n (1), {[Pb 5 (L) 2 (H 2 O) 2 ]·6H 2 O} n (2) were obtained by taking advantage of 2,4-di(3′,5′-dicarboxylphenyl)benzoic acid (H 5 L) and Cd(Ⅱ), Pb(Ⅱ) metal ions under solvothermal conditions. The coordination diversity of the H 5 L ligand gives rise to two distinct coordination modes in 1 – 2 , which contributes to the MOFs with multifarious structures. Complex 1 exhibits a 3D 5-connected topology, and Cd(Ⅱ) metal ions of 1 show three different coordination geometries. 2 displays a 3D (2,3,4,7)-connected net on the basis of penta-nuclear [Pb 5 (μ 1 -COO) 5 (μ 2 -COO) 5 ] clusters, as well the structure of complex 2 contains specific 1D Pb– O –Pb chains. A room temperature, 1 – 2 shows eminent solid-state luminescence properties and the maximum emission peaks are ∼416 ​nm & ∼429 ​nm respectively. At the same time, due to the luminescence quenching effect of complex 1 , it reveals excellent selectivity and sensitivity for Fe3+ cations and Cr 2 O 7 2− anions with low detection limit. The fluorescence quenching mechanisms of complex 1 were also lucubrated. In this paper, two unique 3D MOFs, namely, {[Cd 5 (L) 2 (H 2 O) 16 ]·4H 2 O} n (1), {[Pb 5 (L) 2 (H 2 O) 2 ]·6H 2 O} n (2) were obtained by taking advantage of 2,4-di(3′,5′-dicarboxylphenyl)benzoic acid (H 5 L) and Cd(Ⅱ), Pb(Ⅱ) metal ions under solvothermal conditions. The coordination diversity of the H 5 L ligand gives rise to two distinct coordination modes in 1 – 2 , which contributes to the MOFs with multifarious structures. Complex 1 exhibits a 3D 5-connected topology, and Cd(Ⅱ) metal ions of 1 show three different coordination geometries. 2 displays a 3D (2,3,4,7)-connected net on the basis of penta-nuclear [Pb 5 (μ 1 -COO) 5 (μ 2 -COO) 5 ] clusters, as well the structure of complex 2 contains specific 1D Pb– O –Pb chains. A room temperature, 1 – 2 shows eminent solid-state luminescence properties and the maximum emission peaks are ∼416 ​nm & ∼429 ​nm respectively. At the same time, due to the luminescence quenching effect of complex 1 , it reveals excellent selectivity and sensitivity for Fe3+ cations and Cr 2 O 7 2− anions with low detection limit. The fluorescence quenching mechanisms of complex 1 were also lucubrated. [Display omitted] • Two novel 3D LMOFs were constructed based on a symmetrical V-shaped rigid pentacarboxylic acid ligand. • Complexes 1 and 2 feature 3D frameworks based on diverse metal chains and clusters with high open metal sites. • 1 – 2 shows eminent solid-state luminescence properties at room temperature. • Complex 1 has high selectivity and sensitivity to detect Fe3+ and Cr 2 O 7 2− ions with low detection limit. [ABSTRACT FROM AUTHOR]

Abstract Four new coordination polymers, namely, [Zn 2 (L) 2 (1,3-bdc)(H 2 O) 2 ] n (1) , [Cd 2 L 2 (Cl) 2 ] n ·0.5nH 2 O (2) , [Cd 2 L 2 (adip)] n ·2nH 2 O (3) , and [CdLCl] n (4) were solvothermally synthesized by reaction of Zn(NO 3) 2 ·6H 2 O, CdCl 2 ·H 2 O with an asymmetrical rigid N-heterocyclic carboxylatic acid (HL), where HL = 1-(4-carboxylphenyl)-3-(prazin-2-yl)-1H-1,2,4-triazole, 1,3-bdc = benzene- 1,3-dicarboxylic acid, H 2 adip = adipic acid, H 2 glu = glutaric acid. Compound 1 is a 1D ladder chain. Compound 2 is a (3,6)-connected network with the Point symbol of (42·6) 2 (44·62·88·10). Compound 3 displays a intriguing (3,3,4,4)-connected topological net with the Point symbol of (4·64·8)(4·72)(42·6·72·9)(42·6). Compound 4 presents a new (3,5)-connected topological net with the Point symbol of (3·4·5)(32·4·5·62·74). In addition, the thermal stabilities and photoluminescence properties of these compounds were also studied. Dramatically, compound 3 shows the high selectivity and sensitivity for Fe3+ cation via a luminescence quenching effect. Graphical abstract In this paper, we have synthesized four new Zn/Cd compounds based on HL, namely, [Zn 2 (L) 2 (1,3-bdc)(H 2 O) 2 ] n (1) , [Cd 2 L 2 (Cl) 2 ] n ·0.5nH 2 O (2) , [Cd 2 L 2 (adip)] n ·2nH 2 O (3) , [CdLCl] n (4). Meanwhile, the luminescence properties and thermal stabilities of 1 – 4 were also studied. Compound 3 shows the high selectivity and sensitivity for Fe3+ cation, via a luminescence quenching effect. fx1 Highlights • Four new coordination polymers were solvothermally synthesized. • HL ligand displays multiple coordination modes. • Compound 3 shows the high selectivity and sensitivity for Fe3+ cation. [ABSTRACT FROM AUTHOR]

In this paper, two new H 2 ZTO-Co(II) coordination polymers (H 2 ZTO = 4,4′-azo-1,2,4-triazol-5-one), [Co(H 2 ZTO) 2 (H 2 O) 4 ](NO 3 ) 2 (1) and {[Co(H 2 ZTO)(H 2 O) 4 ](NO 3 ) 2 ·2H 2 O} n (2), have been synthesized and characterized. Polymer 2 is derived from 1 and undergoes a multistage transformation by soaking 1 in distilled water. X-ray single crystal structure analyses showed that 2 exhibit a one-dimensional (1D) chain geometry coordinated by 0D units of 1 through uncoordinated nitrogen atoms of H 2 ZTO ligands. The thermal decomposition behaviors and magnetic properties of 1 and 2 were discussed. In addition, the low-temperature (1.9–300 K) heat capacities of 1 and 2 were measured using the heat capacity option of a Quantum Design Physical Property Measurement System (PPMS). The thermodynamic functions of 1 in the experimental temperature range were derived by fitting the heat capacity data to a series of theoretical and empirical models. Using the fitted heat capacity results, the standard molar entropy and standard molar enthalpy have been respectively calculated to be (871.1 ± 8.7) J·mol −1 ·K −1 and (132.7 ± 1.3) kJ·mol −1 for 1 . [ABSTRACT FROM AUTHOR]

Two water-stable Cd(II)-MOFs, [CdL 0.5 (H 2 O)] (1) and {[Cd 3 (H 2 L)(dtb) 2 (H 2 O)]·3H 2 O} n (2) [H 4 L ​= ​1,1'-(ethane-1,2-diyl)bis (1H-imidazole-4,5-dicarboxylic acid); H 2 dtb ​= ​1,4-di (1H-tetrazol-5-yl)benzene) has been hydrothermally synthesized and characterized by elemental analyses, IR, TG, and X-ray single-crystal diffraction. Complex 1 exhibits a 3D 6-connected framework based on L4− ligands μ 6 -linking [Cd 2 O 2 ] unit, and complex 2 possesses a 3D (3,8)-connected porous framework built by H 2 L2− and dtb2− ligands bridging [Cd 3 O 2 ] units. The luminescence properties were investigated, showing that 1 and 2 can display high sensitivity and selectivity for detecting Fe3+, Cr(VI) and MnO 4 − ions in aqueous solutions via luminescence quenching effects. Furthermore, possible sensing mechanism was investigated in this paper. Two water-stable luminescent Cd(II)-MOFs has been hydrothermally synthesized by using a new flexible ligand (H 4 L) containing two H 2 IDC groups. Complex 1 exhibits a 3D 6-connected framework based on L4− ligands μ 6 -linking [Cd 2 O 2 ] unit, and complex 2 possesses a 3D (3,8)-connected porous framework built by H 2 L2− and dtb2− ligands bridging [Cd 3 O 2 ] units. Luminescence sensing performances reveal that two complexes behave satisfactory recognition and detection effect toward Fe3+, Cr(VI) and MnO 4 − ions with low detection limit and high sensitivity, which may be acted as potential multi-responsive luminescence sensing materials. Furthermore, possible sensing mechanism was investigated in this paper. [Display omitted] • A new ligand containing two H 2 IDC groups was firstly employed to construct MOFs. • Two water-stable Cd(II)-MOFs have been hydrothermally synthesized. • Complexes 1 and 2 exhibited 3D porous frameworks, respectively. • Both 1 and 2 displayed potential multi-responsive luminescence sensing capabilities. [ABSTRACT FROM AUTHOR]

