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  • Chemistry  (108,909)
  • Inorganic Chemistry  (11,128)
  • Wiley-Blackwell  (108,906)
  • Massachusetts Institute of Technology and Woods Hole Oceanographic Institution  (3)
  • 2015-2019  (3)
  • 1995-1999  (38,447)
  • 1990-1994  (50,825)
  • 1950-1954  (9,223)
  • 1925-1929  (10,411)
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  • 1
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    Massachusetts Institute of Technology and Woods Hole Oceanographic Institution
    Publication Date: 2022-05-25
    Description: Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy at the Massachusetts Institute of Technology and the Woods Hole Oceanographic Institution September 2018
    Description: Many chemical constituents are removed from the ocean by attachment to settling particles, a process referred to as “scavenging.” Radioisotopes of thorium, a highly particle-reactive element, have been used extensively to study scavenging in the ocean. However, this process is complicated by the highly variable chemical composition and concentration of particles in oceanic waters. This thesis focuses on understanding the cycling of thorium as affected by particle concentration and particle composition in the North Atlantic. This objective is addressed using (i) the distributions 228,230,234Th, their radioactive parents, particle composition, and bulk particle concentration, as measured or estimated along the GEOTRACES North Atlantic Transect (GA03) and (ii) a model for the reversible exchange of thorium with particles. Model parameters are either estimated by inversion (chapter 2-4), or prescribed in order to simulate 230Th in a circulation model (chapter 5). The major findings of this thesis follow. In chapters 2 and 3, I find that the rate parameters of the reversible exchange model show systematic variations along GA03. In particular, 𝑘1, the apparent first-order rate "constant" of Th adsorption onto particles, generally presents maxima in the mesopelagic zone and minima below. A positive correlation between 𝑘1 and bulk particle concentration is found, consistent with the notion that the specific rate at which a metal in solution attaches to particles increases with the number of surface sites available for adsorption. In chapter 4, I show that Mn (oxyhydr)oxides and biogenic particles most strongly influence 𝑘1 west of the Mauritanian upwelling, but that biogenic particles dominate 𝑘1 in this region. In chapter 5, I find that dissolved 230Th data are best represented by a model that assumes enhanced values of 𝑘1 near the seafloor. Collectively, my findings suggest that spatial variations in Th radioisotope activities observed in the North Atlantic reflect at least partly variations in the rate at which Th is removed from the water column.
    Description: This work was supported by the US National Science Foundation. Two US NSF grants have supported the research in this thesis (OCE-1232578 and OCE-155644).
    Keywords: Thorium ; Chemistry
    Repository Name: Woods Hole Open Access Server
    Type: Thesis
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  • 2
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    Massachusetts Institute of Technology and Woods Hole Oceanographic Institution
    Publication Date: 2022-05-25
    Description: Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy at the Massachusetts Institute of Technology and the Woods Hole Oceanographic Institution June 2017
    Description: This thesis documents the origin, distribution, and fate of methane and several of its isotopic forms on Earth. Using observational, experimental, and theoretical approaches, I illustrate how the relative abundances of 12CH4, 13CH4, 12CH3D, and 13CH3D record the formation, transport, and breakdown of methane in selected settings. Chapter 2 reports precise determinations of 13CH3D, a “clumped” isotopologue of methane, in samples collected from various settings representing many of the major sources and reservoirs of methane on Earth. The results show that the information encoded by the abundance of 13CH3D enables differentiation of methane generated by microbial, thermogenic, and abiogenic processes. A strong correlation between clumped- and hydrogen-isotope signatures in microbial methane is identified and quantitatively linked to the availability of H2 and the reversibility of microbially-mediated methanogenesis in the environment. Determination of 13CH3D in combination with hydrogen-isotope ratios of methane and water provides a sensitive indicator of the extent of C–H bond equilibration, enables fingerprinting of methane-generating mechanisms, and in some cases, supplies direct constraints for locating the waters from which migrated gases were sourced. Chapter 3 applies this concept to constrain the origin of methane in hydrothermal fluids from sediment-poor vent fields hosted in mafic and ultramafic rocks on slow- and ultraslow-spreading mid-ocean ridges. The data support a hypogene model whereby methane forms abiotically within plutonic rocks of the oceanic crust at temperatures above ca. 300 C during respeciation of magmatic volatiles, and is subsequently extracted during active, convective hydrothermal circulation. Chapter 4 presents the results of culture experiments in which methane is oxidized in the presence of O2 by the bacterium Methylococcus capsulatus strain Bath. The results show that the clumped isotopologue abundances of partially-oxidized methane can be predicted from knowledge of 13C/12C and D/H isotope fractionation factors alone.
