Search Results
{N,N-Bis[bis(2,2,2-trifluoroethoxy)phosphanyl]methylamine- κ2 P,P′}bis(η5-cyclopentadienyl) titanium(II)
2013, Haehnel, M., Hansen, S., Spannenberg, A., Beweries, T.
The title compound, [Ti(C5H5)2(C 9H11F12NO4P2)], is a four-membered titanacycle obtained from the reaction of Cp2Ti(η 2-Me3SiC2SiMe3) and CH 3N[P(OCH2CF3)2]2 {N,N-bis[bis(trifluoroethoxy)phosphanyl]methylamine, tfepma}. The Ti II atom is coordinated by two cyclopentadienyl (Cp) ligands and the chelating tfepma ligand in a strongly distorted tetrahedral geometry. The molecule is located on a mirror plane.
Long-term trends in the ionospheric F2 region with different solar activity indices
2013, Mielich, J., Bremer, J.
A new comprehensive data collection by Damboldt and Suessmann (2012a) with monthly foF2 and M(3000)F2 median values is an excellent basis for the derivation of long-term trends in the ionospheric F2 region. Ionospheric trends have been derived only for stations with data series of at least 22 years (124 stations with foF2 data and 113 stations with M(3000)F2 data) using a twofold regression analysis depending on solar and geomagnetic activity. Three main results have been derived: Firstly, it could be shown that the solar 10.7 cm radio flux F10.7 is a better index for the description of the solar activity than the relative solar sunspot number R as well as the solar EUV proxy E10.7. Secondly, the global mean foF2 and
Tandem dinucleophilic cyclization of cyclohexane-1,3-diones with pyridinium salts
2013, Kiamehr, M., Moghaddam, F.M., Mkrtchyan, S., Semeniuchenko, V., Supe, L., Villinger, A., Langer, P., Laroshenko, V.O.
The cyclization of cyclohexane-1,3-diones with various substituted pyridinium salts afforded functionalized 8-oxa-10-aza-tricyclo[7.3.1.0 2,7]trideca-2(7),11-dienes. The reaction proceeds by regioselective attack of the central carbon atom of the 1,3-dicar-bonyl unit to 4-position of the pyridinium salt and subsequent cyclization by base-assisted proton migration and nucleophilic addition of the oxygen atom to the 2-position, as was elucidated by DFT computations. Fairly extensive screening of bases and additives revealed that the presence of potassium cations is essential for formation of the product.
Quantification of waves in lidar observations of noctilucent clouds at scales from seconds to minutes
2013, Kaifler, N., Baumgarten, G., Fiedler, J.
We present small-scale structures and waves observed in noctilucent clouds (NLC) by lidar at an unprecedented temporal resolution of 30 s or less. The measurements were taken with the Rayleigh/Mie/Raman lidar at the ALOMAR observatory in northern Norway (69 N) in the years 2008-2011. We find multiple layer NLC in 7.9% of the time for a brightness threshold of δ β 12 × 10-10 m-1 sr-1. In comparison to 10 min averaged data, the 30 s dataset shows considerably more structure. For limited periods, quasi-monochromatic waves in NLC altitude variations are common, in accord with ground-based NLC imagery. For the combined dataset, on the other hand, we do not find preferred periods but rather significant periods at all timescales observed (1 min to 1 h). Typical wave amplitudes in the layer vertical displacements are 0.2 km with maximum amplitudes up to 2.3 km. Average spectral slopes of temporal altitude and brightness variations are-2.01 ± 0.25 for centroid altitude,-1.41 ± 0.24 for peak brightness and-1.73 ± 0.25 for integrated brightness. Evaluating a new single-pulse detection system, we observe altitude variations of 70 s period and spectral slopes down to a scale of 10 s. We evaluate the suitability of NLC parameters as tracers for gravity waves.
Self-propelled micromotors for cleaning polluted water
2013, Soler, L., Magdanz, V., Fomin, V.M., Sanchez, S., Schmidt, O.G.
