Department of Chemical & Environmental Engineering, The University of Arizona, 1133 James E. Rogers Way, P.O. Box 210011, Tucson, AZ, 85721, USA.
Department of Environmental Science & Arizona Laboratory for Emerging Contaminants, The University of Arizona, AZ, 85721, Tucson, USA.
Environ Sci Pollut Res Int. 2022 Apr;29(17):25988-25994. doi: 10.1007/s11356-022-19376-8. Epub 2022 Feb 26.
Aryl-iodonium salts are utilized as photoacid generators (PAGs) in semiconductor photolithography and other photo-initiated manufacturing processes. Despite their utilization and suspected toxicity, the fate of these compounds within the perimeter of semiconductor fabrication plants is inadequately understood; the identification of photolithography products is still needed for a comprehensive environmental impact assessment. This study investigated the photolytic transformation of a representative iodonium PAG cation, bis-(4-tert-butyl phenyl)-iodonium, under conditions simulating industrial photolithography. Under 254-nm irradiation, bis-(4-tert-butyl phenyl)-iodonium reacted rapidly with a photolytic half-life of 39.2 s; different counter ions or solvents did not impact the degradation kinetics. At a semiconductor photolithography-relevant UV dosage of 25 mJ cm, 33% of bis-(4-tert-butyl phenyl)-iodonium was estimated to be transformed. Six aromatic/hydrophobic photoproducts were identified utilizing a combination of HPLC-DAD and GC-MS. Selected photoproducts such as tert-butyl benzene and tert-butyl iodobenzene had remarkably higher acute microbial toxicity toward bacterium Aliivibrio fischeri compared to bis-(4-tert-butyl phenyl)-iodonium. Octanol-water partition coefficients estimated using the Estimation Programs Interface Suite™ indicated that the photoproducts were substantially more hydrophobic than the parent compound. The results fill a critical data gap hindering the environmental impact assessment of iodonium PAGs and provide clues on potential management strategies for both iodonium compounds and their photoproducts.
芳基碘𬭩盐被用作半导体光刻和其他光引发制造工艺中的光酸产生剂 (PAG)。尽管它们被使用且被怀疑具有毒性,但这些化合物在半导体制造工厂范围内的命运仍未被充分了解;为了进行全面的环境影响评估,仍需要识别光刻产品。本研究在模拟工业光刻的条件下研究了代表性的碘𬭩 PAG 阳离子双-(4-叔丁基苯基)-碘𬭩的光解转化。在 254nm 照射下,双-(4-叔丁基苯基)-碘𬭩迅速反应,光解半衰期为 39.2s;不同的抗衡离子或溶剂不会影响降解动力学。在与半导体光刻相关的 25mJ cm 的 UV 剂量下,估计有 33%的双-(4-叔丁基苯基)-碘𬭩被转化。利用 HPLC-DAD 和 GC-MS 的组合,鉴定了六种芳香族/疏水性光产物。一些光产物,如叔丁基苯和叔丁基碘苯,对细菌 Aliivibrio fischeri 的急性微生物毒性比双-(4-叔丁基苯基)-碘𬭩高得多。使用 Estimation Programs Interface Suite™ 估算的辛醇-水分配系数表明,光产物比母体化合物的疏水性显著增加。该结果填补了阻碍碘𬭩 PAG 环境影响评估的关键数据空白,并为碘𬭩化合物及其光产物的潜在管理策略提供了线索。