Polymers 2013, 5(4), 1229-1240; doi:10.3390/polym5041229
Article

Surface Initiated Polymerizations via e-ATRP in Pure Water

1,2email and 3,4,* email
Received: 24 August 2013; in revised form: 11 October 2013 / Accepted: 21 October 2013 / Published: 25 October 2013
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Here we describe the combined process of surface modification with electrochemical atom transfer radical polymerization (e-ATRP) initiated from the surface of a modified gold-electrode in a pure aqueous solution without any additional supporting electrolyte. This approach allows for a very controlled growth of the polymer chains leading towards a steady increase in film thickness. Electrochemical quartz crystal microbalance displayed a highly regular increase in surface confined mass only after the addition of the pre-copper catalyst which is reduced in situ and transformed into the catalyst. Even after isolation and washing of the modified electrode surface, reinitiation was achieved with retention of the controlled electrochemical ATRP reaction. This reinitiation after isolation proves the livingness of the polymerization. This approach has interesting potential for smart thin film materials and offers also the possibility of post-modification via additional electrochemical induced reactions.
Keywords: atom transfer radical polymerization; electro-chemistry; surface polymerization; thin films; surface chemistry
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MDPI and ACS Style

Hosseiny, S.S.; van Rijn, P. Surface Initiated Polymerizations via e-ATRP in Pure Water. Polymers 2013, 5, 1229-1240.

AMA Style

Hosseiny SS, van Rijn P. Surface Initiated Polymerizations via e-ATRP in Pure Water. Polymers. 2013; 5(4):1229-1240.

Chicago/Turabian Style

Hosseiny, Seyed S.; van Rijn, Patrick. 2013. "Surface Initiated Polymerizations via e-ATRP in Pure Water." Polymers 5, no. 4: 1229-1240.


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