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  • 1
    ISSN: 1572-8862
    Keywords: Iron ; ynamine ; aminoalkyne ; N-sulfinylaniline ; carbene ; structure ; insertion ; nitrene ; sulfur
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The diiron ynamine complexes [Fe2(CO)7{μ-C(R)C(NEt2)}] (1) (R=Me, Ph, C3H5, SiMe3) react with theN-sulfinylaniline, PhNSO, in refluxing hexane to yield the complexes [Fe2(CO)6{μ-N(Ph)C(Me)S}] (2), [Fe2(CO)6{μ-N(Ph)C(NEt2)C(Ph)S}] · 0.5C6H12 (3), [Fe2(CO)6{μ-C(C3H5)C(NEt2)N(Ph)SO}] · 0.5CH2Cl2 (4), and [Fe2(CO)6{μ-C(SiMe3)C(NEt2)S)}] (5). Compound 5 was found to be identical to the previously reported product obtained from the reaction of 1 with sulfur. Compounds 2, 3, and 4 were characterized by single crystal X-ray diffraction analyses. Crystal data: for 2: space group = P21/n,a=9.533(1) Å,b=18.830(4) Å,c=12.705(4) Å, β=107.01(2)°,Z=4, 2687 reflections,R=0.027; for 3: space group=P21/n,a=13.660(2) Å,b=19.096(8) Å,c=10.972(2) Å, β=90.62(1)°,Z=4, 2821 reflections,R=0.036; for 4: space group=P21/a,a=18.098(5) Å,b=16.564(4) Å,c=18.548(2) Å, β=115.44(2)°,Z=4, 3569 reflections,R=0.041. Complexes 2 and 3 result from fragmentation of theN-sulfinylaniline ligand and insertion of the nitrene grouping into the Fe=C(aminocarbene) bond, whereas the sulfur atom inserts into one Fe-C bond of the bridging carbene. Compound 4 is formed by insertion of the entireN-sulfinyl aniline ligand into the Fe=C(aminocarbene) bond. All three complexes have basket-like arachno structure isolobal to the benzvalene one.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 987-994 
    ISSN: 1434-193X
    Keywords: Addition reactions ; Octahydroacridine ; Polypyridines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A new octahydroacridine with a tert-butoxypropyl group in the 9-position was prepared and was used in the synthesis of new soluble annelated polypyridines. Quinquepyridine with 11 adjacent rings was prepared in 17-25% yield by condensation of an α-methylene ketone and an enolisable ketone in the presence of ammonium acetate under basic conditions.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 2001-2001 
    ISSN: 1434-193X
    Keywords: Addition reactions ; Octahydroacridine ; Polypyridines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A new octahydroacridine with a tert-butoxypropyl group in the 9-position was prepared and was used in the synthesis of new soluble annelated polypyridines. Quinquepyridine with 11 adjacent rings was prepared in 17-25% yield by condensation of an α-methylene ketone and an enolisable ketone in the presence of ammonium acetate under basic conditions.
    Type of Medium: Electronic Resource
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