# ALBERT

## All Library Books, journals and Electronic Records Telegrafenberg

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• 1
Electronic Resource
Springer
ISSN: 1618-2650
Source: Springer Online Journal Archives 1860-2000
Topics: Chemistry and Pharmacology
Type of Medium: Electronic Resource
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• 2
Electronic Resource
Springer
ISSN: 1618-2650
Source: Springer Online Journal Archives 1860-2000
Topics: Chemistry and Pharmacology
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• 3
Electronic Resource
Springer
ISSN: 1588-2780
Source: Springer Online Journal Archives 1860-2000
Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
Notes: Abstract The split-root technique was used to study the effect of varying the growth media on the elemental content of nutrient elements in the roots of grape vines. The varieties 2-1 (R99 x Jacquez) and Sauvignon blanc (Vitis vinifera) were grown in Hoagland water culture with and without added aluminium. The elemental concentrations of Mg, Al, Si, P. S, Cl, K and Ca in the dried roots were determined by PIXE. Roots grown in Al-rich media were deficient in Mg and Ca, but enriched in Al. There was a correlation between Al and Si but the uptake differed in the two varieties.
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• 4
Electronic Resource
Springer
International journal of thermophysics 19 (1998), S. 719-730
ISSN: 1572-9567
Keywords: bromomethanes ; bromomethyl radicals ; enthalpies of formation ; thermodynamic properties
Source: Springer Online Journal Archives 1860-2000
Topics: Physics
Notes: Abstract Thermochemical data on volatile organic compounds containing bromine are needed for atmospheric modeling, in view of their ozone depletion potential upon photodissociation and the release of atomic bromine. Yet even for the bromomethane series, with the exception of CH3Br, thermodynamic properties are not well established. Similarly, structural and thermochemical information on brominated methyl radicals is incomplete or not available. In this paper we have adopted a computational approach to obtain this needed information. Equilibrium geometries for the molecules CH4−n Br n (n = 0–4) and radicals CH3−m Br m (m = 0–3) were optimized at both HF/6-31G* and MP2/6-31G* levels of theory. Moments of inertia, harmonic vibrational frequencies, and thermodynamic functions were determined at the HF/6-31G* level. Electron correlation contributions were performed by single-point calculations at both second- and fourth-order Møller–Plesset perturbation theory for derived MP2/6-31G*geometries. Enthalpies of formation were obtained from a consideration of applicable isodesmic reactions using the derived MP4/6-31G**//MP2/6-31G* total energies in conjunction with experimentally established enthalpies of formation for CH3Br, CH4, and CH3. These data were then used in the determination of $$\Delta {\rm H}^ \circ _{{\text{f, T}}} ,{\text{ }}\Delta G^ \circ _{{\text{f,T}}} ,{\text{ and }}K_{f,\Upsilon }$$ and K f, T for all species over the temperature range 0 to 1500K. A comparison was made to the existing standard enthalpies of formation at 298 K, both experimentally measured and theoretically estimated, for CH2Br2, CHBr3, CBr4, CH2Br•, CHBr2•, and CBr3•.
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• 5
Electronic Resource
Springer
Cell biology and toxicology 12 (1996), S. 245-249
ISSN: 1573-6822
Keywords: acrolein ; bronchial hyperresponsiveness ; calcium ; ozone ; excitation-contraction coupling
Source: Springer Online Journal Archives 1860-2000
Topics: Biology , Medicine
Notes: Abstract The aims of this work were (1) to determine the dose-response relationship between ex vivo exposure to oxidizing pollutants such as nitrogen dioxide (NO2), the aldehyde acrolein, and ozone (O3), and the reactivity to agonists in isolated human bronchial smooth muscle; and (2) to investigate the alterations in the cellular mechanisms of human airway smooth muscle contraction induced by such exposures. Experiments were performed in isolated human bronchi obtained at thoracotomy. Isometric contraction in response to a variety of agonists was compared between pollutant-exposed preparations and paired controls. Short exposures to NO2, acrolein, or O3 altered the subsequent airway smooth muscle responsiveness in a dose-dependent manner. The cellular mechanisms producing the airway hyperresponsiveness observed in vitro are shared by the three pollutants and include alterations in airway smooth muscle excitation-contraction coupling as well as indirect effects on neutral endopeptidase activity.
