6,042 research outputs found

    The Microchannel X-ray Telescope for the Gamma-Ray Burst mission SVOM

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    We present the Microchannel X-ray Telescope, a new light and compact focussing telescope that will be flying on the Sino-French SVOM mission dedicated to Gamma-Ray Burst science. The MXT design is based on the coupling of square pore micro-channel plates with a low noise pnCCD. MXT will provide an effective area of about 50 cmsq, and its point spread function is expected to be better than 3.7 arc min (FWHM) on axis. The estimated sensitivity is adequate to detect all the afterglows of the SVOM GRBs, and to localize them to better then 60 arc sec after five minutes of observation.Comment: 12 pages, 8 figures, to be published in SPIE Astronomical Telescopes + Instrumentation, Montreal, June 201

    Longitudinal spin transport in diluted magnetic semiconductor superlattices: the effect of the giant Zeeman splitting

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    Longitudinal spin transport in diluted magnetic semiconductor superlattices is investigated theoretically. The longitudinal magnetoconductivity (MC) in such systems exhibits an oscillating behavior as function of an external magnetic field. In the weak magnetic field region the giant Zeeman splitting plays a dominant role which leads to a large negative magnetoconductivity. In the strong magnetic field region the MC exhibits deep dips with increasing magnetic field. The oscillating behavior is attributed to the interplay between the discrete Landau levels and the Fermi surface. The decrease of the MC at low magnetic field is caused by the sds-d exchange interaction between the electron in the conduction band and the magnetic ions.Comment: 6 pages, 9 figures, submitted to Phys. Rev.

    Tuning Carbon Dioxide Adsorption Affinity of Zinc(II) MOFs by Mixing Bis(pyrazolate) Ligands with N-Containing Tags

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    The four zinc(II) mixed-ligand metal-organic frameworks (MIXMOFs) Zn(BPZ)x(BPZNO2)1-x, Zn(BPZ)x(BPZNH2)1-x, Zn(BPZNO2)x(BPZNH2)1-x, and Zn(BPZ)x(BPZNO2)y(BPZNH2)1-x-y (H2BPZ = 4,4′-bipyrazole; H2BPZNO2 = 3-nitro-4,4′-bipyrazole; H2BPZNH2 = 3-amino-4,4′-bipyrazole) were prepared through solvothermal routes and fully investigated in the solid state. Isoreticular to the end members Zn(BPZ) and Zn(BPZX) (X = NO2, NH2), they are the first examples ever reported of (pyr)azolate MIXMOFs. Their crystal structure is characterized by a three-dimensional open framework with one-dimensional square or rhombic channels decorated by the functional groups. Accurate information about ligand stoichiometric ratio was determined (for the first time on MIXMOFs) through integration of selected ligands skeleton resonances from 13C cross polarized magic angle spinning solid-state NMR spectra collected on the as-synthesized materials. Like other poly(pyrazolate) MOFs, the four MIXMOFs are thermally stable, with decomposition temperatures between 708 and 726 K. As disclosed by N2 adsorption at 77 K, they are micro-mesoporous materials with Brunauer-Emmett-Teller specific surface areas in the range 400-600 m2/g. A comparative study (involving also the single-ligand analogues) of CO2 adsorption capacity, CO2 isosteric heat of adsorption (Qst), and CO2/N2 selectivity in equimolar mixtures at p = 1 bar and T = 298 K cast light on interesting trends, depending on ligand tag nature or ligand stoichiometric ratio. In particular, the amino-decorated compounds show higher Qst values and CO2/N2 selectivity vs the nitro-functionalized analogues; in addition, tag "dilution" [upon passing from Zn(BPZX) to Zn(BPZ)x(BPZX)1-x] increases CO2 adsorption selectivity over N2. The simultaneous presence of amino and nitro groups is not beneficial for CO2 uptake. Among the compounds studied, the best compromise among uptake capacity, Qst, and CO2/N2 selectivity is represented by Zn(BPZ)x(BPZNH2)1-x

    Tetrazine-Triggered Release of Carboxylic-Acid-Containing Molecules for Activation of an Anti-inflammatory Drug.