In this paper, two isostructural Co/Ni-based coordination polymers [Co(Htzbt)(bpy)] n (1) and [Ni(Htzbt)(bpy)] n (2) have been synthesized by solvothermal method using 2-(1H-1,2,4-triazol-1-yl)benzene-1,3,5-tricarboxylic acid (H 3 tzbt) and 4,4′-Bipyridine (bpy) as mixed ligands. The two compounds exhibited three dimensional (3D) pillared-layer structure and relative high water-stability. Interestingly, through rationally selection of functional ligand and metal ions, isolated N sites and carboxylic acid sites as well as unsaturated metal sites were combined in the structure of the final compounds. Benefit from these multiple active centers in the framework, the as-synthesized compounds exhibit enhanced catalytic activity in both cycloaddition of CO 2 with epoxides and hydrogenation of 4-nitrophenol (4-NP) to 4-aminophenol. In particular, compound 1 showed superior catalytic performance under mild conditions. Additionally, 1 could maintain relative high efficiency for at least four cycles, exhibiting potential application in practical catalysis. In this paper, two isostructural 3D pillared-layer Co/Ni-based coordination polymers, namely [M(Htzbt)(bpy)] n (M ​= ​Co2+, 1 ; M ​= ​Ni2+, 2) have been synthesized, which show good catalytic activity in both cycloaddition of CO 2 with epoxides and hydrogenation of 4-nitrophenol to 4-aminophenol, due to the multiple active sites inside their structures. Image 1 • Two Co/Ni-based coordination polymers have been successfully synthesized based on H 3 tzbt and bpy ligands. • The two compounds ​present similar 3D pillared-layer frameworks, which are stable against hot and humid conditions. • Multiple active centers have been designed within the frameworks as potential catalytic sites. • The two compounds ​also exhibit good catalytic properties. • The unique structures endow ​the compounds ​with multifunctional applications. [ABSTRACT FROM AUTHOR]

In this paper, we reported the fabrication of Co-embedded nitrogen-doped carbon nanotube (Co-NCNT) by using Co-melamine coordination polymer (CP) as precursor. The sample was well characterized via SEM, TEM, XRD, XPS and BET methods. The Co-NCNT shows excellent and stable catalytic performance for OER. The overpotential of Co-NCNT at 10 mA cm -2 is 370 mV (vs RHE). The current density of Co-NCNT could reach 100 mA cm -2 at overpotential of 520 mV, which showed much better performance than RuO 2 , while the largest current density of RuO 2 could reach is only 44 mA cm -2 . The Tafel slope of Co-NCNT is 56 mV dec -1 , which is smaller than that of commercial RuO 2 (58 mV dec -1 ). The results indicate that metal-melamine based CPs or MOFs can be promising precursors for the preparation of efficient metal-embedded nitrogen-doped carbon materials for electrocatalysis. [ABSTRACT FROM AUTHOR]

In this paper, two novel 1D uranyl coordination polymers, [(UO 2)(HPDTC)(H 2 O)]Cl (1) and [(UO 2)(DPA)(H 2 O) (2) based on pyridine acid have been synthesized using hydrothermal method. The structure was obtained with the help of a Single Crystal X-ray diffraction meter and further characterized by IR, UV–vis, TG and others. The compounds show good luminescence properties and the uranium center exhibits the same pentagonal bipyramid coordination geometry among the compounds. Their electrochemical properties have been investigated through Cyclic Voltammetry (CV) and Galvanostatic Charge/Discharge (GCD). It reveals the counterion ions in compound 1 improve the electrical properties as the capacity is 56.94 ​F ​g−1. Two novel 1D uranyl coordination polymers based on pyridine acids have been synthesized using the hydrothermal method and further characterized by IR, UV–vis, TG and others. The uranium center of the two compounds exhibits the same pentagonal bipyramid coordination geometry according to the results of the Single-crystal X-ray diffraction. Their electrochemical properties have been investigated through Cyclic Voltammetry (CV) and Galvanostatic Charge/Discharge (GCD), and it reveals the counterion ions in compound 1 improve the electrical properties as the capacity is 56.94 ​F ​g−1. [Display omitted] • Two novel uranium derivatives based on pyridine carboxylic have been synthesized. • The compounds with charming fluorescence properties because of the uranium. • The electrochemistry properties were studied and compound 1 with a capacity of 56.94 Fg-1. [ABSTRACT FROM AUTHOR]

