Related Experiment Video
Updated: Aug 31, 2025

Synthesis of Soft Polysiloxane-urea Elastomers for Intraocular Lens Application
Published on: March 8, 2019
Nonlinear Optical Properties of Pyrene Derivatives Based on a Donor-Acceptor Structure and Its Polyurethane
Lijun Gao1, Biyu Li1, Haoyue Yi1
1Henan Provincial Key Laboratory of Surface & Interface Science, College of Material and Chemical Engineering, Zhengzhou University of Light Industry, Zhengzhou 450000, China.
Abstract:
Two pyrenyl Schiff base derivatives with π conjugated structures (B2 and B3) were designed and synthesized. Then, B2 and B3 were added into polyurethane to obtain doped and bonded polyurethane nonlinear optical materials (B2/PU and B3/PU), respectively. The synthesized B2, B3, and polyurethane nonlinear optical materials were tested by a nanosecond (ns) and picosecond (ps) pulse Z-scan at a 532 nm wavelength. Due to the two-photon absorption-induced excited state absorption (TPA-ESA), B2, B3, and polyurethane nonlinear optical materials show reverse saturable absorption (RSA). From a quantum chemistry calculation, it can be concluded that the RSA of B2 and B3 comes from the large π conjugated system and intramolecular charge transfer. Furthermore, B2, B3, and the polyurethane nonlinear optical materials show good optical limiting. B2/PU and B3/PU not only have excellent nonlinear optical properties but also have good transmittance, thermal stability, and processability of polyurethane materials. The combination of pyrenyl Schiff base derivatives and polyurethane materials greatly improves the application of nonlinear small molecules in the field of optical limiting and all-optical switching.
Related Concept Videos
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...
Polymer Classification: Architecture
UV–Vis Spectroscopy: Woodward–Fieser Rules
Polymer Classification: Stereospecificity
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation