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    In addition to its use for the study of biomolecules in living systems, bioorthogonal chemistry has emerged as a promising strategy to enable protein or drug activation in a spatially and temporally controlled manner. This study demonstrates the application of a bioorthogonal inverse electron-demand Diels-Alder (iEDDA) reaction to cleave trans-cyclooctene (TCO) and vinyl protecting groups from carboxylic acid-containing molecules. The tetrazine-mediated decaging reaction proceeded under biocompatible conditions with fast reaction kinetics (<2 min). The anti-inflammatory activity of ketoprofen was successfully reinstated after decaging of the nontoxic TCOprodrug in live macrophages. Overall, this work expands the scope of functional groups and the application of decaging reactions to a new class of drugs

    Cobalt(II) Bipyrazolate Metal-Organic Frameworks as Heterogeneous Catalysts in Cumene Aerobic Oxidation: A Tag-Dependent Selectivity

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    "This document is the Accepted Manuscript version of a Published Work that appeared in final form in Inorganic Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acs.inorgchem.0c00481"[EN] Three metal-organic frameworks with the general formula Co(BPZX) (BPZX(2-) = 3-X-4,4'-bipyrazolate, X = H, NH2, NO2) constructed with ligands having different functional groups on the same skeleton have been employed as heterogeneous catalysts for aerobic liquid-phase oxidation of cumene with O-2 as oxidant. O-2 adsorption isotherms collected at p(O2) = 1 atm and T = 195 and 273 K have cast light on the relative affinity of these catalysts for dioxygen. The highest gas uptake at 195 K is found for Co(BPZ) (3.2 mmol/g (10.1 wt % O-2)), in line with its highest BET specific surface area (926 m(2)/g) in comparison with those of Co(BPZNH(2)) (317 m(2)/g) and Co(BPZNO(2)) (645 m(2)/g). The O-2 isosteric heat of adsorption (Q(2)) trend follows the order Co(BPZ) > Co(BPZNH(2)) > Co(BPZNO(2)). Interestingly, the selectivity in the cumene oxidation products was found to be dependent on the tag present in the catalyst linker: while cumene hydroperoxide (CHP) is the main product obtained with Co(BPZ) (84% selectivity to CHP after 7 h, p(O2) = 4 bar, and T = 363 K), further oxidation to 2-phenyl-2-propanol (PP) is observed in the presence of Co(BPZNH(2)) as the catalyst (69% selectivity to PP under the same experimental conditions).S.G., R.V., and M.M. acknowledge Universita dell'Insubria for partial funding. G.G. thanks the Italian MIUR through the PRIN 2017 Project Multi-e: Multielectron Transfer for the Conversion of Small Molecules: an Enabling Technology for the Chemical Use of Renewable Energy (20179337R7) for financial support. G.G. thanks the TRAINER project (Catalysts for Transition to Renewable Energy Future) ref. ANR-17-MPGA-0017 for support. C.P. thanks the University of Camerino and the Italian MIUR throughout the PRIN 2015 Project Towards a Sustainable Chemistry (20154 x 9ATP_002). This project has also received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No. 641887 (project acronym: DEFNET) and the Spanish Government through projects MAT2017-82288-C2-1-P and Severo Ochoa (SEV-2016-0683). Professor Norberto Masciocchi (University of Insubria, Como, Italy) is acknowledged for fruitful discussions. The authors are also grateful to Dr. Giulia Tuci (CNR-ICCOM Florence, Italy) for help with the XPS curve fitting. The Microscopy Service of the Universitat Politècnica de València is gratefully acknowledged for the electron microscopy measurements.Nowacka, AE.; Vismara, R.; Mercuri, G.; Moroni, M.; Palomino Roca, M.; Domasevitch, K.; Di Nicola, C.... (2020). Cobalt(II) Bipyrazolate Metal-Organic Frameworks as Heterogeneous Catalysts in Cumene Aerobic Oxidation: A Tag-Dependent Selectivity. Inorganic Chemistry. 