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• 6
Electronic Resource
Springer
Cell biology and toxicology 12 (1996), S. 377-377
ISSN: 1573-6822
Source: Springer Online Journal Archives 1860-2000
Topics: Biology , Medicine
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• 7
Electronic Resource
s.l. : American Chemical Society
Journal of the American Chemical Society 81 (1959), S. 1081-1083
ISSN: 1520-5126
Source: ACS Legacy Archives
Topics: Chemistry and Pharmacology
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• 8
Electronic Resource
New York, NY : Wiley-Blackwell
ISSN: 0538-8066
Keywords: Chemistry ; Physical Chemistry
Source: Wiley InterScience Backfile Collection 1832-2000
Topics: Chemistry and Pharmacology
Notes: The room temperature photolysis of 1,1-dichloroethane at 147 nm in the pressure range of 1.34-196.2 torr is characterized almost entirely by the molecular elimination of HCl, Cl2, and small quantities of H2. Acetylene is also produced. While it is possible that the C2H2 arises, in part, from the decomposition of vibrationally excited ground states of C2H3Cl and/or C2H4, in this particlar case serious consideration has to be given to alternative explanations where the products of the primary processes are formed in electronically excited states. The ±, elimination of molecular chlorine is not inconsistent with an increased degree of Cl—Cl interaction predicted for a «Rydberg «state of 1,1-C2H4Cl2. Varying small yields of CH4 are observed in the presence and absence of NO. The effect of large pressures of CF4 on the quantum yields of the major products is extremely small. The extinction coefficient for 1,1-C2H4Cl2 at 147 nm and 296°K is 246 ± 29 cm-1 ± atm-1.
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• 9
Electronic Resource
New York, NY : Wiley-Blackwell
ISSN: 0538-8066
Keywords: Chemistry ; Physical Chemistry
Source: Wiley InterScience Backfile Collection 1832-2000
Topics: Chemistry and Pharmacology
Notes: 1,1,1-Difluorochloroethane (Freon 142) was photolyzed at 147 nm in the pressure range of 3.6-20.6 torr. The effects of added NO, H2S, and CF4 were investigated. The extinction coefficient at 147 nm and 296°K was determined to be 64 ± 8 atm-1 · cm-1.The molecule photodecomposes largely by α,β elimination of HCl to give 1,1-difluoroethylene (Φ = 0.74 ± 0.06). There is no observable elimination of HF, but there is strong evidence for the elimination of the elements of FCl though the relative importance of this process is minor, as are contributions from carbon—carbon and carbon—halogen bond fission.The 1,1-difluoroethylene formed is undoubtedly vibratonally excited and is the source of a pressure-dependent small yield of fluoroacetylene. Over the pressure range studied there is no evidence that the major primary process itself is affected by changes in total pressure as is the case in the 147-nm photolysis of ethyl chloride.
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• 10
Electronic Resource
New York, NY : Wiley-Blackwell
ISSN: 0538-8066
Keywords: Chemistry ; Physical Chemistry
Source: Wiley InterScience Backfile Collection 1832-2000
Topics: Chemistry and Pharmacology
Notes: 1,2-Fluorochloroethane was photolyzed at 147 nm in the pressure range of 3.8-20.9 torr. The effects of added NO, H2S, and large pressures of CF4 were also investigated. The exponential extinction coefficient at 147 nm and 296°K was found to be 147 ± 4 atm-1 · cm-1.The photochemistry in some respects is similar to that of ethyl chloride. The primary processes again appear to involve at least two excited states. One of these yields ethylene by FCl elimination (Φ ≃ 0.3) and has a lifetime of ∼3.2 × 10-10 sec, with respect to an internal conversion to the vibrationally excited ground state or, more probably, a collisionally induced crossover to a state decomposing mainly by carbon—halogen bond fission. The molecular elimination of HCl, H2, and small amounts of HF also occurs but not apparently from the same state as does FCl. The quantum yields of products with radical precursors, however, are not large, and hence little, if any, of the FCl and probably none of HCl, H2, and HF subsequently dissociates. The vinyl fluoride and vinyl chloride, accompanying the elimination of HF and HCl, are postulated as possible sources of the secondary production of acetylene.