We describe the use of catalytically self-propelled microjets (dubbed micromotors) for degrading organic pollutants in water via the Fenton oxidation process. The tubular micromotors are composed of rolled-up functional nanomembranes consisting of Fe/Pt bilayers. The micromotors contain double functionality within their architecture, i.e., the inner Pt for the self-propulsion and the outer Fe for the in situ generation of ferrous ions boosting the remediation of contaminated water.The degradation of organic pollutants takes place in the presence of hydrogen peroxide, which acts as a reagent for the Fenton reaction and as main fuel to propel the micromotors. Factors influencing the efficiency of the Fenton oxidation process, including thickness of the Fe layer, pH, and concentration of hydrogen peroxide, are investigated. The ability of these catalytically self-propelled micromotors to improve intermixing in liquids results in the removal of organic pollutants ca. 12 times faster than when the Fenton oxidation process is carried out without catalytically active micromotors. The enhanced reaction-diffusion provided by micromotors has been theoretically modeled. The synergy between the internal and external functionalities of the micromotors, without the need of further functionalization, results into an enhanced degradation of nonbiodegradable and dangerous organic pollutants at small-scale environments and holds considerable promise for the remediation of contaminated water.
Carbonyl{3,3′-di-tert-butyl-5,5′-dimethoxy-2,2′-bis[(4,4, 5,5-tetramethyl-1,3,2-dioxaphospholan-2-yl)oxy]biphenyl-κ2 P,P′}hydrido(triphenylphosphane-κP)rhodium(I) diethyl ether trisolvate
2013, Selent, D., Spannenberg, A., Börner, A.
In the title compound, [RhH(C74H68O8P2)(C18H15P)(CO)]·3C4H10O, the CHP3 coordination set at the RhI ion is arranged in a distorted trigonal-bipyramidal geometry with the P atoms adopting equatorial coordination sites and the C atom of the carbonyl ligand as well as the H atom adopting the axial sites. The asymmetric unit contains two very similar molecules of the rhodium complex, two half-occupied diethyl ether molecules and further diethyl ether solvent molecules which could not be modelled successfully. Therefore contributions of the latter were removed from the diffraction data using the SQUEEZE procedure in PLATON [Spek (2009). Acta Cryst. D65, 148-155].
Airborne high spectral resolution lidar observation of pollution aerosol during EUCAARI-LONGREX
2013, Groß, S., Esselborn, M., Abicht, F., Wirth, M., Fix, A., Minikin, A.
Airborne high spectral resolution lidar observations over Europe during the EUCAARI-LONGREX field experiment in May 2008 are analysed with respect to the optical properties of continental pollution aerosol. Continental pollution aerosol is characterized by its depolarisation and lidar ratio. Over all, the measurements of the lidar ratio and the particle linear depolarization ratio of pollution aerosols provide a narrow range of values. Therefore, this data set allows for a distinct characterization of the aerosol type "pollution aerosol" and thus is valuable both to distinguish continental pollution aerosol from other aerosol types and to determine mixtures with other types of aerosols.
Simultaneous observations of a Mesospheric Inversion Layer and turbulence during the ECOMA-2010 rocket campaign
2013, Szewczyk, A., Strelnikov, B., Rapp, M., Strelnikova, I., Baumgarten, G., Kaifler, N., Dunker, T., Hoppe, U.-P.
From 19 November to 19 December 2010 the fourth and final ECOMA rocket campaign was conducted at Andøya Rocket Range (69 N, 16 E) in northern Norway. We present and discuss measurement results obtained during the last rocket launch labelled ECOMA09 when simultaneous and true common volume in situ measurements of temperature and turbulence supported by ground-based lidar observations reveal two Mesospheric Inversion Layers (MIL) at heights between 71 and 73 km and between 86 and 89 km. Strong turbulence was measured in the region of the upper inversion layer, with the turbulent energy dissipation rates maximising at 2 W kg-1. This upper MIL was observed by the ALOMAR Weber Na lidar over the period of several hours. The spatial extension of this MIL as observed by the MLS instrument onboard AURA satellite was found to be more than two thousand kilometres. Our analysis suggests that both observed MILs could possibly have been produced by neutral air turbulence.
