Abstract

The kinetics of aminolysis between two different active ester polymer brush platforms, poly(4-pentafluorophenyl acrylate) (poly(PFPA)) and poly(N-hydroxysuccinimide-4-vinyl benzoate) (poly(NHS4VB)), are compared using primary and aromatic amines with varying reactivity toward postpolymerization modification. UV–vis was used to monitor the aminolysis of both brush platforms with 1-aminomethylpyrene (AMP), 1-aminopyrene (AP), and Ru(bpy)2(phen-5-NH2)(PF6) (Ru2+A). Using a pseudo-first-order kinetics model, the pseudo-first-order rate constant (k′) was calculated for each system. The k′ of poly(PFPA) modified with AMP, AP, and Ru2+A were 2.46 × 10–1, 5.11 × 10–3, and 2.59 × 10–3 s–1, respectively, while poly(NHS4VB) can only be functionalized with the alkyl amine, albeit at a slower rate constant, k′ of 3.49 × 10–3 s–1, compared to that of poly(PFPA) with AMP. The kinetics of surface-initiated photopolymerization of PFPA from oxide surfaces was also investigated as an effective method to control grafting den...

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