KeYu Shi

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Name: 石可瑜; KeYu Shi
Organization: Nankai Univerisity , China
Department:
Title: Professor(PhD)

TOPICS

Co-reporter:Heng Zhou, Chonggao Liu, Yaqing Qu, Chengqiang Gao, Keyu Shi, and Wangqing Zhang
Macromolecules 2016 Volume 49(Issue 21) pp:8167-8176
Publication Date(Web):October 14, 2016
DOI:10.1021/acs.macromol.6b01756
Polymerization-induced self-assembly (PISA) is proven to be a powerful approach of in situ synthesis of block copolymer (BCP) nanoassemblies, and polymerization conditions are found to be correlative to the block copolymer morphology. In this study, three PISA formulations, e.g., the poly(ethylene glycol) macro-RAFT agent mediated dispersion RAFT polymerization, seeded dispersion RAFT polymerization, and seeded emulsion RAFT polymerization, are comparatively investigated. Our results reveal that dispersion RAFT polymerization undergoes much slower than other two PISA formulations of seeded dispersion RAFT polymerization and seeded emulsion RAFT polymerization. Besides, the results reveal that the BCP morphology of poly(ethylene glycol)-block-polystyrene (PEG45-b-PS) produced via three PISA cases is much different. That is, dispersion RAFT polymerization affords vesicles, seeded dispersion RAFT polymerization affords the mixture of vesicles and porous nanospheres, and seeded emulsion RAFT polymerization affords porous nanospheres of PEG45-b-PS. The reason for formation of porous nanospheres by seeded RAFT polymerization is discussed, and the fed styrene monomer swelling the seeded vesicles is ascribed. Our study clarifies how the PISA procedures affect the morphology of BCP nanoassemblies, and it is expected to be effective to prepare BCP nanoassemblies with interesting morphology.
Co-reporter:Heng Zhou;Chonggao Liu;Chengqiang Gao;Yaqing Qu;Wangqing Zhang
Journal of Polymer Science Part A: Polymer Chemistry 2016 Volume 54( Issue 11) pp:1517-1525
Publication Date(Web):
DOI:10.1002/pola.28002

ABSTRACT

Polymerization-induced self-assembly of block copolymer through dispersion RAFT polymerization has been demonstrated to be a valid method to prepare block copolymer nano-objects. However, volatile solvents are generally involved in this preparation. Herein, the in situ synthesis of block copolymer nano-objects of poly(ethylene glycol)-block-polystyrene (PEG-b-PS) in the ionic liquid of 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIN][PF6]) through the macro-RAFT agent mediated dispersion polymerization is investigated. It is found that the dispersion RAFT polymerization of styrene in the ionic liquid of [BMIN][PF6] runs faster than that in the alcoholic solvent, and the dispersion RAFT polymerization in the ionic liquid affords good control over the molecular weight and the molecular weight distribution of the PEG-b-PS diblock copolymer. The morphology of the in situ synthesized PEG-b-PS diblock copolymer nano-objects, e.g., nanospheres and vesicles, in the ionic liquid is dependent on the polymerization degree of the solvophobic block and the concentration of the fed monomer, which is somewhat similar to those in alcoholic solvent. It is anticipated that the dispersion RAFT polymerization in ionic liquid broads a new way to prepare block copolymer nano-objects. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016, 54, 1517–1525

Benzaldehyde, 3,4,5-tris[2-(2-methoxyethoxy)ethoxy]-
1,4-BENZENEDICARBOXYLIC ACID, BIS[4-(CHLOROCARBONYL)PHENYL] ESTER
2,6-Pyridinedimethanol, 4-(phenylmethoxy)-
POLY[OXY[2-METHYL-2-[[[6-[[4'-[[6-[(1-OXO-3-PHENYL-2-PROPENYL)OXY]HEXYL]OXY][1,1'-BIPHENYL]-4-YL]OXY]HEXYL]OXY]METHYL]-1,3-PROPANEDIYL]]
2,6-Pyridinedicarboxylic acid, 4-(phenylmethoxy)-, dimethyl ester
2-Propenoic acid, 3-phenyl-,6-[[4'-[[6-[(3-methyl-3-oxetanyl)methoxy]hexyl]oxy][1,1'-biphenyl]-4-yl]oxy]hexyl ester
Urea, N,N-bis(1-methylethyl)-N'-phenyl-
Dodecanol
Cyanamide, N-cyano-
Pentanoyl chloride, 2-chloro-3-methyl-, (2S,3S)-