

FOLLOWUS
State Key Laboratory of Fine Chemicals, Department of Polymer Science and Engineering, Liaoning key Laboratory of Polymer Science and Engineering, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, China
hanli@dlut.edu.cn
Received:26 August 2025,
Accepted:27 September 2025,
Published Online:18 December 2025,
Published:15 January 2026
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Wang, Y. H.; Zhang, R. X.; Leng, H. T.; Xu, J. X.; Li, X. W.; Wang, Y. S.; Ma, H. W.; Li, Y.; Han, L. Anionic copolymerization of α-methylstyrene (AMS) and styrene (St) under the mild temperature. Chinese J. Polym. Sci. 2026, 44, 57–67
Yun-Han Wang, Rui-Xue Zhang, Hai-Tao Leng, et al. Anionic Copolymerization of
Wang, Y. H.; Zhang, R. X.; Leng, H. T.; Xu, J. X.; Li, X. W.; Wang, Y. S.; Ma, H. W.; Li, Y.; Han, L. Anionic copolymerization of α-methylstyrene (AMS) and styrene (St) under the mild temperature. Chinese J. Polym. Sci. 2026, 44, 57–67 DOI: 10.1007/s10118-025-3468-6.
Yun-Han Wang, Rui-Xue Zhang, Hai-Tao Leng, et al. Anionic Copolymerization of
The anionic copolymerization of
α
-methylstyrene (AMS) and styrene (St) was investigated under mild conditions (−25 °C to 25 °C). Using a stepwise feeding strategy to suppress depolymerization enabled efficient AMS incorporation
resulting in a single
composition-dependent
T
g
that enhanced the heat resistance of polystyrene (PS).
An effective strategy for enhancing the heat resistance of polystyrene (PS) with regard to its glass transition temperature (
T
g
) involves the anionic solution copolymerization of
α
-methylstyrene (AMS) with styrene (St)
typically requires much lower temperature (−25 °C) and multi-step monomer feeding to achieve higher number-average molecular weight (
M
n
) block copolymers. However
the anionic copolymerization of AMS and St under the mild temperature remains largely unexplored. This study systematically investigated the anionic copolymerization of AMS and St using
n
-BuLi in nonpolar solvent (−25 °C to 25 °C) through both one-step and two-step approaches. We demonstrated that one-step copolymerization at 25 °C yielded only 1−3 terminal AMS units
with higher feed ratios (5 wt%−20 wt%) increasing AMS incorporation but reducing the exact molecular weight (MW) due to enhanced depolymerization
as evidenced by MALDI-TOF MS. Temperature-controlled AMS conversion at −15 °C achieved 98% AMS conversion (5 wt% feed) by suppressing side reactions and lowering the [M
]
ₑ
while 50 °C (near
T
c
) almost prevented incorporation. Despite t-BuOK regulation induced broader PDI (1.24)
via
reactive [(polymer-Li)OR
]
K intermediates
while other systems showed narrow distributions
t-BuOK outperformed THF in enhancing AMS incorporation
via
efficient ion pair dissociation. In comparison
the two-step polymerization approach demonstrated superior performance
achieving both higher AMS conversion efficiency and preferential incorporation at the initiation end. At a 20 wt% AMS feed ratio
this method yielded copolymer chains containing up to 6 AMS units on average. Thermal analysis revealed a composition-dependent single
T
g
which exhibited a systematic increase with higher AMS incorporation content. These results collectively
demonstrate the precise control over AMS incorporation and heat resistance achievable through the manipulation of polymerization conditions.
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