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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Cell Biochemistry and Function 9 (1991), S. 193-199 
    ISSN: 0263-6484
    Keywords: Calcium ; translocase ; mitochondria ; electrophoresis ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: ATP translocation into mitochondria isolated from halothane-sensitive pig (HP) muscle was dramatically reduced compared with normal pigs (NP). To determine if this was due to a decreased amount of ATP translocase in the mitochondrial membranes, or a structural modification of this protein, an electrophoretic study was undertaken. Total proteins and purified translocase preparations from (NP) and (HP) mitochondria were analysed by SDS gel electrophoresis. In the two type of mitochondria no significant differences were observed either in the amount of ATP translocase or in the molecular weight. Also, neither nonequilibrium pH gradient gel electrophoresis nor the analysis of peptides produced by limited proteolysis revealed any structural difference between the two types of protein. On the basis of these results, the depressed translocase activity observed in (HP) mitochondria cannot be explained by a reduced amount of the nucleotide translocase, nor a structural alteration of this protein. Possible inhibition of (HP) translocase activity by Ca2+ accumulation or by other mechanisms is discussed.
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 42 (1998), S. 341-346 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 108 (1996), S. 2922-2937 
    ISSN: 0044-8249
    Keywords: Aromatizität ; Chemiegeschichte ; Hückel ; Erich ; Pericyclische Reaktionen ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zwischen 1930 und 1937 kamen von Erich Hückel, einem theoretisch arbeitenden Physiker, mit den quantenmechanischen Beschreibungen ungesättigter und konjugierter Moleküle wesentliche Beiträge zur Organischen Chemie. Hier folgt einem kurzen Überblick über seine wissenschaftliche Laufbahn aus der Sicht eines Organikers eine vereinfachte Darstellung der stark approximativen theoretischen Methoden, die er verwendete. Für cyclische Moleküle der Klasse CnHn ist die Aussage, daß im Fall von (4N + 2) π-Elektronen (N = 0,1,2,…) abgeschlossene Schalen vorliegen, von besonderer Bedeutung. Die Analyse von Schlüsselanwendungen der Ideen Hückels zeigt, wie sie schließlich die Erforschung neuer Gebiete in der organischen Synthese und bei organischen Reaktionsmechanismen anregten. Ein weiterer bedeutsamer (aber bis vor kurzem kaum beachteter) Beitrag von Hückel war die Erkenntnis, daß die Konnektivität der Atome ein entscheidender Faktor für die Spinmultiplizität in Nicht-Kekulé-Molekülen ist. Sie liefert, wie jüngere theoretische und experimentelle Befunde bestätigen, im Prinzip eine Basis für die Voraussage von Verstößen gegen die Hundsche Regel. Darüber hinaus werden die Wechselwirkung von Experimenten mit den unterschiedlichen Ausprägungen der Quantentheorie und die Auswirkung dieser Wechselwirkung auf die Entwicklung der Chemie kurz betrachtet. Schließlich werden Mutmaßungen angestellt, warum das Werk Hückels jahrzehntelang einen so geringen Einfluß auf die Organische Chemie ausübte, bis man endlich anfing, seine Bedeutung zu erkennen.
    Additional Material: 4 Ill.
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  • 4
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei vielen Carboniumionen-Umlagerungen, die in Lösung über mehrere aufeinander-folgende Zwischenstufen verlaufen, bestimmt die stereochemische Konfiguration am Ausgangspunkt der Heterolyse zwei Reaktionsschritte später die Spezifität der Wanderung. Diese Erinnerungseffekte (memory effects) können kleinen, bislang unbeobachtbaren Minima in der Energieoberfläche zugeschrieben werden. Durch Markierungsmethoden aller Art wird gezeigt, daß Erinnerungseffekte allgemein bei der Bildung bicyclischer Carboniumionen durch Ringerweiterung auftreten. Die Zwischenstufen bei diesen Reaktionen verhalten sich unsymmetrisch, obwohl sie im Gleichgewichtszustand notwendigerweise symmetrisch oder quasi-symmetrisch sind. Der Erinnerungseffekt benutzt die Geschwindigkeit einer intramolekularen Carboniumionen-Umlagerung als Bezugsgröße, mit der die Geschwindigkeit der Symmetrieeinstellung verglichen wird. Auf diese Weise dient das System zum Nachweis von Subspezies.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 35 (1996), S. 2750-2764 
    ISSN: 0570-0833
    Keywords: aromaticity ; history of chemistry ; Hückel ; Erich ; pericyclic reactions ; Aromaticity ; History of chemistry ; Hückel, Erich ; Pericyclic reactions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the period between 1930 and 1937, Erich Hückel, a theoretical physicist, made profound contributions to organic chemistry in his quantum mechanical descriptions of unsaturated and conjugated compounds. A brief account of his academic career is followed by simplified expositions, from the point of view of an organic chemist, of the highly approximate theoretical methods he used. Of special significance in the case of cyclic molecules of the class CnHn is the concept of filled shells when the number of π electrons is (4 N + 2) (N = 0,1,2,…). Examinations of key applications of Hückel's ideas reveal how they eventually motivated the exploration of new fields in organic synthesis and organic reaction mechanism. Another significant (but until recently, virtually ignored) contribution by Hückel was the recognition that atomic connectivity is a strong determinant of spin multiplicity in non-Kekulé molecules. This idea provides, in principle, a basis for predicting violations of Hund's rule, as recent computational and experimental developments confirm. The interaction of experiment with different styles of quantum theory, and the impact of this relationship on the development of chemistry, are briefly considered. Speculations are given on why Hückel's work exerted so little influence on organic chemistry for decades before its importance finally began to be recognized.
    Additional Material: 4 Ill.
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  • 6
    ISSN: 0570-0833
    Keywords: Memory effects ; Stereochemistry ; Rearrangement ; Carbocations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereochemical configuration at the initial site of heterolysis in a carbonium ion process in solution controls the specificity of migration two steps later in many sequential multiple rearrangements. These “memory effects” are attributable to the presence on the potential energy surface of small, hitherto undetectable minima. A variety of structural, stereochemical, and isotopic marking techniques are used to demonstrate that memory effects are a general feature of the ring-expansion route to bicyclic carbonium ions. The intermediates formed in these reactions, although necessarily symmetrical or quasi-symmetrical at equilibrium, act unsymmetrically. The memory effect uses the rate of an intramolecular carbonium ion rearrangement as a calibration with which to compare the rate of symmetrization. In this way, the system functions as a sensor of sub-species.
    Additional Material: 3 Ill.
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