Search Results - "Aicher, Frederik S. W."

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  1. 1

    Cationic Stannylenes: In Situ Generation and NMR Spectroscopic Characterization by Sindlinger, Christian P, Aicher, Frederik S. W, Wesemann, Lars

    Published in Inorganic chemistry (03-01-2017)
    “…The reaction of MeNHC (MeNHC = 1,3,4,5-tetramethylimidazolylidene, where NHC = N-heterocyclic carbene) adducts to organotin­(II) hydrides Ar*SnH and Ar′SnH…”
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  2. 2

    Reductive Elimination and Oxidative Addition of Hydrogen at Organostannylium and Organogermylium Cations by Diab, Fatima, Aicher, Frederik S. W., Sindlinger, Christian P., Eichele, Klaus, Schubert, Hartmut, Wesemann, Lars

    Published in Chemistry : a European journal (21-03-2019)
    “…Bulkily substituted organodihydrogermylium and ‐stannylium cations [Ar*EH2]+ (E=Ge, Sn; Ar*=2,6‐Trip2C6H3, Trip=2,4,6‐triisopropylphenyl) were characterized as…”
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  3. 3

    Access to Base Adducts of Low-Valent Organotin-Hydride Compounds by Controlled, Stepwise Hydrogen Abstraction from a Tetravalent Organotin Trihydride by Sindlinger, Christian P., Grahneis, Wiebke, Aicher, Frederik S. W., Wesemann, Lars

    Published in Chemistry : a European journal (23-05-2016)
    “…Hydrogen can be selectively removed from organotin trihydrides to generate the corresponding organohydrostannylene intermediates. Depending on the size of the…”
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  4. 4

    Molecular Ln(III)−H−E(II) Linkages (Ln=Y, Lu; E=Ge, Sn, Pb) by Widemann, Max, Aicher, Frederik S. W., Bonath, Martin, Eichele, Klaus, Maichle‐Mössmer, Cäcilia, Schubert, Hartmut, Sirsch, Peter, Anwander, Reiner, Wesemann, Lars

    Published in Chemistry : a European journal (10-08-2022)
    “…Following the alkane‐elimination route, the reaction between tetravalent aryl tintrihydride Ar*SnH3 and trivalent rare‐earth‐metallocene alkyls…”
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  5. 5

    Complete Hydrogen Transfer: Tin Hydride Reactivity toward Adamantylisonitrile and Benzonitrile by Aicher, Frederik S. W, Eichele, Klaus, Schubert, Hartmut, Wesemann, Lars

    Published in Organometallics (11-06-2018)
    “…Adamantylisonitrile and benzonitrile were reacted with bulky substituted organotin trihydride [Ar*SnH3] [Ar* = (C6H3-2,6-Trip2), Trip =…”
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  6. 6

    Reductive Dehydrogenation of a Stannane via Multiple Sn−H Activation by Frustrated Lewis Pairs by Sindlinger, Christian P., Aicher, Frederik S. W., Schubert, Hartmut, Wesemann, Lars

    Published in Angewandte Chemie International Edition (13-02-2017)
    “…A bulky substituted stannane Ar*SnH3 (Ar*=2,6‐(2′,4′,6′‐triisopropylphenyl)phenyl) was treated with the well‐known frustrated Lewis pair (FLP) PtBu3/B(C6F5)3…”
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  7. 7

    Reduktive Dehydrierung eines Stannans durch mehrfache Sn‐H‐Aktivierung mit einem frustrierten Lewis‐Paar by Sindlinger, Christian P., Aicher, Frederik S. W., Schubert, Hartmut, Wesemann, Lars

    Published in Angewandte Chemie (13-02-2017)
    “…Ein sterisch anspruchsvoll substituiertes Stannan Ar*SnH3 (Ar*=2,6‐(2′,4′,6′‐Triisopropylphenyl)phenyl) wurde mit dem bekannten frustrierten Lewis‐Paar (FLP)…”
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  8. 8

    Reduktive Dehydrierung eines Stannans durch mehrfache Sn-H-Aktivierung mit einem frustrierten Lewis-Paar by Sindlinger, Christian P, Aicher, Frederik S W, Schubert, Hartmut, Wesemann, Lars

    Published in Angewandte Chemie (13-02-2017)
    “…Ein sterisch anspruchsvoll substituiertes Stannan Ar*SnH3 (Ar*=2,6-(2',4',6'-Triisopropylphenyl)phenyl) wurde mit dem bekannten frustrierten Lewis-Paar (FLP)…”
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