59(12):8161-8172. https://doi.org/10.1021/acs.inorgchem.0c00481S816181725912Fortuin, J. P., & Waterman, H. I. (1953). Production of phenol from cumene. Chemical Engineering Science, 2(4), 182-192. doi:10.1016/0009-2509(53)80040-0Luyben, W. L. (2009). Design and Control of the Cumene Process. Industrial & Engineering Chemistry Research, 49(2), 719-734. doi:10.1021/ie9011535Matsui, S., & Fujita, T. (2001). New cumene-oxidation systems. Catalysis Today, 71(1-2), 145-152. doi:10.1016/s0920-5861(01)00450-3Opeida, I. A., Kytsya, A. R., Bazylyak, L. I., & Pobigun, O. I. (2017). Silver Nanoparticle Catalysis of the Liquid-Phase Radical Chain Oxidation of Cumene by Molecular Oxygen. Theoretical and Experimental Chemistry, 52(6), 369-374. doi:10.1007/s11237-017-9492-zTsodikov, M. V., Kugel, V. Y., Slivinskii, E. V., Bondarenko, G. N., Maksimov, Y. V., Alvarez, M. A., … Navio, J. A. (2000). Selectivity and mechanism of cumene liquid-phase oxidation in the presence of powdered mixed iron–aluminum oxides prepared by alkoxy method. Applied Catalysis A: General, 193(1-2), 237-242. doi:10.1016/s0926-860x(99)00438-xZhang, M., Wang, L., Ji, H., Wu, B., & Zeng, X. (2007). Cumene Liquid Oxidation to Cumene Hydroperoxide over CuO Nanoparticle with Molecular Oxygen under Mild Condition. Journal of Natural Gas Chemistry, 16(4), 393-398. doi:10.1016/s1003-9953(08)60010-9Hsu, Y. F., & Cheng, C. P. (1998). Mechanistic investigation of the autooxidation of cumene catalyzed by transition metal salts supported on polymer. Journal of Molecular Catalysis A: Chemical, 136(1), 1-11. doi:10.1016/s1381-1169(98)00016-8Hsu, Y. F., & Cheng, C. P. (1997). Polymer supported catalyst for the effective autoxidation of cumene to cumene hydroperoxide. Journal of Molecular Catalysis A: Chemical, 120(1-3), 109-116. doi:10.1016/s1381-1169(96)00442-6Ying Fang, H., Mei Huei, Y., & Cheu Pyeng, C. (1996). Autooxidation of cumene catalyzed by transition metal compounds on polymeric supports. Journal of Molecular Catalysis A: Chemical, 105(3), 137-144. doi:10.1016/1381-1169(95)00205-7Narulkar, D. D., Srivastava, A. K., Butcher, R. J., Ansy, K. M., & Dhuri, S. N. (2017). Synthesis and characterization of N3Py2 ligand-based cobalt(II), nickel(II) and copper(II) catalysts for efficient conversion of hydrocarbons to alcohols. Inorganica Chimica Acta, 467, 405-414. doi:10.1016/j.ica.2017.08.027Wang, R.-M., Duan, Z.-F., He, Y.-F., & Lei, Z.-Q. (2006). Heterogeneous catalytic aerobic oxidation behavior of Co–Na heterodinuclear polymeric complex of Salen-crown ether. Journal of Molecular Catalysis A: Chemical, 260(1-2), 280-287. doi:10.1016/j.molcata.2006.07.049Rogovin, M., & Neumann, R. (1999). Silicate xerogels containing cobalt as heterogeneous catalysts for the side-chain oxidation of alkyl aromatic compounds with tert-butyl hydroperoxide. Journal of Molecular Catalysis A: Chemical, 138(2-3), 315-318. doi:10.1016/s1381-1169(98)00207-6Konopińska, A. (2017). &lt;i&gt;N&lt;/i&gt;-Hydroxyphthalimide as a Catalyst of Cumene Oxidation with Hydroperoxide. Modern Chemistry, 5(2), 29. doi:10.11648/j.mc.20170502.12VARMA, G. (1973). Heterogeneous catalytic oxidation of cumene (isopropyl benzene) in liquid phase. Journal of Catalysis, 28(2), 236-244. doi:10.1016/0021-9517(73)90006-7Collom, S. L., Bloomfield, A. J., & Anastas, P. T. (2016). Advancing Sustainable Manufacturing through a Heterogeneous Cobalt Catalyst for Selective C–H Oxidation. Industrial & Engineering Chemistry Research, 55(12), 3308-3312. doi:10.1021/acs.iecr.5b03674Scognamiglio, J., Jones, L., Letizia, C. S., & Api, A. M. (2012). Fragrance material review on 2-phenyl-2-propanol. Food and Chemical Toxicology, 50, S130-S133. doi:10.1016/j.fct.2011.10.011Rossin, A., Tuci, G., Luconi, L., & Giambastiani, G. (2017). Metal–Organic Frameworks as Heterogeneous Catalysts in Hydrogen Production from Lightweight Inorganic Hydrides. ACS Catalysis, 7(8), 5035-5045. doi:10.1021/acscatal.7b01495Chughtai, A. H., Ahmad, N., Younus, H. A., Laypkov, A., & Verpoort, F. (2015). Metal–organic frameworks: versatile heterogeneous catalysts for efficient catalytic organic transformations. Chemical Society Reviews, 44(19), 6804-6849. doi:10.1039/c4cs00395kLiu, J., Chen, L., Cui, H., Zhang, J., Zhang, L., & Su, C.-Y. (2014). Applications of metal–organic frameworks in heterogeneous supramolecular catalysis. Chem. Soc. Rev., 43(16), 6011-6061. doi:10.1039/c4cs00094cGascon, J., Corma, A., Kapteijn, F., & Llabrés i Xamena, F. X. (2013). Metal Organic Framework Catalysis: Quo vadis? ACS Catalysis, 4(2), 361-378. doi:10.1021/cs400959kLuo, S., Zeng, Z., Zeng, G., Liu, Z., Xiao, R., Chen, M., … Jiang, D. (2019). Metal Organic Frameworks as Robust Host of Palladium Nanoparticles in Heterogeneous Catalysis: Synthesis, Application, and Prospect. ACS Applied Materials & Interfaces, 11(36), 32579-32598. doi:10.1021/acsami.9b11990Deng, X., Li, Z., & García, H. (2017). Visible Light Induced Organic Transformations Using Metal-Organic-Frameworks (MOFs). Chemistry - A European Journal, 23(47), 11189-11209. doi:10.1002/chem.201701460Dhakshinamoorthy, A., Asiri, A. M., & Garcia, H. (2016). Metal-Organic Frameworks as Catalysts for Oxidation Reactions. Chemistry - A European Journal, 22(24), 8012-8024. doi:10.1002/chem.201505141Song, X., Hu, D., Yang, X., Zhang, H., Zhang, W., Li, J., … Yu, J. (2019). Polyoxomolybdic Cobalt Encapsulated within Zr-Based Metal–Organic Frameworks as Efficient Heterogeneous Catalysts for Olefins Epoxidation. ACS Sustainable Chemistry & Engineering, 7(3), 3624-3631. doi:10.1021/acssuschemeng.8b06736Zhang, T., Hu, Y.-Q., Han, T., Zhai, Y.-Q., & Zheng, Y.-Z. (2018). Redox-Active Cobalt(II/III) Metal–Organic Framework for Selective Oxidation of Cyclohexene. ACS Applied Materials & Interfaces, 10(18), 15786-15792. doi:10.1021/acsami.7b19323Ma, Y., Peng, H., Liu, J., Wang, Y., Hao, X., Feng, X., … Li, Y. (2018). Polyoxometalate-Based Metal–Organic Frameworks for Selective Oxidation of Aryl Alkenes to Aldehydes. Inorganic Chemistry, 57(7), 4109-4116. doi:10.1021/acs.inorgchem.8b00282Othong, J., Boonmak, J., Ha, J., Leelasubcharoen, S., & Youngme, S. (2017). Thermally Induced Single-Crystal-to-Single-Crystal Transformation and Heterogeneous Catalysts for Epoxidation Reaction of Co(II) Based Metal–Organic Frameworks Containing 1,4-Phenylenediacetic Acid. Crystal Growth & Design, 17(4), 1824-1835. doi:10.1021/acs.cgd.6b01788Wang, J.-C., Ding, F.-W., Ma, J.-P., Liu, Q.-K., Cheng, J.-Y., & Dong, Y.-B. (2015). Co(II)-MOF: A Highly Efficient Organic Oxidation Catalyst with Open Metal Sites. Inorganic Chemistry, 54(22), 10865-10872. doi:10.1021/acs.inorgchem.5b01938Tuci, G., Giambastiani, G., Kwon, S., Stair, P. C., Snurr, R. Q., & Rossin, A. (2014). Chiral Co(II) Metal–Organic Framework in the Heterogeneous Catalytic Oxidation of Alkenes under Aerobic and Anaerobic Conditions. ACS Catalysis, 4(3), 1032-1039. doi:10.1021/cs401003dHamidipour, L., & Farzaneh, F. (2013). Cobalt metal organic framework as an efficient heterogeneous catalyst for the oxidation of alkanes and alkenes. Reaction Kinetics, Mechanisms and Catalysis, 