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  • 1
    Electronic Resource
    Electronic Resource
    Komplexierung von 1,4-Dihydro-1,4-diborafulvenen mit Ni(cod)- und Pt(cod)-FragmentenHerrn Professor Hubert Schmidbaur zum 60. Geburtstag gewidmet. (1994)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2393-2396 
    Details
    ISSN: 0009-2940
    Keywords: 1,4-Diborafulvenes, 1,4-dihydro- ; Slipped triple-decker ; Nickel complexes ; platinum complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexation of 1,4-Dihydro-1,4-diborafulvenes with Ni(cod) and Pt(cod) Fragments*Reactions of the 1,4-diborapentafulvene derivatives 1 and 2a, b with M(cod)2 (M = Ni, Pt) yield the complexes [(η5-1)Ni-(cod)] (8), [(μ,η2η5-2a){Ni(cod)}2] (9a), [(μ,η2,η5-2b){Ni(cod)}2] (9b), and [(μ,η2,η5-2a){Pt(cod)}2] (10). Compounds 9 and 10 are the first examples of complexes with 2a, b as a μ,η2,η5-ligand. The X-ray structure analyses of 9b and 10 are described.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19941271209
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  • 2
    Electronic Resource
    Electronic Resource
    Ein neuer Zugang zu 1,2- und 1,3-DiborolHerrn Prof. Dr. Joachim Knappe zum 65. Geburtstag gewidmet. (1994)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1363-1368 
    Details
    ISSN: 0009-2940
    Keywords: 1,2-Diboroles, 2,5-dihydro- ; 1,3-Diboroles, 2,3-dihydro- ; Cobalt complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A New Approach to 1,2- and 1,3-DiboroleHerrn Prof. Dr. Joachim Knappe zum 65. Geburtstag gewidmet.Diaminoborylation of 1,3-dilithiopropenes leads to the (Z)-1,3-bis(diaminoboryl)propenes 4a, b, which are transformed by an amine/chlorine exchange to the (Z)-1,3-bis(aminochloroboryl)propenes 5a, b. These react with sodium to yield the 2,5-dihydro-1H-1,2-diboroles 2c, d, whereas the reaction with potassium leads to the 2,3-dihydro-1H-1,3-diboroles 6a, b by rearrangement of the C3B2 skeleton. The constitutions of the heterocycles 2c, d and 6a, b are established by X-ray structure analyses. Reaction of the 1,2-diboroles 2c, d with (C5H5)Co(C2H4)2 leads to the red (1-borabutadiene)cobalt complexes 3c, d. In 3c a sigmatropic rearrangement is studied by NMR spectroscopy.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19941270807
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  • 3
    Electronic Resource
    Electronic Resource
    Darstellung und Komplexierung von 1,4-Dimethyl-2,3-bis(isopropyliden)-1,4-diboratetralinHerrn Professor Nils Wiberg zum 60. Geburtstag gewidmet. (1995)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 183-185 
    Details
    ISSN: 0009-2940
    Keywords: 1,4-Diboranaphthalines ; 2,7-Diboradodeca-1,3,9,11-tetraenes ; Cobalt complexes ; Rhodium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Complexation of 1,4-Dimethyl-2,3-bis(isopropylidene)-1,4-diboratetraline1,4-Dimethyl-2,3-bis(isopropylidene)-1,4-diboratetraline (2) is obtained from o-dilithiumbenzene and 2,5-dimethyl-3,4-bis(chloromethylboryl)-2,4-hexadiene in 61% yield. Its complexation with cyclopentadienylbis(ethene)cobalt leads to the triple-decker bis(η5-cyclopentadienylcobalt)-μ-η6,η6-1,4-dimethyl-2-isopropenyl-3-isopropyl-1,4-dihydro-1,4-dibora-naphthaline (3) in low yield. However, the reaction of 2 with (C5H5)Rh(C2H4)2 and (C5Me5)Co(C2H4)2 originates complexes of a tricyclic ligand formed from 2 via conrotatoric [2 + 2] cycloaddition of the isopropylidene groups. (η5-Cyclo-pentadienylrhodium)-η6-tricyclo-[6.4.0.03,6]-2,4,4,5,5,7-hexamethyl-2,7-diboradodeca-1,3,9,11-tetraene (4), (η5-pentamethylcyclopentadienylcobalt)-η6-tricyclo-[6.4.0.03,6]-2,4,4,5,5,7-hexamethyl-2,7-diboradodeca-1,3,9,11-tetraene (5) and its related dinuclear complex 6 could be isolated in 29, 10, and 31%, respectively. Their constitutions are derived from spectroscopic data and proven by X-ray structure analysis of 4.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19951280216
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  • 4
    Electronic Resource
    Electronic Resource
    Nickelkomplexe eines 1,4-Dihydro-1,4-Diboranaphthalin-DerivatesHerrn Professor Dr. Anton Meller zum 60. Geburtstag gewidmet. (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 993-997 
    Details
    ISSN: 0009-2940
    Keywords: 1,4-Diboranaphthalenes, 1,4-dihydro- ; Nickel complexes ; Double-decker ; Triple-decker ; Tetradecker, slipped ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Nickel Complexes of a 1,4-Dihydro-1,4-diboranaphthalene Derivative*2,3-Diethyl-1,4-dihydro-1,4-dimethyl-1,4-diboranaphthalene (1) reacts with bis(1,5-cyclooctadiene)nickel to form the complexes 2 and 3. The latter is also obtained from 1 and bis(allyl)nickel. However, the reaction of 1 with Ni(C3H5)2 in a 1:1 ratio leads to 4 containing the 1,5-hexadiene ligand. The bis(allylnickel) triple-decker 5 is obtained from the dianion 12- and [(C3H5)NiBr]2. In addition, the diamagnetic 44-VE tetradecker 6 is formed in low yield. The constitutions of the complexes 2, 3, 4, and 6 are derived from spectroscopic data and are proven by X-ray structure analyses.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921250503
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