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Multifunctional materials with a coexistence of proton conduction properties, single–molecule magnet (SMM) behaviors and magneto–optical Faraday effects have rarely been reported. Herein, a new pair of Cu(II)–Dy(III) enantiomers, [DyCu2(RR/SS–H2L)2(H2O)4(NO3)2]·(NO3)·(H2O) (R–1 and S–1) (H4L = [RR/SS] –N,N′–bis [3–hydroxysalicylidene] –1,2–cyclohexanediamine), has been designed and prepared using homochiral Schiff–base ligands. R–1 and S–1 contain linear Cu(II)–Dy(III)–Cu(II) trinuclear units and possess 1D stacking channels within their supramolecular networks. R–1 and S–1 display chiral optical activity and strong magneto–optical Faraday effects. Moreover, R–1 shows a zero–field SMM behavior. In addition, R–1 demonstrates humidity– and temperature–dependent proton conductivity with optimal values of 1.34 × 10−4 S·cm−1 under 50 °C and 98% relative humidity (RH), which is related to a 1D extended H–bonded chain constructed by water molecules, nitrate and phenol groups of the RR–H2L ligand.

Rare-earth doped phosphors with negative thermal expansion (NTE) may display thermally-enhanced emission, but their performance is generally limited. Here the authors report thermally-boosted green upconversion luminescence and near-infrared downshifting luminescence in Sc2(MoO4)3:Yb/Er phosphors with two-dimensional NTE, and their application in temperature sensing.

via simple hydrothermal method, CeO2 was in-situ grown onto the CNTs to form CeO2/CNTs nanocomposites were synthesized with cerium nitrate as Ce resource. The morphology and structure were characterized by transmission electron microscopy and X-ray diffraction. The characterizations reveal that CeO2 nanoparticles are uniformly dispersed onto the surface of the pre-acidified CNTs. The electrochemical property of the synthesized nanocomposite was investigated in 0.1 M KCl electrolyte containing 2 mM [Fe(CN)6]3-/4-. The nanocomposites were employed to fabricate electrochemical sensor for phenol detection. The linear range for phenol detection measured by the differential pulse voltammetry method is 1–500 μM. The sensor also exhibits good selectivity, reproducibility and stability. When applied for the river and tap water analysis, it shows good recovery rate.

Diketopyrrolopyrrole (DPP) is an important type of π-conjugated building block for high-performance organic electronic materials. DPP-based conjugated materials are usually synthesized via Suzuki, Stille, or Negishi cross-coupling reactions, which require organometallic precursors. In this paper, a series of novel phenyl-cored DPP molecules, including five meta-phenyl-cored molecules and four para-phenyl-cored molecules, have been synthesized in moderate to good yields, in a facile manner, through the Pd-catalyzed direct arylation of C−H bonds, and their optoelectrical properties have been investigated in detail. All new molecules have been fully characterized by NMR, MALDI-TOF MS, elemental analysis, UV−visible spectroscopy, and cyclic voltammetry. This synthetic strategy has evident advantages of atom- and step-economy and low cost, compared with traditional cross-coupling reactions.

The construction of multifunctional metal-organic frameworks (MOFs) has attracted considerable attention. Two novel Dy-MOFs namely [Dy2(TPTC-2OMe)1.5(H2O)4·H2O]n (1) and {[Dy2(TPTC-2OMe)(H2TPTC-2OMe) (H2O)2]·2H2O}n (2) were obtained by a solvothermal method using 2′,5′-dimethoxy-[1,1′:4′,1″-terphenyl]- 4,4″-dicarboxylic acid (H4TPTC-2OMe) as the ligand. Structure analysis demonstrates that both MOFs 1 and 2 displayed three-dimensional framework structures, in which MOF 1 was with Dy(III) metal chains as nodes, while MOF 2 was with Dy2 binuclear metal clusters as nodes. Interestingly, MOFs 1 and 2 exhibited high thermal and chemistry stabilities and presented relatively high proton conductivity (σ) values of 1.69 × 10-4 S cm-1 and 3.52 × 10-6 S cm-1 at 50 °C and 98% RH. Although there exist a large number of coordinated or free H2O molecules in both structures, it is easier to form an ordered hydrogen-bonding network between the coordinated H2O molecules in the structure of MOFs, resulting in a more excellent proton conductivity of MOF 1. Moreover, MOF 1 exhibited field-induced single-molecule magnet (SMM) behavior with energy barriers (Ueff) of 37.22 K (τ0 = 9.27 × 10-8 s). Furthermore, MOF 1 exhibits obvious second-order nonlinear optical properties. This research provides guidance for the design of novelty multifunctional MOF materials. [ABSTRACT FROM AUTHOR]