    Description: The research activities documented in this thesis were made possible by grants to my advisor from the U.S. National Science Foundation (NSF award EAR-1250394), the National Aeronautics and Space Administration (NASA) Astrobiology Institute (NAI, University of Colorado, Boulder, CAN 7 under Cooperative Agreement NNA15BB02A), the Department of Energy (DOE, Small Business Innovation Research program, contract DE-SC0004575), the Alfred P. Sloan Foundation via the Deep Carbon Observatory, and a Shell Graduate Fellowship through the MIT Energy Initiative. I completed the bulk of the work in this thesis while being supported by a National Defense Science and Engineering Graduate (NDSEG) Fellowship awarded through the Office of Naval Research of the U.S. Department of Defense. The StanleyW.Watson Fellowship Fund provided support during my first summer term at WHOI.The Charles M. Vest Presidential Fellowship at MIT supported me in the first year of my Ph.D. studies. I received additional support that year through NSF award EAR-1159318 (to S. Ono and T. Bosak) and theWalter & Adel Hohenstein Graduate Fellowship of Phi Kappa Phi. The MIT Earth Resources Laboratory and PAOC Houghton Fund funded my attendance at several conferences.
    Keywords: Methane ; Chemistry ; Isotopes ; Oxidation
    Repository Name: Woods Hole Open Access Server
    Type: Thesis
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  • 3
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    Massachusetts Institute of Technology and Woods Hole Oceanographic Institution
    Publication Date: 2022-05-26
    Description: Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy at the Massachusetts Institute of Technology and the Woods Hole Oceanographic Institution February 2017
    Description: Salt marshes are physically, chemically, and biologically dynamic environments found globally at temperate latitudes. Tidal creeks and marshtop ponds may expand at the expense of productive grass-covered marsh platform. It is therefore important to understand the present magnitude and drivers of production and respiration in these submerged environments in order to evaluate the future role of salt marshes as a carbon sink. This thesis describes new methods to apply the triple oxygen isotope tracer of photosynthetic production in a salt marsh. Additionally, noble gases are applied to constrain air-water exchange processes which affect metabolism tracers. These stable, natural abundance tracers complement traditional techniques for measuring metabolism. In particular, they highlight the potential importance of daytime oxygen sinks besides aerobic respiration, such as rising bubbles. In tidal creeks, increasing nutrients may increase both production and respiration, without any apparent change in the net metabolism. In ponds, daytime production and respiration are also tightly coupled, but there is high background respiration regardless of changes in daytime production. Both tidal creeks and ponds have higher respiration rates and lower production rates than the marsh platform, suggesting that expansion of these submerged environments could limit the ability of salt marshes to sequester carbon.
    Description: Financial support for my doctoral research was provided by the United States Department of Defense through the National Defense Science and Engineering Graduate Fellowship Program, the National Science Foundation under grant OCE-1233678, and the Woods Hole Oceanographic Institution (WHOI) under grants from the WHOI Coastal Ocean Institute, Ocean and Climate Change Institute, and Ocean Life Institute. WHOI Academic Programs Office also provided funding support for research, through the Ocean Ventures Fund, and for my stipend, as graduate research assistantships including an assistantship from the United States Geological Survey administered by WHOI.
