期刊
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
卷 45, 期 14, 页码 2913-2924出版社
WILEY
DOI: 10.1002/pola.22047
关键词
atom transfer radical polymerization (ATRP); block copolymers; functionalization of polymers
Heterotelechelic polystyrene (PS), poly(tert-butyl acrylate) (PtBA), and poly (methyl acrylate) (PMA), containing both azide and triisopropylsilyl (TIPS) protected acetylene end groups, were prepared in good control (Mw/Mn <= 1.24) by atom transfer radical polymerization (ATRP). The end groups were independently applied in two successive click reactions, that is: first the azide termini were functionalized and, after deprotection, the acetylene moieties were utilized for a second conjugation step. As a proof of concept, PS was consecutively functionalized. with propargyl alcohol and azido-acetic acid, as confirmed by MALDI-ToF MS. In addition, the same methodology was employed to modularly build up an ABC type triblock terpolymer. Size exclusion chromatography measurements demonstrated first coupling of PtBA to PS and, after the deprotection of the acetylene functionality on PS, connection of PMA, yielding a PMA-b-PS-b-PtBA triblock terpolymer. The reactions were driven to completion using a slight excess of azide functionalized polymers. Reduction of the residual azide groups into amines allowed easy removal of this excess of polymer by column chromatography. (c) 2007 Wiley Periodicals, Inc.
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