Related Experiment Video
Updated: Jan 17, 2026

Synthesis of Soft Polysiloxane-urea Elastomers for Intraocular Lens Application
Published on: March 8, 2019
Bleaching effect of high refractive index xylylic poly(thiourea)s with "de-conjugated" polarizable hydrogen bonds
Seigo Watanabe1, Yoshino Tsunekawa2, Kenichi Oyaizu1,2
1Research Institute for Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555, Japan. oyaizu@waseda.jp.
Abstract:
Poly(p-xylylene thiourea) (pX-PTU) exhibits high visible-light transparency (%T ≧ 99), a high refractive index (nD = 1.71), and a reasonable Abbe number (νD = 26) owing to "de-conjugated" hydrogen bonds, which inhibit orbital interactions between the polarizable phenylene and thiourea units through sandwiched methylene spacers. Upon blending pX-PTU with all-aromatic poly(thiourea)s, their refractive index increased up to nD = 1.80.
Related Concept Videos
π Electron Effects on Chemical Shift: Overview
Stability of Conjugated Dienes
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
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.
Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene

