Related Experiment Video
Updated: Mar 26, 2026

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
Published on: January 19, 2016
Mechanochromism and Mechanical-Force-Triggered Cross-Linking from a Single Reactive Moiety Incorporated into Polymer
Huan Zhang1, Fei Gao1, Xiaodong Cao1
1Department of Chemistry, College of Chemistry and Engineering, Xiamen University, 422 South Siming Road, Xiamen, Fujian, 361005, P.R. China.
Abstract:
Incorporation of small reactive moieties, the reactivity of which depends on externally imposed load (so-called mechanophores) into polymer chains offers access to a broad range of stress-responsive materials. Here, we report that polymers incorporating spirothiopyran (STP) manifest both green mechanochromism and load-induced addition reactions in solution and solid. Stretching a macromolecule containing colorless STP converts it into green thiomerocyanine (TMC), the mechanically activated thiolate moiety of which undergoes rapid thiol-ene click reactions with certain reactive C=C bonds to form a graft or a cross-link. The unique dual mechanochemical response of STP makes it of potentially great utility both for the design of new stress-responsive materials and for fundamental studies in polymer physics, for example, the dynamics of physical and mechanochemical remodeling of loaded materials.
More Related Videos
Related Concept Videos
Cationic Chain-Growth Polymerization: Mechanism
Radical Chain-Growth Polymerization: Overview
Radical Chain-Growth Polymerization: Mechanism
Anionic Chain-Growth Polymerization: Mechanism
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Anionic Chain-Growth Polymerization: Overview