    Keywords: Marshes ; Chemistry ; Metabolism ; Knorr (Ship : 1970-) Cruise KN210-04
    Repository Name: Woods Hole Open Access Server
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  • 4
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    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999) 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 5
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    Chemie in unserer Zeit 33 (1999), S. 45-50 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A variety of demonstration experiments can be shown to a large audience with a minimum amount of chemicals by using an ordinary slide projector and easily mounted cuvettes. A detailed instruction for assembling the cuvettes is given as m d l as examples for suitable demonstration experiments in general, inorganic, organic and physical chemistry.
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  • 6
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    Chemie in unserer Zeit 33 (1999), S. 61-61 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 7
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    Chemie in unserer Zeit 33 (1999), S. 66-66 
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    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 8
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    Chemie in unserer Zeit 33 (1999), S. 67-67 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 9
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    Chemie in unserer Zeit 33 (1999) 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 10
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    Chemie in unserer Zeit 33 (1999), S. 95-103 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Natural events as well as human activities are affecting the environment and even with largescale monitoring programs it is not possible to completely assess the state of the environment. But a documentation of the environmental status with respect to its chemical composition can be realized with systematically collected representative environmental samples, which can be stored for decades at very low temperatures almost without degradation. Such ‘banking activity’ allows a current environmental monitoring and also a retrospective analysis for the determination of components which have not been analyzed at the time of sampling because of ta lack in analytical techniques or because they have not been known or considered environmentally relevant. The concept of environmental specimen banking and general procedures are described. Various examples illustrate the many facets of such activities.
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  • 11
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    Chemie in unserer Zeit 33 (1999), S. 128-128 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Arbeitsmarktsituation in der Chemie hat sich in den letzten Jahren spürbar entspannt. Dennoch gibt es auf etlichen, nicht hundertprozentig dem Trend der Zeit entsprechenden Spezialgebieten immer noch einen beträchtlichen Überhang an Stellensuchenden. Entsprechende Mobilität vorausgesetzt, kann das Internet bei der Stellensuche hilfreich sein.
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  • 12
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    Chemie in unserer Zeit 33 (1999), S. 135-135 
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    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 13
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    Chemie in unserer Zeit 33 (1999) 
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    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 14
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    Chemie in unserer Zeit 33 (1999), S. 165-166 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 15
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    Chemie in unserer Zeit 33 (1999), S. 158-164 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Atmospheric aerosol particles cause one of the largest uncertainties in estimates of human influence on climate - a good reason to take a closer look at the atmospheric life cycle of the aerosols and its effects. Besides a number of primary and secondary natural aerosol sources we need to consider since the beginning of industrialisation strong manmade particle sources. During its residence in the atmosphere the aerosol interacts in many physical and chemical ways with other atmospheric trace substances, most importantly with water vapor and its liquid and solid phases. Through its direct effect on solar and thermal radiation and through its influence on clouds the atmospheric aerosol exerts a climate forcing. To data we cannot predict the ensuing climate response because of our limited understanding of essential atmospheric processes and of the many possible feedbacks within the climate system. However, already our present knowledge of the role of the atmospheric aerosol in the climate system makes strictly global views of anthropogenic climate changes questionable.
    Notes: Der Stand unseres Wissens zum Kreislauf des Atmosphärischen Aerosols und von seiner Rolle im Klimasystem läßt sich wie folgt zusammenfassen: 1Unser Verständnis des globalen Aerosolkreislaufs und vor allem des menschlichen Eingriffs in denselben ist noch sehr unvollständig. Dies gilt in hohem Maße auch für die mit diesem Kreislauf verbundenen chemischen Mehrphasenprozesse.2Ein negativer direkter Klimaantrieb anthropogener Aerosole existiert über die Streuung und Absorption, hat aber noch große Unsicherheiten und kann über hoch mit Rußpartikeln belasteten Gebieten auch positive Werte annehmen.3Ein indirekter Klimaantrieb anthropogener Aerosole existiert wahrscheinlich und hat ebenfalls ein negatives Vorzeichen. Seine Größenordnung und Unsicherheiten lassen sich noch nicht quantifizieren.
