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Development of luminescent coordination polymers (LCPs) for effective detection of the environmental pollutants is urgent and important for human health and environmental protection. Three novel Zn-LCPs, {[Zn1(L)(4,4′-bbibp)]–[Zn2(L)(4,4′-bbibp)]}n [YMUN6 (for Youjiang Medical University for Nationalities)], [Zn(L)(1,4-bimb)]n (YMUN7), and [Zn(L)(4,4′-bidpe)]n (YMUN8), were fabricated from flexible dicarboxylic acid 1,3-bis(4′-carboxylphenoxy)benzene (H2L) and different imidazole ligands [4,4′-bbibp = 4,4′-bis(benzimidazol-1-yl)biphenyl, 1,4-bimb = 1,4-bis(imidazol-1ylmethyl)benzene, 4,4′-bidpe = 4,4′-bis(imidazolyl)diphenyl ether] using solvothermal conditions. They were characterized using X-ray diffraction (XRD), infrared (IR), thermogravimetric (TG), powder X-ray diffraction (PXRD), and photoluminescence (PL) spectroscopic techniques. YMUN6 possessed the "ABAB" interpenetrating 2D complanate structure. YMUN7 showed a three-interpenetrating 2D network. YMUN8 displayed a hcb 3-connected 3-fold interpenetrated 2D network. Photoluminescent properties of YMUN6–8 were investigated, and 6–8 served as "turn off" sensors that could detect chlortetracycline (Chl), Ag+, and Cr2O72− in an aqueous solution with simultaneous high efficiency and sensitivity. Notably, the investigation of Ag+ sensing was most focused on lanthanide metal LCPs, and Zn-LCPs have rarely been reported in this direction. Furthermore, selectivity and recyclability were also investigated. [ABSTRACT FROM AUTHOR]

Recently, lots of organic dye adsorbents were introduced; the pollution of water bodies caused by adsorbents was an urgent problem to be solved. The modified metal–organic frameworks with magnetic properties provided a great platform for solving this disadvantage. In this study, a novel magnetic material Fe3O4@PmPD–[Co-BT] (Co-BT = [Co(bcpo)0.5(tib)(H2O)2]n, bcpo = 2,5-bis(4-carboxylphenyl)-1,3,4-oxadiazole, tib = 1,3,5-tris(1-imidazolyl)benzene)) was prepared using Fe3O4 modified by mPDs (mPD = m-phenylenediamine). This material was successfully characterized by transmission electron microscopy (TEM) and powder X-ray diffraction (PXRD), and it was confirmed that Co-BT was adhered to the Fe3O4 surface by PmPDs. The dye adsorption performance of magnetic Fe3O4@PmPD–[Co-BT] was investigated in detail with selectivity, capacity, thermodynamics and kinetics studies, and with respect to influence factors including the pH value, solvent types, and ionic strength. Notably, the saturated adsorption capacity of magnetic Fe3O4@PmPD–[Co-BT] for CR dyes could reach 347.8 mg g−1. The dye removal mechanism was investigated by zeta potential analyses and Fourier transform infrared (FTIR) spectroscopy. [ABSTRACT FROM AUTHOR]

Two novel Co (II)‐ coordination polymers (CPs) based on 2,5‐bis(4‐carboxylpheny)‐1,3,4‐oxadiazole (bcpo), namely [Co/(bcpo)0.5(tib)(H2O)2]n (1) and [Co (bcpo)0.5(bidpe)(H2O)2]n (2) (tib = 1,3,5‐tirs(1‐imidazolyl)benzene, bidpe = 4,4′‐bis (imidazolyl)diphenyl ether) have been synthesized under solvothermal conditions and characterized by powder X‐ray diffraction (PXRD), single crystal X‐ray diffraction, photochemistry as well as electrochemistry. The investigation of the photo‐degradation methyl blue and methyl violet (MB, MV) properties of CPs 1–2 demonstrates that CP 1 shows great performance for the degradation of MB, and CP 2 could efficiently degrade MB/MV. Meanwhile, the possible photo‐degradation mechanism has been proposed and explored. Simultaneously, electrochemistry studies show that both CPs 1 and 2 can catalyze water oxidation under an alkaline condition at the potential around 1.20 V vs. NHE with relatively low overpotential of 330–510 mV vs. NHE. [ABSTRACT FROM AUTHOR]

