Debromination of ATRP-made Wang soluble polymer supports
Debromination of ATRP-made Wang soluble polymer supports
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DOI:
10.1016/j.polymer.2015.02.057
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发表时间:
2015-08
期刊:
影响因子:
4.6
通讯作者:
L. Oswald;Thanh Tam Trinh;Delphine Chan-Seng;Jean‐François Lutz
中科院分区:
文献类型:
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作者:
L. Oswald;Thanh Tam Trinh;Delphine Chan-Seng;Jean‐François Lutz
This article describes two convenient methods for removing the ω-terminal bromine atom of well-defined soluble polymer supports prepared by atom transfer radical polymerization (ATRP). The targeted soluble supports are linear polystyrene chains that contain an acid-labile p-alkoxybenzyl ester linker (i.e. Wang linker) at their α-chain end. These polymers are synthesized by ATRP using a fluorenylmethoxycarbonyl (Fmoc)-protected amino functional ATRP initiator, namely 3-(Fmoc-amino)propyl 2-bromoisobutyrate. After polymerization and before Wang functionalization, the bromine-atom of the ATRP-made soluble supports was removed. Two different debromination approaches were considered. The first one consists in reducing the terminal alkyl bromide in the presence of a trialkyltin hydride. This method can be applied directly in the ATRP medium at the end of the polymerization or can be performed on a purified polymer sample. The latter conditions were found to be more suitable. It was also observed that the use of tributyltin hydride in the absence of additional radical initiator led to the best results. Indeed, well-defined polymer supports with controlled chain-length, molecular weight distribution and fully dehalogenated chain-ends were obtained. The second dehalogenation approach consisted in removing the terminal bromide by nucleophilic substitution with sodium azide. Afterwards, the formed terminal azide group was reacted with 1-pentyne by copper-catalyzed azide-alkyne 1, 3-dipolar Huisgen cycloaddition. This method was also found to be valid for preparing bromine-free polystyrene supports. After ω-chain-end debromination, Fmoc-deprotection was performed on the α-chain-end and the resulting amine function was reacted with 4-(hydroxymethyl)phenoxyacetic acid. Further esterification of the Wang linker is also possible.