Hilschmann Jessica, Wenz Gerhard, Kali Gergely
Organic Macromolecular Chemistry, Saarland University, Campus C4.2, 66123 Saarbrücken, Germany.
Beilstein J Org Chem. 2017 Jul 3;13:1310-1315. doi: 10.3762/bjoc.13.127. eCollection 2017.
The aqueous reversible addition fragmentation chain-transfer (RAFT) copolymerization of isoprene and bulky comonomers, an acrylate and an acrylamide in the presence of methylated β-cyclodextrin was employed for the first time to synthesize block-copolyrotaxanes. RAFT polymerizations started from a symmetrical bifunctional trithiocarbonate and gave rise to triblock-copolymers where the outer polyacrylate/polyacrylamide blocks act as stoppers for the cyclodextrin rings threaded onto the inner polyisoprene block. Statistical copolyrotaxanes were synthesized by RAFT polymerization as well. RAFT polymerization conditions allow control of the composition as well as the sequence of the constituents of the polymer backbone which further effects the CD content and the aqueous solubility of the polyrotaxane.
首次采用甲基化β-环糊精存在下异戊二烯与大分子单体(一种丙烯酸酯和一种丙烯酰胺)的水相可逆加成断裂链转移(RAFT)共聚反应来合成嵌段共聚轮烷。RAFT聚合反应从对称双官能三硫代碳酸酯开始,生成三嵌段共聚物,其中外部的聚丙烯酸酯/聚丙烯酰胺嵌段充当环糊精环的封端剂,这些环糊精环套在内部的聚异戊二烯嵌段上。也通过RAFT聚合反应合成了统计共聚轮烷。RAFT聚合条件能够控制聚合物主链成分的组成以及序列,这进而影响聚轮烷的环糊精含量和水溶性。