A novel CdII-based two-fold interpenetrated metal--organic framework (MOF), namely {[Cd2(BTDB)2(4,4-bpy)]·DMF}n (JXUST-14), (H2BTDB = 4,4'-(benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzoic acid and 4,4-bpy = 4,4-bipyridine), has been prepared and characterized. Single-crystal structure determination reveals that JXUST-14 has a tetranuclear cluster based 6-connected pcu topological network with Schlafli symbol {412·63}. When soaked in common organic solvents and aqueous solutions with diverse pH values of 2-12 for 48 h, JXUST-14 remains stable. JXUST-14 is a highly selective and sensitive luminescent sensor for L-histidine (His) with a detection limit of 11.1 ppm. JXUST-14 is the first CdII-based MOF for the detection of His via turn-on and fluorescence blue-shift effects. Experimental study and theoretical calculation suggest that the sensing process can be mainly attributed to a charge transfer and energy transfer mechanism. More interestingly, LED lamps of JXUST-14 and JXUST-14@His were successfully developed, which endowed efficient sensitivity for His detection and thus provide great potential for future applications. [ABSTRACT FROM AUTHOR]

Two new cyano-bridged one-dimensional heterobimetallic coordination polymers and a trinuclear complex are synthesized using tailored tricyanometalate precursor. Complex [(bpca)2Fe(super III)2(CN)6Mn(CH3OH)2(H2O)2] displays metamagnetic behavior with a Neel temperature of T(sub N) = 2.2 K and a weak critical field of 250 Oe at 1.8 K.

One-dimensional chiral copper(II) and manganese(II) coordination polymers with single asymmetric end-to-end azide bridges are synthesized, using azide ions as bridging groups and chiral Schiff bases as auxiliary ligands. The findings reveal that they all crystallize in the chiral space group P2I.

The synthesis and properties of a highly conducting neural nickel complex with a pi-conjugated dithiolate ligand, tetrathiafulvalenedithiolate is presented. Results indicated that it has a different packing mode from that of [Ni(tmdt)2] which leads to the variance of conductivity.

The syntheses, crystal structures, and magnetic properties of four one-dimensional cyanobridged heterobimetallic chain complexes are presented. Complexes [(TP)2[Fe.sub.2.sup.III](CN)6Cu(CH3OH).2CH3OH]n and [(TP)2[Fe.sub.2.sup.III](CN)6Cu(DMF).DMF]n ( Tp=tris(pyrazolyl)hydroborate ) show single chain magnets behavior.

The synthesis and characterization of two enantiopure one-dimensional complexes with helical structures, [[M[n.sub.3][((R,R).Salcy).sub.3][([H.sub.2]O].sub.2]Fe[(CN).sub.6].2[H.sub.2]O].sub.n] and [[M[n.sub.3][((S,S).Salcy).sub.3][([H.sub.2]O].sub.2]Fe[(CN).sub.6].2[H.sub.2]O].sub.n] is reported. Magnetic studies reveal both complexes to be ferrimagnets with their magnetic transition temperature at 3 K.

Abstract In corneal epithelium, tight junctions play a vital role in its barrier function. Human cornea is highly susceptible to damage by dust. Continued daily exposure to dust has been associated with increased risks of corneal injury. Studies demonstrated that water extract of dust induced cytotoxicity in human corneal epithelial cells (HCECs); however, its effects on corneal epithelial barrier function are unknown. In this study, we determined the concentrations of heavy metals in water extracts of dust, with office dust having higher concentrations of heavy metals than housedust, and Cu and Zn being highest among metals for both dust. Changes in barrier function and its associated mechanism after exposing HCECs to water extracts of dust at 48 μg/100 μ L for 7 d were evaluated. Water extracts of both dust caused decrease of TEER value (39–73%), down-regulation of gene expression related to tight junction and mucin (0.2–0.8 fold), and loss of ZO-1 immunoreactivity from cellular borders, with office dust having greater potential than housedust to disrupt corneal epithelial barrier function. Our data implied the importance to reduce heavy metals in dust to reduce their adverse impacts on human eyes. Graphical abstract Image 1 Highlights • Human corneas are countinually exposed to dust on a daily basis. • First report on effects of dust water extract on corneal epithelial barrier function. • Extracts decreased TEER value, tight junction and mucin related gene expression. • More loss of ZO-1 immunoreactivity was found in water extract of office dust. • Need to evaluate impact of dust on corneal barrier function. Water extract of office dust had more impact than housedust on disruption of tight junction in normal human corneal epithelial cells. [ABSTRACT FROM AUTHOR]

Six new coordination polymers (CPs) based on the V-shaped 1,3-bis(benzimidazolyl)benzene (bbib) have been synthesized under solvothermal conditions: [Zn(bbib)(ip)]n (1), {[Zn(bbib)(oba)]·solvents}n (2), {[Zn(bbib)(tp)]·DMF}n (3), [Cd(bbib)(ip)]n (4), {[Cd(bbib)(oba)]·H2O·solvents}n (5) and {[Cd(bbib)(tp)]·DMF}n (6) (ip = isophthalate, oba = 4,4′-oxybisbenzoate and tp = terephthalate). Complexes 1-3 display a plane minimal net, (4,4) sheet and a hexagonal plane net, respectively. The structures of 4-6 range from a 1D zigzag chain (4), 2D (4,4) sheet (5) to a 3D "pillar-layer" coordination framework with pcu α-Po topology (6). The structural transition from 1D to 3D among these complexes is realized with the aid of different auxiliary ligands. The results demonstrate that the conformations and coordination modes of dicarboxylate ligands make an impact on the structural diversity of ZnII/CdII coordination polymers. To the best of our knowledge, the CPs based on the bbib ligand have been successfully prepared for the first time. Moreover, complex 2 is a good bifunctional chemosensor for the detection of both Fe3+ and MnO4 - with the detection limits of 3.31 ppm and 8.81 ppm, respectively, indicating that 2 could be used as an efficient fluorescent sensor with high sensitivity and selectivity for Fe3+ and MnO4-. [ABSTRACT FROM AUTHOR]

The effect of dust particle size on the distribution and bioaccessibility of flame retardants (FRs) in indoor dust remains unclear. In this study, we analyzed 20 FRs (including 6 organophosphate flame retardants (OPFRs), 8 polybrominated diphenyl ethers (PBDEs), 4 novel brominated flame retardants (NBFRs), and 2 dechlorane plus (DPs)) in composite dust samples from offices, public microenvironments (PME), and cars in Nanjing, China. Each composite sample (one per microenvironment) was separated into 6 size fractions (F1–F6: 200–2000 µm, 150–200 µm, 100–150 µm, 63–100 µm, 43–63 µm, and <43 µm). FRs concentrations were the highest in car dust, being 16 and 6 times higher than those in offices and PME. The distribution of FRs in different size fractions was Kow-dependent and affected by surface area (Log Kow=1–4), total organic carbon (Log Kow=4–9), and FR migration pathways into dust (Log Kow>9). Bioaccessibility of FRs was measured by the physiologically-based extraction test, with OPFR bioaccessibility being 1.8–82% while bioaccessible PBDEs, NBFRs, and DPs were under detection limits due to their high hydrophobicity. The OPFR bioaccessibility in 200–2000 µm fraction was significantly higher than that of <43 µm fraction, but with no difference among the other four fractions. Risk assessment was performed for the most abundant OPFR-tris(2-chloroethyl) phosphate. The average daily dose (ADD) values were the highest for the <43 µm fraction for all three types of dust using total concentrations, but no consistent trend was found among the three types of dust if based on bioaccessible concentrations. Our results indicated that dust size impacted human exposure estimation of FRs due to their variability in distribution and bioaccessibility among different fractions. For future risk assessment, size selection for dust sampling should be standardized and bioaccessibility of FRs should not be overlooked. [ABSTRACT FROM AUTHOR]

