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  • 1
    ISSN: 0009-2940
    Keywords: Manganese-mediated cyclization ; Nine-membered carbocycles ; Manganese complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photochemical Reactions of Transition Metal Organyl Complexes with Olefines, 31). - [4 + 5] Cycloaddition of Conjugated Dienes to Tricarbonyl(η5-2,4-dimethyl-2,4-pentadienyl)manganeseTricarbonyl(η5-2,4-dimethyl-2,4-pentadienyl)manganese [1] reacts photochemically with the acyclic conjugated dienes 1,3-butadiene [A], 2-methyl-1,3-butadiene [B], (E)-1,3-pentadiene (C), (E,E)-2,4-hexadiene (D), 2,4-dimethyl-1,3-pentadiene (E), 2,4-hexadien-1-ol (F), and methyl 2,4-hexadienoate (G) in a formal [4 + 5] cycloaddition to give tricarbonylmanganese complexes with η3:2-2,6-cyclononadien-1-yl ligands (2A-2G). In addition, the reaction of 1 with A yields thermolabile [η3:2:2-1-(3-butene-1,2-diyl)-1,3-dimethyl-2,6-cyclononadiene]dicarbonylmanganese (3A) and E,E and E,Z isomers of [η3-1-(2-butene-1,1-diyl)-1,3-dimethyl-2,6-cyclononadiene]tetracarbonylmanganese (4A, 4A] as byproducts. Similarly, 1 reacts with B to form tetracarbonyl[η3-1-(3-methyl-2-butene-1,1-diyl)-1,3,6-trimethyl1-2,6-cyclononadiene]manganese (4B) in a side reaction. The crystal and molecular structures of tricarbonyl(η3:2-1,3,5,5,7-pentamethyl-2,6-cyclononadien-1-yl]manganese (2E) and of 3A are determined by X-ray structure analyses. In each of the formally octahedral complexes unusual long manganese-carbon bonds are found for one coordinated CC double bond of the hydrocarbon ligands.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 3 (1990), S. 459-469 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: N-[2,3-Bis(dimethylamino)cyclopropenylio]- and N-(tetramethylamidinio)pyridinium salts (trifluoromethanesulphonates and tetrafluoroborates) form 1:1 and 1:2 charge-transfer complexes with the pentakis(methoxycarbonyl)cyclopentadienide anion. The x-ray crystal structures of 1-[2,3-bis(dimethylamino)cyclopropenylio] pyridinium pentakis(methoxycarbonyl)cyclopentadienide tetrafluoroborate hydrate and of 1-[2,3-bis(dimethylamino)cyclopropenylio] pyridinium bis[pentakis(methoxycarbonyl)cyclopentadienide] were determined. In constrast, the tetra-cyano-p-quinodimethane (TCNQ) radical anion reacts with the first-mentioned salts by C—C bond formation to give novel dicationic salts. Thereby, the radical anion attacks the pyridinium γ-position of the N-(tetramethylamidinio)-pyridinium dication, but the three-membered ring of the N-[2,3-bis(dimethylamino)cyclopropenylio] pyridinium system.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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