A new XRD experiment and crystal structure refinement was performed for the earlier published compound in the paper “Heterobimetallic coordination polymers involving 3d metal complexes and heavier transition metals cyanometallates” by Peresypkina et al. (2015) [1]. A choice of a crystal cell taking in consideration the superstructural reflections allowed to obtain more reliable data about the symmetry and bond distances in the heterometallic 2D framework {[Ni(cyclam)] 2 [ReO(OH) 0.5 (MeOH) 0.5 (CN) 4 ]} 2.5+ . Additionally, doubling of the parameter c permitted to get more details about interlayer space. As a result, disordered perchlorate anions and solvate molecules were located. [ABSTRACT FROM AUTHOR]

The synthesis of crystalline homochiral MOF materials is very important for their potential application in enantioselective processes and asymmetric catalysis. In this paper, four novel zinc based chiral boron imidazolate frameworks (BIFs), Zn 2 [BH(2-eim) 3 ](BA) 2 (OH) (BIF-132-BA , 2-eim ​= ​2-ethylimidazolate, BA ​= ​benzoate), Zn[HBH(2-ipim) 3 ](OHBA)(Ac) (BIF-133-OHBA , 2-ipim ​= ​2-isopropylimidazolate, OHBA ​= ​ o -hydroxybenzoate, Ac ​= ​acetate), Zn[HBH(2-ipim) 3 ](PHBA)(Ac) (BIF-133-PHBA , PHBA ​= ​ p -hydroxybenzoate), and Zn[HBH(2-ipim) 3 ](DHBA)(Ac) (BIF-133-DHBA , DHBA ​= ​2,4-dihydroxybenzoate) were prepared via solvothermal synthesis. Single-crystal X-ray diffraction demonstrated that the existence of hydrogen bonds between adjacent chains results in two different structure features of BIF-131 : a chiral ladder-like 1D chain (BIF-133-OHBA) and two supramolecular 2D layers (BIF-133-PHBA and BIF-133-DHBA). Then, the optical activities of as-synthesied crystals were preliminarily studied by circular dichroism (CD) spectroscopy. In addition, because they crystallized in noncentrosymmetric space groups, the powder second-harmonic generation (SHG) measurements were carried out and the SHG response of BIF-133-PHBA was almost comparable to potassium dihydrogen phosphate (KDP). Four novel zinc based chiral boron imidazolate frameworks (BIFs), were prepared from the potential chiral substrate of tridentate boron imidazoate ligands. The solid-state CD spectra indicate that the as-synthesized crystals of are optically active. Furthermore, due to their noncentrosymmetric space group, samples of BIF-133-PHBA were selected for the SHG measurements, which is the first example for BIFs used in NLO materials. [Display omitted] • Four novel zinc based chiral boron imidazolate frameworks (BIFs), were prepared from the potential chiral substrate of tridentate boron imidazoate ligands. • The solid-state CD spectra indicate that the as-synthesized crystals of are optically active. • The first examples for BIFs used in NLO materials. [ABSTRACT FROM AUTHOR]

Abstract: One new compound, [Ag(p-bix)]3[Ag(Hbtc)2]·2H2O (H3btc=1,2,4-benzenetricarboxylate, p-bix=1,4-bis(imidazol-1-ylmethyl)-benzene), has been synthesized under hydrothermal conditions and characterized by elemental analysis, IR, PXRD, luminescent analysis, and single-crystal X-ray diffraction. X-ray structural analysis revealed that 0-D unit [Ag(Hbtc)2]3− and two kinds of 1-D linear chain [Ag(p-bix)] ∞ +, can be found within the crystal structure. The combination of 0-D [Ag(Hbtc)2]3− unit and 1-D undulated chain [Ag1(p 1-bix)] ∞ + through weak Ag–O bond gave rise to 2-D anionic supramolecular doublelayer. Then the grids of the 2-D layer are threaded by 1-D linear cationic chain [Ag2(p 2-bix)] ∞ + to generate entangled 3-D architecture with unusual poly(pseudo-rotaxane)-type arrangements. Luminescent properties of the title complex were also studied in this paper. [Copyright &y& Elsevier]

