Related Experiment Video
Updated: Jan 4, 2026

Synthesis of Soft Polysiloxane-urea Elastomers for Intraocular Lens Application
Published on: March 8, 2019
Organic Glasses of High Glass Transition Temperatures Due To Substitution with Nitrile Groups
Felix Krohn1, Christian Neuber1, Ernst A Rössler2
1Department of Macromolecular Chemistry I and Bavarian Polymer Institute , University of Bayreuth , 95440 Bayreuth , Germany.
Abstract:
The glass transition temperature (Tg) of a molecular glass depends on its molar mass. However, the nature of intermolecular interactions also plays a major role in both the glass transition temperature and its glass-forming ability. In this context, we report on novel molecular glasses containing nitrile groups and investigate the influence of this highly polar group on Tg and the glass-forming ability. As reference compounds, we studied the thermal properties of synthesized molecular glasses with C-C-bonded phenyl rings. The molar mass of the studied compounds ranges from 341 to 568 g/mol. Despite their relatively low molar mass, glass transition temperatures from 347 K (74 °C) to 471 K (198 °C) were observed. Most of the compounds possess high Tg/Tmratios between 0.7 and 0.8. By introducing highly interacting nitrile groups, the dependence of the molar mass on Tg could be increased by a factor of 2-3.
Related Concept Videos
Ziegler–Natta Chain-Growth Polymerization: Overview
Polymer Classification: Stereospecificity
IR Frequency Region: Alkyne and Nitrile Stretching
Comparing the stretching vibrational frequency of C≡C triple bonds with that of double and single bonds, it is evident that C≡C triple bonds exhibit a higher stretching frequency than C=C double and C–C single bonds. Similarly, the C≡N triple bond...
Polymer Classification: Crystallinity
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
2° Amines to N-Nitrosamines: Reaction with NaNO2
Diazonium Group Substitution: –OH and –H

