Related Experiment Video
Updated: May 12, 2026

1,3,5-Triphenylbenzene and Corannulene as Electron Receptors for Lithium Solvated Electron Solutions
Published on: October 10, 2016
π-Electron ring-currents and bond-currents in [10,5]-Coronene and related structures conforming to the
1University Chemical Laboratory, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, England, UK. tkd25@cam.ac.uk
Abstract:
A series of hypothetical conjugated structures is defined; the series is called the p-Coronenes and the first four members of it are shown to respect the 'Annulene-Within-an-Annulene' (AWA) model when tested by means of Hückel-London-Pople-McWeeny (HLPM) π-electron ring-current and bond-current calculations. The first member of this series, 5-Coronene, is also a member of the regular [r,s]-Coronene series, where it is known as [10,5]-Coronene. It is shown that, as p is varied (with p always odd, and with p > 3) through the values 5, 7, 9, 11, etc., the resulting structures alternate between a '[4n + 2]-Annulene-Within-a-[4m]-Annulene' (if (p- 1) is divisible by 4) and a '[4n]-Annulene-Within-a-[4m + 2]-Annulene' (if (p- 1) is not divisible by 4). It is therefore claimed that the p-Coronenes constitute an ideal series for testing the AWA model. It is also remarked that each member of the p-Coronene series has only four Kekulé structures, and that the 'spokes' or 'transverse' bonds connecting the central [p(p- 3)]-membered ring to the outer [p(p- 1)]-membered periphery always have a Pauling bond-order of zero, ensuring that the outer and inner rings are 'decoupled'; such bonds also bear zero bond-current, by symmetry. It is argued that the former property of these transverse bonds, rather than the latter, determines that the p-Coronenes obey the AWA rule-which is in fact an exception, rather than a 'rule'per se. The paper concludes by explicitly stating our philosophy that a conceptually simple model depending on no subjective (or any other) parameters whatsoever can give intuitive chemical insight for certain systems equal to that available from far-more complex methods such as ab initio calculations-what Coulson once famously called 'primitive patterns of understanding'.
More Related Videos
09:35Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
08:44Measurements of Long-range Electronic Correlations During Femtosecond Diffraction Experiments Performed on Nanocrystals of Buckminsterfullerene
Published on: August 22, 2017
Related Concept Videos
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
Structure and Bonding of Alkenes
Doubly bonded carbons are sp2 hybridized and have a trigonal planar geometry. The double bond is composed of a σ bond formed by the overlap of hybrid orbitals and a π bond produced by the lateral overlap of unhybridized 2p orbitals on both the carbons. Each carbon atom is bonded to two hydrogen atoms...
Bond Energies and Bond Lengths
Structure of Benzene: Molecular Orbital Model
Structure of Conjugated Dienes
Conjugated dienes are compounds characterized by the presence of alternating double and single bonds. In a conjugated system like 1,3-butadiene, the unhybridized 2p orbital on each carbon overlaps continuously, allowing the π electrons to be delocalized across the entire molecule. In contrast, this type of overlap does not occur in cumulated and isolated dienes, such as 2,3-pentadiene and 1,4-pentadiene, respectively. Instead, the π electrons remain localized between the double...
Structure of Benzene: Kekulé Model
He proposed that benzene has a cyclic structure of six carbon atoms attached to one hydrogen atom each, with three alternating pi bonds.