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  • 16
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    Chemie in unserer Zeit 33 (1999), S. 177-185 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemical concepts are important to gain a qualitative understanding of chemistry. They are needed to find interesting questions to which experimental research as well as quantum-chemical investigations and computer simulations can contribute. We point out why chemical concepts should be seen as an important and from fundamental physical theories to a certain degree independent part of chemistry. An overview and analysis of some concepts - which are often introduced only in connection with special examples instead of a discussion for their own sake - are given. We take a closer look at some concepts to illustrate our assertions. An analysis of the stability of the cyclic (MoNL3)-trimer demonstrates how these concepts work and what they can tell us about this special case.
    Notes: Wir haben versucht, deutlich zu machen, wie wichtig theoretische Konzepte in der Chemie sind. Dabei gelangen wir zu folgenden Schlußfolgerungen über die Konzepte, die in der Chemie herangezogen werden, um Beobachtungen zu deuten und zu verstehen: Qualitativ chemische Konzepte sind für ein Verständnis der Chemie unverzichtbar. Eine quantenchemische Berechnung liefert nicht automatisch Verständnis und Einordnung in einen Gesamtzusammenhang.Erst die vereinfachende Beschreibung chemischer Konzepte ermöglicht eine unmittelbare Diskussion chemischer Fragestellungen.Die Konzepte sind trotz grundlegender physikalischer Theorien bis zu einem gewissen Grade eigenständig.
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  • 17
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    Chemie in unserer Zeit 33 (1999) 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 18
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    Chemie in unserer Zeit 33 (1999), S. 213-220 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The article commemorates the centenary of the protection of the proprietary mine of Aspirin. The early medicinal uses of salicylic acid derivatives in herbal remedies arc summarised as well as the biosynthesis of these derivatives. The history of the synthesis of salicylic acid and of acetyl salicylic acid (ASS) is described in detail as is the discovery of additional therapeutic applications and the basic pharmacology of ASS.
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  • 19
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    Chemie in unserer Zeit 33 (1999), S. 234-235 
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    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 20
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
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  • 21
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    Chemie in unserer Zeit 33 (1999), S. 246-246 
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    Keywords: Chemistry ; Chemistry
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  • 22
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    Chemie in unserer Zeit 33 (1999), S. 250-250 
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    Keywords: Chemistry ; Chemistry
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  • 23
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    Chemie in unserer Zeit 33 (1999), S. 308-309 
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    Keywords: Chemistry ; Chemistry
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  • 24
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    Chemie in unserer Zeit 33 (1999), S. 312-312 
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    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 25
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    Chemie in unserer Zeit 33 (1999), S. 314-314 
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    Keywords: Chemistry ; Chemistry
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    Topics: Chemistry and Pharmacology
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  • 26
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    Chemie in unserer Zeit 33 (1999), S. IX 
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    Keywords: Chemistry ; Chemistry
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  • 27
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    Chemie in unserer Zeit 33 (1999), S. 318-318 
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    Keywords: Chemistry ; Chemistry
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  • 28
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    Chemie in unserer Zeit 33 (1999), S. 354-358 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemical Biology is a rapidly growing field at the interface of organic chemistry and cell biology. Chemical strategies are used to address biological questions not amenable to traditional genetic and biochemical techniques alone. Thc enormous potential of Chemical Biology is illustrated by four recent examples.
    Notes: Chemische Biologie ist eine junge Forschungsrichtung im Grenzgebiet zwischen Organischer Cherme und Zellbiologie, welche aus einem Bedarf nach neuen Techniken zur Untersuchung zellbiologischer Mechanismen entstanden ist. Chemische Methoden werden mit biochemischen und molekularbiologischen Methoden kombiniert, um neuartige Möglichkeiten für die biologische Grundlagenforschung zu schaffen. So werden synthetische Oligosaccharide kovalent an die Oberfläche lebender Zellen gebunden, die Konzentration von Calciumionen im Zytosol künstlich reguliert und Rezeptoren künstlich aktiviert.
