

FOLLOWUS
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai 200438, China
jphe@fudan.edu.cn
Received:09 January 2019,
Revised:2019-2-25,
Accepted:01 March 2019,
Online First:12 April 2019,
Published:2019-09
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Citation: Zheng, K.; He, J. P. Amphiphilic dendrimer-like copolymers with high chain density by living anionic polymerization. Chinese J. Polym. Sci. 2019, 37, 875–883
Ke Zheng, Jun-Po He. Amphiphilic Dendrimer-like Copolymers with High Chain Density by Living Anionic Polymerization[J]. Chinese Journal of Polymer Science, 2019, 37(9): 875-883.
Citation: Zheng, K.; He, J. P. Amphiphilic dendrimer-like copolymers with high chain density by living anionic polymerization. Chinese J. Polym. Sci. 2019, 37, 875–883 DOI: 10.1007/s10118-019-2247-7.
Ke Zheng, Jun-Po He. Amphiphilic Dendrimer-like Copolymers with High Chain Density by Living Anionic Polymerization[J]. Chinese Journal of Polymer Science, 2019, 37(9): 875-883. DOI: 10.1007/s10118-019-2247-7.
We report here a method for the preparation of amphiphilic dendrimer-like copolymers with dendritic polystyrene (PS) core and protonated poly(2-vinyl pyridine) (P2VP) or poly(methacrylic acid) (PMAA) shell. The method employed the efficient coupling reaction of anionic living polymer chains and chlorosilane. The synthesis started from a functionalized 3
rd
generation dendritic polystyrene
G3PS-
g
-SiCl
used as the precursor. The dendrimer-like copolymer of styrene and 2-vinyl pyridine
G3PS-
g
-P2VP
was synthesized by direct coupling of living P2VPLi to the precursor. The dendrimer-like copolymer of styrene and
tert
-butyl methacrylate
G3PS-
g
-P
t
BMA
was synthesized by an indirect procedure in which a living polymer containing mainly P
t
BMA segment was attached to the precursor. Both methods resulted in the formation of dendrimer-like copolymers with the high molecular weights (up to 8.5 × 10
6
Da)
large molecular sizes (diameter up to 73 nm)
and dense shells (number of arms up to 1300). These products
G3PS-
g
-P2VP and G3PS-
g
-P
t
BMA
were protonated with trifluoroacetic acid and acidic hydrolyzed
respectively. After transformation
amphiphilic dendrimer-like copolymers
G3PS-
g
-P2VPH
+
and G3PS-
g
-PMAA
were obtained. Preliminary results on the solution properties of the amphiphilic products were presented.
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