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  • A novel class of chiral superbases derived from the 2,2 '-bipyridyl-N,N-dioxide skeleton are presented. Combined experimental and theoretical data reveal that their proton affinities are on the order of 1050 kJ mol(-1), with protonation occurring at the oxygen atoms in a chelating manner. In the free bases, the oxygen atoms form a strongly polar binding site hidden in a hydrophobic envelope formed by the hydrocarbon backbone of the superbases. This chiral molecular structure can entrap polar intermediates or polarized transition structures and stabilize them in nonpolar solvents. Specifically, this mode of catalysis is shown for the coupling of benzaldehyde and allyltrichlorosilane.
  • A novel class of chiral superbases derived from the 2,2 '-bipyridyl-N,N-dioxide skeleton are presented. Combined experimental and theoretical data reveal that their proton affinities are on the order of 1050 kJ mol(-1), with protonation occurring at the oxygen atoms in a chelating manner. In the free bases, the oxygen atoms form a strongly polar binding site hidden in a hydrophobic envelope formed by the hydrocarbon backbone of the superbases. This chiral molecular structure can entrap polar intermediates or polarized transition structures and stabilize them in nonpolar solvents. Specifically, this mode of catalysis is shown for the coupling of benzaldehyde and allyltrichlorosilane. (en)
Title
  • Oxygen Superbases as Polar Binding Pockets in Nonpolar Solvents
  • Oxygen Superbases as Polar Binding Pockets in Nonpolar Solvents (en)
skos:prefLabel
  • Oxygen Superbases as Polar Binding Pockets in Nonpolar Solvents
  • Oxygen Superbases as Polar Binding Pockets in Nonpolar Solvents (en)
skos:notation
  • RIV/00216208:11310/10:10062507!RIV11-MSM-11310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • S, Z(MSM0021620857)
http://linked.open...iv/cisloPeriodika
  • 36
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 277894
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11310/10:10062507
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • mass spectrometry; DFT methods; Superbases (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [8795EE6CB1C7]
http://linked.open...i/riv/nazevZdroje
  • Journal of the American Chemical Society
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 132
http://linked.open...iv/tvurceVysledku
  • Kadlčíková, Aneta
  • Kotora, Martin
  • Roithová, Jana
  • Ducháčková, Lucie
http://linked.open...ain/vavai/riv/wos
  • 000282074200029
http://linked.open...n/vavai/riv/zamer
issn
  • 0002-7863
number of pages
http://localhost/t...ganizacniJednotka
  • 11310
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