General Papers ARKIVOC 2016 (iii) 23-35 Divinyl isophthalate. White solid, mp 65 °C; (lit.14 mp 59–60 °C). UV: λmax (EtOH): 260 nm. 1H NMR (300 MHz, CDCl3, δ ppm): 8.85 (1H, m, H1), 8.36–8.39 (2H, m, H3,5), 7.65 (1H, t, J 6 Hz, H4), 7.53–7.60 (2H, dd, J 6 Hz and J 15 Hz, H9,9'), 5.16–5.21(2H, dd, J 3 Hz and J 12 Hz H12,12'), 4.79–4.82 (2H, dd, J 3 Hz and J 9 Hz, H11,11'). 13C (75 MHz, CDCl3, δ ppm): 162.71, 141.26, 134.78, 131.45, 129.67, 129.03, 123.25, 98.93. Divinyl dodecanedioate. Liquid, 1H NMR (300 MHz, CD3OD, δ ppm) : 7.26-7.33 (2H, dd, J 6 Hz and J 15 Hz, H2, 2’), 4.85-4.90 (2H, dd, J 3 Hz and J 6 Hz, H5, 5’), 4.60-4.57(2H, dd, J 3 Hz and J 6 Hz, H4, 4’), 2.41 (4H, t, J 6 Hz, H6, 6’), 1.59-1.70 (4H, m, H7, 7’), 1.34-1.39 (12H, m, H8, 8’,9 13 ,9’,10 ,10’). C (75 MHz, CD3OD δ ppm): 25.80, 30.20, 30.37, 30.44, 34.70, 97.89, 142.53, 172.28. Acknowledgements This work was partly funded by the French National Research Agency (ANR) through a grant (HIPERM) to IB. References 1. Faber, K.; Riva, F. Synthesis 1992, 895. http://dx.doi.org/10.1055/s-1992-26255 2. Uyama, H.; Kobayashi, S. Adv. Polym. Sci. 2006, 194, 133. http://dx.doi.org/10.1007/12_031 3. Husar. B.; Heller, C.; Schwentenwein, M.; Mautner, A.; Varga, F.; Koch, T.; Stampfl, J.; Liska, R. J. Polym. Sci. Part A. Polym. Chem. 2011, 49, 4927. http://dx.doi.org/10.1002/pola.24933 4. Murray, R. E.; Lincoln, D. M. Catal. Today 1992, 13, 92. http://dx.doi.org/10.1016/0920-5861(92)80189-T 5. Heller, C.; Schwentenwein, M.; Russmueller, G.; Varga, F.; Stampfl, J.; Liska, R. J. Polym. Sci. Part A Polym. Chem. 2009, 47, 6941. http://dx.doi.org/10.1002/pola.23734 6. Waller, F. J. In: Kosak, J. R.; Johnson, T. A. Eds. Catalysis of Organic Reactions, M. Dekker: NY 1994, p 397. 7. Swern, D.; Jordan, E. F. Jr. Org. Synth. Coll. 1963, 4, 977. http://dx.doi.org/10.15227/orgsyn.030.0106 Page 34 © ARKAT-USA, Inc.
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