A novel metal organic framework, namely, {[Zn3(btc)2(bimmb)2.5]·2H2O·CH3CN}n (1) (btc = 1,3,5-benzenetricarboxylic acid), bimmb = 1,4-bis(imidazol-l-ylmethyl) benzene), has been reasonably designed, successfully solvothermally synthesized, and characterized. The complex is characterized by elemental analysis, IR spectroscopy, single-crystal X-ray diffraction, thermogravimetric analysis, and powder X-ray diffraction. Complex 1 exhibits a 5-nodal 3,3,4,4,6-connected 3D framework with a (5·6·7)2(52·8)2(52·92·102)2(53·82·9)2(54·62·72·84·92·11) topology. The photodegradation studies reveal that complex 1 displays highly sensitive photodegradation sensing toward methylene blue, rhodamine B, and methyl violet under UV irradiation. [ABSTRACT FROM AUTHOR]

Two novel 3D functional CPs based on the flexible 4-(4-carboxylphenylmethylthio)benzoic acid ligand have been successively synthesized. Complex 2 that is composed of Co(II), 4,4′-H 2 cpmb and 1,3-Hbib ligand displays good photo-degradation and adsorption properties for the organic dyes. Two new coordination polymers (CPs) based on transition metals, namely [Ni 2 (4,4′-cpmb) 2 (4,4′-bbibp) 2 (H 2 O) 4 ] n (1) and [Co(4,4′-Hcpmb)(1,3-bib)] n (2) (flexible 4,4′-H 2 cpmb = 4-(4-carboxylphenylmethylthio)benzoic acid, rigid 4,4′-bbibp = 4,4′-bis(benzoimidazo-1-ly)biphenyl and 1,3-Hbib = 1,3-bis(1-imidazo-1-ly)benzoic acid), have been designed and successfully synthesized under solvothermal conditions, which have been characterized by elemental analysis, infrared spectra, thermogravimetric (TG) analysis, powder X-ray diffraction (PXRD) and single-crystal X-ray diffraction. Single-crystal X-ray diffraction analysis reveals that 1 features a 3D supermolecular structure in ABAB mode by H bonds (O⋯H⋯O) with a 2-fold interpenetrating sql topology framework and 2 displays a 3D supermolecular framework by H bonds (O⋯H⋯O) with a rarely fes topology. Moreover, the photo-degradation and dye adsorption properties of CPs 1 – 2 have been investigated. Importantly, 2 shows good photo-degradation and dye adsorption properties. [ABSTRACT FROM AUTHOR]

