Kaur Supreet, Lesea-Pringle Benjamin, Marjit Surya, Hong Hyukhun, Rahman Aqib, Ma Boran, Favaro Denize C, DelRe Christopher
Nanoscience Initiative, CUNY Advanced Science Research Center, New York, New York 10031, USA.
Ph.D. Program in Biochemistry, The Graduate Center of the City University of New York, 365 fifth Ave, New York, New York 10016, USA.
J Am Chem Soc. 2025 Jun 25;147(25):22245-22252. doi: 10.1021/jacs.5c07556. Epub 2025 Jun 9.
Blends of polymers with microporous particles are essential to many modern technologies, including membranes, catalysts, nanocomposites, and porous liquids. However, the design space and performance of these technologies are substantially limited because it is difficult to quantify and control how polymers thread into the particles' sub-2 nm micropores. Here, we address these issues with two new strategies. First, we show that traditional solution-state NMR can be used to directly monitor polymer chains and quantify their diffusivities as they thread into microporous particles from the surrounding solvent. This label-free, high-resolution, in situ monitoring is possible because once a polymer chain enters the particles, its NMR signal becomes invisible due to excessively slow molecular tumbling. Second, we show that threading rates can be tuned across at least 6 orders of magnitude─without changing the particle size, micropore topology, or polymer chain length─by rationally modifying the particles' external surface with different coatings that form via noncovalent self-assembly after simple mixing. The strategies described here to quantify and control polymer threading are simple and generalizable to a wide range of polymer/particle combinations, solvents, temperatures, and concentrations; thus, they may spark advances in diverse technological and fundamental areas that rely on blends of polymers with microporous particles.
聚合物与微孔颗粒的混合物对于许多现代技术至关重要,包括膜、催化剂、纳米复合材料和多孔液体。然而,这些技术的设计空间和性能受到很大限制,因为难以量化和控制聚合物如何穿入颗粒小于2纳米的微孔中。在此,我们用两种新策略解决这些问题。首先,我们表明传统的溶液态核磁共振可用于直接监测聚合物链,并量化它们从周围溶剂穿入微孔颗粒时的扩散率。这种无标记、高分辨率的原位监测是可行的,因为一旦聚合物链进入颗粒,由于分子翻滚过慢,其核磁共振信号就会变得不可见。其次,我们表明通过在简单混合后用不同涂层对颗粒外表面进行合理修饰,这些涂层通过非共价自组装形成,穿入速率可在至少6个数量级范围内调节 ── 而不改变颗粒大小、微孔拓扑结构或聚合物链长度。这里描述的量化和控制聚合物穿入的策略简单且可推广到广泛的聚合物/颗粒组合、溶剂、温度和浓度;因此,它们可能会推动依赖聚合物与微孔颗粒混合物的各种技术和基础领域取得进展。