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  • LUNAR AND PLANETARY EXPLORATION  (13)
  • Chemistry  (9)
  • 2015-2019
  • 1985-1989  (11)
  • 1980-1984  (11)
  • 1955-1959
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 23 (1984), S. 707-718 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An electric birefringence study was carried out on aqueous suspensions of the purple membrane of Halobacterium halobium. In addition to the characterization of both native and modified membrane samples, the dependence of electric birefringence on pH and ionic strength was also investigated. The results indicate that purple membrane shows electric birefringence at a field strength as low as 200 V/cm. The permanent dipole moment and polarizability ranged from 20,500 debyes and 1.01 × 10-14 cm3 for a purple membrane concentration of 0.40 mg/mL to 41,000 debyes and 2.05 × 10-14 cm3 for a concentration of 0.80 mg/mL. It was also found that removal of the retinyl group of bacteriorhodopsin substantially decreases but does not eliminate the electric birefringence of the membrane. The solubilization of the membrane by Triton X-100, however, completely abolishes the electric birefringence. These experiments indicate that there is an interaction between adjacent bacteriorhodopsin molecules within the purple membrane via the retinyl chromophore moiety that builds up the permanent dipole moment. They also suggest that there are two types of response when purple membrane suspensions are placed in an electric field. One is an alignment of the disk-shaped particles with the field. The other is a stacking of the particles following their alignment by the electric field, which is promoted by the induced dipole moment.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: These studies compare the voltammetric behavior of solutions and adsorbed layers of the following unsaturated alcohols: benzyl alcohol (BZA), 4-pyridylcarbinol (4PC), allyl alcohol (AA), propargyl alcohol (PGA), cis-2-butene-1,4-diol (CBED), and 2-butyne-1,4-diol (BYD). They were undertaken for well-characterized Pt(111) electrode surfaces which were either annealed in an ultrahigh vacuum (UHV) or electrochemically cycled, as well as for annealed (UHV) Pt(poly). Electrochemical oxidation of BZA, AA, PGA, CBED, and BYD in aqueous fluoride electrolyte proceeds in two stages: first the alcohol moiety is oxidized to CO2 (0.4 V), followed by oxidation of the resulting adsorbed hydrocarbon (alkene, alkyne, or phenyl, 1.0 V); 4PC is relatively inert. The alcohol moiety in 4PC, which is located opposite the pyridine ring from the surface, does not undergo oxidation at an appreciable rate. in fact, 4PC effectively passivates the surface and poisons the electrochemical activity. Electrochemical cycling of the annealed Pt(111) single-crystal surface greatly increases the oxidation rates of the aliphatic alcohols and, to a lesser extent, increases the oxidation rate of BZA. The oxidation rate enhancement is somewhat smaller if the electrode is electrochemically cycled in the presence of the alcohol. The majority of the difference effected by cycling can be observed after only one cycle. Voltammetry on polycrystalline Pt surfaces resembles that on cycled Pt(111) surfaces for PGA and AA, but resembles that on cycled Pt(111) surfaces for PGA and AA, but resembles that on annealed Pt(111) more closely for the diols CBED and BYD.
