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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 239 (1996), S. 33-41 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Der neuartige dikationische Komplex [dppfNi(MeCN)4][BF4]2 (dppf = 1,1′-Bis(diphenylphosphin)ferrocen) zeigte in Anwesenheit von Diethylaluminiumchlorid (AIEt2CI) hohe Aktivität für die Polymerisation von 1,3-Butadien. Reaktionsdauer, Temperatur und das Aluminium/Nickel-Verhältnis wurden auf maximale Aktivität und Selektivität optimiert. Umsätze über 90% konnten erreicht werden. Im Vergleich zu Polybutadienen, die mit anderen Nickel-Phosphin-Systemen hergestellt wurden, zeigten die synthetisierten Polybutadiene höhere cis-1,4-Anteile (〈80%) und eine geringe Bildung von 1,2-Einheiten (2%). Alle Polymeren hatten niedrige mittlere Molekulargewichte (Mw 〉 11 800).
    Notes: The new dicationic nickel complex [dppfNi(MeCN)4][BF4]2 (dppf = 1,1′-bis(diphenylphosphino)ferrocene) in the presence of diethylaluminium chloride (AIEt2CI) exhibited high activity on the 1,3-butadiene polymerization. Reaction time, temperature and aluminium/nickel molar ratio were optimized in order to achieve maximum activity and selectivity. Conversions higher than 90% were obtained in contrast to other nickel-based systems using phosphine ligands, the resulting polybutadiene showed high cis-1,4 (〈80%) content and only small amount of 1,2-units (2%). All polymers presented low molecular weights (Mw 〉 11 800).
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  • 2
    Publication Date: 2013-12-18
    Description: River systems connect the terrestrial biosphere, the atmosphere and the ocean in the global carbon cycle. A recent estimate suggests that up to 3 petagrams of carbon per year could be emitted as carbon dioxide (CO2) from global inland waters, offsetting the carbon uptake by terrestrial ecosystems. It is generally assumed that inland waters emit carbon that has been previously fixed upstream by land plant photosynthesis, then transferred to soils, and subsequently transported downstream in run-off. But at the scale of entire drainage basins, the lateral carbon fluxes carried by small rivers upstream do not account for all of the CO2 emitted from inundated areas downstream. Three-quarters of the world's flooded land consists of temporary wetlands, but the contribution of these productive ecosystems to the inland water carbon budget has been largely overlooked. Here we show that wetlands pump large amounts of atmospheric CO2 into river waters in the floodplains of the central Amazon. Flooded forests and floating vegetation export large amounts of carbon to river waters and the dissolved CO2 can be transported dozens to hundreds of kilometres downstream before being emitted. We estimate that Amazonian wetlands export half of their gross primary production to river waters as dissolved CO2 and organic carbon, compared with only a few per cent of gross primary production exported in upland (not flooded) ecosystems. Moreover, we suggest that wetland carbon export is potentially large enough to account for at least the 0.21 petagrams of carbon emitted per year as CO2 from the central Amazon River and its floodplains. Global carbon budgets should explicitly address temporary or vegetated flooded areas, because these ecosystems combine high aerial primary production with large, fast carbon export, potentially supporting a substantial fraction of CO2 evasion from inland waters.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Abril, Gwenael -- Martinez, Jean-Michel -- Artigas, L Felipe -- Moreira-Turcq, Patricia -- Benedetti, Marc F -- Vidal, Luciana -- Meziane, Tarik -- Kim, Jung-Hyun -- Bernardes, Marcelo C -- Savoye, Nicolas -- Deborde, Jonathan -- Souza, Edivaldo Lima -- Alberic, Patrick -- Landim de Souza, Marcelo F -- Roland, Fabio -- England -- Nature. 2014 Jan 16;505(7483):395-8. doi: 10.1038/nature12797. Epub 2013 Dec 15.