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  • 1980-1984  (10)
  • 1980  (10)
  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 286 (1980), S. 638-640 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Intact cattle rod outer segments have been isolated according to Schnetkamp etal.9. Disk vesicles were obtained by sonication of intact rod outer segments in a medium containing sucrose, 600 mM; Ficoll 400, 5% v/v; HEPES, pH 7.0 2 mM, for 30 s at 40 W. The suspension also contained about 3-4 ,? of ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European biophysics journal 6 (1980), S. 18-19 
    ISSN: 1432-1017
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1458-1471 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Polar and Non-polar Cycloadditions of 1,3-Butadiene and Cyclopentadiene to AnthracenesThe photoadditions of anthracene (1a) and 9-anthracenecarbonitrile (1b) with 1,3-butadiene (2) lead to very different ratios of [4 + 2]- and [4 + 4]-adducts. This and, in contrast to the behavior of 1a, the complete suppression of photo-Diels-Alder additions between 1b,c,d and cyclopenta-diene (9) at 0°C are readily rationalized as an effect of hybridization in terms of the well established and successful diradical mechanism. At higher temperatures the [4 + 4]-adducts 11 undergo suprafacial 1,3-shifts into Diels-Alder adducts 12 and [4 + 4]-cycloreversions into 1 and 9. At such temperatures, added 1,3-dienes (or 1 and 9 generated in situ) combine with 11 to give well defined polycyclic adducts. Spectroscopic and quenching data are discussed.
    Notes: Die Photoadditionen von Anthracen (1a) und 9-Anthracencarbonitril (1b) mit 1,3-Butadien (2) führen zu deutlich verschiedenen Verhältnissen an [4 + 2]- und [4 + 4]-Addukten. Dies und die  -  im Gegensatz zu 1a  -  völlige Unterdrückung der Photo-Diels-Alder-Addition zwischen 1b,c,d und Cyclopentadien (9) bei 0°C ist als Hybridisierungseffekt beim vielfach bewährten Diradikalmechanismus zu verstehen. Bei höheren Temperaturen gehen die [4 + 4]-Addukte 11 durch suprafaciale 1,3-Verschiebung in Diels-Alder-Addukte 12, durch [4 + 4]-Cycloreversion in 1 und 9, oder mit zugesetzten 1,3-Dienen (bzw. in situ gebildetem 1 und 9) in wohldefinierte poly-cyclische Addukte über. Spektroskopische und Löschdaten werden diskutiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1626-1631 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoadditions of Dibenz[a,c]- and Dibenz[a,h]anthracene to CyclopentadieneThe electronically excited carcinogens and mutagens 1 and 5 react with cyclopentadiene (2) at 0°C to give the stereochemically well defined [4 + 2]- (3) and [4 + 4]- (4) or [4 + 2]- (6) and [2 + 4]-adducts (7), resp. The products are characterized by UV, fluorescence, and 1H NMR spectra which reveal transannular interactions. 4 gives the cage compound 10 on photolysis.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 3669-3674 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diene-Catalyzed Photodimerization via Excimers (Exciplexes) or Diene Addition to Anthracene and 9-PhenylanthraceneThe [4 + 4]-photodimerization of anthracene (1) is not enhanced by 2,4-hexadiene (3) but impeded due to formation of [4 + 2]- (4) and [4 + 4]-adducts (5, 6). 6 and 1 combine to give the bisadduct 7 at room temperature. The selective photolysis of 9-phenylanthracene (8) leads to the anti-[4 + 4]-dimer (9). This can be compared with the [4 + 4]-photodimerization of 9-methylanthracene which affords the anti- and the thermolabile syn-product. 1,3-Dienes such as 1,3-pentadiene (10) or 1,3-cyclohexadiene (13) are not necessary for the formation of 9 but undergo cycloadditions with 8 to yield [4 + 2]- (11, 12, 14), [4 + 4]- (15), and [2 + 2]-adducts (16, 17). The structures of the products are established primarily by high field 1H-NMR spectroscopy.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 3932-3936 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemiluminescence of Diradicals from Lepidopterene, Dibenzylidenetriasterane, and DiphenylbicyclooctadieneThe hydrocarbons lepidopterene (1), sym-dibenzylidene-dimethyltriasterane (5), and 2,6-diphenylbicyclo[3.3.0]octa-2,6-diene (8) are sources of intense emission of red light upon UV-excitation under specified experimental conditions (solutions, glassy media, crystals). These unusual observations are interpreted in terms of initial diradical formation and their subsequent decay to intramolecular exciplexes and triplet excimers, resp., which undergo the radiative decay.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 92 (1980), S. 245-276 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In diesem Aufsatz werden die zahlreichen, häufig nur in der Originalliteratur genannten intramolekularen Reaktionen elektronisch angeregter Benzolderivate - geordnet nach Reaktionstypen - systematisch analysiert. Es können alle bekannten Reaktionstypen berücksichtigt werden. Sie gliedern sich in Reaktionen des Benzolrings (Ionisierung, Ringöffnung, Ringveränderung), Reaktionen mit Seitenkettenbeteiligung (α-, β-, γ-Spaltungen, Homolyse, Heterolyse), Reaktionen von Substituenten mit Seitenketten (Cyclisierung, Entalkylierung, Schutzgruppenabspaltung) und Reaktionen von Seitenketten mit dem aromatischen Ring (Substitution, Addition, Entaromatisierung, Cyclisierung). Die Wahl zwischen energetisch möglichen konkurrierenden Reaktionen wird überwiegend von geometrischen Faktoren bestimmt. Die Anwendungen der empirischen Effekte in der präparativen Chemie sind sehr vielseitig. Zahlreiche hier besprochene Reaktionen werden bereits industriell ausgewertet (z. B. in der Photochromie, UV-Stabilisierung, Photographie, Informationsspeicherung, Druck-, Lackierungs- und Polymertechnologie sowie Pharmazie).
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 19 (1980), S. 243-275 
    ISSN: 0570-0833
    Keywords: Rearrangement ; Fragmentation ; Benzene derivatives ; Photochemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this article the numerous intramolecular reactions of electronically excited benezene derivatives, which in many instances are only mentioned in original papers, are systematically analyzed and arranged according to reaction types. All known reaction types can be classified, and subdivided into reactions of the benzene ring (ionization, ring opening, ring alteration), reactions with participation of side chains (α-, β-, γ-cleavage, homolysis, heterolysis), reactions of substituents with side chains (cyclization, dealkylation, cleavage of protective groups), and reactions of side chains with the aromatic ring (substitution, addition, dearomatization, cyclization). The selectivity of the energetically feasible competing reactions is primarily determined by geometric factors. Applications of the empirical effects are numerous and varied in preparative organic chemistry. Many of the reactions under discussion are already utilized industrially (e.g. in photochromism, UV stabilization, photography, information storage, printing, coating and polymer technology, and pharmacy).
    Additional Material: 1 Tab.
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