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    Chemie in unserer Zeit 33 (1999), S. 373-374 
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    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eine neue Elektrosynthese erfüllt erstmals den Traum der Elektrochemiker, gleichzeitig Anoden- und Kathodenreaktion für organische Synthesen technisch zu nutzen.
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    Chemie in unserer Zeit 33 (1999), S. 377-377 
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    Chemie in unserer Zeit 33 (1999), S. 380-380 
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    Chemie in unserer Zeit 33 (1999), S. 382-384 
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    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Around the world, BASF has been preparing for Y2K since 1996. The Information services and the Process Control Technology divisions, as well as embedded systems and logistics, not to mention the company's customers and suppliers have all been systenmatically tested for Y2K capability. In addition, special precautionary measures in particular, at large Verbund sites - will be in place during the switchover period.
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    Chemie in unserer Zeit 33 (1999), S. 4-4 
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    Chemie in unserer Zeit 33 (1999), S. 66-66 
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    Chemie in unserer Zeit 33 (1999), S. 104-109 
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    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Fonds of German Chemical Industry (FCI) has produced an instrumental kit named „Blue Genes“ which enables High School teachers to perform in their school environment basic experiments of gene analysis and cloning. In particular, the kit contains all necessary equipment and reagents to perform a restriction analysis, and cloning and expression of a bacterial gene.
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    Chemie in unserer Zeit 33 (1999), S. 152-157 
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    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A few physical phenomena believed to be religious miracles are considered, and scientific explanations for them are proposed.
    Notes: Einige physikalische Phänomene, von denen man glaubte, sie seien religiöse Wunder, werden vorgestellt und wissenschaftliche Erklärungen hierfür vorgeschlagen.
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    Chemie in unserer Zeit 33 (1999), S. 173-173 
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    Chemie in unserer Zeit 33 (1999), S. VIII 
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    Keywords: Chemistry ; Chemistry
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    Chemie in unserer Zeit 33 (1999), S. XIV 
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    Chemie in unserer Zeit 33 (1999), S. 334-341 
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    Notes: The essential trace element copper plays a key role in living systems. Its metalloproteins are involved in various reactions. The IT ononuclear blue copper type-1 proteins take, part in electron transfer processes. Type-2 proteins can either act as oxidases, oxygenases, dioxygenases, or superoxide dismutases, containing one copper core. Dinuclear copper centers of Type-3 proteins are the oxygen transport system hemocyanin, oxidases and oxygenases. Due to this variety of functions copper deficiency and also abundance can cause severe damage of any life form.
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    Chemie in unserer Zeit 33 (1999), S. 359-364 
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    Notes: It is tried to fix the limits between the notions high pressure synthesis and high temperature chemistry. The work of Fritz Haber to apply high pressure to synthetise ammonia and of Friedrich Bergius to liquify coal to synthetise petrol is described. Special attention is given to the merits of Carl Bosch and his coworkers at BASF for applying the high pressure synthesis into industrial scale. The consequences of thc work of Haber, Bergius und Bosch on chemistry, social and political life and their importance for the present are considered.
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    Chemie in unserer Zeit 33 (1999), S. 376-376 
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    Chemie in unserer Zeit 33 (1999), S. 390-390 
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    Notes: Diatoms are unicellular organisms which possess a unique silicified cell wall. Their intricate structures have inspired the imagination of naturalists and scientists throughout centuries. However, molecular biological details about silica metabolic pathways still are obscure. To find out how soft matter can selforganize and create finite solid shapes and complex patterns is certainly one of the most challenging scientific problems today. Especially chemists just have started to unravel the mysteries of chemical morphogenesis.
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    Notes: Cyclopentadienyl (Cp) complexes of maingroup elements are classified and compared in terms of structural types, bonding features, and characteristic reactions. Halfsandwich, sandwich and multidecker sandwich arrangements of different type are observed including cluster species with weak or strong metal-metal bonds. The Cp-El bonding ranges from mainly covalent to purely ionic with important structure-determining intermolecular contacts in the latter. π-Complexation allows the stabilisation of compounds with low-valent elements such as AI(I), Ga(I), and Si(I1). Important reaction principles and applications are shortly described.
