Dendrimers Based on Thermally Reversible Furan−Maleimide Diels−Alder Adducts
- 19 January 2007
- journal article
- research article
- Published by American Chemical Society (ACS) in Macromolecules
- Vol. 40 (4) , 818-823
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Anthracene−Maleimide-Based Diels−Alder “Click Chemistry” as a Novel Route to Graft CopolymersMacromolecules, 2006
- Exploiting Chemical Switching in a Diels–Alder Polymer for Nanoscale Probe Lithography and Data StorageAdvanced Functional Materials, 2006
- Thermally Cleavable Surfactants Based on Furan−Maleimide Diels−Alder AdductsLangmuir, 2005
- Electrical and mechanical behavior of filled elastomers 2: The effect of swelling and temperatureJournal of Polymer Science Part B: Polymer Physics, 2004
- Synthesis and Photomodulation of Rigid Polyphenylene Dendrimers with an Azobenzene CoreMacromolecules, 2003
- Diels−Alder Reactions with Novel Polymeric Dienes and Dienophiles: Synthesis of Reversibly Cross-Linked ElastomersMacromolecules, 2002
- Protein Nanoarrays Generated By Dip-Pen NanolithographyScience, 2002
- Optically Active Polymer Synthesis by Diels−Alder Polymerization with Chirally Modified Lewis Acid CatalystMacromolecules, 1999
- endo- and exo-Stereochemistry in the Diels-Alder Reaction: Kinetic versus Thermodynamic ControlJournal of Chemical Education, 1997
- Stimuli-Responsive Hybrid Macromolecules: Novel Amphiphilic Star Copolymers With Dendritic Groups at the PeripheryJournal of the American Chemical Society, 1996