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Verfasst von:Hartmann, Deborah [VerfasserIn]   i
 Schädler, Marcel [VerfasserIn]   i
 Greb, Lutz [VerfasserIn]   i
Titel:Bis(catecholato)silanes
Titelzusatz:assessing, rationalizing and increasing silicon's Lewis superacidity
Verf.angabe:Deborah Hartmann, Marcel Schädler, Lutz Greb
E-Jahr:2019
Jahr:14th June 2019
Umfang:10 S.
Fussnoten:Accepted 14th June 2019 ; Gesehen am 21.04.2020
Titel Quelle:Enthalten in: Chemical science
Ort Quelle:Cambridge : RSC, 2010
Jahr Quelle:2019
Band/Heft Quelle:10(2019), 31, Seite 7379-7388
ISSN Quelle:2041-6539
Abstract:Although bis(catecholato)silanes have been known for several decades, their substantial Lewis acidity is not yet well described in the literature. Herewith, the synthesis and characterization of multiple substituted bis(catecholato)silanes and their triethylphosphine oxide, fluoride and chloride ion adducts are reported. The Lewis acidity of bis(catecholato)silanes is assessed by effective (Gutmann-Beckett, catalytic efficiency), global (theoretical and relative experimental fluoride (FIA) and chloride (CIA) ion affinities) and intrinsic (electrophilicity index) scaling methods. This comprehensive set of experimental and theoretical results reveals their general Lewis acidic nature and provides a consistent Lewis acidity trend for bis(catecholato)silanes for the first time. All experimental findings are supported by high-level DLPNO-CCSD(T) based thermochemical data and the Lewis acidity is rationalized by complementary chemical bonding analysis tools. Against the common belief that inductive electron withdrawal is the most important criterion for strong Lewis acidity, the present work highlights the decisive role of π-back bonding effects in aromatic ring systems to enhance electron deficiency. Thus, bis(perbromocatecholato)silane is identified and synthesized as the new record holder for silicon Lewis superacids.
DOI:doi:10.1039/C9SC02167A
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1039/C9SC02167A
 Volltext: https://pubs.rsc.org/en/content/articlelanding/2019/sc/c9sc02167a
 DOI: https://doi.org/10.1039/C9SC02167A
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:169527900X
Verknüpfungen:→ Zeitschrift

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