Church Derek C, Takiguchi Lauren, Pokorski Jonathan K
Department of NanoEngineering, Jacobs School of Engineering, University of California San Diego, La Jolla, CA 92093, USA.
Polym Chem. 2020 Jul 21;11(27):4492-4499. doi: 10.1039/d0py00716a. Epub 2020 Jun 18.
Ring opening metathesis polymerization (ROMP) is widely considered an excellent living polymerization technique that proceeds rapidly under ambient conditions and is highly functional group tolerant when performed in organic solvents. However, achieving the same level of success in aqueous media has proved to be challenging, often requiring an organic co-solvent or a very low pH to obtain fast initiation and high monomer conversion. The ability to efficiently conduct ROMP under neutral pH aqueous conditions would mark an important step towards utilizing aqueous ROMP with acid-sensitive functional groups or within a biological setting. Herein we describe our efforts to optimize ROMP in an aqueous environment under neutral pH conditions. Specifically, we found that the presence of excess chloride in solution as well as relatively small changes in pH near physiological conditions have a profound effect on molecular weight control, polymerization rate and overall monomer conversion. Additionally, we have applied our optimized conditions to polymerize a broad scope of water-soluble monomers and used this methodology to produce nanostructures via ring opening metathesis polymerization induced self-assembly (ROMPISA) under neutral pH aqueous conditions.
开环易位聚合(ROMP)被广泛认为是一种出色的活性聚合技术,它在环境条件下能快速进行,且在有机溶剂中进行时对官能团具有高度耐受性。然而,事实证明,要在水性介质中取得同样的成功具有挑战性,通常需要有机共溶剂或极低的pH值才能实现快速引发和高单体转化率。在中性pH值的水性条件下高效进行ROMP的能力,将是朝着在具有酸敏官能团的情况下或在生物环境中利用水性ROMP迈出的重要一步。在此,我们描述了我们在中性pH条件下优化水性环境中ROMP的努力。具体而言,我们发现溶液中过量氯离子的存在以及生理条件附近pH值的相对微小变化对分子量控制、聚合速率和整体单体转化率有深远影响。此外,我们已将优化后的条件应用于聚合多种水溶性单体,并使用该方法在中性pH水性条件下通过开环易位聚合诱导自组装(ROMPISA)制备纳米结构。