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. 2016 Jun 13;55(30):8680–8685. doi: 10.1002/anie.201602930

Table 2.

Selected data for the rac‐LA polymerization using 46 and 13 under immortal conditions (the complete Table can be found in Table S1).

Cat [mol %] Conv [%][a] M n (exp) [kg⋅mol−1][b] Ð[b] M n(cld) [kg⋅mol−1][c] TOF [h1][d]
4 (0.1) 48 50 1.10 70 30
5 (0.1) 93 53 1.04 67 13 000
6 (0.1) 97 49 1.09 70 14 000
1 (0.1) 97 14 1.07 14 60 000
2 (0.1) 91 13 1.03 13 50 000
3 (0.1) 92 13 1.08 13 35 000
2 [e] (0.005) 80 45 1.03 57 16 000
2 [f] (0.002) 42 48 1.02 61 12 600
A[ g] (0.2) 97 38 1.10 28 600
B [h] (0.1) 99 100 1.40 142 4430
C [i] (0.1) 63 13 1.11 13 18 900
D [j] (0.009) 83 900 2.00 1344 1170

Polymerization conditions as per Figure 1 (LHS for 46 and RHS for 13, immortal conditions) [a] Determined by 1H NMR spectroscopy (CDCl3, 298 K). [b] Determined by SEC versus polystyrene standards, and corrected by a factor of 0.58.16 [c] M n(cld)=(conversion/100)×loading/[number of metal centers]×RMM(LA). [d] TOF=(conversion/100)×loading/(time×number of metal centers). [e] 40 equiv. of IPA per mol of catalyst. [f] 50 equiv. of IPA per mol of catalyst. [g] A=BDIZnOiPr, [rac‐LA]=0.4 m, T=20 °C in CH2Cl2. 8 [h] B=halfsalenZnEt, CH2Cl2.9 [i] C=bis(morpholinomethyl)phenoxyZnEt, 10 equiv. of IPA per mol of catalyst, T=60 °C in toluene.17 [j] D=Sn(Oct)2, T=110 °C in octanoate, neat.18