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High-ThroughputSmall-Scale Platform for Synthesis,Characterization, and Modeling of Per- and Polyfluoroalkyl SubstancesAnalogs 高通量小型平台合成,表征,和模拟的每和多氟烷基物质类似物
Pub Date : 2025-09-18 DOI: 10.1021/acs.estlett.5c00699.s001
Kai-Hung Huang (5334098), Namita Narendra (22272754), Kaili Yap (16993749), Nicolás M. Morato (22272757), Kitmin Chen (13725014), Yunfei Feng (10268318), R. Graham Cooks (1278798), Tillmann Kubis (8443497), Christina R. Ferreira (461379)
Per- and polyfluoroalkyl substances (PFAS) are a global challenge due to their exceptional thermal and chemical durability which leads to environmental persistence, bioaccumulation, and toxicity. Tackling this challenge is a complex endeavor as the ever-expanding number of emerging PFAS hinders their monitoring while current countermeasures remain limited. Thus, there is a need for rapid strategies that can transform PFAS into safer, degradable analogs or expand libraries for untargeted monitoring. Here, we describe the implementation of a high-throughput (1 Hz) desorption electrospray ionization mass spectrometry (HT-DESI-MS) platform for the chemical transformation of perfluorocarboxylic acids (PFCAs) via a data-driven workflow that led to 915 new PFCA analogs (89% success rate) and revealed reactivity trends. Tandem mass spectrometry (MS/MS) enabled online structural confirmation and diagnostic fragment identification, supporting standard-free LC-MS/MS analysis. Further integration with ion mobility spectrometry (IMS) provided drift time measurements correlating with molecular size and shape, adding a new dimension that can improve feature annotation in untargeted PFAS analysis. Complementary quantum mechanical calculations of dipole moment and HOMO–LUMO gap predicted polarity and electronic reactivity, guiding analog selection. Collectively, this workflow combines rapid synthesis, structural annotation, and multidimensional profiling, with potential to discover safer PFAS and enhance environmental monitoring.
全氟烷基和多氟烷基物质(PFAS)由于其特殊的热和化学耐久性而导致环境持久性、生物蓄积性和毒性,是一项全球性挑战。应对这一挑战是一项复杂的努力,因为不断增加的新兴PFAS数量阻碍了对它们的监测,而目前的对策仍然有限。因此,需要一种快速的策略,将PFAS转化为更安全、可降解的类似物,或扩展库以进行非目标监测。在这里,我们描述了一个高通量(1hz)解吸电喷雾质谱(HT-DESI-MS)平台的实施,该平台通过数据驱动的工作流程,用于全氟羧酸(PFCAs)的化学转化,从而产生915个新的PFCA类似物(89%的成功率),并揭示了反应性趋势。串联质谱(MS/MS)实现了在线结构确认和诊断片段鉴定,支持无标准LC-MS/MS分析。与离子迁移率光谱(IMS)的进一步集成提供了与分子大小和形状相关的漂移时间测量,增加了一个新的维度,可以改善非靶向PFAS分析中的特征注释。偶极矩和HOMO-LUMO间隙的互补量子力学计算预测极性和电子反应性,指导模拟选择。总的来说,该工作流程结合了快速合成、结构注释和多维分析,具有发现更安全的PFAS和加强环境监测的潜力。
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