Preparative Macromolecular Chemistry, Institut für Technische Chemie und Polymerchemie and Centre for Functional Nanostructures, Karlsruhe Institute of Technology, Engesserstrasse 18, 76128 Karlsruhe, Germany.
J Am Chem Soc. 2012 May 2;134(17):7274-7. doi: 10.1021/ja301762y. Epub 2012 Apr 20.
Tailor-made water-soluble macromolecules, including a glycopolymer, obtained by living/controlled RAFT-mediated polymerization are demonstrated to react in water with diene-functionalized poly(ethylene glycol)s without pre- or post-functionalization steps or the need for a catalyst at ambient temperature. As previously observed in organic solvents, hetero-Diels-Alder (HDA) conjugations reached quantitative conversion within minutes when cyclopentadienyl moieties were involved. However, while catalysts and elevated temperatures were previously necessary for open-chain diene conjugation, additive-free HDA cycloadditions occur in water within a few hours at ambient temperature. Experimental evidence for efficient conjugations is provided via unambiguous ESI-MS, UV/vis, NMR, and SEC data.
通过活性/可控 RAFT 介导聚合获得的定制水溶性大分子,包括糖聚合物,在无需预或后功能化步骤或催化剂的情况下,在环境温度下可与二烯官能化的聚(乙二醇)在水中反应。正如以前在有机溶剂中观察到的那样,当涉及环戊二烯基部分时,杂 Diels-Alder(HDA)偶联在几分钟内达到定量转化。然而,虽然之前需要催化剂和升高的温度来进行开链二烯键合,但在环境温度下,在无添加剂的情况下,HDA 环加成可在数小时内发生。通过明确的 ESI-MS、UV/vis、NMR 和 SEC 数据提供了有效偶联的实验证据。