Related Experiment Video
Updated: Jan 12, 2026

Gradient Echo Quantum Memory in Warm Atomic Vapor
Published on: November 11, 2013
Pentagonal/Heptagonal-Lock Strategy Enables Narrowband Red Multiple Resonance Emitters Through Temperature-Controlled
Jiahao Zhang1, Jiahui Liu2, Zhenlong Li1
1Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu, 610064, P.R. China.
None:
Although π-extension has shown considerable success in achieving red-shifted emission in multiple resonance (MR) emitters, it often induces substantial spectral broadening, thereby limiting its utility for developing high-performance red MR materials. Herein, we report a straightforward naphthalene-based pentagonal/heptagonal-lock π-extension strategy that enables a significant redshift of 116 nm while maintaining a narrow emission bandwidth. By controlling the Scholl reaction at different temperatures, we achieved precise π-extension through sequential pentagonal and heptagonal ring formation, enabling broad color tuning via fine adjustment of frontier molecular orbital energy gaps. As a result, a red fluorescent emitter was obtained, exhibiting an emission peak at 600 nm and a narrow full-width-at-half-maximum of 30 nm. Furthermore, the corresponding OLED devices exhibited a high external quantum efficiency of 21.3% with minimal efficiency roll-off.
Related Concept Videos
Double Resonance Techniques: Overview
Spin decoupling is usually achieved by...
Cycloaddition Reactions: MO Requirements for Thermal Activation
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals

