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. 2015 Mar 5;6(5):2979–2988. doi: 10.1039/c5sc00477b

Fig. 9. 1H NMR spectrum of PMA synthesized by visible light-initiated polymerization with Xe lamp irradiation at ambient temperature. [MA]0 = 1.0 M, [MA]0/[(salen)Co–CO2CH3]0 = 200/1, conversion = 50%. M n,GPC = 10 300, M n,th = 9270, M n,NMR = 9530, M w/M n = 1.10. M n,th = M w( I ) + M w(MA) × ratio × conv. (%); M n,NMR = I 2.3ppm/(I 7.9ppm/2) × M w(MA) + M w( I ), where I 2.3ppm and I 7.9ppm are the integrals of the signals at δ 2.3 ppm and 7.9 ppm corresponding to the methane group of MA and the imine group of salen, respectively.

Fig. 9