Cancerous human liver cell line has been used to test the hepatic toxicity of indoor dust, showing its organic extract decreases cell viability. However, little is known about its impact on normal human liver cell line. In the present study, we compared the cellular responses between carcinoma cell line (HepG2) and normal cell line (HL-7702) after exposing to 10–640 μg/100 μL organic dust extract for 24 h. The dust extract caused cytotoxicity, oxidative damage, inflammatory response and loss of mitochondrial transmembrane potential (MMP) in both cells. The inhibition of cell viability in HL-7702 cells was stronger than that in HepG2 cells, with HL-7702 cells having lower LC 50 . Higher production of oxidative stress, more loss of MMP and stronger suppression of antioxidant enzymes mRNA level occurred in HepG2 cells, while mRNA expression and hepcidin secretion were enhanced in HL-7702 cells at 40/100 μL, indicating the dust extract probably perturbed their liver Fe homeostasis. Our data showed considerable differences in cellular responses between normal and cancerous cell lines. To obtain accurate data, normal hepatocytes should be employed as they better match with the in vivo tissue than cancerous cell lines. [ABSTRACT FROM AUTHOR]

Human cornea is highly susceptible to damage by dust. Continued daily exposure to housedust has been associated with increasing risks of corneal injury, however, the underlying mechanism has not been elucidated. In this study, a composite housedust sample was tested for its cytotoxicity on primary human corneal epithelial (PHCE) cells, which were exposed to dust at 5–320 μg/100 μL for 24 h. PHCE cell viability showed a concentration-dependent toxic effect, attributing to elevated intracellular ROS. Moreover, when exposed at > 20–80 μg/100 μL, dust-induced oxidative damage was evidenced by increased malondialdehyde and 8-hydroxy-2-deoxyguanosine (1.3–2.3-fold) and decreased antioxidative capacity (1.6–3.5-fold). Alteration of mRNA expression of antioxidant enzymes ( SOD1 , CAT , HO-1 , TRXR1 , GSTM1 , GSTP1 , and GPX1 ) and pro-inflammatory mediators ( IL-1β , IL-6 , IL-8 , TNF-α , and MCP-1 ) were also observed. Furthermore, the mitochondrial transmembrane potential was dissipated from 9.2 to 82%. Our results suggested that dust-induced oxidative stress probably played a vital role in the cytotoxicity in PHCE cells, which may have contributed to dust-induced impairment of human cornea. [ABSTRACT FROM AUTHOR]

The mono- and dinuclear Cu(I) complexes [CuI(PPh)(pmtz)] ( 1) and [{Cu(PPh)}( μ-pmtz)](ClO) ( 2), where pmtz is 3-(2-pyrimidinyl)-1,2,4-triazine, have been synthesized and characterized. Single-crystal X-ray diffraction analysis reveals that the pmtz acts as a bidentate ligand in complex 1, whereas in complex 2 the pmtz coordinates as a bis-bidentate chelate, assembling two identical {Cu(PPh)} moieties into a copper(I) dimer with a triple-decker sandwich structure involving phenyl/pmtz/phenyl π-π interactions. The UV-vis spectra of complexes 1 and 2 show low-energy absorptions at 350-550 nm, assigned to the Cu(I) to pmtz MLCT transition, probably mixed with some XLCT character for 1. The absorption of 2 is blue-shifted relative to that of 1 due to the substitution of the iodide of 1 with the π-acceptor ligand PPh. Complexes 1 and 2 are non-emissive, both in solution and in the solid state, most likely owing to the electronic effects induced by the additional nitrogen donor of pmtz compared to 2,2′-bipyrimidine. [ABSTRACT FROM AUTHOR]

