Zobrazeno 1 - 10
of 2 349
pro vyhledávání: '"Holger Braunschweig"'
Autor:
Iemhoff, Andree, Vennewald, Maurice, Artz, Jens, Asmelash, Chalachew Mebrahtu, Meledin, Alexander, Weirich, Thomas E., Hartmann, Heinrich, Besmehn, Astrid, Aramini, Matteo, Venturini, Federica, Mosselmans, Fred, Held, Georg, Arrigo, Rosa, Palkovits, Regina
Publikováno v:
ChemCatChem 14(9), e202200179 (2022). doi:10.1002/cctc.202200179 special issue: "Surface organometallic and heterogeneous single-atom catalysts"
ChemCatChem 14(9), e202200179 (2022). doi:10.1002/cctc.202200179 special issue: "Surface organometallic and heterogeneous single-atom catalysts"
Published by WILEY-VCH Verlag, Weinheim
Published by WILEY-VCH Verlag, Weinheim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcf18e94bfc573a4fbe9571505c385be
Autor:
Chakrabortty, Soumyadeep, Konieczny, Katharina, Müller, Bernd H., Spannenberg, Anke, Kamer, Paul C. J., de Vries, Johannes G.
Publikováno v:
Catalysis Science & Technology; 2022, Vol. 12 Issue: 5 p1392-1399, 8p
Autor:
Marcel Härterich, Alexander Matler, Rian D. Dewhurst, Andreas Sachs, Kai Oppel, Andreas Stoy, Holger Braunschweig
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-7 (2023)
Abstract The Fischer carbene synthesis, involving the conversion of a transition metal (TM)-bound CO ligand to a carbene ligand of the form [=C(OR’)R] (R, R’ = organyl groups), is one of the seminal reactions in the history of organometallic chem
Externí odkaz:
https://doaj.org/article/dbab5c0d08d0411180aed3b43ba0cd1d
Publikováno v:
Angewandte Chemie. Nov2012, Vol. 124 Issue 47, p11838-11839. 2p.
Autor:
Zhu Wu, Nikolai Hippchen, Jie Han, Lei Ji, Alexandra Friedrich, Ivo Krummenacher, Holger Braunschweig, Johannes Krebs, Michael Moos, Philipp Biegger, Olena Tverskoy, Steffen Maier, Christoph Lambert, Andreas Dreuw, Todd B. Marder, Jan Freudenberg, Uwe H. F. Bunz
Publikováno v:
The Journal of Organic Chemistry. 88:2742-2749
Autor:
Silvia Huynh, Merle Arrowsmith, Lukas Meier, Maximilian Dietz, Marcel Härterich, Maximilian Michel, Annalena Gärtner, Holger Braunschweig
Publikováno v:
Dalton Transactions. 52:3869-3876
NMR-spectroscopic, structural and theoretical data of cyclic alkyl(amino)iminate (CAAI)-stabilised boranes synthesised by halosilane elimination from CAAI–SiMe3 and haloborane precursors highlight the excellent σ- and π-electron donor ability of
Autor:
Younes K. J. Bejaoui, Frederik Philippi, Hans-Georg Stammler, Krzysztof Radacki, Ludwig Zapf, Nils Schopper, Kateryna Goloviznina, Kristina A. M. Maibom, Roland Graf, Jan A. P. Sprenger, Rüdiger Bertermann, Holger Braunschweig, Tom Welton, Nikolai V. Ignat'ev, Maik Finze
Publikováno v:
Chemical Science. 14:2200-2214
Room temperature ionic liquids of cyclic sulfonimide anions ncPFSI (ring size: n = 4-6) with the cations [EMIm]+ (1-ethyl-3-methylimidazolium), [BMIm]+ (1-butyl-3-methylimidazolium) and [BMPL]+ (BMPL = 1-butyl-1-methylpyrrolidinium) have been synthes
Autor:
Julian Böhnke, Theresa Dellermann, Mehmet Ali Celik, Ivo Krummenacher, Rian D. Dewhurst, Serhiy Demeshko, William C. Ewing, Kai Hammond, Merlin Heß, Eckhard Bill, Eileen Welz, Merle I. S. Röhr, Roland Mitrić, Bernd Engels, Franc Meyer, Holger Braunschweig
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-7 (2018)
Attempts to bend and twist multiple bonds in order to alter their reactivities have thus far been met with only modest success. Here, Braunschweig and colleagues isolate double-bond-containing boron-based species and their 90°-twisted diradical anal
Externí odkaz:
https://doaj.org/article/58a8fc7cef4c4b33ac6d1678b54a97f7
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Annalena Gärtner, Lukas Meier, Merle Arrowsmith, Maximilian Dietz, Ivo Krummenacher, Rüdiger Bertermann, Felipe Fantuzzi, Holger Braunschweig
Publikováno v:
Journal of the American Chemical Society. 144:21363-21370
The stepwise reduction of a doubly cyclic alkyl(amino)carbene (CAAC)-stabilized 2,3-bis(dibromoboryl)naphthalene enables the isolation of the corresponding mono- and bis(boryl) radicals (one- and two-electron reduction), a 2π-aromatic 1,2-diborete (