Related Experiment Video
Updated: May 13, 2026

An Electrochemical Cholesteric Liquid Crystalline Device for Quick and Low-Voltage Color Modulation
Published on: February 27, 2019
Pressure-Induced Controllable Multicolor Emission in Ethyl 7-hydroxy-2-oxo-2H-chromene-3-carboxylate
Jingkai Bi1, Wenfei Xu1,2, Jiaxiang Wang2
1Institute of Quantum Materials and Physics, Henan Academy of Sciences, Zhengzhou, China.
Ethyl 7-hydroxy-2-oxo-2H-chromene-3-carboxylate (EHC) shows significant color changes under pressure, making it a promising material for advanced pressure sensors. Its sensitivity and color contrast dramatically increase after a phase transition at 1.0 GPa.
Area of Science:
- Materials Science
- Organic Chemistry
- Spectroscopy
Background:
- Organic piezochromic materials are crucial for pressure-sensing applications.
- High sensitivity and color contrast are essential for practical use.
Purpose of the Study:
- To investigate the piezochromic behavior and phase transition of ethyl 7-hydroxy-2-oxo-2H-chromene-3-carboxylate (EHC).
- To evaluate EHC's potential as a colorimetric pressure sensor.
Main Methods:
- Studied the piezochromic response of EHC under varying pressure conditions.
- Analyzed phase transitions and their effect on optical properties.
Main Results:
- EHC undergoes a pressure-induced phase transition at 1.0 GPa.
- Exhibits multicolor emission shifts from blue to green and yellow with increasing pressure.
- Sensitivity increased from 1.12 nm·GPa⁻¹ to 11.63 nm·GPa⁻¹ and color contrast from 1 nm to 186 nm post-transition.
Conclusions:
- EHC demonstrates excellent potential as a colorimetric sensor for external pressure.
- Enhanced intermolecular interactions, particularly π-π interactions, drive the improved performance.
- Provides insights into structure-property relationships for developing new piezochromic materials.
More Related Videos
05:51Fabrication of White Light-emitting Electrochemical Cells with Stable Emission from Exciplexes
Published on: November 15, 2016
06:08Time-resolved Photophysical Characterization of Triplet-harvesting Organic Compounds at an Oxygen-free Environment Using an iCCD Camera
Published on: December 27, 2018
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Variables Affecting Phosphorescence and Fluorescence
Thermal and Photochemical Electrocyclic Reactions: Overview
UV–Vis Spectroscopy of Conjugated Systems
One of the factors influencing λmax is the extent of conjugation in the...
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.