Particle hygroscopicity during atmospheric new particle formation events: Implications for the chemical species contributing to particle growth
2013, Wu, Z., Birmili, W., Poulain, L., Poulain, L., Merkel, M., Fahlbusch, B., Van Pinxteren, D., Herrmann, H., Wiedensohler, A.
This study examines the hygroscopicity of newly formed particles (diameters range 25-45 nm) during two atmospheric new particle formation (NPF) events in the German mid-level mountains during the Hill Cap Cloud Thuringia 2010 (HCCT-2010) field experiment. At the end of the NPF event involving clear particle growth, we measured an unusually high soluble particle fraction of 58.5% at 45 nm particle size. The particle growth rate contributed through sulfuric acid condensation only accounts for around 6.5% of the observed growth rate. Estimations showed that sulfuric acid condensation explained, however, only around 10% of that soluble particle fraction. Therefore, the formation of additional water-soluble matter appears imperative to explain the missing soluble fraction. Although direct evidence is missing, we consider water-soluble organics as candidates for this mechanism. For the case with clear growth process, the particle growth rate was determined by two alternative methods based on tracking the mode diameter of the nucleation mode. The mean particle growth rate obtained from the inter-site data comparison using Lagrangian consideration is 3.8 (± 2.6) nm h-1. During the same period, the growth rate calculated based on one site data is 5.0 nm h-1 using log-normal distribution function method. In light of the fact that considerable uncertainties could be involved in both methods, we consider both estimated growth rates consistent.
Formation of organic aerosol in the Paris region during the MEGAPOLI summer campaign: Evaluation of the volatility-basis-set approach within the CHIMERE model
2013, Zhang, Q.J., Beekmann, M., Drewnick, F., Freutel, F., Schneider, J., Crippa, M., Prevot, A.S.H., Baltensperger, U., Poulain, L., Wiedensohler, A., Sciare, J., Gros, V., Borbon, A., Colomb, A., Michoud, V., Doussin, J.-F., Denier Van Der Gon, H.A.C., Haeffelin, M., Dupont, J.-C., Siour, G., Petetin, H., Bessagnet, B., Pandis, S.N., Hodzic, A., Sanchez, O., Honoré, C., Perrussel, O.
Simulations with the chemistry transport model CHIMERE are compared to measurements performed during the MEGAPOLI (Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation) summer campaign in the Greater Paris region in July 2009. The volatility-basis-set approach (VBS) is implemented into this model, taking into account the volatility of primary organic aerosol (POA) and the chemical aging of semi-volatile organic species. Organic aerosol is the main focus and is simulated with three different configurations with a modified treatment of POA volatility and modified secondary organic aerosol (SOA) formation schemes. In addition, two types of emission inventories are used as model input in order to test the uncertainty related to the emissions. Predictions of basic meteorological parameters and primary and secondary pollutant concentrations are evaluated, and four pollution regimes are defined according to the air mass origin. Primary pollutants are generally overestimated, while ozone is consistent with observations. Sulfate is generally overestimated, while ammonium and nitrate levels are well simulated with the refined emission data set. As expected, the simulation with non-volatile POA and a single-step SOA formation mechanism largely overestimates POA and underestimates SOA. Simulation of organic aerosol with the VBS approach taking into account the aging of semi-volatile organic compounds (SVOC) shows the best correlation with measurements. High-concentration events observed mostly after long-range transport are well reproduced by the model. Depending on the emission inventory used, simulated POA levels are either reasonable or underestimated, while SOA levels tend to be overestimated. Several uncertainties related to the VBS scheme (POA volatility, SOA yields, the aging parameterization), to emission input data, and to simulated OH levels can be responsible for this behavior. Despite these uncertainties, the implementation of the VBS scheme into the CHIMERE model allowed for much more realistic organic aerosol simulations for Paris during summertime. The advection of SOA from outside Paris is mostly responsible for the highest OA concentration levels. During advection of polluted air masses from northeast (Benelux and Central Europe), simulations indicate high levels of both anthropogenic and biogenic SOA fractions, while biogenic SOA dominates during periods with advection from Southern France and Spain.