Monodispersed spheres (1-4 μm in diameter) of BaWO:Eu (hereafter BWO:Eu) red-phosphor exhibiting intense emission at 615 nm were synthesized via a mild hydrothermal method. X-ray diffraction, scanning electron microscope, photoluminescence excitation and emission spectra, and decay curve were used to characterize the properties of BWO:Eu phosphors. An intense red emission was obtained by exciting either into the L state with 394 nm or the D state with 465 nm, that correspond to two popular emission lines from near-UV and blue LED chips, respectively. The values of Ω experimental intensity parameters (13.8 × 10 and 8.2 × 10 cm) are determined. The high-emission quantum efficiency of the BWO:Eu phosphor suggests this material could be promising red phosphors for generating white light in phosphor-converted white light-emitting diodes. [ABSTRACT FROM AUTHOR]

The article describes how a previously unreported dianion can affect the crystallization of polymeric metal complex cations. The structures of both title compounds are described in detail. It examines the two-coordinate Ag structure features of the title compounds. Also illustrated are the two-dimensional supramolecular layered architectures of the title compounds.

In the title compound, C6H7N3O2·H2O, all atoms of 2-ureidopyridine N-oxide molecule are approximately coplanar and adjacent molecules are connected by strong hydrogen bonds, resulting in a three-dimensional network. [ABSTRACT FROM AUTHOR]

The title complex, [Cu(C7H2N2O7)(C4H8N2O2)(H2O)], is a mononuclear copper(II) compound. The CuII ion is five-coordinated in a distorted pyramidal geometry by two N atoms from one dimethylglyoxime molecule, two O atoms from one 3,5-dinitro-2-oxidobenzoate ligand and one O atom from a water molecule. Strong hydrogen bonds connect adjacent molecules into a three-dimensional network. [ABSTRACT FROM AUTHOR]

With the use of the tailored cyanometalate precursor, (Bu4N)[(Tp)Fe(CN)3] (Tp = Tris(pyrazolyl)hydroborate) as the building block to react with fully solvated CuII, CoII, and NiII cations, four one-dimensional (1D) heterobimetallic cyano-bridged chain complexes of squares, [(Tp)2FeII2(CN)6Cu(CH3OH)·2CH3OH]n (1), [(Tp)2FeII2(CN)6Cu(DMF)·DMF]n (2), [(Tp)2FeIII2(CN)6M(CH3OH)2·2CH3OH]n (M = Co (3) and Ni (4)), have been prepared. In complexes 1 and 2, the CuII ions are pentacoordinated in the form of a slightly distorted square-based pyramid, and they are linked by distorted octahedrons of [(Tp)Fe(CN)3]- to form 1D chains of squares. In complexes 3 and 4, both the central CoII and NiII ions have a slightly distorted octahedral coordination geometry, and they are bridged by [(Tp)Fe(CN)3]- to form similar 1D chains of squares. There are weak interchain π-π stacking interactions through the pyrazolyl groups of the Tp ligands for complexes 3 and 4. The crystal structures and magnetic studies demonstrate that complexes 1 and 2 exhibit intrachain ferromagnetic coupling and single-chain magnets behavior, and the blocking temperature is ca. 6 K for complex 1 and ca. 3 K for complex 2. Complexes 3 and 4 show significant metamagnetic behavior, where the cyanides mediate the intrachain ferromagnetic coupling between FeIII and CoII or NiII ions and the interchain π-π stacking interactions lead to antiferromagnetic couplings. The field dependence of the magnetization measurements shows that the critical field is around 1 kOe for complex 3 and 0.8 kOe for complex 4 at 1.8 K. [ABSTRACT FROM AUTHOR]