Abstract: Two new energetic compounds, [M(BTE)(H2O)5] n (M=Sr(1), Ba(2)) [H2BTE=1,2-bis(tetrazol-5-yl)ethane], have been hydrothermally synthesized and structurally characterized. Single-crystal X-ray diffraction analyses reveal that they are isomorphous and exhibit 2D (4,4) net framework, generated by 4-connected Sr2(H2O)10/Ba2(H2O)10 SBUs linked up by two independent binding modes of H2BTE, and the resulting 2D structure is interconnected by hydrogen-bond and strong face to face π–π stacking interactions between two tetrazole rings to lead to a 3D supramolecular architecture. DSC measurements show that they have significant catalytic effects on thermal decomposition of ammonium perchlorate. Moreover, the photoluminescence properties, thermogravimetric analyses, and flame colors of the as-prepared compounds are also investigated in this paper. [Copyright &y& Elsevier]

In this paper, a zinc(II)-based coordination polymer, Zn 2 [(C 6 H 8 (COOH) 2 ] 2 (1) [(C 6 H 8 (COOH) 2 ​= ​1,2-cyclopentanedicarboxylic acid, CPDA)], was successfully synthesized by solvothermal method. Thereafter, 1 was characterized by single crystal and powder X-ray diffraction, elemental analysis, thermogravimetric analysis and infrared spectrum techniques. In the hypoglycemic experiment, the results showed that 1 could effectively increase the glucose uptake in insulin resistance (IR)-type HepG2 cells. Besides, 1 displayed favorable antidiabetic activity in contrast to the Zinc nitrate and the CPDA ligand. The mechanism of 1 to alleviate insulin resistance might be related to the reduction of the intracellular reactive oxygen species (ROS) level and the regulation of the ROS/JNK/AKT signaling pathway. Zn 2 (CPDA) 2 alleviated the insulin resistance by reducing of the intracellular reactive oxygen species (ROS) level and the regulation of the ROS/JNK/AKT signaling pathway. [Display omitted] •A zinc-based coordination polymer, [Zn 2 (CPDA) 2 ] (1), was synthesized. • 1 was found to have high antidiabetic effect to HepG2 cells. •The antidiabetic mechanism might be related to the ROS production. [ABSTRACT FROM AUTHOR]

The three multi-dimensional coordination polymers, [Mn 2 (μ 4 -dttpa)(μ 6 -dttpa)(H 2 O) 2 ] n (1), {[Co(μ 4 -dttpa)(H 2 O) 2 ]·2H 2 O} n (2), and {[Zn 3 (μ 4 -dttpa) 2 (μ 2 -dttpa)(phen) 2 (H 2 O) 2 ]·2H 2 O} n (3) (H 2 dttpa ​= ​2,5-di(1H-1,2,4-triazol-1-yl)terephthalic acid; phen ​= ​1,10- phenanthroline), are successfully synthesized and characterized by X-ray single crystal diffraction, powder X-ray diffraction (PXRD), FT-IR spectra, elemental analysis and thermogravimetric analysis. Structurally, complex 1 is a three-dimensional structure with the 3-nodal Schläfli point symbol of {4·63·82} 2 {42·62·82}{62·84}. Complex 2 displays a two-dimensional network with a 6-connected uninodal net. With the point symbol of {4·62} 2 ·{43·63} 2 ·{44·62}{6}, complex 3 shows the two-dimensional stacking pattern. Temperature-dependent magnetic data of complexes 1 and 2 indicate antiferromagnetic behaviors between adjacent metal ions from 2 ​K to 300 ​K. Further magnetic studies show that the best fitting parameters of comple× 1 are obtained using the dinuclear Mn(II) model. From 50K to 300K, complex 2 displays antiferromagnetism over its mononuclear analogue with the zero-field splitting parameter (|D| ​= ​35.2 ​cm−1). The luminescent intensity of complex 3 is much stronger than that of free ligand (H 2 dttpa) and auxiliary ligand (phen). Moreover, the photoluminescence mechanism of complex 3 has been analyzed by theoretical calculation at ωB97XD/6–311++g(2d,p) level with DFT and TDDFT, which reveals that luminescence emission of 3 is attributed to the ligand-to-ligand charge transfer (π∗ phen -π dttpa2-). Compared with the free ligand, the enhancement of the luminescent intensity of compound 3 might occur due to the construction of Zn(II) ion, dttpa2− and phen increases the efficiency of charge transfer between LUMO and HOMO in the solid state. [Display omitted] • The luminescence mechanism of Zinc(II) compound has been elaborated by DFT and TDDFT analysis. • Summary and comparison of dttpa2− complexes in this paper and published in literature. • A new coordination mode μ 2 -(η1)-(η1) of dttpa2− in the solid state is first published. [ABSTRACT FROM AUTHOR]

