Related Experiment Video
Updated: Aug 13, 2026

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Molecular size insensitivity of optical gap of [n]cycloparaphenylenes (n = 3-16)
Yoshifumi Noguchi1, Osamu Sugino1
1Institute for Solid State Physics, The University of Tokyo, 5-1-5 Kashiwanoha, Kashiwa, Chiba 277-8581, Japan.
Abstract:
The first-principles GW+Bethe-Salpeter method is applied to [n]cycloparaphenylenes ([n]CPPs, n = 3-16) to explain why the experimental UV-vis absorption spectra for n = 7-16 are roughly size-insensitive, unlike the fluorescence spectra. Having confirmed that the calculated absorption spectra consistently exhibit size-insensitivity, the exciton properties are investigated in detail using a novel analysis method based on the two-particle picture. The size-insensitivity of large-sized [n]CPPs (n≥9) is found due to a common spatial distribution of the wave functions involved with the first dark exciton and the first bright exciton, which are characterized primarily by a number of the wave function nodes. The exciton wave function as well as other properties of smaller molecules of n = 7 and 8 is, on the contrary, size-sensitive, although and the peak positions are essentially size-insensitive because of the cancellation of size-dependence of exciton binding energy and orbital energy. Different size-sensitivity between absorption and fluorescence can thus be explained unless such cancellation also occurs for fluorescence.
More Related Videos
06:55Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
09:22Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Related Concept Videos
Conformations of Cycloalkanes
Criteria for Aromaticity and the Hückel 4n + 2 Rule
For the first time, Eric Hückel, a German chemical physicist, derived a set of structural features for a compound to be classified as aromatic. This is now known as Hückel’s rule or the 4n + 2 rule.
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous overlap of p...
Frost Circles for Different Conjugated Systems
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR