Fig. 2: 1H and 13C NMR chemical shifts comparison of the E/AM polymers, E/hex-5-enenitrile polymer and E/undec-10-enamide polymer (C2D2Cl4, 110 oC). | Nature Communications

Fig. 2: 1H and 13C NMR chemical shifts comparison of the E/AM polymers, E/hex-5-enenitrile polymer and E/undec-10-enamide polymer (C2D2Cl4, 110 oC).

From: Cyano-functionalized polyethylenes from ethylene/acrylamide copolymerization

Fig. 2

a 1H and 13C NMR chemical shifts of the E/AM polymer obtained in run 1 of Table 1. b 1H and 13C NMR chemical shifts of the E/AM polymer obtained in run 4 of Table 1. c 1H and 13C NMR chemical shifts of the E/hex-5-enenitrile polymer obtained in run 1 of Supplementary Table 1 (1.6 mol% comonomer content; see Supplementary Figs. 25-27 and section 1.4 in Supplementary Information for synthesis and characterization). d 1H and 13C NMR chemical shifts of the E/undec-10-enamide polymer obtained in run 1 of Supplementary Table 2 (1.8 mol% comonomer content; see Supplementary Figs. 28-30 and section 1.4 in Supplementary Information for synthesis and characterization).

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