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Ring-Opening Metathesis Polymerization in Miniemulsion Using a TEGylated Ruthenium-Based Metathesis Catalyst
被引:6
|作者:
Zhu, Chunyang
[1
]
Wu, Xiaowei
[2
]
Zenkina, Olena
[2
]
Zamora, Matthew T.
[2
]
Moffat, Karen
[3
]
Crudden, Cathleen M.
[2
]
Cunningham, Michael F.
[1
,2
]
机构:
[1] Queens Univ, Dept Chem Engn, 19 Div St, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Dept Chem, 90 Bader Lane, Kingston, ON K7L 3N6, Canada
[3] Xerox Res Ctr Canada Ltd, 2660 Speakman Dr, Mississauga, ON L5K 2L1, Canada
基金:
加拿大自然科学与工程研究理事会;
关键词:
CONTROLLED/LIVING RADICAL POLYMERIZATION;
EMULSION POLYMERIZATION;
LATEX-PARTICLES;
ROMP;
CARBENE;
NORBORNENE;
STYRENE;
COMPLEX;
STRAIN;
D O I:
10.1021/acs.macromol.8b02240
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
Ring-opening metathesis polymerization (ROMP) of 1,5-cyclooctadiene (COD) in miniemulsion was conducted utilizing a water-soluble TEGylated ruthenium alkylidene catalyst that was designed to undergo phase transfer from the aqueous phase to the monomer droplets or polymer particles following activation. The catalyst yielded colloidally stable latexes with, similar to 100% conversion, often in less than 1 h. Kinetic studies revealed first-order kinetics with good livingness as confirmed by the shift of gel permeation chromatography (GPC) traces. Depending on the surfactants used, the particle sizes ranged from 100 to 300 nm with monomodal distributions. The more strained cyclic olefin norbornene (NB) could also be efficiently polymerized in miniemulsion with full conversion and without coagulum formation.
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页码:9088 / 9096
页数:9
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