Počet záznamů: 1  

Aromatic C-H bond activation revealed by infrared multiphoton dissociation spectroscopy

  1. 1.
    0377947 - ÚOCHB 2013 RIV GB eng J - Článek v odborném periodiku
    Jašíková, L. - Hanikýřová, E. - Schröder, Detlef - Roithová, J.
    Aromatic C-H bond activation revealed by infrared multiphoton dissociation spectroscopy.
    Journal of Mass Spectrometry. Roč. 47, č. 4 (2012), s. 460-465. ISSN 1076-5174. E-ISSN 1096-9888
    Grant ostatní: GA ČR(CZ) GAP207/11/0338; Seventh Framework Program(XE) 226716
    Výzkumný záměr: CEZ:AV0Z40550506
    Klíčová slova: C-H activation * density functional theory calculations * ion spectroscopy * metal oxides * rearrangements
    Kód oboru RIV: CC - Organická chemie
    Impakt faktor: 3.214, rok: 2012

    Metal-oxide cations are models of catalyst mediating the CH bond activation of organic substrates. One of the most powerful reagents suggested in the gas phase is based on CuO+. Here, we describe the activation of the aromatic CH bonds of phenanthroline in its complex with CuO+. The reaction sequence starts with a hydrogen atom abstraction by the oxygen atom from the 2-position of the phenanthroline ring, followed by OH migration to the ring. Using infrared multiphoton spectroscopy, it is shown that the reaction can be energetically facilitated by additional coordination of a water ligand to the copper ion. As the reaction is intramolecular, a spectroscopic characterization of the product is mandatory in order to unambiguously address the reaction mechanism.
    Trvalý link: http://hdl.handle.net/11104/0209957

     
     
Počet záznamů: 1  

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