Polymer Brush Covalently Attached to OH-Functionalized Mica Surface via Surface-Initiated ATRP: Control of Grafting Density and Polymer Chain Length

被引:55
作者
Lego, Beatrice [1 ]
Francois, Marion
Skene, W. G. [1 ]
Giasson, Suzanne [1 ,2 ,3 ]
机构
[1] Univ Montreal, Dept Chem, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Fac Pharm, Montreal, PQ H3C 3J7, Canada
[3] Univ Montreal, Ctr Self Assembled Chem Struct, Montreal, PQ H3C 3J7, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
TRANSFER RADICAL POLYMERIZATION; SILICON SURFACES; BLOCK-COPOLYMERS; AREA MICA; NANOPARTICLES; MONOLAYERS; GROWTH; ENHANCEMENT; STYRENE; FORCES;
D O I
10.1021/la804060s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The controlled grafting density of poly(tert-butyl acrylate) was studied on OH-activated mica substrates via surface-initiated atom-transfer radical polymerization (ATRP). By properly adjusting parameters such as the immobilization reaction time and the concentration of an ATRP initiator, a wide range of initiator surface coverages and hence polymer densities on mica were possible. The covalently immobilized initiator successfully promoted the polymerization of tert-butyl acrylate on mica surfaces. The resulting polymer layer thickness was measured by AFM using a step-height method. Linear relationships of the polymer thickness with respect to the molecular weight of the free polymer and with respect to the monomer conversion were observed, suggesting that ATRP is well controlled and relatively densely end-grafted layers were obtained. The polymer grafting density controlled by adjusting the initiator surface coverage was confirmed by the polymer layer swelling capacity and film thickness measurements.
引用
收藏
页码:5313 / 5321
页数:9
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