Nucleophilicities and Nucleofugalities of Thio- and Selenoethers

Maji, Biplab; Duan, Xin-Hua; Juestel, Patrick M.; Byrne, Peter A.; Ofial, Armin R. und Mayr, Herbert (2021): Nucleophilicities and Nucleofugalities of Thio- and Selenoethers. In: Chemistry - A European Journal, Bd. 27, Nr. 44: S. 11367-11376

Abstract

Rate constants for the reactions of dialkyl chalcogenides with laser flash photolytically generated benzhydrylium ions have been measured photometrically to integrate them into the comprehensive benzhydrylium-based nucleophilicity scale. Combining these rate constants with the previously reported equilibrium constants for the same reactions provided the corresponding Marcus intrinsic barriers and made it possible to quantify the leaving group abilities (nucleofugalities) of dialkyl sulfides and dimethyl selenide. Due to the low intrinsic barriers, dialkyl chalcogenides are fairly strong nucleophiles (comparable to pyridine and N-methylimidazole) as well as good nucleofuges;this makes them useful group-transfer reagents.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Chemie und Pharmazie
• Themengebiete: 500 Naturwissenschaften und Mathematik > 540 Chemie
• ISSN: 0947-6539
• Sprache: Englisch