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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.
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  • 3
    ISSN: 1434-1948
    Keywords: Molybdenum ; μ-Oxo ; Conformational equilibrium ; X-ray diffraction ; NMR spectroscopy ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new thiocyanatomolybdenum(VI) dioxo-μ-oxo complex dimer bearing a 4,4′-di-tert-butyl-2,2′-bipyridine ligand (2) is shown to exist in the crystal cell unit as a meso (Mo-O-Mo angle of 180°) and d,l, pair (Mo-O-Mo angle of 155.7°). These conformers are in equilibrium in solution and have been observed clearly by 1H NMR spectroscopy.
    Additional Material: 4 Ill.
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  • 4
    ISSN: 1434-1948
    Keywords: Rhodium ; Phosphanes ; Ligand redistribution ; Dichloromethane activation ; Oxidative addition ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dichloromethane reacts with dinuclear rhodium complexes [{(PR3)2Rh}2(μ-Cl)2] to give the bridging-methylene complexes [{(PR3)2RhCl}2(μ-Cl)2(μ-CH2)] (PR3 = PEt3, PPh2Me). The structure of the PEt3 complex has been established by X-ray diffraction study. The early stages of the reaction of [{(C8H14)2Rh}2(μ-Cl)2] with monophosphanes have been monitored by 31P NMR, evidencing chloride bridges cleavage and phosphane redistribution processes.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 2907-2912 
    ISSN: 1434-193X
    Keywords: Polyaza heterocycles ; Enaminones ; Pyrimidines ; Carboxamidines ; Guanidines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple and efficient method for the synthesis of larger polyaza heterocyclic structures 6a, 6b and 8 with 1,3-pyrimidine units has been developed, based on the reaction of enaminones with appropriate guanidines or carboxamidines under basic conditions. Using this procedure, several new, optically active polyaza heterocycles 10, 12 and 13 have been prepared in good yields, from enantiomerically pure Nα-Boc-L-arginine as guanidine reagents.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2485-2490 
    ISSN: 1434-193X
    Keywords: Molecular recognition ; Host-guest chemistry ; Polypyridines ; Condensation reactions ; Michael additions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Highly soluble annelated bi- and terpyridines were prepared in 46-60% yields by a two-step procedure which combines the Michael addition of an enolizable cyclic ketone with an α,β-unsaturated ketone and the cyclization of the resulting 1,5-diketone in the presence of ammonium acetate.
    Additional Material: 3 Ill.
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  • 7
    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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