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. 2019 Aug 20;141(34):13301–13305. doi: 10.1021/jacs.9b06259

Table 2. Synthesis of Poly(cis-1-b-trans-1-b-cis-1).

entry n:CTA cis/trans Mtheo (g mol–1)b Mn,NMR (g mol–1)c Mn, SECd (g mol–1)d ĐMd
1 20:1 54:46 (3:97) 4650 (2370) 3700 (2200) 4600 (2100) 2.06 (2.02)
2 40:1 54:46 (3:97) 9210 (4650) 10 000 (5000) 8900 (4700) 1.60 (1.67)
a

Sequential procedure outlined in Scheme 2, with [1]0 = 1 mol L–1. Monomer conversion quantitative for each step. Values in brackets were obtained after the ROMP step.

b

Calculated as Mr(CTA) + (2 × n × Mr(1)).

c

Calculated by the relative integration of the methylene protons in the CTA (δ = 4.19–4.27 ppm) and the polymer (δ = 4.60 – 4.80 ppm).

d

Calculated by SEC relative to polystyrene standards in THF eluent.