Related Experiment Video
Updated: Aug 4, 2026

A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
Published on: November 12, 2016
Contact ion-pair SN2 reactions activated by Lewis Base Phase transfer catalysts
Ju Gyeong Jeong1, Young-Ho Oh2, Tae Hyun Park1
1Department of Chemistry, Inha University, 100 Inha-ro, Nam-gu, Incheon, 402-751, Republic of Korea.
Abstract:
We present experimental probes of contact ion-pair (CIP) SN2 reactions for simplest prototype systems by 19F-NMR spectroscopy. This study provides crucial evidences for the reactions of CIP metal salts facilitated by Lewis base phase transfer catalysts (PTCs) [2,2,2]-cryptand, 18-crown-6, pentaethylene glycols (pentaEGs) and BINOL-based pentaEG. The 19F-NMR spectra of MF (M = K, Cs) ion-pairs in various solvents are used as fingerprinting tools to identify the CIP CsF/PTC/substrate complexes in SN2 reactions. Examination of the prototype reactions demonstrates that the novel CIP mechanism, which is in sharp contrast to the conventional perspectives, may account for the observed phenomenal efficiency of the SN2 processes using the alkali metal salts under the influence of various PTCs. In this extremely efficient and selective protocol of wide applicability, the CIP MF is activated by the Lewis base PTCs acting on the counter-cation M+ to drastically mitigate the latter's retarding Coulomb forces on the adjacent nucleophile F-, with or without the participation of hydrogen bonds.
Related Concept Videos
Lewis Acids and Bases
A coordinate covalent bond (or dative bond) occurs when one of the atoms in the bond provides both bonding electrons. For example, a coordinate covalent bond occurs when a water molecule combines with a hydrogen ion to form a hydronium ion. A coordinate covalent bond also results when...
Formation of Complex Ions
SN2 Reaction: Mechanism
The presence of the more electronegative halogen in the substrate creates a polarized carbon-halide bond. The halide pulls the electron cloud generating an electrophilic center at the carbon atom. Thus, the carbon atom carries a partial positive charge while the halide has a...
SN2 Reaction: Transition State
When the nucleophile approaches the electrophilic carbon with its lone pairs, the halide acts as a leaving group and moves away with the electron-pair bonded to the carbon. Dotted partial bonds represent the bonds being formed or broken...
SN1 Reaction: Mechanism
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
E2 Reaction: Kinetics and Mechanism

