Related Experiment Video
Updated: May 30, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Cycloolefin Copolymers With a Multiply Rigid Structure for Protecting Triplet Exciton From Thermo- and
Shiman Tang1, Shunnan Jiang1, Kaiti Wang1
1School of Materials Science and Engineering, Chongqing University of Technology, Chongqing, 400054, China.
Abstract:
Polymeric room temperature phosphorescence (RTP) materials have been well developed and utilized in various fields. However, their fast thermo- and moisture-quenching behavior highly limit their applications in certain harsh environments. Therefore, the preparation of materials with thermo- and moisture-resistant phosphorescence is greatly attractive. Compared with common water-soluble polymers, cycloolefin copolymers (COC) show outstanding hydrophobicity and higher rigidity, even at elevated temperatures, being as a promising candidate to prepare phosphorescence materials with suppressed thermo- and moisture-quenching behavior. Herein, a type of COC bearing hydroxyl, ester, and adamantanyl side groups is synthesized. After dispersing various phosphors into this matrix, the resultant composites exhibit full-color RTP with lifetimes of 249-590 ms. Their luminescence does not show obvious quenching in water, acid, alkalinous, reductive, and oxidative environments. In the presence of both rigid COC matrix and rigid phosphors, the corresponding composite displays high-temperature phosphorescence performance. Even at 378 K, the composite can emit phosphorescence with a lifetime of 40-98 ms. The applications of these COC-based composites for imaging, information encryption, and anti-counterfeiting are thus explored.
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
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
Thermal and Photochemical Electrocyclic Reactions: Overview
Cycloaddition Reactions: MO Requirements for Photochemical Activation
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.
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...