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. 2023 Oct 2;14(40):11228–11236. doi: 10.1039/d3sc03827k

Library of alternating and statistical styrene–propylene and styrene–ethylene copolymers prepared by RAFT copolymerizations of the corresponding saccharin (meth)-acrylamide followed by hydrolysis and photocatalytic decarboxylation.

Entry Copolymer Copolymer compositiona StyX/P or E (mol%) Catalyst M n,app b (g mol−1) Đ b T g c (°C) T g breadthc (°C)
1 P(Sty-alt-P) 50/50 A1 9800 1.15 71 ± 1 17
2 P(Sty-stat-P) 54/46 A1 12 000 1.39 63 ± 1 20
3 P(StyOMe-alt-P) 51/49 A1 12 300 1.21 70 ± 1 14
4 P(StyOMe-stat-P) 51/49 A1 8000 1.23 64 ± 1 17
5 P(StyCl-alt-P) 50/50 A1 10 600 1.32 110 ± 1 19
6 P(StyCl-stat-P) 47/53 A1 14 500 1.37 80 ± 0 20
7 P(Sty-alt-E) 50/50 A2 9700 1.37 26 ± 1 13
8 P(Sty-stat-E) 47/53 A2 14 800 1.30 24 ± 0 16
9 P(StyOMe-alt-E) 50/50 A2 9600 1.69 39 ± 2 17
10 P(StyOMe-stat-E) 54/46 A2 10 500 1.19 46 ± 0 20
11 P(StyCl-alt-E) 50/50 A2 11 000 1.22 47 ± 1 18
12 P(StyCl-stat-E) 49/51 A2 8800 1.34 56 ± 0 21
a

Copolymer composition was determined by 1H NMR spectroscopy of the copolymer before decarboxylation.

b

Apparent molecular weights and dispersities were estimated by SEC in N,N-dimethylacetamide with a polystyrene calibration.

c

Glass transition temperatures and breadths were determined by differential scanning calorimetry (DSC).