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Laboratoire Environnements et Paleoenvironnements Oceaniques et Continentaux (EPOC), CNRS, Universite Bordeaux 1, Avenue des Facultes, 33405 Talence, France [2] Laboratoire Geosciences et Environnement de Toulouse, Institut de Recherche pour le Developpement, Universite Paul Sabatier, 14 avenue Edouard Belin, 31400 Toulouse, France. ; Laboratoire Geosciences et Environnement de Toulouse, Institut de Recherche pour le Developpement, Universite Paul Sabatier, 14 avenue Edouard Belin, 31400 Toulouse, France. ; Laboratoire d'Oceanologie et Geosciences, CNRS, Universite du Littoral Cote d'Opale, 32 avenue Foch, 62930 Wimereux, France. ; Equipe Geochimie des Eaux, Institut de Physique du Globe de Paris, Universite Paris Diderot, Sorbonne Paris Cite, 35 rue Helene Brion, 75205 Paris Cedex 13, France. ; Laboratorio de Ecologia Aquatica, Departamento de Biologia, Universidade Federal de Juiz de Fora, Rua Jose Lourenco Kelmer, MG 36036-900 Juiz de Fora, Brazil. ; Laboratoire Biologie des Organismes et Ecosystemes Aquatiques (BOREA), Museum National d'Histoire Naturelle, CNRS, IRD, UPMC, 61 rue Buffon, 75005, Paris, France. ; NIOZ (Royal Netherlands Institute for Sea Research), Department of Marine Organic Biogeochemistry, Texel, 1790 AB Den Burg, The Netherlands. ; Programa de Geoquimica, Universidade Federal Fluminense, Outeiro Sao Joao Batista, RJ 24020015 Niteroi, Brazil. ; Laboratoire Environnements et Paleoenvironnements Oceaniques et Continentaux (EPOC), CNRS, Universite Bordeaux 1, Avenue des Facultes, 33405 Talence, France. ; Instituto de Geociencias, Universidade de Brasilia, Campus Universitario Darcy Ribeiro, DF 70.910-900 Brasilia, Brazil. ; Institut des Sciences de la Terre d'Orleans, 1A rue de la Ferollerie, 45071 Orleans Cedex 2, France. ; Laboratorio de Oceanografia Quimica, Universidade Estadual de Santa Cruz, Rodovia Ilheus-Itabuna, 45662-900 Ilheus, Bahia, Brazil.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24336199" target="_blank"〉PubMed〈/a〉
    Keywords: Atmosphere/chemistry ; Brazil ; Carbon Cycle ; Carbon Dioxide/*analysis ; Lakes/chemistry ; Plants/metabolism ; Rivers/*chemistry ; Water Movements ; *Wetlands
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic ecology 28 (1994), S. 441-451 
    ISSN: 1573-5125
    Keywords: Bacterioplankton ; oxygen consumption ; sub-tropic ; estuarine ; lagoon ; Brazil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Water samples were taken monthly in 1976 at three sites along the Cananéia estuarine-lagoon system (25°S 48°W), on the southern coast of São Paulo State, Brazil. After screening through a 100 μm mesh silk screen, samples from two sites were size fractionated in classes between 100–50 μm, 50–10 μm and 10–0.45 μm and, concentrated. Oxygen consumption rates (OCR) of the fractionated and unfractionated surface samples were estimated after incubating in dark bottles at ‘in situ’ temperature. OCR varied from 0.26±0.95 to 41.61±2.56 μl O2 l−1 h−1. Highest OCR was observed in summer, at the site under fresh-water influence. At this site, for most of the year, the smallest size category contributed mostly to total OCR. Bacteria attached to particulate matter appear to be responsible for most of the oxygen consumption measured. At the more saline waters, OCR was found to be associated with organisms in the 10–100 μm size class. At this site, size analysis of chlorophylla showed that the 0.45–10 μm size category comprised the major portion of total chlorophyll. The lack of association between the OCR dominant size class and the prevailing phytoplankton and bacteria size categories, suggests the oxygen consumption to be due to other organisms, probably nano- and microzooplankton. OCR measured in the unfractionated samples, at site 2, showed the same order of magnitude to those of the fractionated ones. At this site the importance of the bacterial metabolism in relation to the total OCR measured is discussed. It is concluded that in the surface waters of the Cananéia estuarine lagoon system the contribution of bacterial metabolism to total oxygen consumption differs along the system, being significant at the upper reaches of the estuary, where the inputs of organic matter are larger. In saline waters, in spite of high bacterial densities, oxygen consumption seems to reflect the metabolism of larger organisms.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 46 (1998), S. 403-415 
    ISSN: 0006-3525
