

FOLLOWUS
a.Chinese Academy of Sciences Key Laboratory of Soft Matter Chemistry, Hefei National Laboratory for Physical Sciences at the Microscale, Department of Polymer Science and Engineering, University of Science and Technology of China, Hefei 230026, China
b.Institutes of Physical Science and Information Technology, Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Anhui University, Hefei 230026, China
tcchem@mail.ustc.edu.cn (C.T.)
changle@ustc.edu.cn (C.L.C.)
Received:16 August 2020,
Revised:2020-9-13,
Accepted:17 September 2020,
Online First:16 October 2020,
Published:01 January 2021
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Behzadi, S.; Zou, C.; Yang, B. P.; Tan, C.; Chen, C. L. Styrene-containing phosphine-sulfonate ligands for nickel- and palladium-catalyzed ethylene polymerization. Chinese J. Polym. Sci. 2021, 39, 447–454
Shabnam Behzadi, Chen Zou, Bang-Pei Yang, et al. Styrene-containing Phosphine-sulfonate Ligands for Nickel- and Palladium-catalyzed Ethylene Polymerization[J]. Chinese Journal of Polymer Science, 2021, 39(4): 447-454.
Behzadi, S.; Zou, C.; Yang, B. P.; Tan, C.; Chen, C. L. Styrene-containing phosphine-sulfonate ligands for nickel- and palladium-catalyzed ethylene polymerization. Chinese J. Polym. Sci. 2021, 39, 447–454 DOI: 10.1007/s10118-021-2509-z.
Shabnam Behzadi, Chen Zou, Bang-Pei Yang, et al. Styrene-containing Phosphine-sulfonate Ligands for Nickel- and Palladium-catalyzed Ethylene Polymerization[J]. Chinese Journal of Polymer Science, 2021, 39(4): 447-454. DOI: 10.1007/s10118-021-2509-z.
A series of phosphine-sulfonate ligands bearing 2-
3- and 4-vinylphenyl on the phosphorus atom were designed
synthesized
characterized and investigated in Ni- and Pd-catalyzed ethylene polymerization. The structure of the phosphine-sulfonate Pd complex bearing 2-vinylphenyl on the phosphorus atom showed 2
1-insertion for the 2-vinyl group. The phosphine-sulfonate Ni complex bearing 2-vinylphenyl resulted in significantly increased thermal stability and polyethylene molecular weights (
M
n
=3.69×10
4
g·mol
−1
at 80 °C) versus the counterparts bearing 3-/4-vinyl groups as well as previously reported phosphine-sulfonate Ni complexes bearing bulky biaryl substituents.
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