109(1), 67-75. doi:10.1007/s11144-012-0533-2Luz, I., León, A., Boronat, M., Llabrés i Xamena, F. X., & Corma, A. (2013). Selective aerobic oxidation of activated alkanes with MOFs and their use for epoxidation of olefins with oxygen in a tandem reaction. Catal. Sci. Technol., 3(2), 371-379. doi:10.1039/c2cy20449eSantiago-Portillo, A., Navalón, S., Cirujano, F. G., Xamena, F. X. L. i, Alvaro, M., & Garcia, H. (2015). MIL-101 as Reusable Solid Catalyst for Autoxidation of Benzylic Hydrocarbons in the Absence of Additional Oxidizing Reagents. ACS Catalysis, 5(6), 3216-3224. doi:10.1021/acscatal.5b00411Nowacka, A., Briantais, P., Prestipino, C., & Llabrés i Xamena, F. X. (2019). Selective Aerobic Oxidation of Cumene to Cumene Hydroperoxide over Mono- and Bimetallic Trimesate Metal–Organic Frameworks Prepared by a Facile «Green» Aqueous Synthesis. ACS Sustainable Chemistry & Engineering, 7(8), 7708-7715. doi:10.1021/acssuschemeng.8b06472Vismara, R., Tuci, G., Tombesi, A., Domasevitch, K. V., Di Nicola, C., Giambastiani, G., … Galli, S. (2019). Tuning Carbon Dioxide Adsorption Affinity of Zinc(II) MOFs by Mixing Bis(pyrazolate) Ligands with N-Containing Tags. ACS Applied Materials & Interfaces, 11(30), 26956-26969. doi:10.1021/acsami.9b08015Vismara, R., Tuci, G., Mosca, N., Domasevitch, K. V., Di Nicola, C., Pettinari, C., … Rossin, A. (2019). Amino-decorated bis(pyrazolate) metal–organic frameworks for carbon dioxide capture and green conversion into cyclic carbonates. Inorganic Chemistry Frontiers, 6(2), 533-545. doi:10.1039/c8qi00997jMosca, N., Vismara, R., Fernandes, J. A., Tuci, G., Di Nicola, C., Domasevitch, K. V., … Galli, S. (2018). Nitro-Functionalized Bis(pyrazolate) Metal-Organic Frameworks as Carbon Dioxide Capture Materials under Ambient Conditions. Chemistry - A European Journal, 24(50), 13170-13180. doi:10.1002/chem.201802240Pettinari, C., Tăbăcaru, A., & Galli, S. (2016). Coordination polymers and metal–organic frameworks based on poly(pyrazole)-containing ligands. Coordination Chemistry Reviews, 307, 1-31. doi:10.1016/j.ccr.2015.08.005Pettinari, C., Tăbăcaru, A., Boldog, I., Domasevitch, K. V., Galli, S., & Masciocchi, N. (2012). Novel Coordination Frameworks Incorporating the 4,4′-Bipyrazolyl Ditopic Ligand. Inorganic Chemistry, 51(9), 5235-5245. doi:10.1021/ic3001416Colombo, V., Montoro, C., Maspero, A., Palmisano, G., Masciocchi, N., Galli, S., … Navarro, J. A. R. (2012). Tuning the Adsorption Properties of Isoreticular Pyrazolate-Based Metal–Organic Frameworks through Ligand Modification. Journal of the American Chemical Society, 134(30), 12830-12843. doi:10.1021/ja305267mTăbăcaru, A., Pettinari, C., Masciocchi, N., Galli, S., Marchetti, F., & Angjellari, M. (2011). Pro-porous Coordination Polymers of the 1,4-Bis((3,5-dimethyl-1H-pyrazol-4-yl)-methyl)benzene Ligand with Late Transition Metals. Inorganic Chemistry, 50(22), 11506-11513. doi:10.1021/ic2013705Colombo, V., Galli, S., Choi, H. J., Han, G. D., Maspero, A., Palmisano, G., … Long, J. R. (2011). High thermal and chemical stability in pyrazolate-bridged metal–organic frameworks with exposed metal sites. Chemical Science, 2(7), 1311. doi:10.1039/c1sc00136aMasciocchi, N., Galli, S., Colombo, V., Maspero, A., Palmisano, G., Seyyedi, B., … Bordiga, S. (2010). Cubic Octanuclear Ni(II) Clusters in Highly Porous Polypyrazolyl-Based Materials. Journal of the American Chemical Society, 132(23), 7902-7904. doi:10.1021/ja102862jGalli, S., Masciocchi, N., Colombo, V., Maspero, A., Palmisano, G., López-Garzón, F. J., … Navarro, J. A. R. (2010). Adsorption of Harmful Organic Vapors by Flexible Hydrophobic Bis-pyrazolate Based MOFs. Chemistry of Materials, 22(5), 1664-1672. doi:10.1021/cm902899tBoldog, I., Sieler, J., Chernega, A. N., & Domasevitch, K. V. (2002). 