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  • iron phosphine  (2)
  • Wiley-Blackwell  (2)
  • American Chemical Society
  • 1990-1994  (2)
  • 1970-1974
  • 1
    Electronic Resource
    Electronic Resource
    The structure and dynamics of FeH(DMPE)2(BH4), FeH(DEPE)2(BH4) and FeH(DPrPE)2(BH4): Iron complexes containing monodentate borohydride ligands (1990)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 4 (1990), S. 543-549 
    Details
    ISSN: 0268-2605
    Keywords: Borohydride ; iron phosphine ; organoiron ; NMR spectroscopy ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: FeH(DMPE)2(BH4) [DMPE = 1,2-bis(dimethylphosphino)ethane] is a stable, diamagnetic complex which can be synthesized readily by borohydride reduction of FeH(DMPE)2Cl or by treatment of Fe(DMPE)2H2 with borane. The complex contains an unsupported B—H—Fe hydrogen bridge. Analogous complexes with bulkier ligands, FeH(DEPE)2(BH4), [DEPE = 1,2-bis(diethylphosphino)ethane] and FeH(DPrPE)2(BH4) [DPrPE = 1,2-bis(di-n-propylphosphino)ethane], are less stable. In all complexes, in solution the borohydride ligand undergoes rapid internal motion, with all four boron-bound hydrogens interchanging environments. The barriers for BH4 reorientation (measured by NMR spectroscopy) are in the sequence FeH(DMPE)2(BH)4 〉 FeH(DEPE)2(BH)4 〉 FeH(DPrPE)2(BH4).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aoc.590040516
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  • 2
    Electronic Resource
    Electronic Resource
    Synthesis and properties of bis(dialkylphosphino)ethane iron dihydrides (1990)
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 4 (1990), S. 551-556 
    Details
    ISSN: 0268-2605
    Keywords: Metal hydride ; iron phosphine ; organoiron ; NMR spectroscopy ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses and properties of the iron bisphosphinoethane complexes FeH2(PP)2 and FeHCl(PP)2[PP=R2PCH2CH2CH2PR2, where R=Me (PP=DMPE), Et(PP=DEPE), and n-Pr (PP=DprPE)] are reported. The complexes can be formed by reduction of the corresponding dichlorides FeCl2(PP)2 with lithium aluminium hydride in THF solution provided that ethanol or more acidic reagents are not employed during the reaction work-up. The dihydrides are notably basic compounds and can be protonated reversibly by alcohols.The dihydrides exist as equilibrating mixtures of cis and trans isomers in solution. The cis isomers of each of the dihydrides are fluxional on the NMR timescale and NMR studies indicate that the interconversion of cis isomers does not necessarily proceed via the trans isomer.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aoc.590040517
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