Abstract: In this paper, treatment of N-ethyl-benzo[f]quinolium (ebq) iodide and CuI with excess KI afforded an unusual coordination polymer [(ebq)2(Cu3I4)(CuI2)] n (1). 1 crystallizes in tetragonal system, space group P4(2)bc with cell parameters of , , , , , and . A highly interesting feature of 1 is its presence of mixed types of chains [ and chain] in one crystal lattice based on supramolecular self-assembly directed by cations. The infinite chains and in 1 could be described as the edge-sharing arrangement of CuI4 tetrahedron. Furthermore, IR, EA, UV–Vis, thermal analysis and optical limiting measurements were adopted to characterize polymer 1. The optical limiting experiment shows that the present polymer exhibits a large optical limiting capacity. [Copyright &y& Elsevier]

Molecule-based room temperature phosphorescence (RTP) materials have attracted considerable attention owing to their extensive applications in the optoelectronic and biological field. In this paper, two isostructural coordination polymers [Zn 3 (TIB) 2 X 6 ] (X ​= ​Cl, 1-Cl ; X ​= ​Br, 1-Br) have been synthesised and characterized by the assemble of triangular D-A-D ligand 1,3,5-tri(1H-imidazol-1-yl)benzene (TIB) and ZnX 2 salts. The incorporation of halogen atoms play significant role in the formation of abundant C-H···X hydrogen-bonding interactions and dense structures, enable high thermal stability of the two complexes. 1-Br shows phosphorescence lifetime three order of magnitude longer than that of 1-Cl , and obviously phosphorescence emission recognized by naked eyes. The theory calculations reveal complete separation of molecular orbitals between halogen atoms and TIB ligand. Photoelectron response performance have also been studied. This work provides an efficient way to achieve long-last RTP by the incorporation of metal-bromide units in the coordination polymers. Herein, two [ZnX 2 ] based isostructural coordination polymers (X ​= ​Cl, 1-Cl ; X ​= ​Br, 1-Br) have been reported. 1-Br shows obviously phosphorescence emission by naked eyes and lifetime three order of magnitude longer than that of 1-Cl. [Display omitted] • Two [ZnX 2 ] based isostructural MOFs (X ​= ​Cl, 1-Cl ; X ​= ​Br, 1-Br) have been successfully synthesised. • 1-Br shows long-lived phosphorescence lifetime three orders of magnitude longer than 1-Cl. • The long-last yellow-green emission can be directly observed by naked eyes after removing the light source. [ABSTRACT FROM AUTHOR]

Application to the photo catalytic oxidation of orange II under solar lightL. DermÃche, G. Rekhila, C. Rabia and M. TrariContents121973Features of solid-phase mechanochemical synthesis of hydroxyapatite doped by copper and zinc ionsNatalia V. Bulina, Olga B. Vinokurova, Natalia V. Eremina, Igor Y. Prosanov, Vyacheslav R. Khusnutdinov and Marina V. ChaikinaThe paper shows the possibility of solid-phase mechanochemical synthesis of hydroxyapatite doped by copper or zinc ions with a high degree of doping.121963Ab initio prediction of thermoelectric performance of monolayer BiSbTe3Qiong Xia, Qi Xu, Bin Xu and Lin YiOur ZT estimate should be more accurate. Magnetic investigations have suggested that there is antiferromagnetic coupling between neighboring metal ions in the two compounds. [Extracted from the article]

