Výsledky vyhledávání - "Kristina A. M. Maibom"

Insights into structure–property relationships in ionic liquids using cyclic perfluoroalkylsulfonylimides

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::189e29f67270ed29c7713e821ebfc834
https://doi.org/10.1039/d2sc06758g

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Stable and Storable N(CF 3 ) 2 Transfer Reagents

Autor: Johannes Landmann, Tanja Knuplez, Christoph Kerpen, Nikolai V. Ignat'ev, Ludwig Zapf, Rüdiger Bertermann, Kristina A. M. Maibom, Tobias Bischof, Fabian Keppner, Eva-Maria Tanzer Krauel, Carl Deutsch, Leon Schneider, Klaus Urbahns, Michael Hailmann, Maik Finze

Publikováno v: Chemistry (Weinheim an Der Bergstrasse, Germany)

Fluorinated groups are essential for drug design, agrochemicals, and materials science. The bis(trifluoromethyl)amino group is an example of a stable group that has a high potential. While the number of molecules containing perfluoroalkyl, perfluoroa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc4a7cbb2b72ad5af348d43556e67a89
https://doi.org/10.1002/chem.202101436

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Hydrogen-bond-induced selectivity of a head-to-head photo-dimerisation of dialkynylanthracene - access to tetradentate Lewis acids

Autor: Kristina A. M. Maibom, Philipp Niermeier, Hans-Georg Stammler, Beate Neumann, Jan-Hendrik Lamm, Norbert W. Mitzel

Publikováno v: Chemical Science

Using 2-hydroxypropyl-protecting groups, 1,8-dialkynylanthracene photo-dimers were prepared in head-to-head-configuration by UV irradiation on a multi-gram scale. In non-polar solvents, the combination of non-covalent hydrogen bonds and π–π-inter

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5365a97d87ea9cbbd75ad5aa7af6137
https://pubmed.ncbi.nlm.nih.gov/34257857

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