Two new cyano-bridged one-dimensional heterobimetallic coordination polymers, [(bpca)2FeIII2(CN)6Cu(H2O)2·1.5H2O]n (2) and [(bpca)FeIII(CN)3Cu(bpca)(H2O)·H2O]n (3), and a trinuclear complex, [(bpca)2FeIII2(CN)6Mn(CH3OH)2(H2O)2]·2H2O (4), have been synthesized using the tailored tricyanometalate precursor (Bu4N)[Fe(bpca)(CN)3]·H2O (1) (Bu4N+ = tetrabutylammonium cation; bpca = bis(2-pyridylcarbonyl)amidate anion) as a building block and structurally characterized. In complex 2, the CuII ions are six-coordinated in an elongated distorted octahedral environment, and they are linked by distorted octahedrons of [Fe(bpca)(CN)3]- to form 1D chain of squares. Complex 3 is an unexpected chiral heterobimetallic helical chain complex, in which the helical chain consists of the asymmetric unit of [(bpca)Fe(CN)3Cu(bpca)(H2O)]. In complex 4, there are two independent trinuclear clusters in one asymmetric unit, and the coordination modes of the two methanol and two water molecules coordinating to the central Mn(II) ion are different (cis and trans). Complex 2 shows metamagnetic behavior with a Neel temperature of TN = 2.2 K and a critical field of 250 Oe at 1.8 K, where the cyanides mediate the intrachain ferromagnetic coupling between the CuII and FeIII ions. Complex 3 shows ferromagnetic coupling between CuII and FeIII ions, the best-fit for χMT versus T using a 1D alternating chain model leads to the parameters J1 = 7.9(3) cm-1, J2 = 1.03(2) cm-1, and g = 2.196(3). Complex 4 exhibits ferrimagnetic behavior caused by the noncompensation of the local interacting spins (SMn = 5/2 and SFe = 1/2) which interact antiferromagnetically through bridging cyano groups. [ABSTRACT FROM AUTHOR]

Cleanup goals for sites contaminated with persistent organic pollutants (POPs) are often established based on total contaminant concentrations. However, mounting evidence suggests that understanding contaminant bioavailability in soils is necessary for accurate assessment of contaminant exposure to humans via oral ingestion pathway. Animal-based in vivo tests have been used to assess contaminant bioavailability in soils; however, due to ethical issues and cost, it is desirable to use in vitro assays as alternatives. Various in vitro methods have been developed, which simulate human gastrointestinal (GI) tract using different digestion fluids. These methods can be used to predict POP bioavailability in soils, foods, and indoor dust after showing good correlation with in vivo animal data. Here, five common in vitro methods are evaluated and compared using PAHs and PBDEs as an example of traditional and emerging POPs. Their applications and limitations are discussed while focusing on method improvements and future challenges to predict POP bioavailability in different matrices. The discussions should shed light for future research to accurately assess human exposure to POPs via oral ingestion pathway. [ABSTRACT FROM AUTHOR]

Human corneal epithelial (HCE) cells are continually exposed to dust in the air, which may cause corneal epithelium damage. Both water and organic soluble contaminants in dust may contribute to cytotoxicity in HCE cells, however, the associated toxicity mechanisms are not fully elucidated. In this study, indoor dust from residential houses and commercial offices in Nanjing, China was collected and the effects of organic and water soluble fraction of dust on primary HCE cells were examined. The concentrations of heavy metals in the dust and dust extracts were determined by ICP-MS and PAHs by GC–MS, with office dust having greater concentrations of heavy metals and PAHs than house dust. Based on LC 50 , organic extract was more toxic than water extract, and office dust was more toxic than house dust. Accordingly, the organic extracts induced more ROS, malondialdehyde, and 8-Hydroxydeoxyguanosine and higher expression of inflammatory mediators ( IL-1β , IL-6 , and IL-8 ), and AhR inducible genes ( CYP1A1 , and CYP1B1 ) than water extracts ( p < 0.05). Extracts of office dust presented greater suppression of superoxide dismutase and catalase activity than those of house dust. In addition, exposure to dust extracts activated NF-κB signal pathway except water extract of house dust. The results suggested that both water and organic soluble fractions of dust caused cytotoxicity, oxidative damage, inflammatory response, and activation of AhR inducible genes, with organic extracts having higher potential to induce adverse effects on primary HCE cells. The results based on primary HCE cells demonstrated the importance of reducing contaminants in indoor dust to reduce their adverse impacts on human eyes. [ABSTRACT FROM AUTHOR]