    Keywords: molecular dynamics ; DNA curvature ; DNA flexibility ; TATA box functionality ; TATA box binding protein (TBP) ; TBP recognition ; TBP binding ; TBP transcriptional activation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four 1.5 ns molecular dynamics (MD) simulations were performed on the d(GCTATAAAAGGG) · d(CCCTTTTATAGC) double helix dodecamer bearing the Adenovirus major late promoter TATA element and three iso-composition mutants for which physical and biochemical data are available from the same laboratory. Three of these DNA sequences experimentally induce tight binding with the TATA box binding protein (TBP) and induce high transcription rates; the other DNA sequence induces much lower TBP binding and transcription. The x-ray crystal structures have previously shown that the duplex DNA in DNA-TBP complexes are highly bent. We performed and analyzed MD simulations for these four DNAs, whose experimental structures are not available, in order to address the issue of whether inherent DNA structure and flexibility play a role in establishing these observed preferences. A comparison of the experimental and simulated results demonstrated that DNA duplex sequence-dependent curvature and flexibility play a significant role in TBP recognition, binding, and transcriptional activation. © 1998 John Wiley & Sons, Inc. Biopoly 46: 403-415, 1998
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  • 5
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A convenient method for the synthesis of 11-[(4-cyano-4′- trans-α-cyanostilbene) oxy]- undecanyl vinyl ether (6) which is the first member of a new class of mesogenic monomers is described. The polymerization of 6 initiated with CF3SO3H/S (CH3)2 in methylene chloride at 0°C proceeds through a living cationic mechanism leading to polymers with controllable molecular weights and polydispersities narrower than 1.10. The mesomorphic behavior of both 6 and poly(6)s with various molecular weights was determined by using a combination of thermal optical polarized microscopy and differential scanning calorimetry. 6 is only crystalline. Poly(6)s with degrees of polymerization from 4 to 30 exhibit an enatiotropic smectic A mesophase and side chain crystallization.
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  • 6
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 353-363 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Block copolymers of styrene and α-methylstyrene were obtained by a cationic mechanism involving a single-step addition in the m-chloroperbenzoic acid/liquid sulfur dioxide system. This result was possible because of the difference in the reactivity of these monomers in the temperatures of -40°C, -60°C, and -78°C. Under these temperature conditions α-methylstyrene is more reactive than styrene. The composition of the block copolymers was determined by NMR and TGA analysis in fractionated samples.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1105-1108 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 19 (1998), S. 409-411 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: RuHCl(CO)(PCy3)2 (1) dissolved in 1-butyl-3-methylimidazolium tetrafluoroborate (2) molten salt is able to reduce selectively NBR to HNBR under hydrogen partial pressures between 10 and 40 bar at 100-160°C in a typical two-phase catalytic reaction. Reaction rates between 0.059 (mmol Ru)-1 · min-1 and 1.65 (mmol Ru)-1 · min-1 were obtained depending on the reaction parameters and increasing with the volume of the molten salt. The overall process has an apparent activation energy of 47 ± 3 kJ · mol-1. The recovered ionic catalyst solution can be reused several times without significant changes in the catalytic performance (selectivity and activity).
    Additional Material: 5 Ill.
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  • 10
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The complex [η3-methallyl-nickel-dad]PF6 is a new catalyst precursor for ethylene polymerization. The system is active in the presence of usual organoaluminium compounds like diethylaluminium chloride, at low Al/Ni ratios and under mild reaction conditions (temperatures between -10°C and 25°C, ethylene partial pressure from 1 to 15 atm). The polymers show extensive methyl branching, whose content is controlled by reaction parameters like temperature and ethylene pressure.
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