2-Propenoic acid, 2-methyl-, (10-methyl-9-anthracenyl)methyl ester

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BASIC PARAMETERS Find an error

CAS: 57504-09-3
MF: C20H18O2
MW: 290.35572
Synonyms: 2-Propenoic acid, 2-methyl-, (10-methyl-9-anthracenyl)methyl ester

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REPORT BY

Juergen Popp

Friedrich-Schiller-Universit?t Jena
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Co-reporter: R. Geitner, J. Kötteritzsch, M. Siegmann, R. Fritzsch, T. W. Bocklitz, M. D. Hager, U. S. Schubert, S. Gräfe, B. Dietzek, M. Schmitt and J. Popp  
pp: 17973-17982
Publication Date(Web):15 Jun 2016
DOI: 10.1039/C6CP03464K
The self-healing polymer P(LMA-co-MeAMMA) crosslinked with C60-fullerene has been studied by FT-Raman spectroscopy in combination with two-dimensional (2D) correlation analysis and density functional theory calculations. To unveil the molecular changes during the self-healing process mediated by the Diels–Alder equilibrium between 10-methyl-9-anthracenyl groups and C60-fullerene different anthracene–C60-fullerene adducts have been synthesized and characterized by time-, concentration- and temperature-dependent FT-Raman measurements. The self-healing process could be monitored via the C60-fullerene vibrations at 270, 432 and 1469 cm−1. Furthermore, the detailed analysis of the concentration-dependent FT-Raman spectra point towards the formation of anthracene–C60-fullerene adducts with an unusual high amount of anthracene bound to C60-fullerene in the polymer film, while the 2D correlation analysis of the temperature-dependent Raman spectra suggests a stepwise dissociation of anthracene–C60-fullerene adducts, which are responsible for the self-healing of the polymer.
Co-reporter: R. Geitner, J. Kötteritzsch, M. Siegmann, R. Fritzsch, T. W. Bocklitz, M. D. Hager, U. S. Schubert, S. Gräfe, B. Dietzek, M. Schmitt and J. Popp
pp: NaN17982-17982
Publication Date(Web):2016/06/15
DOI: 10.1039/C6CP03464K
The self-healing polymer P(LMA-co-MeAMMA) crosslinked with C60-fullerene has been studied by FT-Raman spectroscopy in combination with two-dimensional (2D) correlation analysis and density functional theory calculations. To unveil the molecular changes during the self-healing process mediated by the Diels–Alder equilibrium between 10-methyl-9-anthracenyl groups and C60-fullerene different anthracene–C60-fullerene adducts have been synthesized and characterized by time-, concentration- and temperature-dependent FT-Raman measurements. The self-healing process could be monitored via the C60-fullerene vibrations at 270, 432 and 1469 cm−1. Furthermore, the detailed analysis of the concentration-dependent FT-Raman spectra point towards the formation of anthracene–C60-fullerene adducts with an unusual high amount of anthracene bound to C60-fullerene in the polymer film, while the 2D correlation analysis of the temperature-dependent Raman spectra suggests a stepwise dissociation of anthracene–C60-fullerene adducts, which are responsible for the self-healing of the polymer.

Mitchell A. Winnik

University of Toronto
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Co-reporter: Mitchell A. Winnik;Frank Di Stefano;Jai Vanketessan;Ronghua Liu
pp: 1495-1504
Publication Date(Web):21 MAR 2001
DOI: 10.1002/pola.1126

We describe the synthesis of three anthracene–methacrylate monomers [9-methacryloxymethyl-10-methyl anthracene (4), 9-methacryloxyethyloxymethyl-10-methyl anthracene (5), and 9-methacryloxy-10-methyl anthracene (6)] as well as their emulsion copolymers containing butylacrylate. When films prepared from latex dispersions containing 4 or 5 were heated, the anthracene (An) group was cleaved from the polymer at temperatures above 120 °C. Lower temperatures induced this reaction when strong acids were present. In 4 and 5, the polymerizable group is connected to the An ring via a 9-CH2O[BOND] linkage. The cleavage reaction requires more stringent conditions when the connection involves a benzylic ether (5) instead of a benzylic ester. Polymers prepared from 6, with an An[BOND]O[BOND] bond, were stable for 1 h at 150 °C in the presence of 0.5 wt % p-toluene sulfonic acid. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 1495–1504, 2001