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    Notes: In the last decade, major advances in the understanding of the biology of aging were made. Studies in worms, flies and yeast led to the identification of several life-extending genes. In mammals, two genes were found which, when mutated, shorten life span. Previous studies in rodents reporting life span prolongation by caloric restriction were confirmed and extended to lower organisms. The studies arc consistent with and supportive of the free radical theory of aging, which secs reactive oxygen species as the main contributor to aging. A refinement of this theory puts mitochondrial DNA into the center of the aging process. It appears that mitochondrial DNA may be both, a yardstick for the biological age and a signalling device to tell the organism when to die. A diet low in calories and high in antioxidants promises to lead to a better quality of life at old age and possibly to increased life span for humans.
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    Notes: This first part of „Rechargeable Batteries“ is devoted to materials and reactions in batteries with aqueous electrolytes. Lead-acid, nickelcadmium, nickel-metal hydride, and various zinc systems, such as zinc-manganese oxide, zinc-air, and zinc-bromine cells are discussed. Special attention is paid to the limited electrochemical stability window of the aqueous electrolytes, which enables overcharge and overdischarge protection of the battery but limits cell voltages to less than 2 Volts. In the following part of this article we will focus on nonaqueous electrolyte-based rechargeable batteries. Due to thc wider electrochemical stability window of these electrolytes high specific charge and high cell voltage batteries can be realized, e.g., the „4 V“ lithium ion cell.
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    Notes: Solid solutions arc an area of inorganic chemistry that encompasses a wide variety of natural and synthetic compounds. This article is intended to be a selection of interesting examples which illustrate the importance of solid solutions in everyday life and industrial applications. A short discussion of the theoretical background is given, followed by the description of solid solutions of non-metals in metals such as steel. Furthermore, solid solutions with important optical (e.g. laser materials) and electrical properties (e.g. β-alumina) are discussed, referring to their chemical structure and technological relevance.
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    Notes: Photosynthesis is one of the most fascinating fields of current interdisciplinary research. It seems miraculous that Nature, in the process of evolution, has managed to bring about a 100% quantum yield in charge separation occurring in the primary processes within the photosynthetic reaction centers. In fact, wasteful deactivation of the photoexcited electronic states into the ground state should be favoured and thus prevent charge separation. Biomimetic model compounds have been synthesized, essentially from porphyrins and quinones, resembling the redoxactive cofactors, Nature has developed. The underlying philosophy of this approach is to design and prepare suitable organic molecules allowing the specific properties of the complex electron transfer reactions to be tuned appropriately. Special emphasis is given the through comparison of structures and functions of native and artificial systems. The prominent electron transfer characteristics are discussed in particular by using time-resolved picosecond fluorescence and time-resolved EPR techniques.
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    Notes: In active search for conditions for optimal phototrophic growth, halobacteria respond to light and to a variety of other environmental stimuli by taxis. Light reception is mediated by sensory rhodopsins, seven helix transmembrane retinal proteins that are stably complexed to specific MCP-related transducer proteins. Photoisomerization of the retinal chromophore generates a steric signal which activates the sensory rhodopsin-transducer-complex. Complex activation is relayed to a two component signaling system and transiently changes the cytoplasmic concentration of fumarate which, together with the small cytoplasmic protein CheY controls flagellar motor switching. Dual signaling by CheY and fumarate was also found in Escherichia coli where it mediates metabolic signaling and taxis in cells with disabled two-component system. Sensory integration of different environmental stimuli occurs at the level of the signaling domains of several stimulus-specific transducers constructed through combination of appropriate molecular modules. Irrespective of the complexity of the signaling network, the response to light is quantitatively predictable and stochastic. Its kinetic analysis suggests that time-dependent changes in the activity of signaling components can be resolved even in the context of a complex molecular network.