Five novel Cd(II) metal–organic frameworks (Cd-MOFs), namely [Cd6(L)4(1,3-bit)2(H2O)4]n (1), [Cd(HL)(4,4′-bbibp)]n (2), [Cd3(L)2(1,4-bimb)2(H2O)2]n (3), [Cd(HL)(4,4′-bidpe)]n (4) and [Cd3(L)2(1,1′-bbi)(H2O)4]n (5) (flexible H3L = 5-(2-carboxylphenoxy)isophthalic acid, rigid 1,3-bit = 1,3-bis(l-imidazoly)toluene, rigid 4,4′-bbibp = 4,4′-bis(benzoimidazo-1-ly)biphenyl, semi-flexible 1,4-bimb = 1,4-bis(imidazol-l-ylmethyl)benzene, semi-flexible 4,4′-bidpe = 4,4′-bis(imidazolyl)diphenyl ether, and flexible 1,1′-bbi = 1,1′-(1,4-butanediyl)bis(imidazole)) were synthesized employing a rational design approach under solvothermal conditions and further characterized by elemental analysis, IR spectra, thermogravimetric (TG) analysis, powder X-ray diffraction (PXRD), and single-crystal X-ray diffraction. Diversity architectural topologies have been generated by adjusting the N-donor ligands. They exhibit varied structures: 1 displays an unprecedented 6-nodal (3,3,4,4,8,8)-c 3D topology framework with the point Schläfli symbol of (3·4·5)2(32·42·52·66·78·87·9)(32·63·7)(4·64·8)(410·611·87)(43)2; 2 shows a 2-fold interpenetrating 4-connected cds topology with the point Schläfli symbol of (65·8); 3 exhibits an unprecedented 2-nodal (3,8)-c 3D topology network with the point Schläfli symbol of (42·5)2(44·56·610·75·82·9); 4 shows a 4-connected sql topology with the point Schläfli symbol of (44·62); 5 displays a tfz-d topology 2-nodal (3,8)-c 3D network with the point Schläfli symbol of (43)2(46·618·84). The luminescence studies reveal that MOFs 1–5 display highly sensitive and selective fluorescence sensing towards Fe3+ cations, CrO42− anions and molecular acetone. Meanwhile, the targeted dye adsorption properties of MOFs 1–5 are investigated. [ABSTRACT FROM AUTHOR]

Four novel Zn(ii) metal–organic frameworks (MOFs) including {[Zn(L)0.5(bimb)]·2H2O·0.5(CH3)2NH}n (1), {[Zn(L)0.5(bimmb)]·2H2O}n (2), {[Zn(L)0.5(btdpe)]·H2O}n (3), and [Zn(L)0.5(bidpe)]n (4) (H4L = 5,5′-(1,4-xylylenediamino) diisophthalic acid, bimb = 1,4-bis(imidazol-1-yl)-butane, bimmb = 1,4-bis(imidazol-1-ylmethyl)benzene, btdpe = 4,4′-bis(4H-1,2,4-triazol-4-yl)diphenyl ether, and bidpe = 4,4′-bis(imidazolyl)diphenyl ether) were solvothermally prepared and further characterized by elemental analysis, IR spectroscopy, single-crystal X-ray diffraction, thermogravimetric (TG) analysis and powder X-ray diffraction (PXRD). Single-crystal X-ray diffraction analysis showed that complex 1 features a 3-fold interpenetrated bbf topological framework with the Schläfli symbol of (64·82)(66)2. Complex 2 displayed an unprecedented 2-nodal (4,4)-connected 3D framework with the Schläfli symbol of (86), while complexes 3 and 4 showed 3-nodal (2,4,4)-connected (4·8·104)2(4)2(84·10·12)-unprecedented frameworks. Luminescence studies revealed that complexes 1–4 can be used as high selectivity luminescence sensors for sensing Fe(iii) cations, Cr(vi) anions (Cr2O72− and CrO42−) and nitroaromatic compounds. Furthermore, a possible sensing mechanism was investigated in this paper. [ABSTRACT FROM AUTHOR]

