Related Experiment Video
Updated: Jul 4, 2026

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Thorpe-Ingold effect on the helicity of chiral alternating silylene-divinylarene copolymers
1Department of Chemistry, National Taiwan University, Taipei 106, Taiwan.
Abstract:
The concept of the Thorpe-Ingold effect has been used to rationalize the helicity of the silylene-spaced divinylarene copolymers having chiral substituents. Diisopropylsilylene-spaced divinylbenzene copolymers having chiral 2-methylbutoxy substituents have been shown to exhibit a helical conformation. The presence of the bulky isopropyl substituents on silicon would render each of the monomeric units in these copolymers to favor a syn-syn conformation. The copolymer would thus be more folded to form helical morphology as revealed by the notable enhancement of the circular dichroic intensity. The reversible temperature-dependent circular dichroism (CD) profiles further support the stable helical conformation for the copolymers 4 b and 5 b.
More Related Videos
06:26Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
Published on: May 15, 2017
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
Related Concept Videos
π Electron Effects on Chemical Shift: Overview
Thermal Sigmatropic Reactions: Overview
Sigmatropic shifts are classified based on an order term [i, j ], where i and j indicate the number of atoms across which each end of the σ bond migrates. Below are examples of a [3,3] sigmatropic shift in 1,5-hexadiene, referred to as...
Polymer Classification: Stereospecificity
Chirality at Nitrogen, Phosphorus, and Sulfur
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
Regioselectivity of Electrophilic Additions-Peroxide Effect
Prochirality