Related Experiment Video
Updated: Feb 26, 2026

1,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions
Published on: October 10, 2016
Concave binding of cationic Li to quadrannulene
Jing-Shuang Dang1, Wei-Wei Wang, Xiang Zhao
1Institute for Chemical Physics & Department of Chemistry, School of Science, Xi'an Jiaotong University, Xi'an 710049, China. xzhao@mail.xjtu.edu.cn.
Abstract:
Binding of Li+ to quadrannulene and its influence on buckybowl functionalization are introduced. The concave-trapped Li+ acts as a Lewis acid and the rate of Diels-Alder cycloaddition is enhanced 108 times. A sandwiched bowl-Li+-bowl structure is stabilized via concave-cation-convex interactions, indicating the promoted role of Li+ in buckybowl assembly.
More Related Videos
Related Concept Videos
Ionic Bonding and Electron Transfer
Valence Bond Theory
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...

