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. 2020 Dec 15;10(72):44096–44102. doi: 10.1039/d0ra09280k

Summary of the main properties of the synthesized poly(butadiene-co-myrcene) and poly(butadiene-co-farnesene).

Runa Theoretical terpeneb content-% (Co)polymer compositions (experimental)c Terpene weight fraction A d k app e M w (kg mol−1) Đ f T g g(°C)
Bd-% Terpene-%
PB1 0 100 0 0 364.4 165.5 85 1.9 −107
PBMy1 10 94.7 5.3 0.12 409.3 33.6 119 2.0 −103
PBMy2 25 87.9 12.1 0.26 114.5 30.9 164 2.5 −99
PBMy3 50 72.1 27.9 0.49 103.0 14.7 297 3.4 −87
PBMy4 75 47.9 52.1 0.74 83.8 12.6 560 3.7 −79
PMy 100 0 100 1 109.7 5.1 1259 3.7 −64
PB2 0 100 0 0 242.9 165.4 53 2.8 −106
PBFa1 5 97.3 2.7 0.07 299.8 219.2 n.d. n.d. −103
PBFa2 10 94.9 5.1 0.12 228.0 140.6 59 1.9 −101
PBFa3 30 84.3 15.7 0.32 200.4 99.0 65 1.7 −97
PBFa4 50 63.1 36.9 0.53 291.3 89.4 115 2.1 −88
PBFa5 75 47.4 52.6 0.74 267.9 67.5 145 2.5 −82
PFa 100 0 100 1 n.d. n.d. 375 3.6 −75
a

Synthesis of PBMy and PBFa carried out by an isothermal process, with temperatures of 70 °C and 60 °C respectively, maintaining constant stirring of 100 rpm. n.d. = not determined.

b

Theoretical molar (%) terpene content used for the synthesized of the copolymers.

c

Molar (%) compositions calculated via1H NMR.

d

Catalytic activity (kgpolymer/mol−1 h−1). Calculated after 2 h of reaction for poly(butadiene-co-myrcene) and after 30 min for poly(butadiene-co-farnesene).

e

Apparent first-order rate constant (L mol−1 min−1) calculated considering the kinetic law d[M]/dt = ka[Nd][M], where kapp = k[Nd], and from the plots ln(1 − x)−1 = f(t), where x is the conversion.

f

Dispersity index (Mw/Mn) calculated by SEC.

g

Determined by DSC.