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    Notes: As a matter of fact, most of our technical electrochemical energy storage systems operate outside the limitations of thermodynamics. As in the case of rechargeable batteries with aqueous electrolytes (part I of this article), kinetics control the operation and safety also in batteries with nonaqueous electrolytes (this second and final part).A striking example is the lithium ion battery which possesses an operating voltage of 〉3,5 V and a very high energy density. From a thermodynamic viewpoint such a cell is impossible because the used organic electrolyte is in contact with two lithium insertion electrodes that operate at extreme reducing and oxidizing potentials, respectively. However, a unique mechanism kinetically prevents the decomposition of the electrolyte due to the formation of electronically insulating interphases between electrode and electrolyte that are still permeable to the electrochemically active Li+ cations. Lithium ion batteries have already made their breakthrough into the market as small format systems for portable electronics. The only „kinetically shielded“ high energy density, however, might be a safety complication for large format batteries, which are assembled for electric vehicle (EV) propulsion. Safety concerns are also valid for high temperature (300°C) batteries such as the sodium-sulfur and sodium-nickel chloride systems. These systems are still in the stage of „experimental batteries“, which may find future application in large units for EV's or uninterruptible power systems. The paper is concluded by a performance comparison of various rechargeable battery systems with aqueous and nonaqueous electrolytes. (Possible) applications in consumer electronics and EV's are discussed in more detail.
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    Liebigs Annalen 1999 (1999), S. 57-60 
    ISSN: 1434-193X
    Keywords: Benzyne ; Dehydroanthracene ; Matrix isolation ; Photochemistry ; Bergman reaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -9,10-Didehydroanthracene (1) is an interesting derivative of p-benzyne that has been subject of several studies. In contrast to an earlier report, the photochemical decarbonylation of 9,10-dicarbonyl-9,10-dihydroanthracene (2) does not lead to 1 but rather to the ring-opened ene-diyne 4. The key intermediate for this reaction is keto carbene 7 which is formed by monodecarbonylation of 2. Carbene 7 is labile towards visible-light irradiation and easily looses the second CO molecule to give 4. Carbene 7 and diyne 4 are characterized by IR and UV/Vis spectra, the IR spectra are compared to calculations at the B3LYP/6-31G(d,p) level of theory.
    Additional Material: 2 Ill.
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  • 95
    ISSN: 1434-193X
    Keywords: Nucleophilic addition ; Solvent effect ; Reversal of diastereoselectivity ; Temperature effect ; Imines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Commonly observed, but rarely explored, is the possibility of modifying the diastereomeric excess (de%) by means of temperature. A complete reversal in the diastereofacial selectivity could be obtained whenever the diastereoisomers concerned are differentially favored by enthalpy and entropy. The enthalpic or entropic dominance of a diastereoisomer depends greatly on the reaction solvent used.
    Additional Material: 1 Ill.
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  • 96
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 73-81 
    ISSN: 1434-193X
    Keywords: Donor-acceptor systems ; Cage compounds ; Stelladione ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -A number of condensations could be carried out using tricyclo[3.3.0.03,7]octane-2-one (stellanone, 4) and tricyclo[3.3.0.03,7]octane-2,6-dione (2,6-stelladione, 5) as starting materials. The components for condensations were 2-trimethylsilyl-1,3-dithiane (6), 1,1-bis(trimethylsilyl)-1H-cyclopropa[b]naphthalene (7), its 3,6-dimethoxy-substituted analogue 8, fluorene (12), xanthene (13), diethyl malonate (14), and malononitrile (15). The condensation reactions with 5 yielded mono- and disubstituted products, among them were the donor-acceptor-substituted 2,6-stellanes 33-35. The structures of 18 (prepared from stellanone and fluorene), 19, 24, 27, 31 and 32 (synthesized by condensation of 2,6-stelladione and 2-trimethylsilyl-1,3-dithiane and malononitrile, respectively) were determined by X-ray crystallography.
    Additional Material: 1 Ill.
