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  • 1
    ISSN: 0009-2940
    Keywords: Fullerenes ; Azirines ; Photochemistry ; [3 + 2] Cycloadditions ; Electron transfer reactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoreactions with C60-Fullerene. [3 + 2] Photocycloaddition of 2,3-Diphenyl-2H-azirineUpon irradiation 2,3-Diphenyl-2H-azirine (2) is added to C60 1 with formation of mono and oligo adducts. 1,9-(3,4-Dihydro-2,5-diphenyl-2H-pyrrolo)fulleren-60 (3) has been isolated and identified by standard spectroscopic methods. Mechanistic studies revealed two reaction paths leading to 3, i.e. the classic 1,3-dipolar cycloaddition via the nitrile ylide 4 (direct irradiation) or a route via 2-azaallenyl radical cations 5 (sensitization by photoinduced electron transfer).
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1995 (1995), S. 1455-1461 
    ISSN: 0947-3440
    Keywords: Dienes, chiral ; 1,3-Dioxin-4-ones ; (-)-Menthone ; Diels-Alder reactions, diastereoselective ; Cycloadditions, high-pressure ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and diastereoselective Diels-Alder reactions of new spirocyclic chiral dienes are reported. Starting with diketene and (-)-menthone (1), we prepared the diastereomeric diketene-menthone adducts 2 and 3. Further derivatization and olefination afforded four chiral dienes 12-15. Diastereoselective Diels-Alder reactions of these dienes with N-phenylmaleimide (NPM) under high-pressure conditions yielded the corresponding cycloadducts 16-19. Olefination of 6-diethylphosphonomethyl-2,2-dimethyl-1,3-dioxin-4-one 8 with formaldehyde led to unexpected compounds 9-11 resulting from the originally formed olefination product.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-193X
    Keywords: Sum of free valence numbers ; Benzo[g,h,i]perylenes ; [5]Helicenes ; Photocyclization ; HMO calculations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The syntheses of the new pentahelicenes 5, 11, 17, 21, and 28 with various substituents are described. In the case of 2,13-dicyano-[5]helicene (11) optical resolution was achieved by HPLC using a column packed with γ-cyclodextrin. However, the enantiomers racemized within a few hours. On the other hand, the enantiomers of 28 turned out to be stable after separation on triacetylcellulose using MPLC. The crystal structures of 11, 17, and 21 were solved and indicated the typical distortions which are expected for helicenes. The model of the sum of free valence numbers was applied in order to rationalize the reactivity pattern of the photochemical phenanthrene cyclization.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 26 (1987), S. 825-845 
    ISSN: 0570-0833
    Keywords: Charge transfer ; Radical ions ; Photochemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bimolecular photoreactions usually occur via several steps involving “complex-type” intermediates (excimers or exciplexes). Although physical chemists have investigated them for nearly thirty years (Förster, Weller), and postulated their existence in numerous publications, it is only in the last decade that evidence for an exciplex intermediate in cycloadditions (Caldwell) has been obtained, thereby establishing the link between spectroscopy and synthetic photochemistry. Since then, many investigations have confirmed the role of exciplexes as intermediates in bimolecular photoreactions. The photochemically induced charge transfer from a donor to an acceptor substrate determines not only the bond strengths in the primary exciplex but also influences - via the charge-transfer nature of the complex - the structure of the exciplex and thereby the selectivity of subsequent reactions. Such chemical processes between the donor and the acceptor prevent the reverse transfer of electrons, which usually results in regeneration of the starting materials, thereby only causing the dissipation of energy and occasionally - under specific conditions - the generation of molecules of the starting material in the triplet state. Ionic photodissociation also reduces the probability of a reverse transfer of electrons. This process, which produces solvated radical ions, is promoted by polar solvents and salt effects, particularly special salt effects. By this means it is possible to generate specific radical cations from, for example, alkenes and dienes and to study their reactions. Although in some areas, for example physical and biophysical chemistry, discussions of single electron transfer (SET) processes have long been found in the basic textbooks, organic chemistry lags far behind, although - and this is shown by the numerous recent publications - organic chemists are also aware of the fundamental importance of these processes. In this connection photochemistry plays a central role, since its instruments make it possible to carry out specific SET processes, to analyze them, and to use them in chemical reactions.
    Additional Material: 42 Ill.
    Type of Medium: Electronic Resource
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