Maleimides Designed for Self-Assembly and Reactivity on Graphene
Two new maleimide derivatives have been synthesized, prone to self-assemble and react with graphene as dienophiles. Both compounds bear a long alkyl chain on the carbon-carbon double bond position 3. The maleimide 1 bears a second alkyl chain at the nitrogen, while in compound 2, three maleimide fun...
Main Authors: | Cristina Mattioli, André Gourdon, NanoSciences Group |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2015-10-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/20/10/18856 |
Similar Items
-
Maleimide Self-Reaction in Furan/Maleimide-Based Reversibly Crosslinked Polyketones: Processing Limitation or Potential Advantage?
by: Felipe Orozco, et al.
Published: (2021-04-01) -
Cyclopentadiene-Maleimide Platform for Thermally Reversible Polymers
by: Stegall, Jeremy Brent
Published: (2016) -
The application of the Diels-Alder reaction to polymer syntheses based on furan/maleimide reversible couplings
by: Alessandro Gandini
Published: (2005-06-01) -
Characterization and kinetic study of Diels-Alder reaction: Detailed study on N-phenylmaleimide and furan based benzoxazine with potential self-healing application
by: Z. Stirn, et al.
Published: (2016-07-01) -
Hydrophobilization of Furan-Containing Polyurethanes via Diels–Alder Reaction with Fatty Maleimides
by: Philipp Schmidt, et al.
Published: (2019-07-01)