Related Experiment Video
Updated: Oct 3, 2025

Synthesis of Soft Polysiloxane-urea Elastomers for Intraocular Lens Application
Published on: March 8, 2019
Synthesis and Hydrophilicity Analysis of bis(propane-1,2-diol) Terminated Polydimethylsiloxanes (PDMSs)
Lan-Hee Yang1, Kyeong Eun Park1, Sungho Yoon1
1Department of Chemistry, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul 06974, Korea.
Abstract:
Among silicone oligomers, polydimethylsiloxane (PDMS) is widely used industrially and has the advantage of improving the properties of other compounds, such as flame-retardant polyurethane (PU). However, as there are barriers to the synthesis of PU-grafted siloxane, owing to the polarity difference between isocyanate and PDMS, numerous research efforts are being aimed at improving the hydrophilicity of PDMS. To improve the hydrophilicity and reactivity of hydroxyl PDMS, bis(propane-1,2-diol)-terminated PDMS (G-PDMS-G) with four hydroxy (-OH) groups was synthesized through ring-opening addition to replace both ends of linear α,ω-hydroxyl PDMS (HO-PDMS-OH) with glycidol, resulting in hydrophilic PDMS rather than dihydroxy PDMS. In all cases of G-PDMS-G, the contact angle and viscosity both decreased by more than 20%, confirming the improved hydrophilicity. In particular, G-PDMS-G-3, which has the largest molecular weight, demonstrated the greatest decrease in viscosity and contact angle (33%).
Related Concept Videos
Preparation of Diols and Pinacol Rearrangement
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
Formation of Halohydrin from Alkenes
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.
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Characteristics and Nomenclature of Homopolymers
Polymer Classification: Stereospecificity