4,4′-Bipyrazolyl: new bitopic connector for construction of coordination networks. Inorganica Chimica Acta, 338, 69-77. doi:10.1016/s0020-1693(02)00902-7Domasevitch, K. V., Gospodinov, I., Krautscheid, H., Klapötke, T. M., & Stierstorfer, J. (2019). Facile and selective polynitrations at the 4-pyrazolyl dual backbone: straightforward access to a series of high-density energetic materials. New Journal of Chemistry, 43(3), 1305-1312. doi:10.1039/c8nj05266bTOPAS-Academic 6; Bruker, by Coelho Software: Brisbane, Australia, 2016.Coelho, A. A. (2003). Indexing of powder diffraction patterns by iterative use of singular value decomposition. Journal of Applied Crystallography, 36(1), 86-95. doi:10.1107/s0021889802019878Cheetham, A. K., Bennett, T. D., Coudert, F.-X., & Goodwin, A. L. (2016). Defects and disorder in metal organic frameworks. Dalton Transactions, 45(10), 4113-4126. doi:10.1039/c5dt04392aCliffe, M. J., Wan, W., Zou, X., Chater, P. A., Kleppe, A. K., Tucker, M. G., … Goodwin, A. L. (2014). Correlated defect nanoregions in a metal–organic framework. Nature Communications, 5(1). doi:10.1038/ncomms5176Spirkl, S., Grzywa, M., & Volkmer, D. (2018). Synthesis and characterization of a flexible metal organic framework generated from MnIII and the 4,4′-bipyrazolate-ligand. Dalton Transactions, 47(26), 8779-8786. doi:10.1039/c8dt01185kNazarenko, O. M., Rusanov, E. B., Chernega, A. N., & Domasevitch, K. V. (2013). Cobalt(II) and cadmium(II) square grids supported with 4,4′-bipyrazole and accommodating 3-carboxyadamantane-1-carboxylate. Acta Crystallographica Section C Crystal Structure Communications, 69(3), 232-236. doi:10.1107/s0108270113003405Tăbăcaru, A., Pettinari, C., Marchetti, F., di Nicola, C., Domasevitch, K. V., Galli, S., … Cocchioni, M. (2012). Antibacterial Action of 4,4′-Bipyrazolyl-Based Silver(I) Coordination Polymers Embedded in PE Disks. Inorganic Chemistry, 51(18), 9775-9788. doi:10.1021/ic3011635Sun, Q.-F., Wong, K. M.-C., Liu, L.-X., Huang, H.-P., Yu, S.-Y., Yam, V. W.-W., … Yu, K.-C. (2008). Self-Assembly, Structures, and Photophysical Properties of 4,4′-Bipyrazolate-Linked Metallo-Macrocycles with Dimetal Clips. Inorganic Chemistry, 47(6), 2142-2154. doi:10.1021/ic701344pLozan, V., Solntsev, P. Y., Leibeling, G., Domasevitch, K. V., & Kersting, B. (2007). Tetranuclear Nickel Complexes Composed of Pairs of Dinuclear LNi2 Fragments Linked by 4,4′-Bipyrazolyl, 1,4-Bis(4′-pyrazolyl)benzene, and 4,4′-Bipyridazine: Synthesis, Structures, and Magnetic Properties. European Journal of Inorganic Chemistry, 2007(20), 3217-3226. doi:10.1002/ejic.200700317Bond distances and angles for the rigid body describing the ligand: C–C and C-N of the pyrazole ring 1.36 Å; exocyclic C–C 1.40 Å; C–H of the pyrazole ring 0.95 Å; C–NNH2 1.40 Å; N–H 0.95 Å; pyrazole ring internal and external bond angles 108 and 126°, respectively; angles at the nitrogen atom of the amino group 120°.Coelho, A. A. (2000). Whole-profile structure solution from powder diffraction data using simulated annealing. Journal of Applied Crystallography, 33(3), 899-908. doi:10.1107/s002188980000248xCheary, R. W., & Coelho, A. (1992). A fundamental parameters approach to X-ray line-profile fitting. Journal of Applied Crystallography, 25(2), 109-121. doi:10.1107/s0021889891010804Stephens, P. W. (1999). Phenomenological model of anisotropic peak broadening in powder diffraction. Journal of Applied Crystallography, 32(2), 281-289. doi:10.1107/s0021889898006001Rouquerol, J., Llewellyn, P., & Rouquerol, F. (2007). Is the bet equation applicable to microporous adsorbents? Characterization of Porous Solids VII - Proceedings of the 7th International Symposium on the Characterization of Porous Solids (COPS-VII), Aix-en-Provence, France, 26-28 May 2005, 49-56. doi:10.1016/s0167-2991(07)80008-5Saeidi, N., & Parvini, M. (2015). Accuracy of Dubinin-Astakov and Dubinin-Raduchkevic Adsorption Isotherm Models in Evaluating Micropore Volume of Bontonite. Periodica Polytechnica Chemical Engineering. doi:10.3311/ppch.8374Zhu, X., Tian, C., Veith, G. M., Abney, C. W., Dehaudt, J., & Dai, S. (2016). In Situ Doping Strategy for the Preparation of Conjugated Triazine Frameworks Displaying Efficient CO2 Capture Performance. Journal of the American Chemical Society, 138(36), 11497-11500. doi:10.1021/jacs.6b07644Zhu, X., Mahurin, S. M., An, S.-H., Do-Thanh, C.-L., Tian, C., Li, Y., … Dai, S. (2014). Efficient CO2 capture by a task-specific porous organic polymer bifunctionalized with carbazole and triazine groups. Chemical Communications, 50(59), 7933. doi:10.1039/c4cc01588fSpek, A. L. (2009). Structure validation in chemical crystallography. Acta Crystallographica Section D Biological Crystallography, 65(2), 148-155. doi:10.1107/s090744490804362xBlatov, V. A., Shevchenko, A. P., & Proserpio, D. M. (2014). Applied Topological Analysis of Crystal Structures with the Program Package ToposPro. Crystal Growth & Design, 14(7), 3576-3586. doi:10.1021/cg500498kTonigold, M., Lu, Y., Mavrandonakis, A., Puls, A., Staudt, R., Möllmer, J., … Volkmer, D. (2011). Pyrazolate-Based Cobalt(II)-Containing Metal-Organic Frameworks in Heterogeneous Catalytic Oxidation Reactions: Elucidating the Role of Entatic States for Biomimetic Oxidation Processes. Chemistry - A European Journal, 17(31), 8671-8695. doi:10.1002/chem.201003173Ma, S., & Zhou, H.-C. (2006). A Metal−Organic Framework with Entatic Metal Centers Exhibiting High Gas Adsorption Affinity. Journal of the American Chemical Society, 128(36), 11734-11735. doi:10.1021/ja063538zWang, Z.-J., Lv, J.-J., Yi, R.-N., Xiao, M., Feng, J.-J., Liang, Z.-W., … Xu, X. (2018). Nondirecting Group sp 3 C−H Activation for Synthesis of Bibenzyls via Homo-coupling as Catalyzed by Reduced Graphene Oxide Supported PtPd@Pt Porous Nanospheres. Advanced Synthesis & Catalysis, 360(5), 932-941. doi:10.1002/adsc.201701389CASEMIER, J. (1973). The oxidation of cumene and the decomposition of cumene hydroperoxide on silver, copper, and platinum. Journal of Catalysis, 29(3), 367-373. doi:10.1016/0021-9517(73)90242-xLiao, S., Chi, Y., Yu, H., Wang, H., & Peng, F. (2014). Tuning the Selectivity in the Aerobic Oxidation of Cumene Catalyzed by Nitrogen-Doped Carbon Nanotubes. ChemCatChem, 6(2), 555-560. doi:10.1002/cctc.201300909Silvestre-Albero, J. (2001). Characterization of microporous solids by immersion calorimetry. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 187-188(1-3), 151-165. doi:10.1016/s0927-7757(01)00620-3Everett, D. H. (1972). Manual of Symbols and Terminology for Physicochemical Quantities and Units, Appendix II: Definitions, Terminology and Symbols in Colloid and Surface Chemistry. Pure and Applied Chemistry, 31(4), 577-638. doi:10.1351/pac197231040577Liu, C., Wang, T., Ji, J., Wang, C., Wang, H., Jin, P., … Jiang, J. (2019). The effect of pore size and layer number of metal–porphyrin coordination nanosheets on sensing DNA. Journal of Materials Chemistry C, 7(33), 10240-10246. doi:10.1039/c9tc02778eGong, T., Yang, X., Fang, J.-J., Sui, Q., Xi, F.-G., & Gao, E.