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  • 97
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 87-90 
    ISSN: 1434-193X
    Keywords: Water ; α-Nitrocycloalkanones ; ω-Nitro acids ; Surfactant ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The reaction of various α-nitrocycloalkanones 1 with aqueous 0.05 M NaOH, at 80 °C, in the presence of cetyltrimethylammonium chloride (CTACl) as a cationic surfactant, produces ω-nitro acids 2 in good yields. Reduction of the latter with HCOONH4/Pd-C, in methanol, at 80 °C affords ω-amino acids 3. The synthesis of methyl 9-oxodecanoate (8) is also reported.
    Additional Material: 2 Tab.
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  • 98
    ISSN: 1434-193X
    Keywords: O-Alkylation ; Ambident nucleophile ; Thiazolethione ; Thiohydroxamic acid ; Phase-transfer reaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -O-Alkylation of cyclic thiohydroxamic acids 1 and 3-5 has been studied with a view to developing an efficient method for the synthesis of N-(alkoxy)pyridine-2(1H)-thiones and N-(alkoxy)thiazole-2(3H)-thiones. Four issues have been addressed and the following conclusions can be drawn: (i) Thiones 1 and 5 exist as O-H acids in the solid state. (ii) According to NMR investigations (1H, 13C), the thione structures should be largely retained in CDCl3, [D6]DMSO, and CD3OD solutions of acids 1, 3-5, as is also the case for pyridinethione salts 2a-h. (iii) O-Alkylation of pyridinethione salts occurs in competition with S-alkylation. Selective O-alkylation is however possible, if thiohydroxamate salts with large countercations, such as M = NBu4, are treated with hard alkylating reagents in polar aprotic media. (iv) As tetrabutylammonium thiohydroxamates, such as 2f, are highly useful in the synthesis of cyclic thiohydroxamic acid O-esters, we have developed an efficient protocol for the preparation of N-(alkoxy)pyridine-2(1H)-thiones directly from acid 1 using phase-transfer conditions (alkyl halide or sulfonic acid ester, CH3CN, K2CO3, Bu4NHSO4). This method has proved particularly successful for the synthesis of N-(alkoxy)thiazole-2(3H)-thiones 11, 20-28, which were obtained in yields of up to 87%.
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  • 99
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 129-134 
    ISSN: 1434-193X
    Keywords: Tetrahydro-2-vinylquinoxaline ; Cyclization ; Palladium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Reaction of (Z)-1,2-bis(methoxycarbonyloxy)but-2-ene (2) with various N,N-bis(arylsulfonyl)-o-phenylenediamines 1 was catalyzed by a palladium complex associated with chiral ligands to give optically active 1,4-bis(arylsulfonyl)-1,2,3,4-tetrahydro-2-vinylquinoxalines 3 with up to 62% ee. The use of (S)-MeOBIPHEP as the chiral ligand and N,N-bis(p-tolylsulfonyl)-o-phenylenediamine (1i) as the nucleophile led to the highest ee at 25 °C, regardless of the solvent used. The enantioselectivity of the cyclization is strongly affected by the nature of the substituents at the nitrogen atom.
    Additional Material: 4 Tab.
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  • 100
    ISSN: 1434-193X
    Keywords: Fluorine ; Lactones ; Annulation ; Ketene ; Sulfoxides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Enantiomerically pure α,α-dichloro β-fluoroalkyl γ-p-tolylthio γ-butyrolactones trans-6a-c have been obtained with excellent stereocontrol (〉 98:2) and enantiomeric purity (〉 98:2) by sulfoxide-directed lactonization (Marino's annu-lation reaction) of β-fluoroalkyl vinyl sulfoxides (R)-(E)-5a-c with dichloroketene. Highly chemoselective dechlorination and desulfurization reactions performed on trans-6c efficiently provided the β-chlorodifluoromethyl γ-butyrolactone (S)-8c, the absolute stereochemistry of which was determined by X-ray diffraction analysis of its γ-p-tolylthio precursor (2R,3S)-7c.
    Additional Material: 1 Ill.
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