    Additional Material: 6 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 94 (1982), S. 647-648 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 97 (1985), S. 837-853 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ein Komplex, der zwei oder mehr paramagnetische übergangsmetall-Ionen enthält, kann völlig andere magnetische Eigenschaften haben als Einkernkomplexe dieser Ionen. Die Eigenschaften von Zweikernkomplexen hängen von Art und Stärke der Metall-Metall-Wechselwirkungen über die verbrückenden Liganden ab. Weisen beide Ionen je ein ungepaartes Elektron auf (z. B. Cu2+-Ionen), dann ist der energetische Grundzustand des Moleküls entweder ein Spin-Singulett oder ein Spin-Triplett. Im ersten Fall spricht man von antiferromagnetischer, im zweiten von ferromagnetischer Wechselwirkung. Art und Stärke der Wechselwirkung können durch die Wahl der Metall-Ionen sowie der verbrückenden und der terminalen Liganden und damit durch die Symmetrie und die Delokalisierung der metallzentrierten Orbitale, die von den ungepaarten Elektronen besetzt sind (magnetische Orbitale), gesteuert werden. Dies gelang zuerst bei einem rein ferromagnetischen Cu2+VO2+-Komplex. Die gleiche Strategie konnte zur Herstellung molekularer Ferromagnete genutzt werden, die eine der größten Herausforderungen auf dem Feld molekularer Werkstoffe ist. Man kann das Ausmaß der Wechselwirkung in einer vorgegebenen verbrückten Struktureinheit durch Variation der terminalen Liganden, die die Rolle von „Justierschrauben“ übernehmen, genau abstimmen. Durch die sorgfältige Wahl sowohl der verbrückenden als auch der terminalen Liganden kann eine sehr starke antiferromagnetische Wechselwirkung erreicht werden, sogar im Falle weit voneinander entfernter Metall-Ionen. Einige schwefelhaltige Brücken sind dafür besonders geeignet.
    Additional Material: 29 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 94 (1982), S. 386-386 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract.Das vollständige Manuskript dieser Zuschrift erscheint in: Angew. Chem. Suppl. 1982, 953-960
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 21 (1982), S. 385-385 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract.The complete manuscript of this communication appears in: Angew. Chem. Suppl. 1982, 953. DOI:10.1002/anie.198209530
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 21 (1982), S. 624-625 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 24 (1985), S. 834-850 
    ISSN: 0570-0833
    Keywords: Dinuclear complexes ; Complexes ; Magnetic properties ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When two paramagnetic transition metal ions are present in the same molecular entity, the magnetic properties can be totally different from the sum of the magnetic properties of each ion surrounded by its nearest neighbors. These new properties depend on the nature and the magnitude of the interaction between the metal ions through the bridging ligands. If both ions have an unpaired electron (e.g. Cu2+ ions), then the molecular state of lowest energy is either a spin singlet or a spin triplet. In the former case, the interaction is said to be antiferromagnetic, in the latter case ferromagnetic. The nature and the order of magnitude of the interaction can be engineered by judiciously choosing the interacting metal ions and the bridging and terminal ligands, and, thus, by the symmetry and the delocalization of the orbitals centered on the metal ions and occupied by the unpaired electrons (magnetic orbitals). The first success in this “molecular engineering” of bimetallic compounds was in the synthesis of a Cu2+VO2+ heterobimetallic complex in which the interaction is purely ferro-magnetic. The same strategy could be utilized for designing molecular ferromagnets, one of the major challenges in the area of molecular materials. Another striking result is the possibility of tuning the magnitude of the interaction through a given bridging network by modifying the nature of the terminal ligands, which, in some way, play the role of “adjusting screws”. By careful selection of the bridging and terminal ligands, a very large antiferro-magnetic interaction can be achieved, even if the metal ions are far away from each other. Some sulfur-containing bridges are especially suitable in this respect.
    Additional Material: 29 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 21 (1982), S. 953-960 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 10
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    Unknown
    In:  CASI
    Publication Date: 2014-10-08
    Description: The consequences of the hypothesis that the evolution of CO2 is directly linked to the occurrence of at least transitory pockets of moisture were exposed. The current conditions preclude the existence of open bodies of liquid water and the formation of moisture in disequilibrium is not excluded by any known constraints. The water evaporation rate is inversely proportional to PCO2, and the existence of a limiting value (P*) for which liquid water can form in the Mars environment is postulated. The evolution of PCO2 is controlled largely by relatively rapid aqueous chemistry forming carbon-containing sedimentary rocks, perhaps during early history in open water, but more recently in transitory pockets of moisture in the soil. Once the total atmospheric pressure is reduced to near P*, the occurrence of transitory moisture is inhibited, and atmospheric CO2 is no longer depleted by an efficient mechanism. The role of the carbonate reservoir in the current overall carbon budget on Mars, according to this scheme, is illustrated.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: NASA, Washington Repts. of Planetary Geol. and Geophys. Program; p 232-234
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