Related Experiment Video
Updated: Jun 7, 2026

Characterizing Lewis Pairs Using Titration Coupled with In Situ Infrared Spectroscopy
Published on: February 20, 2020
Structure and dynamic features of an intramolecular frustrated Lewis pair
Kirill V Axenov1, Cornelia M Mömming, Gerald Kehr
1Organisch-Chemisches Institut der Universität Münster, Corrensstrasse 40, 48149 Münster, Germany.
Abstract:
Di(mesityl)cyclohexenylphosphine undergoes hydroboration with Piers' borane [HB(C(6)F(5))(2)] to yield the cyclohexylene-anellated frustrated Lewis pair 5. This P/B pair splits H(2) with the formation of the product 4 and adds to the C=O double bond of phenyl isocyanate to yield 6. In the crystal, compound 5 features a puckered four-membered heterocyclic core structure with a long P-B bond (av. 2.197(5) Å). The activation energy of the P-B cleavage of the frustrated Lewis pair 5 was determined by dynamic (19)F NMR spectroscopy at ΔG(≠)(298 K)=12.1±0.3 kcal mol(-1).
Related Concept Videos
Resonance and Hybrid Structures
Resonance Structures and Resonance Hybrids
The Lewis structure of a nitrite anion (NO2−) may actually be drawn in two different ways, distinguished by the locations of the N–O and N=O bonds.
VSEPR Theory and the Effect of Lone Pairs
VSEPR Theory
Resonance
Molecular Shapes
VSEPR Theory and the Basic Shapes