-Q. (2017). Distinct Chromic and Magnetic Properties of Metal–Organic Frameworks with a Redox Ligand. ACS Applied Materials & Interfaces, 9(6), 5503-5512. doi:10.1021/acsami.6b15540Yamada, Y., Kim, J., Matsuo, S., & Sato, S. (2014). Nitrogen-containing graphene analyzed by X-ray photoelectron spectroscopy. Carbon, 70, 59-74. doi:10.1016/j.carbon.2013.12.061Singhbabu, Y. N., Kumari, P., Parida, S., & Sahu, R. K. (2014). Conversion of pyrazoline to pyrazole in hydrazine treated N-substituted reduced graphene oxide films obtained by ion bombardment and their electrical properties. Carbon, 74, 32-43. doi:10.1016/j.carbon.2014.02.079Dementjev, A. ., de Graaf, A., van de Sanden, M. C. ., Maslakov, K. ., Naumkin, A. ., & Serov, A. . (2000). X-Ray photoelectr

    An evaluation of metal removal during wastewater treatment: The potential to achieve more stringent final effluent standards

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    This is the author's accepted manuscript. The final published article is available from the link below. Copyright @ 2011 Taylor & Francis.Metals are of particular importance in relation to water quality, and concern regarding the impact of these contaminants on biodiversity is being encapsulated within the latest water-related legislation such as the Water Framework Directive in Europe and criteria revisions to the Clean Water Act in the United States. This review undertakes an evaluation of the potential of 2-stage wastewater treatment consisting of primary sedimentation and biological treatment in the form of activated sludge processes, to meet more stringent discharge consents that are likely to be introduced as a consequence. The legislation, sources of metals, and mechanisms responsible for their removal are discussed, to elucidate possible pathways by which the performance of conventional processes may be optimized or enhanced. Improvements in effluent quality, achievable by reducing concentrations of suspended solids or biochemical oxygen demand, may also reduce metal concentrations although meeting possible requirements for the removal of copper my be challenging

    The silicon micro-strip detector plane for the LOFT/Wide Field Monitor

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    The main objective of the Wide Field Monitor (WFM) on the LOFT mission is to provide unambiguous detection of the high-energy sources in a large field of view, in order to support science operations of the LOFT primary instrument, the LAD. The monitor will also provide by itself a large number of results on the timing and spectral behaviour of hundreds of galactic compact objects, Active Galactic Nuclei and Gamma-Ray Bursts. The WFM is based on the coded aperture concept where a position sensitive detector records the shadow of a mask projected by the celestial sources. The proposed WFM detector plane, based on Double Sided micro-Strip Silicon Detectors (DSSD), will allow proper 2-dimensional recording of the projected shadows. Indeed the positioning of the photon interaction in the detector with equivalent fine resolution in both directions insures the best imaging capability compatible with the allocated budgets for this telescope on LOFT. We will describe here the overall configuration of this 2D-WFM and the design and characteristics of the DSSD detector plane including its imaging and spectral performances. We will also present a number of simulated results discussing the advantages that this configuration offers to LOFT. A DSSD-based WFM will in particular reduce significantly the source confusion experienced by the WFM in crowded regions of the sky like the Galactic Center and will in general increase the observatory science capability of the mission.Comment: Proceedings of SPIE, Vol. 8443, Paper No. 8443-89, 201
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