• Six new Zn-MOFs were prepared, and there were four Zn-MOFs showing unparalleled topologies frameworks. • The six Zn-MOFs displayed fluorescence quenching effect on Fe3+ ions and tetracycline antibiotic in aqueous solution. • Complex 1 as a bifunctional fluorescent probe material, showed highly sensitive and selective fluorescence quenching property. Either reduced or excessive metal ions level in biological systems might induce serious metabolic diseases, and the abuse of antibiotics has seriously affected the environment. Despite the significant progress in the development of fluorescence probes over the past decade, the ability to sensitively and selectively detect these metal ions and antibiotics remains a pressing problem. Herein, we demonstrated some effective fluorescence probes for sensing metal ions and antibiotics, six novel and stable Zn(II) metal-organic frameworks (Zn-MOFs), namely [Zn 3 (L) 2 (1,4-bimb) 3 ] n (1), [Zn 3 (L) 2 (4,4′-bbibp) 2 (H 2 O) 2 ] n ·2(CH 3 CN) (2), [Zn(HL)(4,4′-bidpe)] n (3), [Zn(HL)(4,4′-bibp)] n (4), [Zn(HL)(3,5′-bip)] n (5) and [Zn(HL)(1,3′-bit)] n (6) (flexible H 3 L = 5-(2-carboxylphenoxy)isophthalic acid, semi-flexible 1,4-bimb = 1,4-bis(imidazol- l -ylmethyl) benzene, rigid 4,4′-bbibp = 4,4′-bis(benzoimidazo-1-ly)biphenyl, semi-flexible 4,4′-bidpe = 4,4′-bis(imidazolyl)diphenyl ether, rigid 4,4′-bibp = 4,4′-bis(imidazolyl)biphenyl, rigid 3,5′-bip = bis(1-imidazoly)pyridine and rigid 1,3-bit = 1,3-bis(l-imidazoly)toluene) have been successfully synthesized via solvothermal conditions and further characterized by IR spectra, elemental analysis, powder X-ray diffraction (PXRD), single-crystal X-ray diffraction, and thermogravimetric (TG) analysis. These Zn MOFs have exhibited diversely architectural frameworks via the assistant N-donor ligands: 1 , 2 , 5 and 6 show unprecedented topological networks, 1 affords a 3-nodal (3, 4, 4)-connect 2-fold interpenetrating topology structure with the Point Schläfli symbol of (5·6·7·92·10) 2 (5·6·7) 2 (5·73·82), 2 shows a 3-nodal (3, 4, 6)-c topology with (4·82) 2 (42·811·10·12)(86), 5 and 6 display 3-nodal (2, 2, 4)-c topology with (2·44·6)(2)(4). 3 and 4 show 4-connected sql topology with (44·62). As expected, Zn MOFs 1 - 6 not only revealed a highly sensitive and selective fluorescence quenching effect on Fe3+ ions in aqueous solution, but also toughed the interference of a myriad of other metal ions. It is noteworthy that they could also be used as luminescent sensors for detection of tetracycline antibiotic. [ABSTRACT FROM AUTHOR]

• Two novel Zn (II) coordination polymers have been successfully prepared and characterized. • An unprecedented topology with 4-nodal 3, 3, 5, 6-c framework. • Chem-sensors with excellent performance for the detection of Fe3+ ions or TC, high selectivity, extra sensitivity. Environmental issues are the great challenge that human beings are suffering from. Development in coordination polymers (CPs) provides a great platform for tracing hazardous substance by fluorescence detection. In this work, two novel Zn-CPs, namely [Zn(1,1′-bbi)(C 2 O 4)] n (1) and [Zn 3 (1,1′-bbi)(L) 2 (H 2 O)] n (2) (flexible 1,1′-bbi = 1,1′-(1,4-butanediyl)bis(imidazole), and H 3 L = 5-(2-carboxylphenoxy)isophthalic acid) have been synthesized under solvothermal conditions, and further characterized by IR spectra, elemental analyses, thermogravimetric (TG) analyses, powder X-ray diffraction (PXRD), and single-crystal X-ray diffraction. Complex 1 displays a sql topological framework; complex 2 shows an unprecedented 4-nodal (3,3,5,6)-c topological network with Point Schläfli symbol (4·5·6) 2 (42·52·62·73·9) 2 (42·52·64·7·84·9·10)(42·5) 2. CPs 1 – 2 possess good application prospect due to their high thermal, and chemical stability. The selective and sensitive fluorescence sensing of 1 – 2 have been investigated towards Fe3+ ions and tetracycline in detail. [ABSTRACT FROM AUTHOR]