One-pot three-component Arbuzov-type reaction, involving anhydrous cadmium acetate, dimethyl sulfite, and tetraethylammonium iodide, has produced the cadmate salt, [Et 4 N] 2 [Cd(OMs) 4 ] (1) revealing weakly-coordinating methanesulfonate (OMs) ligands inside the metal-coordination sphere. The 'ate' salt 1 was found useful as a precursor in the preparation of coordination polymers with compositions, [Cd(OMs) 2 (MeOH)] n (2) and [Cd(OMs) 2 (H 2 O) 2 ] n (3), when subjected to crystallization in a methanol/chloroform mixture, in dry and ambient conditions, respectively. Compounds 1–3 were characterized by spectroscopic [1H, 13C NMR, FT-IR] techniques, and elemental and thermogravimetric analysis, while the structural attributes of 2 and 3 were investigated using single-crystal X-ray diffraction. The composition of 1 was further scrutinized by electrospray-ionization mass-spectrometry (ESI-MS). The crystal structure of 2 exhibits formation of a two-dimensional (2-D) layer facilitated by the bidentate (μ 2) and tridentate (μ 3) modes of coordination of sulfonate ligands around the metal center. The structure of 3 demonstrates the formation of 1-D linear chains, comprising of eight-membered cyclic [−Cd–O–S–O−] rings, owing to the bridging bidentate (μ 2) mode of coordination of the sulfonate ligands. The involvement of hydrogen-bond interactions in 2 and 3 further perpetuates the assemblies into 2-D and 3-D supramolecular coordination polymers, respectively. This paper reports noticeable features such as, (a) cadmate dianion was afforded by the in situ generation of methanesulfonate ligands and subsequent complexation to the Cd(II) atom; (b) ability of alkanesulfonate ligand to display flexible coordinating behaviour [(μ 2 and uncommon (μ 3)] and prolific H-bond acceptor; (c) competitive ligation between strong coordinating solvents (MeOH and H 2 O) and weakly-coordinating methanesulfonate ligands; (d) effect of types and number of solvent molecules around the metal center with their participation in non-covalent interactions in bringing variation in the structural outcome; (e) the values of distances of Cd–O bonds in 1 and 2 fall in the range of 2.24 Å to 2.29 Å, suggesting the presence of direct metal-sulfonate interactions. The dispersion-corrected density functional theory (DFT-D) and Bader's quantum theory of atoms in molecule (QTAIM) (primary and secondary) studies explored the structures, electronics, and non-covalent interactions of compounds 2 and 3. Additionally, among different involved non-covalent interactions, Hirshfeld surface analysis emphasized the presence of O⋯H/H⋯O contacts as the dominant intermolecular non-covalent interactions as the consolidating factor in crystal packing, in both compounds. Structural variations in Cd(II) coordination polymers based on weakly-coordinating methanesulfonate ligand are tuned by the combined effect of solvents, ligand coordination modes, and non-covalent interactions. Image 1 • Synthesis and characterization of a new cadmate salt used for the construction of coordination polymers. • The compounds are characterized by FT-IR, 1H, 13C, elemental techniques. • Crystallographic study reveals direct Cd(II)-methanesulfonate bonds and non-covalent interactions in construction of 2D/3D supramolecular motifs. • Structural outcomes depend upon the combined effect of solvent molecules, ligand coordination, and non-covalent interactions. • DFT and Hirshfeld surface study are used to understand structural and non-covalent interactions. [ABSTRACT FROM AUTHOR]

[Display omitted] • The iron-based catalyst Fe-N/O@C with Fe-N 2 O 2 coordination was prepared by a simple pyrolysis process. • The Fe-N/O@C + PMS system achieves the degradation of BPA primarily through non-radical pathways dominated by 1O 2 and high-valent iron species. • The doping of O causes a change in the charge distribution of Fe-N. • DFT calculations were used for further analysis to understand the reasons behind the differences in the degradation pathways of Fe-N/O@C and Fe-N@C. Iron-nitrogen co-doped carbon materials as heterogeneous catalysts have attracted much attention in advanced oxidation processes involving peroxymonosulfate (PMS) due to their unique structure and enormous catalytic potential. However, there is limited research on the influence of different coordination structures on the central iron atoms. Through simple pyrolysis, we introduced oxygen atoms into the Fe-N coordination structure, constructing Fe-N/O@C catalysts with Fe-N 2 O 2 coordination structure, and achieved efficient degradation of bisphenol A (BPA). Quenching experiments, electron paramagnetic resonance, and electrochemical analysis indicate that compared to the free radical activation pathway of Fe-N@C, high-valent iron-oxo species (≡Fe(Ⅳ) = O) are the main reactive oxygen species (ROS) in the Fe-N/O@C/PMS system. Meanwhile, we compared the differences in the oxidation states of Fe atoms and electron density in different coordination structures, revealing the formation of high-valent iron-oxo species and the mechanism of interfacial electron transfer. Therefore, this study provides new insights into the design and development of Fe-N co-doped catalysts for resource-efficient and environmentally friendly catalytic oxidation systems. [ABSTRACT FROM AUTHOR]