Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Petra Meixner"'
Autor:
Wolfgang Scherer, Georg Eickerling, Petra Meixner, Andreas Fischer, José Enrique Barquera-Lozada, Klaus Ruhland, Kilian Batke, Klaus Eichele
Publikováno v:
Angewandte Chemie. 128:11846-11850
Autor:
Petra Meixner, Georg Eickerling, Wolfgang Scherer, Klaus Eichele, Kilian Batke, Andreas Fischer, Klaus Ruhland, José Enrique Barquera-Lozada
Publikováno v:
Angewandte Chemie International Edition. 55:11673-11677
We will outline that the sign and magnitude of J(Si,H) coupling constants provide a highly sensitive tool to measure the extent of Si-H bond activation in nonclassical silane complexes. Up to now, this structure-property relationship was obscured by
Autor:
Dominik Schmitz, Kilian Batke, Andreas Fischer, Petra Meixner, Georg Eickerling, Fabio Montisci, Nicola Casati, Klaus Ruhland, Wolfgang Scherer, Marcel Kalter, José Enrique Barquera-Lozada, Piero Macchi, Klaus Eichele
Publikováno v:
Meixner, Petra; Batke, Kilian; Fischer, Andreas; Schmitz, Dominik; Eickerling, Georg; Kalter, Marcel; Ruhland, Klaus; Eichele, Klaus; Barquera-Lozada, José E.; Casati, Nicola P. M.; Montisci, Fabio; Macchi, Piero; Scherer, Wolfgang (2017). J (Si,H) Coupling Constants of Activated Si–H Bonds. Journal of physical chemistry. A, 121(38), pp. 7219-7235. American Chemical Society 10.1021/acs.jpca.7b05830
We outline in this combined experimental and theoretical NMR study that sign and magnitude of J(Si,H) coupling constants provide reliable indicators to evaluate the extent of the oxidative addition of Si–H bonds in hydrosilane complexes. In combina
Autor:
Petra Meixner, Christoph Hauf, José Enrique Barquera-Lozada, Andreas Obenhuber, Dietmar Stalke, Klaus Ruhland, Wolfgang Scherer, Andreas Brück, Dirk Leusser, David J. Wolstenholme
Publikováno v:
Angewandte Chemie. 125:6208-6212
Autor:
David Schmidt, Christoph Hauf, José Enrique Barquera-Lozada, Thomas Zell, Udo Radius, Dietmar Stalke, Petra Meixner, Wolfgang Scherer, Sandra Altmannshofer, Georg Eickerling
In general, it is assumed that the reaction between silanes and late transition metal fragments yields silyl hydride species as oxidative addition products. However, the silane complex Ni(iPr2Im)2(SiHMePh2) (iPr2Im = 1, 3-diisopropylimidazolin-2-ylid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3db3f7d54b4a6e18a0d548becae67ebe
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/48805
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/48805
Autor:
Dirk Leusser, Wolfgang Scherer, Petra Meixner, Klaus Ruhland, Dietmar Stalke, Andreas Obenhuber, Andreas Brück, José Enrique Barquera-Lozada, David J. Wolstenholme, Christoph Hauf
Publikováno v:
Angewandte Chemie (International ed. in English). 52(23)
Experimental and theoretical charge density studies and molecular orbital analyses suggest that the complexes [Cp2Ti(PMe3)SiH2Ph2] (1) and [Cp2Ti(PMe3)SiHCl3] (2) display virtually the same electronic structures. No evidence for a significant interli