Three novel Cu (II) coordination complexes, formulated as [Cu3(C14H8NO3F)2(CH3COO)2]n (1), [Cu2(C14H9NO3F)2(CH3COO)Cl] (2) and [Cu(C14H8NO3F)(CH3OH)2] (3), have been synthesized by 3‐Fluoroanthranilic acid, Salicylaldehyde and Cu (II) salt as sources in different reaction conditions and characterized by single crystal X‐ray diffraction, X‐ray powder diffraction, IR spectroscopy and elemental analysis. Single‐crystal diffraction analysis revealed that the complexes exhibited different coordination modes and conformations which were linked into multidimensional networks through some weak interactions. The biological activities vary greatly on account of the different Cu (II) numbers among the three complexes. In order to discuss the bioactivities, the complexes have been screened for antimicrobial activities against E. coli and S. aureus, antitumor activities against A549 (human lung cancer cells), Hela (human cervical cancer cells) and HepG‐2(human liver hepatocellular carcinoma cells). Their interactions with calf thymus DNA were investigated by UV–visible and fluorescence spectrometry, as well as viscosity measurements. Interestingly, 1 (the rare 3‐core Cu (II) coordination polymer) shows great antibacterial activities and highest DNA binding affinities. Antitumor studies revealed that complex 1 also exhibited highest activity. [ABSTRACT FROM AUTHOR]

One novel metal–organic frameworks (MOFs) has been successfully synthesized under solvothermal condition and characterized by single crystal X-ray diffraction. The electrochemical behaviors of the complex have been studied in 0.1M KOH. Photocatalytic properties have been confired by degrading rhodamine B (RhB), methylene violet (MV), and methylene blue (MB). Possible degradation mechanism and the effect of the variables have been discussed. One novel metal–organic frameworks (MOFs) constructed by one angular ligand and 5-aminoisophthalic acid, namely {[Ni(L)(bpt)(H 2 O)]·2H 2 O} n (H 2 L = 5-aminoisophthalic acid, bpt = 2,5-bis(4-pyridyl)-1,3,4-thiadiazole) has been designed and successfully synthesized under solvothermal condition. This compound was characterized by single crystal X-ray diffraction, elemental analysis, IR spectra, powder X-ray diffraction (PXRD), and thermogravimetric analysis (TGA). Single-crystal X-ray diffraction analysis reveals that the compound possesses a uninodal 3-connected 3D (three-dimensional) hcb topology framework with the point symbol (63). The thermal stabilities and electrochemical behavior in the solid state of the compound have been investigated in detail. Moreover, the photocatalytic degradation of the compound has been investigated. The results show photocatalytic activity of the compound for three dyes is MB > MV > RhB. [ABSTRACT FROM AUTHOR]

Two novel Ni(II) CPs have been successfully synthesized, which could be good candidates for the photocatalytic degradation of organic dyes. • Synthesis of two different Ni(II) coordination polymers by introduction of carboxylic acid ligands. • Frame structure and photodegradation properties of the two complexes have been discussed. • The possible mechanism of photocatalytic degradation of dyes is explored. Two different novel coordination polymers were synthesized under hydrothermal conditions, namely {[Ni(bibp) 3 (H 2 O) 2 ]·2NO 3 ·0.5H 2 O} n (1), [NiL(bibp)] n (2) (H 2 L = 3,3′-azodibenzoic acid, bibp = 4,4′-bis(imidazolyl)biphenyl). Complex 2 is based on the introduction of carboxylic acid ligands on complex 1. These two polymers were characterized by single crystal X-ray diffraction, IR spectra, elemental analysis, powder X-ray diffraction (PXRD), and thermogravimetric (TG) analysis. Single crystal X-ray diffraction analysis showed that complex 1 formed a 3D structure by weak force. Complex 2 possesses a uninodal 4-connected 3D (three-dimensional) sql topology framework with the point symbol (44·62). In addition, the photocatalytic degradation properties of the two complexes are investigated. Significantly, complex 1 is a good photocatalyst for the degradation of organic dyes (RhB/MO), complex 2 is a good photocatalyst for the degradation of organic dyes (MB). And the possible photodegradation mechanism was proposed and explored. [ABSTRACT FROM AUTHOR]