Surface-Initiated Polymerization by Means of Novel, Stable, Non-Ester-Based Radical Initiator

被引:50
作者
Bain, Erich D. [1 ]
Dawes, Keith [1 ]
Oezcam, A. Evren [1 ]
Hu, Xinfang [2 ]
Gorman, Christopher B. [2 ]
Srogl, Jiri [3 ]
Genzer, Jan [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[3] Acad Sci Czech Republ, Inst Chem & Biochem, Prague, Czech Republic
基金
美国国家科学基金会;
关键词
SELF-ASSEMBLED MONOLAYERS; POLY(ACRYLIC ACID) BRUSHES; METHACRYLATE) BRUSHES; COMPUTER-SIMULATION; GRAFTING DENSITY; CHAIN-LENGTH; THICKNESS; BEHAVIOR; PH; IMMOBILIZATION;
D O I
10.1021/ma300491e
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A novel, ester-free initiator for surface-initiated free radical polymerization has been synthesized and tested. The structurally non-symmetrical azo-based initiator features a chemically stable alkane linker between the initiating group and the silane anchoring group, setting it apart from the majority of surface initiators that are linked by hydrolyzable moieties, such as esters. The novel design of the initiator is bolstered by an original synthetic approach, leading to a greater yield and a dramatic reduction in cyanide usage relative to previous methods. Here we demonstrate the capability of this novel initiator for surface-initiated free radical polymerization (SI-FRP), reverse ATRP, and RAFT, noting that Arrhenius behavior of SI-FRP differs significantly from that of FRP in the bulk. Furthermore, we show that polymer brushes formed from the novel initiator are more stable than those formed from ester-based initiators.
引用
收藏
页码:3802 / 3815
页数:14
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