Three new mononuclear copper(I) halide complexes of 2-(2-benzimidazoly)-6-methylpyridine (Hbmp), [Cu(Hbmp)(PPh3)X] (X = I (1); Br (2); Cl (3)), have been synthesized and structurally characterized by X-ray crystallography. It is revealed that the most significant impact of the auxiliary halide ligand on the structure is on the Cu一Npyridyl and Cu一P bond lengths. Complexes 1–3 show a weak low-energy absorption band at 350–600 nm in CH2Cl2, ascribed to the Cu(I) to Hbmp metal-to-ligand charge-transfer (MLCT) transitions, perhaps mixed with some halide-to-ligand charge-transfer (XLCT) character. The solid-state emissions of 1–3 are observed at ambient temperature, markedly depending on the halide ancillary ligand bound to the {Cu(Hbmp)(PPh3)} unit, which are assigned to the MLCT excited states with some mixing of the XLCT characters. [ABSTRACT FROM AUTHOR]

The title polymer, [Cu(C6H5O6PS)(C10H8N2)(H2O)] n, was synthesized by a hydrothermal method. The CuII ion is five-coordinated by one phosphonate O atom, one sulfonate O atom, two N atoms of the bipyridyl ligand and one water molecule. The coordination geometry around the metal centre can be described as slightly distorted square-pyramidal. The CuII ions are connected by bidentate bridging phosphonato-benzenesulfonate ligands, forming one-dimensional helical chains along [010], which are further bridged by bidentate 4,4′-bipyridyl ligands, generating a two-dimensional layered crystal structure. The layered structure features an eight-membered ring including four CuII ions, two [O3S–C6H4–PO3H]2− anions and two 4,4′-bipyridyl ligands. Hydrogen bonds involving aqua ligands, phosphonate O and sulfonate O atoms are observed between the layers, [ABSTRACT FROM AUTHOR]

The title complex, [Co(C12H8N2)(H2O)4](C10H6O6S2)·2H2O, was synthesized hydrothermally. The Co2+ cation, which lies on a twofold rotation axis, is six-coordinate. The anion is located on a centre of inversion. An extensive network of O—H⋯O hydrogen bonds links the components into a threedimensional network. [ABSTRACT FROM AUTHOR]

Indoor dust often contains organic contaminants, which adversely impacts human health. In this study, the organic contaminants in the indoor dust from commercial offices and residential houses in Nanjing, China were extracted and their effects on human breast cancer cells (MCF-7) were investigated. Both dust extracts promoted proliferation of MCF-7 cells at ≤24 μg/100 μL, with cell viability being decreased with increasing dust concentrations. Based on LC 50 , house dust was less toxic than office dust. At 8 μg/100 μL, both extracts caused more MCF-7 cells into active cycling (G2/M + S) and increased intracellular Ca2+ influx, with house dust inducing stronger effects than office dust. Further, the expression of estrogen-responsive genes for TFF1 and EGR3 was enhanced by 3-9 and 4-9 folds, while the expression of cell cycle regulatory genes for cyclin D was enhanced by 2-5 folds. The results suggested that organic dust extract influenced cell viability, altered cell cycle, increased intracellular Ca2+ levels, and activated cell cycle regulatory and estrogen-responsive gene expressions, with house dust showing lower cytotoxicity but higher estrogenic potential on MCF-7 cells. The results indicate the importance of reducing organic contaminants in indoor dust to mitigate their adverse impacts on human health. Unlabelled Image • Effects of organic dust extract on human breast cancer cells (MCF-7) were examined. • Both extracts stimulated proliferation of MCF-7 cells at ≤24 μg/100 μL. • Extracts reduced cell viability, altered cell cycle and enhanced intracellular Ca2+. • Extracts increased expression of estrogen-responsive & cell cycle regulatory genes. • House dust induced lower toxicity but higher estrogenic potential on MCF-7 cells. [ABSTRACT FROM AUTHOR]